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Our Professional Services team has an exciting opportunity for a driven individual, and we're looking for a Project Manager that is passionate about providing IT transformation and implementation services for our clients.
It is mission-critical for the Project Manager to be a leader and a champion that will act as a conduit between the senior management team, key clients, and third-party vendors.
The Project Manager role is project-driven and will support clients by acting as the first point of contact to ensure that their organizational goals are met.
In addition, the Project Manager will be dedicated to monitoring and controlling the scope of work, engagement team priorities and project finances.
Finally, our Project Managers will have the opportunity to travel globally or regionally, based on client locations.
This remote role welcomes candidates from anywhere in Canada or the US.
This role requires travel up to 50% within Canada and the US; a valid passport or visa is required.
What your impact will be:
Project Planning, Scope Management, & PMO Improvements
* Demonstrate outstanding project control, ensuring that project plans/schedules, project budgets, and scope control all exceed expectations.
* Effective project management provided through, impact analysis, leading project scope negotiations, managing expectations of evolving project requirements
* Identify, analyze and assess business opportunities, processes, and workflows for PMO process improvements
Project Delivery & Critical Issue Resolution
* Adhere to the schedule of work for all phases (& refine as a project journey progresses) of the project including start-up and post-implementation follow-up.
* Be knowledgeable on project deliverables and contractual documentation to ensure obligations and expectations are met.
* Prioritize project needs based on tasks outstanding, obstacles or barriers, budgets, resources and deadlines.
* Coordinate resolution of project issues and/or delays to reduce the impact on the project and ensure timely implementation.
* Additional learning opportunities as the project evolves.
Client Management & Leadership
* Responsible for all aspects of the project delivery, including managing the scope of the project and changes to the project deliverables, while ensuring client satisfaction and organizational profitability.
* Regular communication of project updates, critical issues, implications, and progress to our clients and our leadership team.
What we are looking for:
* Ability to manage multiple projects simultaneously
* Experience with project management tools (e.g., Jira, Azure DevOps, Trello)
* Strong communication skills
* Ability to develop strong working relationships with internal and external stakeholders
* Ability to firmly manage scope, schedule and budget
* Ability to travel up to 50% within North America
What would make you stand out:
* P...
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Type: Permanent Location: Edmonton, CA-AB
Salary / Rate: Not Specified
Posted: 2025-07-08 08:16:59
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At Elanco (NYSE: ELAN) – it all starts with animals!
As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets.
We’re driven by our vision of ‘Food and Companionship Enriching Life’ and our approach to sustainability – the Elanco Healthy Purpose™ – to advance the health of animals, people, the planet and our enterprise.
At Elanco, we pride ourselves on fostering a diverse and inclusive work environment.
We believe that diversity is the driving force behind innovation, creativity, and overall business success.
Here, you’ll be part of a company that values and champions new ways of thinking, work with dynamic individuals, and acquire new skills and experiences that will propel your career to new heights.
Making animals’ lives better makes life better – join our team today!
Interested in joining a cause-driven, customer focused company dedicated to positively impacting the health of animals, people and the planet?
An exciting full-time 12-month contract opportunity is available to be part of a friendly, high performing team of researchers in the development of new animal health products globally.
We are actively searching for a Study Manager with experience in companion and/or farm animals to manage and conduct R&D clinical studies.
The role:
As a Study Manager, you will support the operational direction and plan, design, implement, manage and report clinical studies, ensuring optimal output from the site for the development of new animal health products and label extensions for existing products for the global and regional (ANZ) markets.
You will:
* Act as an Investigator and/or Study Director in GxP studies by developing protocols and reports in collaboration with global project teams.
* Be responsible for the conduct of complex studies for the evaluation of compounds and assist in the interpretation of these studies.
* Plan, perform, interpret and report results of field and laboratory studies in both livestock and companion animals.
* Design, review and make recommended changes to scientific protocols and procedures.
* Liaise with external parties in early research projects and implement and oversee disease models.
* Ensure timely availability of information for the AEC (Animal Ethics Committee) and co-operate with the Animal Welfare Officer, to ensure the highest standards of animal welfare are maintained.
* Manage studies, documentation and work according to, and in compliance with, external and internal guidelines (e.g.
SOPs, VICH, FDA, OECD, GxP, HSE and Animal Welfare Code of Practice).
* Collaborate with other associates to facilitate knowledge exchange.
Assist with training and coaching peers as required.
* Assist with the identification, communication and planning of resource requirements.
* Assist with planning opportunities to determine operational prioriti...
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Type: Permanent Location: Yarrandoo, AU-NSW
Salary / Rate: Not Specified
Posted: 2025-07-08 08:16:31
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At Elanco (NYSE: ELAN) – it all starts with animals!
As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets.
We’re driven by our vision of ‘Food and Companionship Enriching Life’ and our approach to sustainability – the Elanco Healthy Purpose™ – to advance the health of animals, people, the planet and our enterprise.
At Elanco, we pride ourselves on fostering a diverse and inclusive work environment.
We believe that diversity is the driving force behind innovation, creativity, and overall business success.
Here, you’ll be part of a company that values and champions new ways of thinking, work with dynamic individuals, and acquire new skills and experiences that will propel your career to new heights.
Making animals’ lives better makes life better – join our team today!
Responsibilities:
* This role supports the needs of the Global Analytics & Insights team, part of the Corporate Strategy Team, with a focus on providing Advanced Analytics (to include statistical modeling, regression analyses, market basket, churn modelling methods) to work on program/promotion design and ROI post program.
Additional project-based work around price elasticity, mixed market modelling, segmentation, game theory modelling and predictive analytics (e.g., customer lifetime value) will be in scope.
The overarching goal of all work will be to find efficiencies in current promotional spend and optimize future business activities.
* This position is responsible for managing all aspects of project-based analyses including data preparation, analysis design, implementation using appropriate methods & results presentation.
* Leading readouts and review with internal customers.
* Lead discussions with customers to uncover needs, design and deliver analytics solutions.
Enable measurement and improved effectiveness of rebates, media spend, pricing and sales force activities leveraging statistics and data science techniques.
* Collaborate with internal stakeholders, descriptive analytics team and cross-functional teams to solve business problems, propose efficiencies and innovative approaches.
* Constantly innovate in data science domain, constantly bringing new expertise to the team and adding to team knowledge
* Guide the junior members on technical and functional aspects, problem formulation, approach design, model building, model refinement and selection, reviewing and storyboarding the results.
* Consistent, constant alignment with all members of team in Greenfield, Indiana.
* Maintain an environment open to change and innovation, recognizing improvements in existing tools and anticipating new technologies to deliver world class analytics and maximize effectiveness
Minimum Qualification (education, experience and/or training, required certifications):
* Bachelor’s Degree in quantitative or manag...
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Type: Permanent Location: Bengaluru, IN-KA
Salary / Rate: Not Specified
Posted: 2025-07-08 08:16:28
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At Elanco (NYSE: ELAN) – it all starts with animals!
As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets.
We’re driven by our vision of ‘Food and Companionship Enriching Life’ and our approach to sustainability – the Elanco Healthy Purpose™ – to advance the health of animals, people, the planet and our enterprise.
At Elanco, we pride ourselves on fostering a diverse and inclusive work environment.
We believe that diversity is the driving force behind innovation, creativity, and overall business success.
