Principal Regulatory Strategy Lead - Ophthalmic Devices
Merck & Co.
Merck & Co. is seeking a Principal Regulatory Affairs Strategy Associate based in Lake Forest, CA. This role involves setting and executing regulatory strategies for health registrations and product approvals, collaborating with cross-functional teams to ensure compliance and drive competitive advantages. The ideal candidate will have a Bachelor’s Degree, at least 7 years of relevant experience, and demonstrated leadership skills. This position requires a self-starter who can manage multiple projects and adhere to GxP regulations. #J-18808-Ljbffr Merck & Co.
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$146.25k - $243.75k
...to join Alcon. As a Sr. Principal, Clinical Development Project Lead , you will be trusted to... ...trials for medical devices and related products, ensuring... ...excellence, and regulatory compliance across global... ...enhance future clinical strategies Supporting Global Medical...PrincipalRegulatoryFlexible hours- ...improvement. The ideal candidate will have expertise in inspection techniques, regulatory compliance, and strong leadership skills. Join Applied Medical to contribute to the excellence in medical devices with competitive compensation and numerous benefits. #J-18808-Ljbffr...Regulatory
- Principal Regulatory Affairs Strategy Associate Exciting development Principal Regulatory... ...brilliantly. The largest device company in the world - with... ...compliance activities for ophthalmic products. This role partners... ...compliance initiatives. Lead regulatory strategy and support...RegulatoryContract work
$160k - $180k
Principal Consultant - Automation Engineering Manager... ...provide outstanding Project Strategy and Delivery. Who We... ..., Biotech, and Med Device clients to make a... ...utilities Strong experience leading large-scale capital... ...cGMP/cGxP requirements, regulatory expectations, and...PrincipalRegulatoryFull timeTemporary workRemote workHome office- Principle Regulatory Affairs Strategy Associate The Principle Regulatory Affairs Strategy Associate, reporting... ...executing the regulatory strategy, leading and managing, acting as a strategist,... .... Support products in the medical device and/or pharmaceutical families,...RegulatoryLocal area
$170k - $200k
...For 45 years, Balt has been leading the way - collaborating... ...to develop elegant medical devices. Our products are being used... ...this opportunity - Senior Principal Regulatory Affairs Specialist Description... ...global regulatory strategies for complex, high-risk medical...PrincipalRegulatory- ## Senior Manager, Regulatory Affairs StrategyApplyremote type: Not applicablelocations... ...Manager, Regulatory Affairs Strategy (Professional Path),... ...the regulatory strategy, leading and managing, acting as a... ...Support products in the medical device and/or pharmaceutical...RegulatoryHourly payTemporary workLocal areaRelocation packageFlexible hours
$104k - $156k
...outcomes. The Principal II, Optical Engineering... ...responsible for leading teams in... ...high-precision and regulatory requirements Apply... ...Engineering in Ophthalmic related Diagnostic... ...for new medical device products. Investigate... ...the corporation strategy development....PrincipalRegulatoryTemporary workVisa sponsorshipRelocation packageFlexible hours- ...Title: Software Engineer, Principal (Test) Department:... ...for innovation, leads to enduring outcomes.... ...and implement testing strategies for our 3D cardiac mapping... ..., traceability, and regulatory submission readiness.... ...processes for medical device software. ~ Track...PrincipalRegulatory
- Alcon MX is seeking a Sr. Principal, Clinical Development Project Lead to manage and lead clinical trials for medical devices. This role includes... ...trial budgets, ensuring regulatory compliance, and driving... ...through impactful clinical strategies. #J-18808-Ljbffr Alcon...Regulatory
- A leading eye care company in Lake Forest, California, is seeking a Director of Regulatory Affairs Strategy. This role involves leading regulatory teams, developing and executing strategies for product approvals, and ensuring adherence to global regulatory requirements....Regulatory
$18 - $23 per hour
A medical device company in California is hiring a Quality Inspector to ensure the safety and compliance of medical devices after clinical... ..., and collaboration with teams to support product quality and regulatory compliance. Candidates should have a high school diploma and a...RegulatoryHourly pay- ...Export Control Principal Specialist A growing, highly regulated organization is seeking... ...Principal Specialist (Direct Hire) to lead and strengthen its global trade compliance... ...subject matter expert, driving regulatory strategy while ensuring adherence to U.S. and international...PrincipalRegulatoryWork at officeRemote work
