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sciAre 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 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 Senior Formulation Scientist to join our Pharmaceutical Development Team…
If any of the below describes you, we would love to meet you!
JOB SUMMARY
The Senior Formulations Scientist will report to the Associate Director of Formulations, and will be expected to develop pharmaceutical dosage forms with an emphasis on immediate and modified-release solid oral dosage forms. This is a client-facing role providing a career path to advancement within Pharmaceutical Development.
RESPONSIBILITIES AND LEARNING OPPORTUNITIES
* Design and perform formulation development studies on immediate and modified release oral solid dosage forms defined by management/customer and assume the responsibility needed to meet the product specific objectives.
* Develop new products utilizing existing and new technologies available within the industry from pre-formulation to manufacturing stage.
* At times, interact directly with Adare’s clients in project update meetings; provide technical expertise, presentation of data
* Write development and cGMP batch records, stability study protocols, in-process and finished product specifications and product development reports
* Assist both Manufacturing and Quality Assurance departments in scale-up and production trouble-shooting
* Perform technology transfer to customer production sites and train/assist customer personnel in scale-up and production.
* Develop and/or locate new technologies that will be of interest to the Company’s product development objectives.
* Supervise/train formulation scientists and ensure their activities comply with CGMP regulations.
* Conducts and manage development projects with manager’s guidance and ensure the successful scale-up of a new product and/or process.
* Comply with all regulations as specified by OSHA, EPA, FDA, DEA, etc., and as defined in the Corporate Hygiene plan.
* Assist in writing and preparation of ...
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Type: Permanent Location: Vandalia, US-OH
Salary / Rate: Not Specified
Posted: 2025-08-07 08:20:39
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At Actus Nutrition, our focus is to create high-quality ingredients designed to optimize health and nutrition.
We are passionate and dedicated people.
Each day, we collectively explore new, innovative ways to enhance product performance and value through our broad human and animal nutrition portfolios. We offer a comprehensive benefits package which includes medical, dental, vision and life insurance as well as a healthy 401(k) company match program.
The EHS Manager has the responsibility for managing the Environmental, Health & Safety programs at the Port Edwards and Wautoma, Wisconsin facilities.
Essential Functions:
* Monitor and assist the facility with compliance of all applicable company environmental, safety and health standards as well as all federal, state and local regulations.
* Develop compliance plans for air and water permits. Manage WPDES permits.
* Oversee and maintain compliance with PSM programs in cooperation with site managers including engineers, maintenance supervisor, plant manager and production manager. Work cooperatively with outside consultants.
* Develop and maintain company environmental, health and safety programs at the facility.
* Work with the highest ethical standard for legal compliance and demonstrate a true passion for employee safety.
* Manage plant safety, health and loss prevention programs.
* Develop policies and procedures to ensure that occupational safety and health standards are maintained throughout the facility.
* Utilize IH equipment to determine employ’s exposures to noise and air contaminants.
* Perform fit-testing for respirator users.
* Maintain all required environmental, health & safety program records and legal documents.
* Regularly inspect plant for unsafe conditions as they relate to equipment, process, and facility.
* Actively participate with the plant management team to develop corrective actions for identified risks.
* Track corrective actions to completion in accordance with the facility corrective action tracking program.
* Professionally train, counsel and advise personnel on all identified safety risks, and establish a proactive approach to providing a safe working environment for everyone at the plant.
* Conduct new employee EHS orientations.
* Lead and oversee the monthly EHS training program.
* Schedule and assist the plant with having monthly safety committee meetings.
* In cooperation with area managers and first-line supervisors investigate all injuries, environmental releases and serious near misses.
* Immediately report all injuries, environmental releases and serious near misses to the Plant Manager. Submit a written notification of all injuries, environmental releases, and serious near misses to the corporate EHS department using the RCI reporting program.
* Complete a first report of injury with Workers Compensation Carrier if required for a w...
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Type: Permanent Location: Wautoma, US-WI
Salary / Rate: Not Specified
Posted: 2025-08-07 08:17:50
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At Actus Nutrition, our focus is to create high-quality ingredients designed to optimize health and nutrition.
We are passionate and dedicated people.
Each day, we collectively explore new, innovative ways to enhance product performance and value through our broad human and animal nutrition portfolios. We offer a comprehensive benefits package which includes medical, dental, vision and life insurance as well as a healthy 401(k) company match program..
The EHS Manager has the responsibility for managing the Environmental, Health & Safety programs at the Fond du Lac, Wisconsin facility.
Essential Functions:
* Monitor and assist the facility with compliance of all applicable company environmental, safety and health standards as well as all federal, state and local regulations.
* Develop compliance plans for air and water permits. Manage WPDES permits.
* Oversee and maintain compliance with PSM programs in cooperation with site managers including engineers, maintenance supervisor, plant manager and production manager.
* Work cooperatively with outside consultants.
* Develop and maintain company environmental, health and safety programs at the facility.
* Work with the highest ethical standard for legal compliance and demonstrate a true passion for employee safety.
* Manage plant safety, health and loss prevention programs.
* Develop policies and procedures to ensure that occupational safety and health standards are maintained throughout the facility.
Utilize IH equipment to determine employ’s exposures to noise and air contaminants.
* Perform fit-testing for respirator users.
* Maintain all required environmental, health & safety program records and legal documents.