Here, you’ll be part of a company that values and champions new ways of thinking, work with dynamic individuals, and acquire new skills and experiences that will propel your career to new heights.
Making animals’ lives better makes life better – join our team today!
Your Role: Senior Specialist - Upstream Operations Technician
The Upstream OpTech is technical process leader on the Upstream operations team responsible for manufacturing execution, changeover, and production control.
The role is dedicated to the execution and oversight of cellular expansion from benchtop through production bioreactor processes.
Your Responsibilities:
* Executes the operation with team serving as process lead, coach, trainer, and responsible party.
* Performs and verifies Maintenance, process setup, troubleshooting, change over, process intervention.
* Serve as the operations representative and subject matter expert for cross-functional process support team.
* Real-time problem solving, process intervention, and technical experiment delivery, and continuous improvement.
* Ensure process documentation is prepared and completed with accuracy and concurrence.
What You Need to Succeed (minimum qualifications):
* Education: High School Diploma / GED
* Experience: minimum of 3 years experience with cellular growth/expansion processes.
What will give you a competitive edge (preferred qualifications):
* Production scale filtration
* Formal Root Cause Investigation training
* Fermentation
* Proficiency with SAP
* GMP manufacturing
* Aseptic experience
Additional Information:
* Travel: Minimal
* Location: Elanco Animal Health Elwood, KS
* Shift: 12 hour Day shift 5a-5:15p 2 week rotation (M,T,F,Sa,Su,W,R)
+ This role currently operates on an 8-hour shift schedule.
Starting in July 2025, the position will transition to the 12-hour shift schedule stated above.
+ Please note that weekend work will have a 4% premium and work outside of your shift hours will have 10% premium.
Don’t meet every single requirement? Studies have shown underrecognized groups are less likely to apply to jobs unless they meet every single qualification.
At Elanco we are dedicated to building a diverse and inclusive work environment.
If you think yo...
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Type: Permanent Location: Elwood, US-KS
Salary / Rate: 37
Posted: 2025-07-08 08:16:17
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Shape Your World
At Alcoa, you will become an essential part of our purpose: to turn raw potential into real progress.
The way we see it, every Alcoan is a work-shaper, team-shaper, idea-shaper, world-shaper.
This is an opportunity for you to bring your wealth of experience to the team and help shape the future of sustainability with world-changing innovations and low carbon technologies.
You have the power to shape things to make them better.
About the Role
Alcoa’s WA Mining operations manage the largest rehabilitation estate globally, spanning 24,000 hectares with areas ranging from newly rehabilitated to over 50 years old.
Due to this immense scale and complexity, we are excited to announce a unique and exciting opportunity for a Spatial Ecologist to pioneer industry-leading rehabilitation monitoring programs for the Northern Jarrah Forest.
We are seeking a highly skilled and innovative Spatial Ecologist to join our team, reporting to the Rehabilitation Monitoring Superintendent.
This pivotal role is responsible for the strategic design, execution, and compliance oversight of spatial data and systems crucial to Alcoa’s rehabilitation monitoring program.
You will be instrumental in demonstrating rehabilitation performance against Completion Criteria for our WA Mining Rehabilitation Estate and providing essential evidence for the handback of rehabilitated land to the State.
This role will be offered on a family-friendly Monday to Friday roster with a paid leisure day off every 4 weeks, allowing you more time doing the things you love.
You will be based predominantly at the WA Mining Hub, with ad hoc site travel to both our Huntly and Willowdale Mine sites as required.
There will be some flexibility to work from home, and our standard hours of operation are 7:30 am – 3:30 pm – but these are flexible to ensure you are able to balance your work and life commitments.
Key responsibilities will include:
* Lead the design and implementation of advanced spatial monitoring standards and methodologies for assessing rehabilitation outcomes.
* Drive the development of cutting-edge, automated spatial analysis software integrating diverse remote sensing data.
* Manage remote sensing survey data collection, QA/QC, geospatial data collation, and database uploads.
* Compile and analyse spatial and non-spatial environmental data to assess rehabilitation performance against Completion Criteria.
* Conduct ecological field surveys to gather essential data and corroborate remote sensing approaches
* Oversee the design and ongoing management of WA Mining’s Rehabilitation Database, providing expert technical advice in spatial ecology
What’s on offer
* Flexible hybrid working options available.
* Employee growth and development opportunities.
* Parental leave support for all caregivers.
* One Paid Leisure day off every 4 weeks.
* Paid employee volunteering hours within our community.
* Em...
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Type: Permanent Location: PINJARRA, AU-WA
Salary / Rate: Not Specified
Posted: 2025-07-08 08:14:24
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POSITION SUMMARY:
The Natural Resource Supervisor will oversee the management, stewardship and program delivery of the Parks & Recreation Department’s natural resources, trails and environmental activities at all Berks County owned Parks and trails.
The employee is responsible for assisting, creating plans and the management of the Park System’s natural areas- including trails, forests, fields, waterways, and gardens.
This position directs and manages park maintenance staff and is required to handle a multitude of tasks including working with other program staff, volunteers, and organizations, as well as administrative functions.
POSITION RESPONSIBILITIES:
Essential Functions
The duties and responsibilities of this position include, but are not necessarily limited to:
Working in close consultation with the Director, Assistant Director and Park Maintenance Supervisor, the Natural Resource Supervisor will be responsible for the following:
* Manage trail maintenance, conduct inspections to ensure proper use and maintenance of County trails.
* Implement cyclical maintenance plans for natural park areas, including vegetation removal, invasive species, hazard trees, erosion control and other factors.
* Prepare scopes of work, develop cost estimates and perform construction and project management and oversight.
* Train, assign and supervise staff and volunteers for maintenance and improvement projects.
* Develop partnerships with volunteer groups, educational institutions, and corporations to develop cooperative projects/activities that benefit the resource.
* Formulates policies and procedures for natural resource management.
Serves as a technical consultant with industry and governmental agencies.
* Oversee the identification and plans for removal of hazardous trees within the Parks system.
* Assure and uphold the protection of the Parks systems natural resources, as they relate to current industry standards.
* Develop guidelines for types of trails uses and carrying capacities. Help to disseminate information to trails users and general public.
* Develop and present general environmental and natural resource programs that highlight the Berks County Parks & Recreation system.
This will include presentations prepared for school groups, adults, Scout troops and others as a community service.
* Work with other Park programming staff to develop programs, workshops and events to be presented as part of the Departments public outreach programming.
* Review and work with the Antietam Lake Park Master Plan to develop and implement proposed phased improvements.
* Seek and apply for grants and other funding sources for projects that will benefit the natural resources or environmental programming of the Parks system and the implementation of Parks projects.
* Develop educational displays and interpretive signage for the Parks systems natural resources.
* A...
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Type: Permanent Location: Reading, US-PA
Salary / Rate: Not Specified
Posted: 2025-07-08 08:12:04
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Overview:
Join the Barber National Institute as a Senior Specialist, Organizational Development and play a key role in shaping employee experience, growth, and engagement across our organization.
In this role, you’ll lead initiatives that support continuous improvement, employee development, and the promotion of a positive, mission-aligned workplace culture.
You’ll collaborate with leadership and departments to drive strategic planning, change management, and employee-focused programming that supports our core commitments and long-term success.
This position will be a remote position in Pennsylvania.
What you’ll bring:
* A growth mindset and passion for building strong organizational culture.
