Senior Regulatory Project Lead - Medical Devices
West Pharmaceutical Services / Progressive Medical
West Pharmaceutical Services is seeking a Senior Specialist, Regulatory Project Management to lead regulatory execution for a global portfolio of medical devices, combination products and SaMDs. The role partners with Regulatory Affairs Leads and cross‑functional SMEs to drive deliverables from development through post‑market lifecycle. The successful candidate will bring expertise in medical device regulatory frameworks, project management, and lifecycle planning to ensure timely, compliant #J-18808-Ljbffr West Pharmaceutical Services / Progressive Medical
- ...Johnson & Johnson seeks a Senior Regulatory Affairs Specialist to coordinate and submit medical device applications to regulatory authorities for orthopaedic products. The role involves managing regulatory submissions, monitoring compliance, and providing strategic input...SeniorRegulatoryMedical device
- ...including parenteral packaging, device, and contract manufacturing... ...-quality execution of all regulatory deliverables and ensures compliance... ...effectively communicate team/project progress/status, decisions,... ...of global pharmaceutical, medical device, and related environmental...SeniorRegulatoryMedical deviceContract workLocal areaRelocationFlexible hours3 days per week
- ...efforts. Job SummaryThe Senior Director, Scientific... ...Affairs is responsible for leading the Scientific Affairs... ..., materials, regulatory expectations, and emerging... ...scientific, technical service, medical affairs, or scientific... ...delivery, medical device, biotechnology, life...SeniorRegulatoryMedical deviceRelocation
- ...sustainability efforts. Job SummaryThe Regulatory Affairs Senior Specialist is responsible for... ...ResponsibilitiesDevelop and implement medical device regulatory strategies for West’s Transfer... ...and effectively communicate team/project progress/status, decisions, timelines...SeniorRegulatoryMedical deviceFull timeTemporary workLocal areaRelocationFlexible hours3 days per week
- ...consistent implementation, regulatory compliance, risk-... ...requirements. The Senior Quality Specialist... ...& Combination Devices. Essential Duties... ....Serve as Quality lead or work package... ...other quality-related projects.Ensure quality... ...environment ideally in the medical device /...SeniorRegulatoryMedical deviceWork at officeLocal areaRelocationFlexible hours3 days per week
- ...Position Overview: The Senior Mechanical Engineer is... ...and coordinating projects internally within... ...Engineer is responsible for leading and mentoring lower-... ...development of marketing, regulatory, and training... ...design and development of medical device systems or other FDA regulated...SeniorRegulatoryMedical deviceFull timeContract workTemporary workApprenticeshipWork at officeLocal areaWork visaFlexible hours
- ...analytical testing to advance R&D clinical projects and deliver commercial supplies.... ...reports, as required. Data Quality and Regulatory Analysis Review analytical release and... ...within the pharmaceutical and/or medical device industries, combination products, peptides...SeniorRegulatoryMedical deviceFull timeContract workWork at office
- ...to business needs, role expectations, regulatory requirements, and West standards. This... ..., content development capability, project management discipline, and the ability... ..., quality, healthcare, pharmaceutical, medical device, or regulated environment. Experience...SeniorRegulatoryMedical deviceWork experience placementWork at officeLocal areaRelocation3 days per week
- Tetra Tech's King of Prussia, PA office is hiring a Senior Project Manager to lead multidisciplinary geology and engineering projects focusing on... ...experience. Join a team delivering hazardous waste assessments, regulatory compliance, and sustainable design using Civil 3D and...SeniorRegulatoryWork at office
- ...our future? Job Summary The Senior Manager, Responsible Sourcing... ..., procurement strategy, and regulatory requirements. This role... ...engagement and compliance actions. Lead development of tools,... ...industries like pharmaceuticals or medical devices. High drive to operate with...SeniorRegulatoryMedical deviceWork experience placementLocal areaRelocationFlexible hours3 days per week
- The QC Senior Scientist - Microbiology is responsible for Test drug... ...analysts, supports product regulatory submissions and inspections,... ...provide YOU the opportunity to lead key activities to progress... ...pharmaceutical, biotechnology, medical device, or healthcare environment.Experience...SeniorRegulatoryMedical deviceFull timeLocal area
$130k - $209k
...Product Manager, MCT Clinical SystemsAs our Senior Product Manager within Philips... ...prioritize value based on market trends and regulatory requirements. Continuously optimize... ...years of experience in product management. Medical Device experience is required.Your skills...SeniorRegulatoryMedical deviceFull timeWork experience placementWork at officeLocal areaImmediate startWork visaRelocation package3 days per week- We Are TevaWe’re Teva, a leading innovative biopharmaceutical company... ...Team, Your ImpactFor the Senior Device Engineer position we are... ...engineer with experience in medical device, pharmaceutical, or combination... ...programs, support regulatory and quality objectives, and...SeniorRegulatoryMedical deviceContract workLocal areaWorldwideFlexible hoursShift work
