Senior Regulatory Affairs Specialist
Experis
Our client, a regulated medical device and life sciences organization is seeking a Senior Regulatory Affairs Specialist to join their team. As a Senior Regulatory Affairs Specialist, you will be part of the Regulatory Affairs and Compliance organization supporting Emerging Regulatory Issues and Global Regulatory Operations. The ideal candidate will have strong cross-functional stakeholder leadership, the ability to manage complex compliance initiatives with clear accountability, and a deep understanding of international regulatory requirements—aligning successfully in the organization.
Job Title: Senior Regulatory Affairs SpecialistLocation:Santa Clara, CA - Hybrid (3 days onsite)
Contract 12 months with possible extension Pay Range: $49/hr on W2
What's the Job?
- Lead pan-franchise implementation of emerging global regulatory requirements across international markets.
- Assess new or changing international regulations to determine business impact, implementation needs, risks, and timelines.
- Coordinate cross-functional gap assessments and implementation plans to ensure regulatory requirements are incorporated into quality systems, procedures, labeling processes, and business operations.
- Support audit readiness by identifying compliance risks, quality system gaps, and remediation opportunities; track observations and commitments through completion.
- Drive regulatory operations and documentation activities, including change management, governance reporting, and process improvements that enhance efficiency, visibility, and compliance.
What's Needed?
- 5-7 years of experience in a regulated medical device, pharmaceutical, biotechnology, or other highly regulated industry within Regulatory Affairs, Regulatory Operations, Regulatory Compliance, Quality Systems, Compliance, or a related function.
- Strong understanding of international regulatory requirements and global compliance frameworks.
- Experience supporting implementation of regulatory or compliance requirements across cross-functional organizations.
- Strong project management, organizational, and stakeholder management skills, including the ability to influence without direct authority.
- Ability to work independently, handle multiple streams simultaneously, and drive issues through resolution with effective mitigations.
What's in it for me?
- Opportunity to support continued market access by translating emerging global regulatory requirements into practical, compliant execution.
- Visibility into compliance governance through KPI dashboards, trackers, and management review metrics.
- Collaboration across Regulatory Affairs, Quality, Labeling, Supply Chain, Legal, and international affiliate teams to drive timely outcomes.
- Experience strengthening audit readiness by tracking remediation and supporting internal, external, and regulatory inspections as needed.
- Chance to serve as an interim lead for the Emerging Issues SME team, supporting prioritization, coordination, and delivery.
Upon completion of waiting period consultants are eligible for:
- Medical
- Dental Plan
- Vision Plan
- 401(k)
- Weekly Pay
If this is a role that interests you and you'd like to learn more, click apply now and a recruiter will be in touch with you to discuss this great opportunity. We look forward to speaking with you!
About ManpowerGroup, Parent Company of: Manpower, Experis, Talent Solutions, and Jefferson Wells.
ManpowerGroup® (NYSE: MAN), the leading global workforce solutions company, helps organizations transform in a fast-changing world of work by sourcing, assessing, developing, and managing the talent that enables them to win. We develop innovative solutions for hundreds of thousands of organizations every year, providing them with skilled talent while finding meaningful, sustainable employment for millions of people across a wide range of industries and skills. Our expert family of brands – Manpower, Experis, Talent Solutions, and Jefferson Wells –creates substantial value for candidates and clients across more than 75 countries and territories and has done so for over 70 years. We are recognized consistently for our diversity - as a best place to work for Women, Inclusion, Equality and Disability and in 2023 ManpowerGroup was named one of the World's Most Ethical Companies for the 14th year - all confirming our position as the brand of choice for in-demand talent.