* Strong communication skills and ability to engage with stakeholders at all levels.
* A strategic approach to process improvement, data-informed decision-making, and change management.
* A collaborative, proactive, and highly organized work style.
* Ability to lead projects independently and contribute to cross-functional teams.
What you’ll have:
* Bachelor's degree in human resources, Organizational Development, Business, or a related field (master's preferred).
* At least 4 years of related experience in organizational development or a related area.
* Experience with project planning, data analysis, and process improvement.
* Familiarity with change management and quality improvement methodologies.
* SHRM-CP or Organizational Development Certification preferred.
* Eligibility for FBI Clearance, State Police Criminal Record Check, and Child Abuse History Clearance.
A typical day may include:
* Leading and supporting cross-departmental organizational development projects.
* Developing and implementing career pathways, mentoring programs, and organizational competencies.
* Facilitating onboarding, orientation, upskilling, and succession planning efforts.
* Conducting organizational assessments and recommending areas for performance and culture improvement.
* Coaching managers and employees on professional development and performance expectations.
* Partnering with Learning & Development to evaluate training impact and identify learning gaps.
* Creating and updating SOPs and documentation for internal organizational processes.
* Driving change initiatives through strategic planning, communication, and staff engagement.
* Optimizing internal systems and processes for improved efficiency and cost savings.
* Presenting data and progress reports to leadership and stakeholders.
* Supporting committees and participating in cross-functional initiatives.
Perks with a Purpose
Our benefits are created with YOU in mind.
Healthcare
• Highmark Medical and Mental Health
• Free Delta Dental Coverage
• Free Davis Vision Coverage
• Short & Long-Term Disability Insurance
• Healthcare Flexible Spending Account
• Tela...
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Type: Permanent Location: Pittsburgh, US-PA
Salary / Rate: Not Specified
Posted: 2025-07-08 08:11:09
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The Capital Area Division (CAD) Applied Research Associates, Inc.
(ARA) is seeking a Fluid Dynamics Subject Matter Expert to be an expert with Computational Fluid Dynamics (CFD) codes such as ANSYS ®, LS-DYNA®, CFX ®, FLUENT ®. The position develops in-depth technical assessments and models of utilities for WMD facilities using multiple intelligence sources and analytical tools.
The successful candidate will perform research and development in advancing models of processes associated with the production of WMD materials and the processes associated with operation of WMD facilities.
The goal of the research is to support investigations into the behavior of those processes and advance investigations into the vulnerabilities of those processes.
The position requires providing technical Reachback support to operational planners to support tactical and strategic planning.
The position also provides occasional training to share expertise with junior counterparts and supports exercises to test new methodologies and analytical tools that are under development.
Required Qualifications:
* Master's degree in Mechanical Engineering or similar.
* Demonstrated ability to work effectively within or lead a team of peers, as well as excellent interpersonal and communications skills.
* Ability to communicate highly technical analyses at a level comprehensible to laymen and senior-level government representatives.
* Ability to clearly express in writing technical analysis results and site characterizations.
* Expertise with ANSYS ®, LS-DYNA®, CFX ®, FLUENT ®.
* 6 - 8 years of experience in solving DoD engineering/science problems.
* Practical experience in mechanical engineering structural modeling or fluid modeling.
* Direct experience supporting reverse engineering, threat analysis and vulnerability assessments of WMD-related facilities, processes and infrastructure (to include underground facilities).
* Expert knowledge and use of Word, Excel and PowerPoint.
* Modeling and simulation expertise with weaponeering and engineering analysis tools or similar.
* Research and Development of new tools and methodologies to understand and reverse engineer processes and support systems at remote WMD-related facilities.
* TS clearance with eligibility for SCI based upon a SSBI in the last five years.
Desired Qualifications:
* D degree in Engineering or Physics.
* 10 years of experience in solving DoD engineering/science problems.
* Military or defense-related experience and an understanding of operational planning and functional defeat of hard targets and underground facilities.
COMPANY INFORMATION:
Applied Research Associates, Inc.
is an employee-owned international research and engineering company recognized for providing technically superior solutions to complex and challenging problems in the physical sciences.
The company, founded in Albuquerque, NM, in 1979, currently employ...
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Type: Permanent Location: Reston, US-VA
Salary / Rate: Not Specified
Posted: 2025-07-08 08:09:58
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The Capabilities, Analysis and Development (CAD) division of Applied Research Associates, Inc.
(ARA) is seeking a Chemical Subject Matter Expert The position provides in-depth technical assessments of technologies emerging for chemical weapons of mass destruction.
The successful candidate will perform research and development in advancing chemistry associated the identification and extraction of trace chemicals associated with the production of chemical WMD materials and the processes in addition to identification and extraction of chemicals associated with commercial industrial processes.
The position also provides occasional training to share expertise with junior counterparts and supports exercises to test new methodologies and analytical tools that are under development.
Required Qualifications:
* Master's degree in Chemistry, Chemical Engineering or similar
* 8-10 years of experience in solving DoD engineering/science problems
* Demonstrated ability to work effectively within or lead a team of peers, as well as excellent interpersonal and communications skills
* Ability to communicate highly technical analyses at a level comprehensible to laymen and senior-level government representatives
* Ability to clearly express in writing technical analysis results
* Practical experience in chemical sciences
* Direct experience supporting characterization of chemical WMD processes
* Expert knowledge and use of Word, Excel and PowerPoint
* Research and Development of new tools and methodologies to understand and reverse engineer processes and support systems at remote WMD-related facilities
* TS clearance with SCI eligibility
Desired Qualifications:
* D degree in Chemistry.
* 5+ years of experience in solving DoD engineering/science problems.
* Military or defense-related experience and an understanding of operational planning and functional defeat of hard targets and underground facilities.
COMPANY INFORMATION:
Applied Research Associates, Inc.
is an employee-owned international research and engineering company recognized for providing technically superior solutions to complex and challenging problems in the physical sciences.
The company, founded in Albuquerque, NM, in 1979, currently employs over 1200 professionals.
ARA offices throughout the United States and Canada provide a broad range of technical expertise in defense technologies, civil technologies, computer software and simulation, systems analysis, environmental technologies, and testing and measurement.
The corporation also provides sophisticated technical products for environmental site characterization, pavement analysis, and robotics.
At ARA, employees are our greatest assets.
The corporation realizes that employee ownership fosters greater creativity and initiative along with higher performance and customer satisfaction levels.
ARA gives its employees the tools, training, and opportunities to take more active ro...
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Type: Permanent Location: Alexandria, US-VA
Salary / Rate: Not Specified
Posted: 2025-07-08 08:09:57
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The Capabilities, Analysis and Development (CAD) division of Applied Research Associates, Inc.
(ARA) has an outstanding opportunity for an exceptional Materials Scientist/Engineer with experience in manufacturing/production systems.
As part of the Counter-WMD Analysis Cell (CWAC), our tightly-knit and highly-focused team conducts detailed technical analyses of foreign, WMD-related industrial facilities, processes, and equipment using multiple intelligence sources, analytical tools, and engineering know-how.
We also support a multi-disciplined team that performs Research & Development on technological applications for detecting, identifying, characterizing, modeling, and defeating WMD threats to support tactical and strategic planning efforts.
In short, our CWAC team provides direct support to elements of the Intelligence Community, Combatant Command planning staffs, and operational units tasked with solving the most difficult problems involving the most dangerous weapons threatening the United States and its allies.