* Regularly inspect plant for unsafe conditions as they relate to equipment, process, and facility.
* Actively participate with the plant management team to develop corrective actions for identified risks.
* Track corrective actions to completion in accordance with the facility corrective action tracking program.
* Professionally train, counsel and advise personnel on all identified safety risks, and establish a proactive approach to providing a safe working environment for everyone at the plant.
* Conduct new employee EHS orientations.
* Lead and oversee the monthly EHS training program.
* Schedule and assist the plant with having monthly safety committee meetings.
* In cooperation with area managers and first-line supervisors investigate all injuries, environmental releases and serious near misses.
* Immediately report all injuries, environmental releases and serious near misses to the Plant Manager. Submit a written notification of all injuries, environmental releases, and serious near misses to the corporate EHS department using the RCI reporting program.
* Complete a first report of injury with Workers Compensation Carrier if required for a workplace i...
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Type: Permanent Location: Fond Du Lac, US-WI
Salary / Rate: Not Specified
Posted: 2025-08-07 08:17:49
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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
A healthier future.
It’s what drives us to innovate.
To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come.
Creating a world where we all have more time with the people we love.
That’s what makes us Roche.
In Roche´s Pharmaceutical Research and Early Development organisation (pRED), we make transformative medicines for patients in order to tackle some of the world’s toughest unmet healthcare needs.
At pRED, we are united by our mission to transform science into medicine.
Together, we create a culture defined by curiosity, responsibility and humility, where our talented people are empowered and inspired to bring forward extraordinary life-changing innovation at speed.
This position is located in Pathology and Applied Safety Science, a chapter within the Pharmaceutical Sciences function, which enables portfolio decisions through integrative immunosafety, investigative safety and pathology expertise.
We closely collaborate with our therapeutic areas and functions to convert hypotheses into innovative therapeutics.
The Opportunity
The Immunosafety team is seeking an Immunosafety Scientist with a focus on Mechanistic Immunomodulation and Immunosafety project support.
* You provide expert immunological insights for drug candidate risk assessment, designing and interpreting studies to identify and mitigate risks of immunoactivation or immunosuppression.
* You participate in developing and implementing risk mitigation strategies for drug candidates.
* You develop, optimize, and validate immunological assays.
* You apply strong practical experience with in vitro and in vivo immunological models, including New Approach Methodologies (NAMs).
* You evaluate new technologies to enhance research and assay capabilities.
* You act as an immunosafety expert on project teams, contributing to translational strategies that bridge preclinical findings to clinical settings.
Please note this position is temporary for 1 year.
Who you are
* You bring a PhD in Immunology, Toxicology or a related field with > 5 years of experience in drug development.
* You bring expertise in investigative immunosafety.
* You have a strong background in immunological assays and model development and validation (in vitro, in vivo, NAMs).
* You bring experience in providing immunological insights for risk assessment and mitigation.
* You can contribute to translational strat...
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Type: Permanent Location: Basel, CH-BS
Salary / Rate: Not Specified
Posted: 2025-08-07 08:17:44
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Job Summary
This is an onsite position at Inogen facilities located in Plano, TX or Beverly, MA.
Responsible for the development and execution of regulatory strategy for Inogen products.
The Director of Regulatory Affairs will lead a team and activities resulting in obtaining and maintaining regulatory approval in support of Inogen business objectives and applicable global medical device regulations.
The position plays a critical role in supporting Inogen’s ambitious global growth objectives and will work closely with internal stakeholders such as R&D, Clinical, Commercial, Operations, and Quality, as well as external stakeholders such as FDA, Notified Bodies, etc.
Responsibilities
* Serve as regulatory subject matter expert providing timely, clear, and consistent regulatory guidance for Inogen products throughout their entire lifecycle
* Prepare and obtain approval for product submissions to FDA and other global regulators
* Ensure compliance with all applicable regulatory requirements
* Maintain site registrations, regulatory files, and records
* Provide regulatory support for Inogen cross-functional regulated activities such as design, manufacturing, clinical trials, audits, post-market surveillance, etc.
* Review and approve product design, labeling, manufacturing, and quality assurance changes, as well as marketing advertising and promotional materials to ensure compliance with internal procedures, applicable regulations and guidelines
* Monitor regulatory trends, regulations, and guidance to inform regulatory strategies and ensure ongoing compliance with changing regulatory requirements
* Lead, mentor, and develop a high-performing team of regulatory professionals, fostering a culture of excellence, collaboration, and continuous improvement
* Build and maintain productive relationships with global regulatory authorities and external stakeholders, consultants, regulatory agencies, and industry groups
* Performs other duties as required
Knowledge, Skills, and Abilities
* Demonstrated proficiency and knowledge of current medical device Good Manufacturing Practices, FDA 510(k), EU MDR, FDA Advertising and Promotion guidance, and other global medical device regulations
* Exceptional leadership and team-building skills, with the ability to work highly effectively in cross-functional teams in a dynamic and fast-paced environment
* Analytical mindset, highly organized, detail oriented, and ability to prioritize
* 10 - 15% domestic and international travel required
* Must have exceptional written, verbal, and interpersonal skills with internal and external stakeholders
Qualifications (Education and Experience)
* Bachelor’s degree in engineering, Life Sciences, or technical discipline is required
* Applicable advanced degree preferred
* RAPS Certification (RAC) preferred
* Minimum of 8 years of Regulatory Affairs experience focusing on submi...