- ...help transform the future of healthcare, you’ll find your purpose here.Job DescriptionPrimary Function of Position The Sr. Regulatory Affairs Specialist’s primary responsibilities include developing regulatory plans, reviewing design input/output documentation,...SeniorLocal areaWorldwideFlexible hours
- ...ID Reference ?Exempt/Non Exempt: Non Exempt • Global Regulatory Affairs & Compliance Expertise: Strong understanding of international... ...Experience: 5-7 Years We are seeking an experienced Senior Regulatory Affairs Specialist to support the implementation of emerging global...SeniorInterim role
- ...Senior Regulatory Affairs SpecialistLocation: California, United StatesType: ContractWork Setting: On-SiteTax Status: W2Senior Regulatory Affairs Specialist 12 month contract Must be able to work on a W2 100% on-site in Santa Clara, CA SUMMARYOur client, a company operating...SeniorContract work
$69.33 - $74.33 per hour
Pay Range: $69.33hr - $74.33hr Job Overview: The Senior Regulatory Affairs Specialist will work with multiple business units to develop, update, and improve regulatory affairs processes. This role assists in implementing strategy and operations for regulatory activities...SeniorTemporary workLocal area- ...Job Description Job Description Description: We are seeking an experienced Senior Regulatory Affairs Specialist to support the implementation of emerging global regulatory requirements across multiple franchises and international markets. This role is responsible...SeniorInterim role
- ...SR. REGULATORY AFFAIRS SPECIALISTWe are searching for an experienced regulatory professional to work within the Companion Diagnostics (CDx) team of Dako North America. Reporting to the Sr. Director, Regulatory Affairs (CDx), the successful candidate must have global regulatory...Senior
- ...Sr. Regulatory Affairs SpecialistBe part of something bigger! BD is one of the largest global medical technology companies in the world and is advancing the world of health by improving medical discovery, diagnostics, and the delivery of care. We have over 65,000 employees...Senior
- ...Senior Regulatory Affairs SpecialistJoin us in pioneering breakthroughs in healthcare. For everyone. Everywhere. Sustainably.Our inspiring and... ...Healthineers company, is hiring a Senior Regulatory Affairs Specialist in either Palo Alto, CA or Austin, TX. The Senior...Senior
- ...Sr. Regulatory Affairs SpecialistEstablished Medical Device company is looking to hire a Sr. Regulatory Affairs Specialist to join their growing team! Must bring a BS Degree and a minimum of 8 years of Regulatory Affairs experience.ResponsibilitiesDevelop regulatory plans...SeniorLocal area
$140k - $180k
...Senior Regulatory Specialist And Project ManagerAt BKF, we're not just growing—we're thriving! As a dynamic multi-service consulting firm, we specialize in planning, environmental compliance, engineering, surveying, and construction management. With more than 20 West...SeniorWork at officeLocal areaRemote work$90k - $180k
...Abbott seeks a Senior International Regulatory Affairs Specialist for its Structural Heart division in Santa Clara. The role involves managing global regulatory submissions, developing submission strategies, and ensuring compliance across international markets for medical...SeniorWork experience placement$121.89k - $143.4k
...that it can be. This role provides expert support for regulatory project management, strategic submissions, and cross-functional... ...that ensures our labels meet the user’s needs, the Senior Regulatory Affairs Specialist (Labeling) will work closely with other departments...SeniorFull timeWork experience placementWork at office$78k - $156k
...California, United StatesEmployment type: full timeCategory: Regulatory AffairsIndustry: HealthcarePosted: 2026-10-05 Working... ...closure devices and peripheral stents. This Senior Regulatory Affairs Specialist position is an on-site opportunity working out of our Santa...SeniorWork experience placementWorldwide- ...Abbott seeks a Principal Regulatory Affairs Specialist for its Vascular Division to lead regulatory strategy and submissions for endovascular medical devices treating peripheral artery disease. The role manages complex regulatory activities across product lifecycle stages...