The work is challenging, dynamic, relevant, and important to the security of the country.
Essential Functions:
* Identify and characterize critical design elements of WMD-related facilities, processes, systems, and equipment
* Integrate an understanding of material properties, mechanical systems, and industrial production processes to identify design flaws, capability limits, and potential failure mechanisms
* Plan, conduct, and identify opportunities for research & development in support of counter-WMD, full-dimensional defeat technologies
* Support exercises that test and/or demonstrate new technologies, methodologies, and analytical tools that are under development
* Produce clearly-written technical analyses and briefings at levels comprehensible to an audience ranging anywhere from the layperson, to senior-level government representatives, to subject matter experts
* Share expertise with junior counterparts
Required Skills:
* Master’s degree or higher in Materials Science, Materials or Mechanical Engineering, or equivalent degree
* 8+ years of experience solving engineering problems
* Must be a US Citizen
* Practical materials science and mechanical systems knowledge gained through design, manufacturing, or other work experience
* Demonstrated ability to work effectively within or lead a team of peers, as well as excellent interpersonal and communications skills
* Willingness and ability to learn and grow into new areas of technical expertise outside of one’s original field
* Expert knowledge and use of Microsoft Word, Excel, and PowerPoint
* An active TOP SECRET clearance and ability to pass a Counter-Intelligence polygraph is required
Preferred Skills:
* Direct experience supporting reverse engineering, threat analysis, and vulnerability/survivability assessments of WMD-related facilities, processes, and infrastructure (to include underground f...
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Type: Permanent Location: Reston, US-VA
Salary / Rate: Not Specified
Posted: 2025-07-08 08:09:57
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Are you ready to join a growing, global drug development and manufacturing organization that puts people first? Come to Adare! We work closely with our pharmaceutical industry partners during all phases of drug development and commercial manufacturing with a mission of improving the lives of patients and medicines essential to people all over the world. Each role and every department within Adare offer you a unique, customized experience with a chance to make a real impact, and is critical to our success. With the help of people like you dedicated to our mission, Adare is transforming lives by transforming drug delivery!
Join our mission at Adare!
What can Adare offer you?
* Medical/dental/vision/life – low employee premiums
* 401k with a highly competitive match
* Generous PTO, including floating holidays
* Career growth and internal opportunities
* Tuition reimbursement
* Relocation assistance
* Performance-based bonus
* Employee Recognition Programs
We are seeking to hire a Raw Materials Chemist I or II to join our Quality Control team…
If any of the below describes you, we would love to meet you!
JOB SUMMARY
The Raw Materials Chemist will perform chemical and physical testing on pharmaceutical raw materials (APIs, Excipients and Packaging components).
RESPONSIBILITIES AND LEARNING OPPORTUNITIES
* Perform sampling, physical testing, and chemical testing of raw materials as described in the documented procedure or compendia with minimal supervision in accordance with cGMP guidelines.
* Compile samples for send out testing and maintain associated documentation.
* Maintain laboratory equipment and work areas in good working condition.
* Ensure Raw Material documentation is accurate and up to date and revise as needed (i.e.
certificates of analysis, test methods, Standard Operating Procedures)
* Monitor compendia for changes that effect current raw materials testing and procedures.
* Perform assigned calibrations and preventative maintenance for equipment in the laboratory.
* Recognize and troubleshoot equipment issues.
* Recognize and investigate Out of Specification results, Out of Trend results and deviations in accordance with cGMP guidelines and report results to supervisor.
* Audit laboratory documentation.
* Assist with training of Raw Material Analysts and temporary personnel.
* Responsible for laboratory systems as assigned (i.e.
logbooks, calibrations, standards)
* Perform new material verifications with minimal supervision.
* Assist with method validations.
* Assist with installation of new laboratory equipment.
* Accurately maintain notebooks and files compliant with current GMPs and internal Standard Operating procedures.
* Observes all safety procedures and regulations.
* Other job-related tasks as required
REQUIRED SKILLS AND QUALIFICATIONS
Level is commens...
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Type: Permanent Location: Vandalia, US-OH
Salary / Rate: Not Specified
Posted: 2025-07-08 08:09:54
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Are you ready to join a growing, global drug development and manufacturing organization that puts people first? Come to Adare! We work closely with our pharmaceutical industry partners during all phases of drug development and commercial manufacturing with a mission of improving the lives of patients and medicines essential to people all over the world. Each role and every department within Adare offer you a unique, customized experience with a chance to make a real impact and is critical to our success. With the help of people like you dedicated to our mission, Adare is transforming lives by transforming drug delivery!
Join our mission at Adare!
What can Adare offer you?
* Medical/dental/vision/life – low employee premiums
* 401k with a highly competitive match
* Generous PTO, including floating holidays
* Career growth and internal opportunities
* Tuition reimbursement
* Relocation assistance
* Performance-based bonus
* Employee Recognition Programs
We are seeking to hire a Quality Control Chemist to join our Laboratory Operations team…
If any of the below describes you, we would love to meet you!
JOB SUMMARY
The QC Chemist performs moderately complex physical and chemical testing of intermediate and finished products according to written procedures and trains less experienced Chemists as required.
Also responsible for testing of cleaning samples for more complex systems and more advanced instrument maintenance.
Responsible for timely analytical data reporting based on project timelines.
RESPONSIBILITIES AND LEARNING OPPORTUNITIES
* Demonstrate a more advanced knowledge of various test methods and instrument analysis techniques and be proficient with all sample types and test methods.
Perform more advanced troubleshooting/maintenance of the instrumentation.
* Responsible for more complex physical and chemical testing of raw material, intermediate, and finished products as described in the documented procedures to support product release and process validation protocols.
* Demonstrate proficient ability to operate the instrument software applications, set up advanced sequences, troubleshoot software and report data while executing the higher complexity test methods that utilize instruments such as UV, FTIR, GC, and HPLC, and IC.
* As required, perform swabbing and analysis of more complex manufacturing equipment with no supervision in accordance with cGMP guidelines.
Provide input on cleaning related issues and investigations.
* Evaluate and maintain assigned calibrations for equipment in the laboratory as required and review the required documentation for compliance.
Review instrument qualification documents to support system change control actions and assist vendors during installation and PM’s.
* Investigate Out of Specification results, Out of Trend results and deviations in accordance with cGMP guidelines.
* Assist Management with writing an...
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Type: Permanent Location: Vandalia, US-OH
Salary / Rate: Not Specified
Posted: 2025-07-08 08:09:53
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Non-Standard
Job Sub Function:
Non-Employee
Job Category:
Non-Standard
All Job Posting Locations:
Suzhou, Jiangsu, China
Job Description:
Contributes to assigned team at J&J.
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Type: Permanent Location: Suzhou, CN-32
Salary / Rate: Not Specified
Posted: 2025-07-08 08:05:25
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At Roche you can show up as yourself, embraced for the unique qualities you bring.
Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally.
This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come.
Join Roche, where every voice matters.
The Position
Unsere Pharma-Vision
Medikamente schnell zu den Patienten zu bringen und das beste Ergebnis für unsere Kunden zu schaffen.
Das ist es, was uns in Sterile Drug Product Manufacturing (SDPM) in Mannheim antreibt.