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Type: Permanent Location: Plano, US-TX
Salary / Rate: Not Specified
Posted: 2025-08-07 08:17:39
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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
A healthier future.
It’s what drives us to innovate.
To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come.
Creating a world where we all have more time with the people we love.
That’s what makes us Roche.
In Roche´s Pharmaceutical Research and Early Development organisation (pRED), we make transformative medicines for patients in order to tackle some of the world’s toughest unmet healthcare needs.
At pRED, we are united by our mission to transform science into medicine.
Together, we create a culture defined by curiosity, responsibility and humility, where our talented people are empowered and inspired to bring forward extraordinary life-changing innovation at speed.
This position is located in Pathology and Applied Safety Science, a chapter within the Pharmaceutical Sciences function, which enables portfolio decisions through integrative immunosafety, investigative safety and pathology expertise.
We closely collaborate with our therapeutic areas and functions to convert hypotheses into innovative therapeutics.
The Opportunity
The Immunosafety team is seeking an experienced Immunologist focused on Translational Immunosafety, Safety Biomarkers, and Immunosafety project support.
This role is crucial for expanding our presence in Translational Immunosafety & Safety Biomarkers to meet the evolving demands of our portfolio.
* You develop strategies to bridge preclinical findings to clinical settings, informing clinical trial design, patient selection, and monitoring.
* You provide comprehensive Immunosafety project support across the drug development value chain.
* You identify and characterize new safety biomarkers for immune-related adverse events (e.g., immunotoxicity, cytokine release syndrome (CRS), autoimmunity).
* You provide immunological insights for integrated risk assessment of drug candidates and contribute to risk mitigation strategies.
* You develop, optimize, and validate immunological assays, applying expertise in in vitro and in vivo immunological models, including New Approach Methodologies (NAMs), and other new technologies.
Who you are
* You bring a PhD in Immunology, Toxicology or a related field with > 5 years of experience in drug development.
* You have expertise in translational immunosafety, including safety biomarker discovery and development.
* You bring expertise in tissue-specific immunology and application in a mechanisti...
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Type: Permanent Location: Basel, CH-BS
Salary / Rate: Not Specified
Posted: 2025-08-07 08:17:31
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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
A healthier future.
It’s what drives us to innovate.
To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come.
Creating a world where we all have more time with the people we love.
That’s what makes us Roche.
In Roche´s Pharmaceutical Research and Early Development organisation (pRED), we make transformative medicines for patients in order to tackle some of the world’s toughest unmet healthcare needs.
At pRED, we are united by our mission to transform science into medicine.
Together, we create a culture defined by curiosity, responsibility and humility, where our talented people are empowered and inspired to bring forward extraordinary life-changing innovation at speed.
This position is located in Pathology and Applied Safety Science, a chapter within the Pharmaceutical Sciences function, which enables portfolio decisions through integrative immunosafety, investigative safety and pathology expertise.
We closely collaborate with our therapeutic areas and functions to convert hypotheses into innovative therapeutics.
The Opportunity
The Immunosafety team is seeking an experienced Immunologist to provide expert immunology support across a diverse portfolio of drug development projects.
This role is critical for maintaining robust portfolio support and introducing new perspectives on addressing immunosafety questions within a drug development setting.
* You serve as a drug safety immunology subject matter expert, staying current with advancements in the field and integrating relevant insights into drug development strategies.
* You provide comprehensive Immunosafety project support and guidance for human risk assessment across the drug development chain.
* You evaluate potential immunotoxicity, design and oversee studies, and interpret data to assess risks in the preclinical space.
* You stay updated on regulatory requirements pertaining to immunotoxicity and integrate them into study designs and interpretations.
* You develop, optimize, and validate immunological assays, demonstrating expertise in both in vitro and in vivo models, including New Approach Methodologies (NAMs).
* You mentor junior scientists within the team, fostering their scientific growth and development.
* You lead cross-functional teams, collaborating effectively with colleagues across various departments.
* You represent the organization at scientific forums, conferences, and external me...
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Type: Permanent Location: Basel, CH-BS
Salary / Rate: Not Specified
Posted: 2025-08-07 08:17:29
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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
A healthier future.
It’s what drives us to innovate.
To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come.
Creating a world where we all have more time with the people we love.
That’s what makes us Roche.
In Roche´s Pharmaceutical Research and Early Development organisation (pRED), we make transformative medicines for patients in order to tackle some of the world’s toughest unmet healthcare needs.
At pRED, we are united by our mission to transform science into medicine.
Together, we create a culture defined by curiosity, responsibility and humility, where our talented people are empowered and inspired to bring forward extraordinary life-changing innovation at speed.
pRED's Pharmaceutical Sciences (PS) group enables discovery and development of safe and effective therapeutics at optimal doses in relevant populations with a vision to power translation, continuously improve the accuracy of our predictions and accelerate the development of tomorrow's medicines.
PS supports discovery and development across the whole value chain from target assessment to on-market and beyond.
This position is located in Pathology and Applied Safety Science, a chapter within the Pharmaceutical Science function, which enables portfolio decisions through proactive and integrative pathology expertise.
We closely collaborate with our therapeutic areas and functions to convert hypotheses into innovative therapeutics.
The Opportunity
We are offering an outstanding opportunity for a veterinary clinical pathologist to work with multidisciplinary teams in preclinical drug discovery and development with a focus on mechanistic, translational and regulatory aspects.
