Senior PM - Medication Process & Regulatory Docs
Ll Oefentherapie
Ll Oefentherapie is seeking a Senior Product Manager to oversee product management, regulatory documentation, and software development across medication processes. The candidate will leverage their extensive experience in healthcare technology to ensure safety and compliance. This role demands collaboration with diverse teams, including engineering, regulatory, and clinical stakeholders. Ideal candidates will possess strong judgment and organizational skills, with a focus on delivering quality and trusted healthcare software. #J-18808-Ljbffr Ll Oefentherapie
- Oracle Health is seeking a Senior Product Manager to drive product management, regulatory and medical device documentation, cross‑functional delivery, and software development... ...lifecycle across Oracle Health’s medication process portfolio. This role will help ensure that...SeniorRegulatory
- Humacyte Inc. is seeking a Senior Medical Writer responsible for crafting clinical and regulatory documents. This role involves writing clinical protocols, study reports, and various regulatory documents, ensuring compliance with guidelines. The ideal candidate will have...SeniorRegulatoryRemote jobWork at office
- ...information, visit JOB SUMMARY: The Senior Medical Writer will be responsible for writing clinical and regulatory documents such as clinical... ...to improve medical writing processes and standards. Other Duties... ...systems (e.g., Google Docs, SharePoint). Familiarity with...SeniorRegulatoryTemporary workFor contractorsWork at officeLocal areaRemote workVisa sponsorship
$288.2k - $360.2k
...Pharmacovigilance and Risk Management (PVRM) Senior Medical Director will be responsible... ...approved labels, RMP/REMS, Regulatory Authorities safety inquiries,... ...Canadian Product Monograph (PM), and Risk Management Plans (... ...to make its application process accessible to all. If you...SeniorRegulatoryWork at officeLocal areaRemote workWorldwideFlexible hours- ...advice and expertise that empowers biotech, medical device, and pharmaceutical organizations... .... With deep domain expertise in regulatory sciences, clinical research solutions, quality... ...in departmental initiatives (e.g., process improvement, lunch and learns, etc.). Other...SeniorRegulatoryContract work
- ...brightest minds to create better, faster, smarter processes to speed therapies to patients that need them the most... ...based anywhere in the US. Summary: Serves as a senior medical writer on clinical study or regulatory project teams. Plans and coordinates report-writing...SeniorRegulatoryContract workWork from home
$95k - $210.9k
Sr. Principal Medical Writer - Regulatory Submission Docs (ISE/ISS/Clinical Overview - Must Have) - Oncology Preferred Syneos Health® is a leading fully... .... Has a broad understanding of clinical research processes and global regulatory document standards. Mentors...SeniorRegulatoryContract workFlexible hours- ...supports the pharmaceutical, biotech, and medical device industries with a proven, scientific approach to complex trial data and regulatory submission challenges. With a global... ...project team who are involved in the writing process Requirements At least 3 years of previous...SeniorRegulatoryRemote jobWorldwide
- Cardinal Health is looking for a Sr Regulatory Affairs Specialist to provide regulatory expertise for medical devices. This remote position involves supporting a diverse portfolio and ensuring compliance with regulations while collaborating with internal teams. The ideal...SeniorRegulatoryRemote job
- Description Discover your exciting role The Lead Process Engineer will serve as the technical... ...compliance with client specifications, regulatory standards, and project objectives.... ...e.g., pregnancy, childbirth and related medical conditions, sexual orientation, gender identity...SeniorRegulatoryLocal area
- ...years in product management, focusing on backend infrastructures, regulatory compliance, and innovative solutions. Candidates should have... ...teams. This position offers competitive benefits, including medical insurance and flexible time off. #J-18808-Ljbffr Inmar Inc.SeniorRegulatoryFlexible hours
$130k - $190k
Veristat, LLC is seeking a Senior Business Development Director to drive growth across Regulatory Science and Medical Writing services in the pharmaceutical and biotechnology sectors. The ideal candidate will have a strong background in sales, with a proven track record...SeniorRegulatoryRemote job$67.9k - $182.55k
...community at a time. A Brief Overview Leads medical underwriting strategy and execution... ...implementations, QLE administration, and regulatory requirements unique to the FI medical... ...benefits are provided during the application process and on Benefits Moments. We anticipate...SeniorRegulatoryHourly payFull timeTemporary workLocal area- A leading engineering consultancy in Raleigh is seeking a Sr. Process Engineer to support capital projects in the life sciences sector... ...in process system engineering and a solid understanding of regulatory standards. Qualified candidates will collaborate with multidisciplinary...SeniorRegulatory