- ...Job Title: Senior Clinical Project Manager Location: Remote... ...Clinical Project Manager to lead complex clinical... ...relationships, and ensure regulatory compliance. The role... ...years Complete medical writing study reports... ...with medical device research, especially...SeniorRegulatoryMedical deviceZero hours contractLocal areaRemote work
- ...planet through our sustainability efforts. Job Summary The Senior Specialist, Regulatory Project Management is responsible for leading regulatory project execution for West’s global portfolio of medical devices, combination products, software-enabled devices/SaMDs, and...SeniorRegulatoryMedical deviceContract workTemporary workWork at office3 days per week
- ...sustainability efforts. Job Summary The Senior Manager, Marketing,... ...solutions. This role leads execution of go‑to‑market programs... ...translate customer needs, regulatory considerations, and West’s... ...pharmaceutical, biotechnology, medical device, or other highly regulated B...SeniorRegulatoryMedical deviceWork experience placementRelocation3 days per week
- ...- Knowledge of basic medical terminology - Proficiency... ...Post Market Regulatory Affairs activities associated... ...determination associated Medical Device Report and/or... ...- Participate in projects and events - Complaint... ...ScienceExperience level: Mid-Senior LevelIndustry:...RegulatoryMedical deviceWork experience placement
- Job Title: Senior Scientist / Principal Scientist - Biotransformation/Metabolite Identification.Location: Exton, PennsylvaniaFull-time... ....Prepare and review scientific reports, presentations, and regulatory documents to ensure accuracy and compliance with industry standards...SeniorRegulatory
- ...Remote50% Remote Job Description: Prepare regulatory documentation to support the market distribution of new and modified medical devices (510(k)/NTF) in US, Canada, and EU.... ...support to Regulatory Manager for special projects as needed. Responsibilities: Compile, prepare...RegulatoryMedical deviceLocal areaRemote work
- ...In this role, you will lead the research,... ...technologies for next‑generation medical devices, with a primary focus... ..., quality, regulatory, and product development... ...for complex research projects, serving as a subject... ...research findings to senior leadership and external...SeniorRegulatoryMedical deviceWork experience placementWork at officeRelocationRelocation packageFlexible hours
- ...will advise on fund formation, governance, regulatory compliance, and strategic initiatives.... ...team environment.Participate in special projects and perform other duties as assigned.... ...financial wellbeing of our clients. To lead through product and services that transform...SeniorRegulatoryFull timeWork experience placementWork at office
- ...through our sustainability efforts. Job SummaryThe Principal Regulatory Affairs Project Manager is responsible for leading complex, high‑visibility regulatory programs across West’s portfolio of medical devices, combination products, and packaging/containment systems....RegulatoryMedical deviceTemporary workRelocationFlexible hours3 days per week
$260k - $300k
...everything possible.The Senior Director, Medical & Scientific Affairs... ...business area and leading daily business operations... ...key strategic projects. This candidate will... ...product development, regulatory submissions, and marketing... ...technology, medical device, or pharmaceutical industry...SeniorRegulatoryMedical deviceFull timeRemote workWork from homeFlexible hours- ...Pharmaceutical Services is seeking a Principal Regulatory Affairs Project Manager for a hybrid role onsite at least 3 days per week. You will lead cross-functional teams to drive global... ..., manage complex submissions for medical devices and combination products, and ensure...RegulatoryMedical device3 days per week
$120k - $210k
...obligations, Treasury market and fixed income regulatory developments, and trading counterparty... ...years of relevant legal experience at a leading law firm and/or in-house. Experience... ...clearly to traders, portfolio managers, and senior management.Nice To Haves:Experience...SeniorRegulatoryFull time$109k - $174.8k
...Senior Scientist position in biomaterials research and development for medical device innovation within orthopaedics. Responsibilities include designing and testing biomaterials... ..., developing test methods, supporting regulatory submissions, and collaborating across cross...SeniorRegulatoryMedical device- WilsonHCG in Exton, PA is seeking a Senior Project Technician to lead execution on new Integrated Security projects. You will service, install, program, integrate and commission a range of security systems on-site for high-profile clients. The role requires hands-on expertise...Senior
- ...client experience, risk management, and operational efficiency.Lead modernization of money movement policies and controls to align... ...movement, banking, payments, or wealth management.Knowledge of regulatory and compliance considerations related to money movement activities...SeniorRegulatoryFull time
$122k - $212.75k
...Senior Manager position responsible for developing... ...and paid channels Lead communications planning... ..., and compliance with regulatory requirements and industry... ...or marketing within medical devices, healthcare, or life sciences... ...multiple simultaneous projects independently ~...SeniorRegulatoryMedical device- Senior Scientist-BiologicsTitle: Senior Scientist, Biologics Location: Exton,PA Full-timeFrontage... ...development of bioanalytical methods and lead sample analysis.Responsibilities:•... ...• Complies with all relevant GLP and FDA regulatory requirements while carrying out assigned...SeniorRegulatoryContract work
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