Your impact:
* You collaborate within an interdisciplinary team of pathologists, scientists and laboratory experts to ensure high-impact clinical pathology assessments are appropriately reported and integrated into investigative and regulatory pathology
* You provide scientific guidance for laboratory activities and participate in the generation of high-quality clinical pathology readouts
* You participate in the establishment and development of emerging safety biomarkers
* You nurture trustful relationships and effective collaboration with internal and external partners to characterize clinical pathology findings and identify potential safety risks
This position is a temporary contract for 2 years.
Who you are
* You are bo...
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Type: Permanent Location: Basel, CH-BS
Salary / Rate: Not Specified
Posted: 2025-08-07 08:17:25
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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
A healthier future.
It’s what drives us to innovate.
To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come.
Creating a world where we all have more time with the people we love.
That’s what makes us Roche.
In Roche’s Pharmaceutical Research and Early Development organization (pRED), we make transformative medicines for patients to tackle some of the world’s toughest unmet healthcare needs.
At pRED, we are united by our mission to transform science into medicine.
Together, we create a culture defined by curiosity, responsibility and humility, where our talented people are empowered and inspired to bring forward extraordinary life-changing innovation at speed.
This position is located in TSAC, a department within the Pharmaceutical Sciences function. We drive the non-clinical safety assessment of drug candidates from small molecules to complex biological products during the discovery and development phases at Roche.
The Opportunity
We are offering an outstanding opportunity for a Senior Toxicologist to serve as the single point of contact for impurities assessments at Roche Basel.
The position is placed in the Translational Safety Assessment chapter (TSAC) within Pharmaceutical Sciences at pRED Basel.
This is a critical role within our team, requiring a strong scientific background and excellent communication skills to collaborate across various departments.
You will play a key role in supporting the safety assessment of impurities and extractables/leachables throughout the value chain from late discovery to clinical development, as well as for established medicines, with compliance to the most current regulatory guidelines.
Utilizing your expertise, you will collaborate with cross-functional teams to ensure the delivery of high-quality and compliant safety evaluations.
Your main responsibilities will be:
* You are the single point of contact for impurity and E&L risk assessments in drug substances and drug products
* You conduct comprehensive risk assessments of genotoxic impurities in line with ICH M7 and related guidance
* You perform toxicological evaluations of E&L profiles associated with container closure systems, devices, and manufacturing components
* You provide guidance on thresholds of toxicological concern (TTC), supporting product compatibility and safety dossiers
* You design and interpret in silico (Q)SAR analyses and, where appropriate, prop...
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Type: Permanent Location: Basel, CH-BS
Salary / Rate: Not Specified
Posted: 2025-08-07 08:17:24
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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
A healthier future.
It’s what drives us to innovate.
To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come.
Creating a world where we all have more time with the people we love.
That’s what makes us Roche.
In Roche´s Pharmaceutical Research and Early Development organisation (pRED), we make transformative medicines for patients in order to tackle some of the world’s toughest unmet healthcare needs.
At pRED, we are united by our mission to transform science into medicine.
Together, we create a culture defined by curiosity, responsibility and humility, where our talented people are empowered and inspired to bring forward extraordinary life-changing innovation at speed.
pRED's Pharmaceutical Sciences (PS) group enables discovery and development of safe and effective therapeutics at optimal doses in relevant populations with a vision to power translation, continuously improve the accuracy of our predictions and accelerate the development of tomorrow's medicines.
PS supports discovery and development across the whole value chain from target assessment to on-market and beyond.
The position is within the Translational Safety Assessment Chapter in Pharmaceutical Sciences.
We drive the non-clinical safety assessment of drug candidates from small molecules to complex biological products through all the discovery and development phases at Roche.
The Opportunity
We are offering an outstanding opportunity for a Project Toxicologist to work with multidisciplinary teams in preclinical drug discovery and development with a focus on mechanistic, translational and regulatory aspects.
Your main responsibilities in this position are:
* The development and execution of an integrated and scientifically sound nonclinical safety strategy from target assessment through clinical trial conduct to registration
* Representing Pharmaceutical Sciences in Global project teams and acting as a key contributor to the selection and timely development of potential new medicines through close interactions with discovery therapeutic areas, and affiliated non-clinical, clinical development and regulatory functions
* Steering non-clinical safety evaluations for potential in-licensing opportunities as well as representing non-clinical safety on collaborations with external partners
* Generating concise safety assessments for internal decision-making, as well as regulatory submission documentation to faci...
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Type: Permanent Location: Basel, CH-BS
Salary / Rate: Not Specified
Posted: 2025-08-07 08:17:23
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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
A healthier future.
It’s what drives us to innovate.
To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come.
Creating a world where we all have more time with the people we love.
That’s what makes us Roche.
In Roche´s Pharmaceutical Research and Early Development organisation (pRED), we make transformative medicines for patients in order to tackle some of the world’s toughest unmet healthcare needs.
At pRED, we are united by our mission to transform science into medicine.
Together, we create a culture defined by curiosity, responsibility and humility, where our talented people are empowered and inspired to bring forward extraordinary life-changing innovation at speed.
pRED's Pharmaceutical Sciences (PS) group enables discovery and development of safe and effective therapeutics at optimal doses in relevant populations with a vision to power translation, continuously improve the accuracy of our predictions and accelerate the development of tomorrow's medicines.