- Qorvo is seeking a Sr Principal Mixed Signal Verification Engineer in San Jose to lead verification for power-management ICs. You will develop metric-driven plans, create constrained-random tests, and build models to support TL simulations, collaborating closely with design...Senior
- Redolent Infotech Pvt. Ltd. in Sunnyvale, CA seeks a Principal Program Manager/Engineering Manager for a 6 to 12+ month engagement. The role requires leading multi-disciplinary, multi-product automation initiatives with hands-on development and test automation expertise...Senior
- Senior Principal Systems Development EngineerHelp architect and deliver Dell's L11 rack-scale AI solutions: fully integrated racks that bring Dell IP and partner technologies together to fuel our customers' AI growth. As a Principal Systems Development Engineer, you'll...Senior
- Hewlett Packard Enterprise in California seeks a Sr. Principal Hardware Engineer to lead the design and development of next‑generation networking hardware. You will drive architecture, schematic design, PCB layout, bring‑up, validation and production, with an onsite...Senior
- R&D Strategy And Project Management Defining, implementing and/or maintaining R&D strategy, guidelines, systems and services for VISHAY Aligning and ensuring implementation of R&D budgets, monitors R&D programs, and allocates resources Planning and coordinating...Senior
$190k - $240k
...portfolio, enabling customers to deploy tailored architectures to meet their unique infrastructure requirements. Discover more at Senior Principal Executive Recruiter Role Overview The Senior Principal Executive Recruiter will serve as a strategic talent advisor...SeniorFull timeFlexible hours- ...Hewlett Packard Enterprise is seeking a Senior Principal Power Hardware Engineer to design and validate high‑voltage power systems in Sunnyvale. The role emphasizes architecture development, multi‑platform coordination, and mentoring teams. This onsite position requires...Senior
- ...Hewlett Packard Enterprise is seeking a Senior Principal Thermal Engineer to define and lead thermal architectures for liquid-cooled hardware across multiple platforms, from concept to production. You will oversee validation plans, mentor engineers, and influence cross...Senior
- KLA, based in Milpitas, CA, is seeking a Senior Export Specialist to drive U.S. export controls, compliance, and related import operations. You... ..., and cross-functional collaboration to maintain regulatory compliance and operational efficiency. #J-18808-Ljbffr KLASenior
- ...Micron Technology, Inc. seeks a Senior Principal CAD Engineer to shape the design automation environment used by global memory teams. You will partner with CAD Software and HPC groups to architect, modernize, and scale platforms, from project setup flows to quality...Senior
- ...QMS Consulting seeks a Regulatory Specialist with direct experience drafting federal rules for the a federal agriculture agency. The specialist will serve as a rulemaking subject matter lead for up to three proposed-rule efforts. Working with QMS analysts and federal...Permanent employment
$45 - $48 per hour
...Regulatory Affairs SpecialistWe are seeking an experienced Senior Regulatory Affairs Specialist to support the implementation of emerging global regulatory requirements across multiple franchises and international markets. This role is responsible for assessing regulatory...Contract workTemporary work$38 - $56 per hour
...LHH Recruitment Solutions is seeking a Regulatory Affairs Specialist for a minimum 6-month remote contract opportunity. This position is open to candidates residing in California who have prior experience in the medical device industry. The ideal candidate will have a...Hourly payContract workLocal areaImmediate startRemote workMonday to Friday- Senior Principal Product Development ManagerInfrastructure Solutions Group (ISG) builds the products that power infrastructure, solutions, and data management our customers need most. Our teams design and develop the hardware and software that connect infrastructure, accelerate...Senior
- ...Northrop Grumman Corp. in Sunnyvale, CA, seeks a Senior Principal Technical Services Project Manager to direct and manage activities for the Strategic Launcher Program Office on-site. You will lead project teams, monitor progress, manage budgets, and serve as primary...SeniorWork at office
- Cadence Design Systems is seeking an expert Digital Implementation and Signoff Field Applications Engineer in California. You will work side-by-side with customers to deploy Cadence technologies in Synthesis, P&R, and Signoff, helping teams meet PPA targets and close designs...Senior
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Senior Regulatory Affairs Specialist. Be the first to apply!
- regulatory officer Santa Clara, CA
- regulatory affairs specialist Santa Clara, CA
- aml compliance analyst Santa Clara, CA
- medicare compliance specialist Santa Clara, CA
- compliance analyst Santa Clara, CA
- senior compliance analyst Santa Clara, CA
- regulatory specialist Santa Clara, CA
- regulatory compliance analyst Santa Clara, CA
- research compliance officer Santa Clara, CA
- compliance consultant Santa Clara, CA