So tragen wir auch dazu bei, bis 2029 unser Ziel zu erreichen: 20 bahnbrechende Medikamente zur Behandlung der Krankheiten mit der größten gesellschaftlichen Belastung bereitzustellen.
Unsere Arbeit, unser täglicher Einsatz und unser Engagement bedeuten für sehr viele große Hoffnung und Zuversicht und deswegen müssen wir anders denken und arbeiten.
Mit dem Patient im Fokus setzen wir auf eine neue Organisation und zwar #WIRGEMEINSAM in SDPM!
Deine Aufgaben
Als Senior Quality Assurance Manager Value Streams / Qualified Person (m/w/d) förderst Du aktiv die Umsetzung unserer Lean-Mindset Kultur unter Berücksichtigung der Pharma Technical Operations (PT) Behaviours und Lean-Methoden und lebst diese vor.
Du bist im Lead bzgl.
der Sicherstellung der Harmonisierung und kontinuierlicher Verbesserung einzelner Prozesse und Vorgehensweisen in Abstimmung und Koordination mit den anderen Value Streams am Standort.
Be a coach! Operatives und strategisches GMP-Coaching aller Funktionen innerhalb und bei Bedarf ausserhalb des Value Streams (VS) sowie die Ausbildung angehender Apotheker im Rahmen des Pharmaziepraktikums in qualitativen Aspekten der Arzneimittelherstellung übernimmst Du ebenfalls im Zuge deiner Tätigkeit
Darüber hinaus übernimmst Du folgende spannenden Aufgaben:
Lokale QA-Tätigkeiten, hierfür bist Du primär in Mannheim vor Ort
* Du unterstützt aktiv die Patientenversorgung mit kommerziellen und klinischen Arzneimitteln durch Sicherstellung einer GMP-konformen und termingerechten Freigabe von Arzneimittelchargen.
Die Berücksichtigung der gesetzlichen, regulatorischen und Roche internen Vorgaben sind Dir hierbei besonders wichtig.
* Selbständige Bearbeitung und Qualitätsbewertung komplexer Unplanned Events (UPE)
* Bei Bedarf Leitung und Koordination des lokalen Triage Teams zur Bearbeitung und Root-Cause-Analyse (RCA) von UPS innerhalb des verantworteten VS
* Coaching und Feedback von/an (Nicht-)Quality Vertretern im VS zur Bearbeitung von UPE sowie bei Bedarf selbständige Bearbeitung und Koordination mit beteiligten Funktionen zur Bearbeitung von Planned Events (PE)
* Erstellung, Aktualisierung und (in Absprache mit Schnittstellen und Kollegen) Umsetzung eines inspektionsfesten Konzepts zur Quality Oversi...
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Type: Permanent Location: Mannheim, DE-BW
Salary / Rate: Not Specified
Posted: 2025-07-08 08:05:00
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Quality Control Inspector
Location: Houston, Texas
Overview:
Bray International is seeking a skilled Quality Control Inspector to join our team in a fast-paced industrial manufacturing environment.
If you are passionate about ensuring product quality and have at least four years of experience in quality inspection, we encourage you to apply.
This is an exciting opportunity to contribute to a leading company in the industrial valve and actuator industry.
Key Responsibilities:
* Perform incoming inspections on purchased parts, subassemblies, and finished products to ensure compliance with engineering drawings and customer standards.
* Review Material Test Reports (MTR) and Certificates of Conformance (CofC) against relevant standards.
* Analyze Non-Conformance Reports (NCR) to identify trends and generate Corrective Action Reports (CAR) as needed.
* Create Non-Conformance Reports and other departmental reports as assigned.
* Evaluate issues and make initial recommendations for corrective actions to supervisors.
* Investigate failures to determine root causes and propose remedial actions.
Qualifications:
* Minimum of four years’ experience in quality control within the industrial manufacturing sector.
* Experience with Positive Material Identification (PMI) preferred.
* Proficient in computerized record-keeping and standard software applications.
* Strong written and verbal communication skills.
* Skilled in using and calibrating precision measuring equipment (e.g., micrometers, height gauges, calipers, dial indicators, bore gauges).
* Knowledge of ISO 9001:2008/2015 and API standards.
* Ability to analyze and determine the best inspection methods for product conformity.
* Proficient in interpreting engineering drawings and understanding Geometric Dimensioning and Tolerancing (GD&T).
* Experience with Coordinate Measuring Machines (CMM).
* Ability to manage multiple tasks in a fast-paced environment while meeting delivery requirements.
* High School Diploma or equivalent required.
Physical Demands:
* Must have 20/20 vision (correctable) without color blindness.
* Ability to lift up to 20 pounds.
Note: Immigration sponsorship is not offered for this position.
Why Work for Us?
At Bray International, we are a global leader in providing industrial valves, actuators, and related control products.
We are known for our innovative flow control solutions and are looking for individuals who share our commitment to excellence, integrity, and collaboration.
What We Offer:
* Career Growth: We offer numerous opportunities for advancement within the organization.
* Comprehensive Benefits: Enjoy benefits such as:
+ Life, medical, dental, and vision insurance
+ Paid holidays and vacation
+ 401(k) plan with matching contributions
* Healthy Work Environment: We provide a smoke-free, drug-free workplace to ensure a sa...
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Type: Permanent Location: Houston, US-TX
Salary / Rate: Not Specified
Posted: 2025-07-07 08:06:25
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Recipe for Success
Reser’s is the leading provider of fresh refrigerated foods for the supermarket and food service industries. Family owned and operated, Reser’s has been a proud sponsor of good times at picnics, BBQs, and affordable family meals since 1950. Reser’s family of brands include Reser’s American Classics, Main Street Bistro, Don Pancho, and more. Reser’s operates facilities in the US, Mexico and actively supports the communities it serves.
Benefits and Culture
We offer a competitive compensation and benefits package designed to help employees live a healthier life, build rewarding careers and save for the future. Reser’s offers choices whenever possible, because we recognize the diverse and ever-changing needs of our employees. Full-time employee benefits include medical, dental, vision, AD&D, life, 401(k) with discretionary match, wellness programs, paid time off, company paid holidays and a variety of voluntary benefit options.
We strive to be Employer of Choice. As one of our five cornerstones, this means that we go all-out to create an environment that shows we are committed to investing in employee growth and creating a culture of belonging where employees what to build a lasting career.
General Summary
Responsible for ensuring compliance with safety regulations and standards within the truck shop.
Administers health and safety programs, including environmental policies in accordance with State and Federal OSHA, FMCSA/DOT regulations.
Under limited supervision, oversees the health and safety of Topeka Truck Shop employees and property.
Principle Duties and Responsibilities
1.
Promotes and supports a culture of safety within the truck shop operations and coordinates truck shop safety meetings. Advises and assists employees in adherence to company and local, state and federal regulatory standards.
2.
Oversees incident investigation and reporting procedures in collaboration with Truck Shop and corporate leadership for follow up to closure including root cause analysis.
3.
Tracks corrective actions, loss sources and trends.
Develops, monitors and communicates to local leadership the associated KPIs.
4.
Utilizing safety management system regular follow up with Truck Shop leadership on incident and case management.
5.
Provides training on use of safety management system to staff who will utilize system.
6.
Applying continuous improvement practices, identifies waste in current processes and programs.
Discusses findings with local leadership and Corporate Risk Management.
7.