PS supports discovery and development across the whole value chain from target assessment to on-market and beyond.
In the Translational PKPD and Clinical Pharmacology chapter, our purpose is to select the right drug to deliver the right dose and dosing schedule to patients to provide a meaningful benefit through strong collaboration, strategic thinking and regulatory and scientific excellence.
The Opportunity
As Neuroscience (NRD) Clinical Pharmacology subchapter leader for the clinical pharmacologists, you oversee the therapeutic area from end to end with a strategic and systems view, and ensure the functional excellence of the deliverables as well as the people leadership. Interacting with key stakeholders is part of your core competencies, as are excellent communication skills. This leadership role is embedded in the Translational PKPD and Clinical Pharmacology chapter, where key contributions to programs are provided from pre-target assessment to established products.
Key areas of impact within this role include:
People leadership
* Line management responsibilities in line with P&C practices to promote development, performance, balanced resourcing and well-being of the colleagues.
* Build a strategy for workforce planning and implement it
* Demonstrate agile leadership skills and exemplary Roche operating practices.
* Embrace agile ways of working and catalyze individual contributor contributions.
...
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Type: Permanent Location: Basel, CH-BS
Salary / Rate: Not Specified
Posted: 2025-08-07 08:17:21
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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: 2025-08-06 08:55:24
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At MTM Transit, it is never just a ride, it's personal.
We understand that our passengers deserve personalized attention and exceptional care and to us, every trip is important.
We have exciting opportunities to join our growing team where your work has a direct impact on the communities we serve.
Our company culture is one of innovation, collaboration, and growth.
If you are passionate, driven, and ready to join a team where your work will directly transform and shape our industry, then we want to talk to you!
What will your job look like?
The Manager, Safety and Training is responsible for implementing safety and training programs as defined by the Leadership of Safety Administration and will ensure compliance with State and Federal regulations, as well as corporate, client guidelines and policies.
Location: 50 E 6th Street Tracy, CA 95376
What you’ll do:
* Manage a consistent safety culture that incorporates various departments, such as operations, safety and maintenance
* Oversee Corporate Safety Incentives and programs effectively and consistently, including assignment of Safety Points
* Implement and support the company and client’s safety management system (SMS) safety plan and initiatives Manage and monitor the FTA’s drug and alcohol DAMIS reporting requirements
* Monitor and support all location insurance claims activities to ensure effective communication with claimants, to help control claims costs and support claims closure
* Lead and support the local safety committee and SMS Ambassador group
* Oversees the locations worker compensation program to ensure compliance and effectively reduce/eliminate claims
* Deliver proper classroom, behind the wheel and mobility management training in accordance with contractual and company requirements
* Promote employee self-responsibility to achieve all safety goals and training requirements
* Ensures all new hires meet minimum qualifications for each division including, background and DMV checks
* Ensure all safety manuals, programs and policies and practices are current and meet the needs of the operating divisions; updating as appropriate
* Successfully complete all related audits including those conducted by the Company, the Client, internal staff members, and state and federal regulatory agencies
* Review, determine and respond to all vehicular, passenger and employee accidents/incidents, indicating the cause and preventability, identifying potential trends to be addressed in future training efforts
* Provide functional expertise in safety regarding hiring of safety department employees
* Collaborate with local Leadership to deliver comprehensive safety meetings and plans
* Act as the location drug program manager, ensuring compliance of FTA/DOT regulations
What you’ll need:
Experience, Education & Certifications:
* High School Diploma or G.E.D.
* Bachelor’s Degree (or equivalent combinati...
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Type: Permanent Location: Tracy, US-CA
Salary / Rate: Not Specified
Posted: 2025-08-06 08:23:58
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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:
Sales Enablement
Job Sub Function:
Sales Operations & Administration
Job Category:
People Leader
All Job Posting Locations:
Shanghai, China
Job Description:
Assistant SO Manager
主要职责：
运营管理
* 快速学习和了解公司规章制度、熟悉并精通相关运营流程。
* 监督呼叫中心日常运营，确保流程高效、合规。
* 有效识别和解决运营中的问题，持续优化工作流程。
* 处理升级的客户投诉和复杂问题，确保及时有效解决问题。
* 负责呼叫中心相关数据报告并能有效分析和洞察，识别提升效率、质量和客户满意度的机会。
* 协助制定和管理呼叫中心运营预算，负责相关费用结算工作。通过监控成本支出，寻求成本优化方案。
* 与跨职能团队进行有效沟通与合作。
供应商管理：
* 能指导和辅导第三方团队成员，定期给与相关培训。
* 设定可衡量的绩效目标，提供定期反馈和辅导，解决人员问题。
* 管理排班和人员配置水平，确保满足服务水平和业务需求。
学历要求：
* 本科及以上学历，商业管理专业优先。
技能和背景要求：
* 5年+项目管理，呼叫中心管理工作优先。
* 具备较强的学习能力和分析能力，了解数据可视化领域； 注重细节，结果导向。
* 出色的团队合作精神和跨团队沟通能力、积极主动的态度以及独立解决问题的能力。有过带人经验者优先。
* 优秀的冲突解决和谈判技巧。
* 精通中英文口语和写作。
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Type: Permanent Location: Shanghai, CN-31
Salary / Rate: Not Specified
Posted: 2025-08-06 08:17:19
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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:
Marketing
Job Sub Function:
Strategic Marketing
Job Category:
Professional
All Job Posting Locations:
Santa Clara, California, United States of America
Job Description:
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/.
Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments.
Ready to join a team that’s pioneering the development and commercialization of Intravascular Lithotripsy (IVL) to treat complex calcified cardiovascular disease.
Our Shockwave Medical portfolio aims to establish a new standard of care for medical device treatment of atherosclerotic cardiovascular disease through its differentiated and proprietary local delivery of sonic pressure waves for the treatment of calcified plaque.
Johnson & Johnson is a leading innovator in cardiovascular medical technology, committed to transforming patient outcomes through cutting-edge solutions.
Our mission is to improve lives by developing and delivering pioneering treatments that address critical cardiovascular conditions.
We are seeking a visionary and strategic Principal Product Manager – Portfolio Marketing to lead market and technology development initiatives for a novel and transformative technology platform.
In this cross-functional leadership role, you will be responsible for driving portfolio-level go-to-market strategies, shaping emerging market opportunities, and aligning technological advancements with customer needs and market trends.
This is a unique opportunity to define the future of an innovative technology in a fast-paced, high-growth environment.
Essential Job Functions
* Develop and refine the value proposition and portfolio strategy for a novel technology platform
* Partner with R&D and clinical to understand the potential applications for novel technology
* Serve as a thought leader and spokesperson for the technology both...
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Type: Permanent Location: Santa Clara, US-CA
Salary / Rate: Not Specified
Posted: 2025-08-06 08:17:06
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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:
Business Support
Job Sub Function:
Administration & Secretarial
Job Category:
Business Enablement/Support
All Job Posting Locations:
High Wycombe, Buckinghamshire, United Kingdom
Job Description:
About Innovative Medicine
Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements.
Visionaries like you work on teams that save lives by developing the medicines of tomorrow.
Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.
Learn more at https://www.jnj.com/innovative-medicine
Johnson & Johnson is currently seeking a Lead Administrative Assistant to join our team of Global Clinical Operations organization, Business Operations, Centralized Admin Team, Executive Support CoE to be based in High Wycombe, UK.
Global Clinical Operations plays a vital role in this mission, supporting the journey to bring medicines to patients and make a real difference in their lives.
Join our team and be part of a global organization dedicated to innovation, impactful initiatives, and creating a healthier future.
Are you an organized, proactive, and dependable professional with proven experience supporting executive leadership?
Johnson & Johnson’s GCO is seeking a dedicated Lead Administrative Assistant to provide top-tier support to our Vice President and a key director.
In this dynamic position, you will be the backbone supporting our leadership team by managing complex calendars, coordinating domestic and international travel, preparing key documentation, and facilitating smooth operations across multiple projects and teams.
Your attention to detail, confidentiality, and ability to prioritize will be integral to your success.
Additionally, you will have the opportunity to engage with peers from around the world and contribute to central administrative activities within the Centralized Admin Network (CAN).
Key Responsibilities:
* Manage the Vice President and one director's complex, dynamic calendars, coordinating meetings and appointments across multiple time zones to optimize their schedules.
* Arrange domestic and international travel, including itineraries, hotel bookings, visas, and transfers, with keen attention to detail and discretion.
* Prepare, reconcile, and submit monthly expense reports efficiently.
* Facilitate clear ...
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Type: Permanent Location: High Wycombe, GB-BKM
Salary / Rate: Not Specified
Posted: 2025-08-06 08:16:44
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Safety & Health Manager
Job Description
The Safety and Health (S&H) Manager is responsible for developing, implementing, and overseeing safety and health programs within a tissue production facility, ensuring that all employees work in a safe environment in compliance with safety standards and regulations.
This role involves identifying potential risks, implementing preventive measures, and investigating incidents to drive continuous improvement.
The Safety and Health Manager will collaborate with various departments to promote a culture of safety and facilitate ongoing improvements.
Primary Location
Taiwan-Chung-Li
Additional Locations
Worker Type
Employee
Worker Sub-Type
Regular
Time Type
Full time
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Type: Permanent Location: Hsin Wu Hsiang, TW-TAO
Salary / Rate: Not Specified
Posted: 2025-08-05 08:35:06
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Job Description
The Postdoctoral Scientist will engage in advanced research in the field of infrastructure systems and disaster resilience within the Department of Civil, Environmental, and Ocean Engineering.
The candidate will contribute to federally funded projects focused on data-driven decision-making, artificial intelligence applications in infrastructure assessment, and risk-informed planning under the supervision of Dr.
Mohammad Ilbeigi.
Responsibilities include designing and conducting experiments, developing analytical and computational models, publishing peer-reviewed journal articles, mentoring graduate students, and contributing to proposal development and collaborative research efforts.
Key Responsibilities:
* Conduct independent and collaborative research on infrastructure systems, AI integration, or resilience modeling
* Analyze large datasets and develop computational tools or machine learning models
* Prepare high-impact publications and conference presentations
* Support the preparation of technical reports and research proposals
* Assist with the supervision and mentoring of graduate and undergraduate researchers
Qualifications:
* Ph.D.
in Civil Engineering, Systems Engineering, Computer Science, or a related field
* Demonstrated experience in data analysis, modeling, or AI/ML applications
* Strong publication record in relevant peer-reviewed journals
* Excellent written and verbal communication skills
* Ability to work independently and collaboratively in a multidisciplinary team
Department
Built Environment
Compensation Range
In compliance with the New Jersey Wage Transparency Act, the annual base range for this position is .