- Applied Medical in Rancho Santa Margarita is seeking an Associate Labeling Specialist to support regulatory labeling strategy and compliance. This position involves managing labeling projects, ensuring alignment with global regulations, and collaborating with cross-functional...Regulatory
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...lives around the world. The Principal Engineer will lead the development of... ...automation, inspection, and regulatory compliance are intentionally... ...functional specifications, control strategies, test plans, and risk... ...for Class III medical devices, balancing innovation with...PrincipalRegulatoryFull time- ...Job Description The Asset Strategy Leader is an experienced and... ..., Commercial, Market Access, Regulatory, Safety, Project Management,... ...broad vision for the asset and leads the effort to create, articulate... ...bodies of Aesthetics Device Governance Board, Tri-Function...RegulatoryFull timeTemporary workLocal area
- ...Job Title: Medical Device Cybersecurity Risk Specialist Work Location: Irvine, California... ...introductions. • Familiarity with regulatory and compliance expectations relevant to... ...validate, and track approved mitigation strategies and alternative risk treatment options where...Regulatory
- ...Health Economics & Outcomes Research (HEOR) leads the strategic development & execution of... ...are reflected in the overall asset strategy. He or she may be accountable for more... ...support. Extensive knowledge of the global regulatory, HTA and PR&A landscape, as well as...RegulatoryFull timeTemporary workWork experience placementLocal area
$121k - $171k
...your knowledge of the medical device industry. Whether your work... ...PMO, Design Assurance (DA), Regulatory, to align on goals and drive... ...successful outcomes for the business. Lead the development and... ...across the business. Drive build strategy, prioritization, and technical...PrincipalRegulatoryFull time$121k - $171k
...transform patient care with devices supported by clinical... ...journey. This Principal Quality Engineer, NPD... ...to meet commitments. · Lead development and drive... ...with functional growth strategies of the individual and... ...Domestic and International regulatory requirements of...PrincipalRegulatoryFull timeLocal area$160k - $210k
...quality, FDA-cleared medical device at scale. The ideal candidate... ...Manufacturing & Production Lead selection and onboarding of... ...levels, including buffer strategies for Year 1 launch. Monitor... ...disruptions. Quality & Regulatory Compliance Maintain and...RegulatoryFull timeContract workWork at officeRemote workFlexible hours$120k - $140k
...Kardion Kardion is a medical device company advancing innovative... ...seeking a Global Logistics Lead to ensure efficient and... ...functional partners in Quality, Regulatory, Clinical, R&D, Finance, and... ...providers. Define and execute strategies to enhance the logistics...RegulatoryFull time- ...drive programs and manage sponsor partnerships in Laguna Hills, California. You will play a pivotal role by developing and executing strategies that ensure collection goals are met, while also providing support to volunteers and maintaining communication channels with...
- ...Manufacturing Team Leader to oversee production operations, guide team members, and ensure the efficient manufacturing of high-quality medical devices. This role involves collaborating with cross-functional teams to implement process improvements and uphold the company's...
- A global technology company seeks a Senior Certification Engineer to lead regulatory compliance and certification for PLC-based products used in hazardous locations. The ideal candidate will have over 8 years of experience in product safety and regulatory compliance, with...Regulatory
$124.7k - $205.8k
...possible with us. Responsibilities The Principal Electrical Engineer, R&D will support Electronic... ...of electronic hardware used in medical device systems. Strong emphasis on Electrical... ...in designing for and testing to Regulatory standards such as IEC/EN60601-1 and IEC/...PrincipalRegulatoryWork at officeRemote workShift work- AVEVA Denmark is looking for a Principal Software Engineer to design Microsoft Azure cloud solutions. The ideal candidate will lead AI adoption, ensuring alignment with Hypervelocity Engineering principles, while using Angular, C#, and AI tools. Qualifications include...Principal
- ...teams. The ideal candidate will have a Bachelor's degree and over 2 years of experience in the medical device industry, focusing on quality assurance and regulatory compliance. Strong communication and problem-solving skills are essential, along with knowledge of ISO standards...Regulatory
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