Utilizing corporate standards and templates, facilitates in the implementation of local and facility specific compliance programs.
8.
Assists with property risk improvement opportunities to identify gaps in life safety and facility protection obligations. Completes actions to established targets and objectives for the site and oversees actions through completion in collaboration with truck shop and corp...
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Type: Permanent Location: Topeka, US-KS
Salary / Rate: Not Specified
Posted: 2025-07-07 08:05:06
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At Johnson & Johnson,â¯we believe health is everything.
Our strength in healthcare innovation empowers us to build aâ¯world where complex diseases are prevented, treated, and cured,â¯where treatments are smarter and less invasive, andâ¯solutions are personal.â¯Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.â¯Learn more at https://www.jnj.com
Job Function:
Medical Affairs Group
Job Sub Function:
Medical Science Liaison
Job Category:
Scientific/Technology
All Job Posting Locations:
Hangzhou, Zhejiang, China
Job Description:
PRINCIPAL RESPONSIBILITIES
External Customer Engagement and Partnering
â¢Â      Actively identify, develop, and engage key KOLs at regional level.
â¢Â      Proactive and reactive communication/interpretation of medical/scientific data/information to KOLs.
â¢Â      Through scientific interactions with KOLs, champion medical benefits of products and contribute to foster innovative therapeutic approaches to benefit patients
â¢Â      Utilizes effective customer engagement strategies, skills, and technology to uncover deep actionable insights on treatment strategies, needs, and priorities that are relevant and important for mutually beneficial value to the customer and Janssen.
â¢Â      Proactively builds a scientific informational resource network
Effectively Scientific Communication with internal/external customers
â¢Â      To help customers and business partners stay abreast of significant advancements through timely identification and dissemination of emerging scientific and medical information from a multitude of sources.
â¢Â      To respond to scientific queries of customers for approved products and products/indications in development, based on Medical Information documents e.g.
literatures, safety records, scientific FAQs etc.
â¢Â      To organize and moderate advisory boards in cooperation with TA groups.
â¢Â      To provide medical and product training and scientific support to Sales Representatives in coordination with Marketing team as appropriate.
â¢Â      To collect insights from external customers and feedback timely to shape Brand/medical strategy    Â
Scientific Communication Effectiveness with external/internal customers
â¢Â      To organize local or regional medical education activities including program development, speaker selection and support in collaboration with ME&MA as appropriate.
â¢Â      To support national and regional medical educational events including material development, speaker selection and support in collaboration with ME&MAs.
â¢Â      Support medical affairs program and activities at local and regional level.
â¢Â      Ensure program implementation 100% in compliance.    Â...
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Type: Permanent Location: Hangzhou, CN-33
Salary / Rate: Not Specified
Posted: 2025-07-07 07:58:46
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Global Human Resources Director
Location: Houston, TX (3-4 days weekly onsite when not traveling)
Reports To: Chief Financial Officer (CFO)
Travel Requirement: Up to 50% international
About Bray International
Bray International is a leading provider of industrial valves, actuators, and related control products, offering innovative flow control solutions worldwide.
As a privately-owned business with over 35 years of engineered excellence, Bray is known for its commitment to excellence, integrity, and collaboration.
Join our team to become part of a dynamic, forward-thinking organization shaping the future of flow control solutions.
About the Role
Bray International, a global leader in flow control solutions, is seeking a hands-on, detail-oriented Global HR Director to lead human resource initiatives across our 40-country footprint.
Reporting directly to the CFO, the successful candidate will have oversight of both solid-line and dotted-line HR teams globally, driving operational efficiency, compliance, and people-centric growth.
This role is heavily focused on tactical execution and project management, ideal for a professional who thrives on implementing process-driven systems, managing international compliance, managing specific employee matters, and collaborating cross-functionally with global finance and operations teams.
Key Responsibilities
* Global Oversight: Manage international HR teams (solid and dotted-line) across 40 countries, ensuring consistency, compliance, and alignment with business goals.
* Tactical Execution: Drive the implementation of process-driven HR projects and initiatives with measurable outcomes, from policy rollouts to process standardization.
* Compliance & Employment Law: Ensure adherence to global labor laws, including GDPR and local country employment regulations; guide U.S.
HR on federal/state compliance matters.
* HR Systems & Payroll: Lead the development of a global HR database and oversee country-specific payroll systems.
* Workforce Strategy: Support global recruitment, visa and immigration processes, and act as an advisor to regional managers on workforce management.
* Employee Engagement & Culture: Lead global engagement, recognition, and retention initiatives tailored to culturally diverse teams.
* Project Leadership: Take active ownership of open HR projects, driving them to completion and ensuring measurable business outcomes.
* Performance & People Management: Coach, mentor, and support HR team members in delivering business-aligned services.
Qualifications
Required:
* Bachelor’s degree in Human Resources, Business Administration, or related field
* 10+ years of progressive HR leadership experience in a global manufacturing, industrial, or engineering environment
* Demonstrated success managing HR operations and compliance across multiple countries
* Strong project management skills and attention to detail
* Profici...
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Type: Permanent Location: Houston, US-TX
Salary / Rate: Not Specified
Posted: 2025-07-06 08:04:35
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At Elanco (NYSE: ELAN) – it all starts with animals!
As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets.
We’re driven by our vision of ‘Food and Companionship Enriching Life’ and our approach to sustainability – the Elanco Healthy Purpose™ – to advance the health of animals, people, the planet and our enterprise.
At Elanco, we pride ourselves on fostering a diverse and inclusive work environment.
We believe that diversity is the driving force behind innovation, creativity, and overall business success.
Here, you’ll be part of a company that values and champions new ways of thinking, work with dynamic individuals, and acquire new skills and experiences that will propel your career to new heights.
Making animals’ lives better makes life better – join our team today!
Your Role: To safely perform laboratory analyses of purchased and manufactured materials, utilities/EM and stability samples to cGMP, Regulatory and Elanco requirements.
Your Responsibilities:
* Maintain laboratory and office areas in compliance with EHS and cGMP requirements. Archive completed laboratory documentation in a timely manner.
* Chemical and/or microbial based analyses of purchased and manufactured materials, utilities/EM, stability samples and non-routine samples.
* Report and approve results using standard laboratory systems ensuring all statistical monitoring charts (paper and electronic) are updated in a timely manner.
* Perform all aspects of sample handling, e.g.
sample receipt, storage and disposal as per procedures.
* If authorised, perform second person verification of analytical data generated in QCL as per procedures.
* Liaise with Supervision and planners to prioritise workload to ensure lead times and expected customer service levels are met.
* Conduct the equipment calibrations, maintenance and IQ/OQ that you are trained to perform.
* Train other QCL staff in these tasks as appropriate.
Write, update and review analytical workbooks, methods and procedures.
* Perform analyses and document results to support method verifications, validations and transfers.
* Assist the QCL Scientist/Equipment group when required, by participating in analytical investigations, investigative testing and method/equipment fault finding and troubleshooting.
* Follow lab purchasing procedures to ensure laboratory remains sufficiently stocked with standards/reagents and consumables.
* If trained and authorised to do so, purchase standards/reagents/consumables.
Communicate with regulatory auditors such as VMD, MHRA, FDA etc in accordance with company policy.
What You Need to Succeed (minimum qualifications):
* Science Degree or Relevant Experience.