This range represents the University’s good faith estimate of possible compensation at the time of posting.
Stevens Institute of Technology determines compensation based on factors including the position’s scope and responsibilities, the candidate’s experience, education, skills, internal equity, market data, and organizational considerations.
The final salary will be set considering departmental budget, qualifications, and relevant credentials.
This pay range represents base pay only and excludes additional forms of compensation, such as incentives, stipends, or other applicable pay components.
For a full overview of our benefits offerings, please refer to the Stevens Institute of Technology Benefits Guidebook, available at:
Benefits Guidebook
General Submission Guidelines:
Please submit an online application to be considered a candidate for any job at Stevens.
Please attach a cover letter and resume with each application.
Other requirements for consideration may depend on the job.
Still Have Questions?
If you have any questions regarding your application, please contact Jobs@Stevens.edu.
EEO Statement:
Stevens Institute of Technology is an Equal Opportunity Employer.
Accordingly, Stevens adheres to an em...
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Type: Permanent Location: Hoboken, US-NJ
Salary / Rate: Not Specified
Posted: 2025-08-05 08:28:42
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ERM is hiring a Construction Safety Manager onsite at a key technology clients Data Center construction project in Port Washinton, Wisconsin. In this critical role, you will be responsible for establishing, implementing, managing, and continuously improving the safety programs.
The Construction Safety Manager will have broad knowledge of Safety compliance programs and, where required, Safety specialty areas.
This is a tactical role for site-wide Safety systems, Safety regulations, and best practices.
This is a full-time (50+ hours a week), limited-term role for a duration of 12 months, extendable.
RESPONBILITIES:
* Champion a strong safety culture across the site and maximize personnel involvement in Safety related activities.
* Provide timely, high quality safety technical support.
* Carry out regular workplace inspections to monitor compliance with site rules, procedures, etc.
* Coordinate the completion of job safety analyses, risk assessments and pre-task plans.
* Prepare and submit local, state, and internal reports as needed.
* Review and track investigations of injuries, illnesses, environmental releases, non-injury accidents and near-misses to ensure that they are effective, and that they identify and resolve root causes.
Lead investigations into serious adverse events.
Monitor and analyze safety performance and initiate action to support or correct trends.
* Coordinate local business continuity, emergency response, and crisis management plans.
Develop and test the plans.
REQUIREMENTS:
* Bachelor’s degree in safety, occupational health, engineering, or related degree is preferred.
* Minimum 5 years’ experience with H&S in the construction industry, 2 years of data center construction project experience preferred.
CHST/CSP certification a plus.
* Proficient with the management of high-risk activities including electrical safety, excavation, fall protection, material handling, and crane operations.
* Experienced in communicating and problem solving as a team with sub-contractors is required.
* A background and knowledge working with specific trades such as electricians, ironworkers, pipefitters etc.
is a plus.
* Understanding of the complexities of multi-employer worksites.
* Experienced trainer on construction safety topics and comfortable working with a wide variety of trades.
* Demonstrated experience conducting construction site safety audits and inspections.
* Experience conducting incident investigations and can follow reporting processes.
* Excellent written and verbal communicator who understands the importance of timely communications and reporting.
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Type: Permanent Location: Milwaukee, US-WI
Salary / Rate: Not Specified
Posted: 2025-08-04 08:18:42
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ERM is hiring a Construction Safety Manager onsite at a key technology clients Data Center construction project in Abilene, Texas. In this critical role, you will be responsible for establishing, implementing, managing, and continuously improving the safety programs.
The Construction Safety Manager will have broad knowledge of Safety compliance programs and, where required, Safety specialty areas.
This is a tactical role for site-wide Safety systems, Safety regulations, and best practices.
This is a full-time (50+ hours a week), limited-term role for a duration of 12 months, extendable.
RESPONBILITIES:
* Champion a strong safety culture across the site and maximize personnel involvement in Safety related activities.
* Provide timely, high quality safety technical support.
* Carry out regular workplace inspections to monitor compliance with site rules, procedures, etc.
* Coordinate the completion of job safety analyses, risk assessments and pre-task plans.
* Prepare and submit local, state, and internal reports as needed.
* Review and track investigations of injuries, illnesses, environmental releases, non-injury accidents and near-misses to ensure that they are effective, and that they identify and resolve root causes.
Lead investigations into serious adverse events.
Monitor and analyze safety performance and initiate action to support or correct trends.
* Coordinate local business continuity, emergency response, and crisis management plans.
Develop and test the plans.
REQUIREMENTS:
* Bachelor’s degree in safety, occupational health, engineering, or related degree is preferred.
* Minimum 5 years’ experience with H&S in the construction industry, 2 years of data center construction project experience preferred.
CHST/CSP certification a plus.
* Proficient with the management of high-risk activities including electrical safety, excavation, fall protection, material handling, and crane operations.
* Experienced in communicating and problem solving as a team with sub-contractors is required.
* A background and knowledge working with specific trades such as electricians, ironworkers, pipefitters etc.
is a plus.
* Understanding of the complexities of multi-employer worksites.
* Experienced trainer on construction safety topics and comfortable working with a wide variety of trades.