- ...Medication Care Manager When you join Sunrise Senior Living, you will be able to use your unique skills to empower residents... ...medications. Follow re-fill process for medications and notify RCD... ...essential duties for safety and regulatory compliance About Sunrise...SeniorRegulatoryLocal areaImmediate startShift work
- ...engineering consulting firm in North Carolina seeks a Principal Process Engineer to lead API and OSD process design. The ideal... ...years of experience in pharmaceutical engineering, expertise in regulatory compliance, and strong business development skills. This position...SeniorRegulatory
- WakeMed, located in Raleigh, North Carolina, is seeking a Medical Laboratory Scientist III. The role involves performing routine and... ...bring leadership experience and be ready to mentor new staff while ensuring compliance with regulatory standards. #J-18808-Ljbffr WakeMedSeniorRegulatory
- ...Core Team Lead - Sr Manager to drive the delivery of a critical medical device product development project. You will manage cross-... ...You’ll play a key role in ensuring all technical, quality, and regulatory standards are upheld, while also managing budgets and resources...SeniorRegulatory
- ProPharma in Raleigh, North Carolina, seeks a skilled medical writer with at least 5 years of experience. The role involves authoring a variety of clinical and regulatory documents while ensuring adherence to regulatory standards. The ideal candidate will demonstrate strong...SeniorRegulatory
- ...This position is on the Digital Process Systems team within the... ...Cybersecurity & OT Analyst or a Senior Cybersecurity & OT Analyst depending... ...necessary to support nuclear regulatory compliance, unit outages, or... ..., childbirth or related medical conditions, including but not...SeniorRegulatoryWork experience placementCasual workWork at officeLocal areaNight shiftWeekend work
- INC Research is seeking a Senior Medical Writer to support clinical study and regulatory project teams. This position is home based anywhere in the US. The ideal candidate will mentor junior writers while managing complex medical writing tasks across various therapeutic...SeniorRegulatoryRemote jobWork from home
- MMS Holdings Inc in Raleigh, North Carolina, is seeking a Medical Writer to critically evaluate and write clinical development documents. Applicants should have at least 3-5 years of regulatory writing experience in the pharmaceutical industry and possess a relevant degree...SeniorRegulatoryRemote job
- ...with applicable regulations and Quality Systems while providing Process and Quality Engineering support. This role includes the... ...facilitate continuous improvement. Responsibilities include preparing regulatory filings, leading risk analysis activities, and providing...SeniorRegulatory
- ...strategies, developing product roadmaps, and ensuring compliance with regulatory standards. Candidates should possess a Bachelor’s degree in... .... This position offers comprehensive benefits, including medical, dental, and 401(k) plans. #J-18808-Ljbffr Dormont Manufacturing...SeniorRegulatory
- We are seeking a Senior Business Process Analyst to join our Business Performance Improvement (BPI... ...internal control validation. Oversee regulatory reporting processes and documentation... ...to travel up to 20%. Benefits Medical Prescription Drug Vision Dependent...SeniorRegulatoryTemporary work
- ...Medication Aide / Med Tech Deliver Safe, Accurate Medication Care for Our Residents At Sunrise Senior Living, we believe meaningful work starts with purpose. Our team members are... ...safety through attention to detail and regulatory compliance. What we're looking for:...SeniorRegulatoryShift work
$169.22k - $253k
...Senior Medical Science Liaison (Associate Director) As an integral member of the ecosystem team for Otsuka's new ecosystem-based customer... ...interactions. Strong understanding of industry legal, regulatory, and compliance landscape. Ability to work in an ambiguous...SeniorRegulatoryTemporary workWork experience placementWork at officeLocal areaRemote workFlexible hours$260k - $295k
...Senior Medical Director, US Immunology Medical Affairs At Sobi, we believe diversity drives innovation and inclusion creates stronger... ...collaborative relationships with internal partners, including Regulatory Affairs, Clinical Operations, Market Access, Medical Information...SeniorRegulatoryTemporary work- ...Medical Office Assistant Administrative Senior - UNC Family Medicine at Kildaire Become part of an inclusive... ...check in and check out procedures, processes financial information, files, answers... ...with established safety and regulatory guidelines, including HIPAA, OSHA...SeniorRegulatoryReliefWork at office
- Senior Healthcare Architect (NCARB Required) | Hospitals, Clinics & Medical Facilities A well-established and growing multidisciplinary Architecture & Engineering firm... ...while ensuring exceptional design quality, regulatory compliance, and successful project execution....SeniorRegulatoryWork at officeFlexible hours
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