* Expertise in Compendial testing (Ph.Eur, USP, JP etc)
* Experience in FTIR, NIR, Spectrophotometry and classical wet c...
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Type: Permanent Location: Liverpool, GB-LIV
Salary / Rate: 30000
Posted: 2025-07-06 07:58:30
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At Elanco (NYSE: ELAN) – it all starts with animals!
As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets.
We’re driven by our vision of ‘Food and Companionship Enriching Life’ and our approach to sustainability – the Elanco Healthy Purpose™ – to advance the health of animals, people, the planet and our enterprise.
At Elanco, we pride ourselves on fostering a diverse and inclusive work environment.
We believe that diversity is the driving force behind innovation, creativity, and overall business success.
Here, you’ll be part of a company that values and champions new ways of thinking, work with dynamic individuals, and acquire new skills and experiences that will propel your career to new heights.
Making animals’ lives better makes life better – join our team today!
Your Role: Quality Control Supervisor, Microbiology
In this role, you will manage and lead the microbiology team in supporting manufacturing, monitoring clean, classified areas and utilities, and in-process and final product release testing.
You will supervise a group of 6-7 individuals at any given time.
Your Responsibilities:
* Leads and schedules a team of Quality Control Microbiologists, delegating tasks effectively.
* Manages all microbiological testing, including environmental monitoring, utilities, and product testing, reviewing, approving, and reporting data.
* Coordinates interdepartmental activities, ensuring seamless collaboration between microbiology and manufacturing, validation, and engineering teams.
* Develops and maintains training programs and records for microbiology staff.
* Creates, reviews, and approves essential documentation, including specifications, validation protocols/reports, study protocols/reports, SOPs, and testing documentation.
Establishes new testing methods as needed.
What You Need to Succeed (minimum qualifications):
* High School Diploma/GED with 8 years of experience, BA or BS degree in Microbiology, Biological Sciences, Pharmaceutical Sciences, or closely related field, or comparable experience.
* Technical skills in microbiology to include, but not limited to aseptic technique, sterile gowning, and pipetting are required.
* Excellent computer, documentation, communication, and organizational skills required.
What Will Give You the Competitive Edge (preferred qualifications):
* Experience in cGMP environment preferred.
* Experience with sterility, mycoplasma, environmental monitoring, and water testing preferred.
* Knowledge of pharmaceutical cGMPs (US and EU), FDA, USDA, VICH, EU as related to QC activities.
* Experience related to method development/validation.
Don’t meet every single requirement? Studies have shown underrepresented groups are less likely to apply to jobs unless they meet every single qualification.
At Elanco, we are dedicated to ...
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Type: Permanent Location: Elwood, US-KS
Salary / Rate: 44.14
Posted: 2025-07-06 07:58:28
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At Elanco (NYSE: ELAN) – it all starts with animals!
As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets.
We’re driven by our vision of ‘Food and Companionship Enriching Life’ and our approach to sustainability – the Elanco Healthy Purpose™ – to advance the health of animals, people, the planet and our enterprise.
At Elanco, we pride ourselves on fostering a diverse and inclusive work environment.
We believe that diversity is the driving force behind innovation, creativity, and overall business success.
Here, you’ll be part of a company that values and champions new ways of thinking, work with dynamic individuals, and acquire new skills and experiences that will propel your career to new heights.
Making animals’ lives better makes life better – join our team today!
Your Role: Quality Control /Environmental Monitoring Technician
Environmental Monitoring / QC Technician Microbiology will report to the QC Supervisor, Microbiology or equivalent.
This position will conduct routine and non-routine environmental monitoring of the manufacturing facilities and associated utilities, as well as microbiology analysis.
Your Responsibilities:
* Conducts Environmental Monitoring: Performs routine and non-routine sampling of manufacturing environments (air and surfaces) and utilities (WFI, USP Water, Pure Steam, Clean Compressed Air).
Maintains gowning qualifications for sterile environments.
* Ensures cGMP Compliance: Upholds cGMP, safety, and environmental standards within the QC lab, generating accurate and compliant data.
Participates in internal assessments and audits.
* Performs Microbiological Testing: Executes routine and non-routine analyses of raw materials, in-process materials, finished goods, and stability samples.
Conducts a variety of microbiology tests, including bioburden, sterility, and microbial identifications.
* Supports Investigations and Deviations: Assists in the investigation of out-of-specification/out-of-trend results, environmental monitoring excursions, and deviations.
Contributes to the preparation of Certificates of Analysis.
* Develops and Maintains QC Methods: Assists in developing, qualifying/validating, and transferring new test methods.
Contributes to the writing and revision of testing methods, specifications, SOPs, and validation protocols/reports.
Maintains lab inventory and performs routine equipment maintenance and cleaning.
What You Need to Succeed (minimum qualifications):
* Education: High School Diploma/GED with 5years experience, BA or BS degree in Microbiology, Biological Sciences, Pharmaceutical Sciences, or closely related field, or comparable experience.
* Experience: Technical skills in Environmental Monitoring to include, but not limited to, monitoring of manufacturing environment and utilities.
* Excellent c...
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Type: Permanent Location: Elwood, US-KS
Salary / Rate: 27
Posted: 2025-07-06 07:58:25
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ERM is seeking a Consultant, Safety and Industrial Hygiene with industry experience, to play a key role in growing our business in the Health and Safety service line.
The ideal candidate will bring H&S technical capability and deep understanding of business processes to help our clients proactively address their EHS risks and challenges.
As a health and safety professional, you will be responsible for supporting on a range of health and safety management projects to build a sustainable business locally, while networking with ERM's global technical team to share best practices across the industry.
This is an excellent opportunity for a senior-level professional looking to advance their career with a global Sustainability leader, and work with a team of outstanding professionals in over 40 countries around the world.
RESPONSIBILITIES:
* Support development and implementation of Safety Management Systems and risk assessments to ensure effective risk control and regulatory compliance.
* Perform incident investigations, development of corrective actions, verification/validation of controls, and learning from incidents. Support root cause analyses in conjunction with client leadership.
* Support life safety programs such as control of hazardous energy, fall protection, electrical safety, machinery safety, powered industrial vehicle, materials lifting, hot work, and fire safety.
* Support client industrial hygiene programs, including leading the qualitative and quantitative assessment of exposure risk.
* Assist in the development of solutions to complex technical and regulatory issues and concerns.
* Contribute to expanding ERM’s Safety Services business.
Identify and develop new opportunities, prepare effective technical proposals, and take active leadership role in developing new business with new and existing clients.
Develop and expand client relationships that generate repeat business.
* Develop and manage innovative, behavior and performance outcome-focused approaches and programs for a variety of clients with complex technical/regulatory issues.
Design and direct corporate H&S strategies and programs in areas such as industrial hygiene, behavior-based safety, safety culture and leadership, serious injury and fatality risk reduction, compliance auditing, EHS management systems, process safety and risk management, construction safety, high-impact training, and general compliance support.
Achieve client’s expectations for scope, budget, schedule, and quality.
* Manage a variety of tasks to achieve scope, budget and schedule targets while ensuring we meet and exceed our clients' expectations on deliverables.
* Build client relationships and nurture repeat business by continuously striving to Build a network within and outside of ERM that will enable you to leverage your skills and solve challenging multi-disciplinary client challenges.
REQUIREMENTS:
* BS/MS degree preferred. Equivalenc...