* Demonstrated experience conducting construction site safety audits and inspections.
* Experience conducting incident investigations and can follow reporting processes.
* Excellent written and verbal communicator who understands the importance of timely communications and reporting.
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Type: Permanent Location: Houston, US-TX
Salary / Rate: Not Specified
Posted: 2025-08-04 08:18:41
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ERM is hiring a motivated hands-on Senior Environmental, Health and Safety (EHS) Consultant to join our growing Performance & Assurance technical team in Sunnyvale, California. This position is expected to involve working a minimum of 3 days on-site. This is a fixed-term, full-time role (40 hours a week) for a duration of 4 months, renewable.
The ideal candidate will have experience developing and supporting implementation of Cal/OSHA requirements, Standard Operating Procedures, Job Hazard Analysis/ Risk Assessments, Emergency Response Plans, Behavioral Safety Programs and Contractor Safety Management. Candidates should also have familiarity with research laboratory safety requirements, waste management (hazardous, non-hazardous, universal/ electronic), environmental reporting (HMBPs), and chemical safety requirements.
RESPONSIBILITIES:
* Oversee and direct team members to effectively manage tasks for on-time delivery and quality of their deliverables.
* Perform compliance audits to assess client compliance with applicable health and safety or environmental regulatory requirements, client standards, or management systems.
* Support our clients’ desire to improve safety performance by providing training, field coaching, and targeted EHS assessments.
* Identify follow-up corrective actions to close audit findings.
* Provide technical assistance on EHS compliance and EHS management system projects on a range of areas such as R&D laboratory safety, chemical safety, machine guarding, laser safety, robotics safety, hazardous materials use/storage/waste, EHS auditing.
* Develop and implement EHS compliance procedures, plans, permits, and reports.
* Manage tasks within assigned scope/budget/schedule and ensure quality standards on project deliverables.
* Build client relationships and nurture repeat business by continuously striving to exceed their expectations.
* Support ERM Partners and Project Managers to effectively manage and deliver projects.
* Build strong collaborative relationships with other ERM employees.
REQUIREMENTS:
* BS in engineering, environmental science, occupational health and safety, or related discipline preferred.
* A minimum of 7 years of applicable experience providing EHS support with an emphasis on health and safety.
* Effective written/verbal communication and organization/analytical skills; experience recording/writing detailed technical data and reports a plus.
* Ability to succeed in a fast-paced consulting environment, handling multiple assignments, meeting strict deadlines, and being able to re-prioritize tasks as-needed.
* Valid driver’s license and good driving record.
Pay Transparency:
For the Environmental, Health and Safety (EHS) Consultant position, we anticipate the annual base pay of $76,000– $97,400, $36.54/hr - $46.82/hr USD, limited-term, non-exempt. An employee’s pay position within this range will be based on ...
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Type: Permanent Location: San Francisco, US-CA
Salary / Rate: Not Specified
Posted: 2025-08-04 08:18:40
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ERM is hiring a Construction Safety Specialist for a key technology client in the Sunnyvale, CA.
In this critical role, you will be responsible for establishing, implementing, managing, and continuously improving the safety programs for several ongoing construction projects.
The Construction Safety Specialist will have broad knowledge of Safety compliance programs and, where required, Safety specialty areas.
This is a tactical role for site-wide Safety systems, Safety regulations, and best practices.
This is a full-time (40 hours), fixed-term position for a duration of six months (6 months).
RESPONBILITIES:
* Champion a strong safety culture across the site and maximize personnel involvement in Safety related activities.
* Act as Owner’s representative while inter-acting with contractors.
* Provide daily observations of on-site safety practices.
* Provide timely, high quality Safety technical support.
* Carry out regular workplace inspections to monitor compliance with site rules, procedures, etc.
* Coordinate the completion of job safety analyses, risk assessments and pre-task plans
* Prepare and submit local, State, and internal reports as needed.
* Review and track investigations of injuries, illnesses, environmental releases, non-injury accidents and near-misses to ensure that they are effective, and that they identify and resolve root causes.
Lead investigations into serious adverse events.
Monitor and analyze Safety performance and initiate action to support or correct trends.
REQUIREMENTS:
* Bachelor’s degree in safety, occupational health, engineering, or related degree is preferred.
* Minimum 5 years’ experience with H&S in the construction industry, preferably with commercial/office building construction or large projects.
CHST certification a plus.
* Proficient with the management of high-risk activities including electrical safety, excavation, confined spaces, fall protection, material handling, rigging and crane operations.
* Experienced in communicating and problem solving as a team with sub-contractors is required.
* A background and knowledge working with specific trades such as electricians, ironworkers, pipefitters etc.
is a plus.
* Understanding of the complexities of multi-employer worksites.
* Experienced trainer on construction safety topics and comfortable working with a wide variety of trades.
* Demonstrated experience conducting construction site safety audits and inspections.
* Experience conducting incident investigations and can follow reporting processes.
* Excellent written and verbal communicator who understands the importance of timely communications and reporting.
Pay Transparency:
For the Field Safety Inspector position we anticipate the annual base pay of $91,998.40 – $109,990.40, $44.23– $52.88/hr, limited-term, non-exempt. An employee’s pay position within this range will be based on several fa...
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Type: Permanent Location: Walnut Creek, US-CA
Salary / Rate: Not Specified
Posted: 2025-08-04 08:18:38