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Type: Permanent Location: Ewing, US-NJ
Salary / Rate: Not Specified
Posted: 2025-07-06 07:55:43
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ERM is seeking a Managing Consultant, Air Quality and Environmental Compliance to join our Ewing, NJ office and specialize in the Air Quality permitting, Emergency Planning and Community Right-to-Know Act (EPCRA), and Toxic Release Inventory (TRI) reporting service areas, and contribute to our nationwide consulting team.
In this role, you will provide senior project management and senior technical leadership and QA/QC review on New Jersey air permitting, EPCRA TRI/Tier II calculation/reporting portfolios, as well as other EHS compliance projects and compliance assurance programs for clients locally, nationally, and internationally.
This is an excellent career opportunity to work with an expert consulting team and center of excellence on challenging environmental reporting and management projects for large industrial and global clients.
Access to ERM's national EHS Management Systems & Compliance experts also provides knowledge sharing of best practices across the industry and ongoing learning opportunities for our team.
RESPONSIBILITIES:
* Manage strategic air permits and compliance assurance programs for a variety of industrial clients with complex technical/regulatory issues. Work closely with clients and develop strong relationships to understand specific processes and develop a permitting and compliance strategy to help clients maintain maximum operating flexibility.
Achieve client’s expectations for scope, budget, schedule, and quality.
* Interact with local regulators to steward permit application review and issuance.
* Effectively manage project teams across the Region, including appropriately delegating project assignments to project teams and mentoring junior staff.
* Work in a collaborative team environment to support the on-going growth and development of ERM’s EPCRA Reporting Program and Portfolio.
* Provide regulatory interpretation and guidance on complex TRI applicability, calculation and reporting issues to the ERM EPCRA team and clients.
* Perform complex facility operational and EHS data analysis and systematic organization/clean-up of large data sets and data manipulation in support of threshold and release calculation preparation.
* Manage multiple large-scale projects and/or reporting programs within scope/budget/schedule expectations and ensure quality standards on project deliverables.
* Provide final QA/QC review of a portfolio of detailed emissions, EPCRA, and TRI threshold and release calculations for multiple industry sectors, including complex chemical plants and oil & gas refineries.
* Ensure on-time quality delivery of calculations and reports.
* Provide environmental compliance support to clients, including on-site assistance as needed.
* Develop and expand client relationships that generate repeat business to grow ERM’s EHS Sustainable Operations practice.
* Prepare technical proposals and participate in business development with existing cli...
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Type: Permanent Location: Ewing, US-NJ
Salary / Rate: Not Specified
Posted: 2025-07-06 07:55:42
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ERM is seeking an experienced Principal Technical Consultant, Ecologist (Scientist or Biologist) with consulting experience to play a key role in implementing our existing programs in our Ewing, New Jersey office.
The ideal candidate will have served as a senior subject matter expert in the ecological field with a proven track record of high-quality outputs, experience working within a variety of ecological media and settings, and excellent client communication skills and responsiveness.
This is a fast-track opportunity for a senior-level professional looking to advance their career with a global environmental leader, on existing contracts.
Business Development will not be required at the onset of this role.
The role will be predominantly desktop with some site visits.
RESPONSIBILITIES:
* Coordinate environmental investigations of surface water, sediments, and wetlands by preparing or reviewing sampling plans in accordance with applicable New Jersey Department of Environmental Protection (NJDEP) regulations and guidance.
* Contribute to preparing technical documents such as Ecological Evaluations and Ecological Remedial Investigation Reports by leading project teams through the data evaluation of soil, groundwater, surface water and sediment sampling results.
* Oversee riparian and wetland restoration projects in New Jersey under the auspices of the NJDEP and Natural Resource Trustees.
* Support ecological risk assessments by coordinating with the data team to process and interpret data for use by the risk assessor.
* Support land use and wetlands permitting efforts pursuant to NJDEP programs.
* Achieve client’s expectations for scope, budget, schedule, and quality.
* Maintain positive relationships with clients and public agencies.
* Other duties may include natural resource surveys, biological monitoring (as necessary), field team management, and providing specialized site assessments.
REQUIREMENTS:
* BS or MS in biology, wetland science, plant ecology or similar field with experience pertaining to a specialized biological training or field.
Or equivalent experience.
* 6+ years (8+ years preferred) of consulting experience that involves oversight, QA/QC, technical writing, ecological evaluations, and multi-media permitting.
* Solid grasp of the key biological or wetland ecology impact assessment and management issues within various industry sectors, as well as a high degree of technical competence and broad knowledge of impact assessment best practices.
* Knowledge of state and federal environmental regulations.
Experience with NJDEP’s Bureau of Environmental Radiation (BER) is a plus.
* Recognized technical expertise by and established reputation in the marketplace, including positive reputation with key regulators relevant to ecological assessment approvals.
* Well-developed team building and influencing skills; unquestioned integrity; and ...
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Type: Permanent Location: Ewing, US-NJ
Salary / Rate: Not Specified
Posted: 2025-07-06 07:55:42
-
At Elanco (NYSE: ELAN) – it all starts with animals!
As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets.
We’re driven by our vision of ‘Food and Companionship Enriching Life’ and our approach to sustainability – the Elanco Healthy Purpose™ – to advance the health of animals, people, the planet and our enterprise.
At Elanco, we pride ourselves on fostering a diverse and inclusive work environment.
We believe that diversity is the driving force behind innovation, creativity, and overall business success.
Here, you’ll be part of a company that values and champions new ways of thinking, work with dynamic individuals, and acquire new skills and experiences that will propel your career to new heights.
Making animals’ lives better makes life better – join our team today!
Your Role: Quality Control Technician
As a Quality Control Technician, you will play a crucial role in ensuring the accuracy and integrity of laboratory testing within our Quality Control and Environmental Control Laboratories.
In this position, you will be responsible for executing precise testing, participating in laboratory investigations, and maintaining equipment in compliance with GMP and safety guidelines.
This position will offer a one-time sign on bonus of $2,500!
Your Responsibilities:
* Perform timely and accurate testing of laboratory samples according to approved methods.
* Adhere to safety protocols and serve as a role model for safety practices on your shift.
* Conduct data entry and verification reviews with high attention to detail.
* Troubleshoot equipment and methodologies as needed.
* Engage in continuous improvement activities and self-inspections.
What You Need to Succeed (minimum qualifications):
* Education: High School Diploma or equivalent.
* Required Experience: Experience in a laboratory environment with a focus on quality control.
* Top 2 skills: Strong attention to detail and ability to work in a highly regulated environment.
What will give you a competitive edge (preferred qualifications):
* Familiarity with GMP and safety guidelines.
* Experience with laboratory investigations and equipment maintenance.
* Ability to work flexible shifts, including 12-hour and 8-hour schedules.
* Previous involvement in safety and ergonomic initiatives.
* Strong problem-solving skills related to laboratory operations.
Additional Information:
* Location: Clinton, IN Manufacturing Site
* Required to work in a laboratory environment (wearing safety glasses and laboratory clothing/PPE required). Some exposure to allergens is possible in the laboratory environment.
* Shift: 12-hour shift that could be days, nights, or swing.
* Unscheduled overtime may be required.
This position is a fixed duration employee with a one-year contract, annually renewable fo...
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Type: Permanent Location: Clinton, US-IN
Salary / Rate: 23
Posted: 2025-07-05 08:53:17
