Global Regulatory Affairs Specialist II
Penumbra
Penumbra, Inc. is seeking a Regulatory Associate to prepare and maintain documentation for worldwide regulatory submissions, ensuring approvals across regions. You will coordinate between teams and regulatory agencies to support clinical research, export, and commercial distribution. The role requires a science degree with 2+ years of regulatory experience, strong communication skills, and proficiency with MS Word/Excel/PowerPoint. On-site work in Alameda, CA with travel likely. #J-18808-Ljbffr Penumbra
$90k - $125k
Alameda, CAGeneral Administration - Regulatory Affairs /External /HybridIn this role, you will work with the team that ensures that Penumbra... ...maintained• Communicate with in-country RA personnel to facilitate global clearance/approvals• Monitor, research, and obtain...SuggestedTemporary workWork at officeLocal areaWorldwide$100k - $200k
...: Full timeAbbott is a global healthcare leader that... ...Opportunity The Principal RA Specialist will work on-site out... ...for leading global regulatory submissions, which include... ...working with Class II, Class III medical devices... .../drugs. Regulatory Affairs Certification (RAC) is...SuggestedShift work- A leading IT staffing company in Emeryville is looking for a qualified candidate to support the maintenance of their Global Regulatory Affairs filing system and RTS database. The role emphasizes effective organization, knowledge of compliance, and project execution skills...SuggestedWork at office
- ...Penumbra, Inc. in Alameda, California seeks a Regulatory Submissions Coordinator to prepare and maintain document packages for worldwide... ...Quality System, and help in-country RA personnel to facilitate global clearances. Occasional travel may be required. #J-18808-Ljbffr...SuggestedWorldwide
$90k - $180k
Senior Regulatory Affairs SpecialistAbbott is a global healthcare leader that helps people live more fully at all stages... ..., the Senior Regulatory Affairs Specialist will support product development... ...regulatory requirements for Class II software medical devicesAssess the...Suggested- Abbott is a global healthcare leader improving lives through diagnostics, medical devices, nutritionals and branded medicines. This role... ...leads the global Compliance PM & ALD portfolio, driving CAPA, regulatory changes, labeling updates, and UDI initiatives with cross-...Worldwide
- Title: Project Manager II Location: Alameda, CA Duration: 6 Months 100% Onsite Summary: The Sr. Business Process Specialist is responsible for developing, implementing, and maintaining... ...Pet Insurance 401(k) Abbott is a global healthcare leader that helps people live...Temporary workFlexible hours
- Job Title: Business Data Analyst II Location Requirements: Hybrid - Oakland, CA Job Type: Contract Role Overview: You will support data-driven business and revenue initiatives within a large technology organization. This role sits at the intersection of data operations...Contract work3 days per week
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- ...California State University - East Bay seeks a Credential Analyst II to maintain oversight of candidate files, interpret credential requirements, and guide students through California certification processes. The role emphasizes accuracy, confidentiality, and collaboration...
- Abbott is a global healthcare leader seeking a senior portfolio leader to own the Compliance/UDI program portfolio, drive CAPA and regulatory initiatives, and guide on-market product changes. You will develop strategies, roadmaps, and ensure alignment with regulatory priorities...
- Penumbra, Inc. in Alameda, CA seeks a Regulatory Affairs coordinator to help bring life-saving technologies to patients worldwide by preparing and maintaining document packages for regulatory submissions. You will assist in preparing submissions (510(k), CE/UKCA, IDE,...Worldwide
$122k - $173k
SUMMARY/JOB PURPOSEThe Contracts Manager II is responsible for drafting, negotiating and managing a variety of contracts supporting Exelixis' research, development, and supply chain functions, providing key support to advance Exelixis' mission.ESSENTIAL DUTIES/RESPONSIBILITIESDraft...Full timeContract workWork at officeLocal areaFlexible hours$100k - $130k
Alameda, CAMarketing - Marketing Operations /External /HybridThe Global Project Manager will play a crucial role in coordinating and... ...operations team, global marketing managers, and Medical, Legal, and Regulatory (MLR) review teams. The Global Project Manager will be...Temporary workWork at officeLocal area3 days per week$86.7k - $173.3k
...working mothers, female executives, and scientistsThis Senior Regulatory Affairs Specialist will work on-site out of our Alameda, CA or Milpitas, CA... ...product lifecycle planning and regulatory requirements for Class II software medical devicesAssess the acceptability of...Shift work$103.4k - $133.76k
...actuarial research by conducting literature reviews with limited direction on standards, assumptions, competition, and the legal and regulatory environment. Analyzes financial risks and opportunities by applying basic actuarial methods; collecting data; and assisting...Full timeTemporary workWork experience placementFlexible hoursShift work- Job Title: Program Manager II Location: Oakland, California, Duration: 1 year Overview: The Social Engineering Training & Testing Program Specialist plays a highly visible role within the Security Communications, Engagement, and Training organization, helping strengthen...For contractorsWork at officeImmediate start
- Job Title: Project Manager II Location: Oakland, CA Job Description: Department Overview The Data, Artificial Intelligence & Security (DAIS) Business Operations team is responsible for the management and governance of Financials for DAIS and for the execution of program...Contract workWork at office
- Exelixis, a leader in oncology, seeks an Executive Director, Regulatory Affairs to guide global regulatory strategies from early development through post-approval. You will oversee program leaders, ensure timely IND/NDAs/BLAs submissions, and maintain strong FDA relationships...
$114k - $228k
...AlamedaJob Type: Full timeCategory: Regulatory AffairsIndustry:... ...HealthcarePosted Date: 2026-08-04Abbott is a global healthcare leader that helps... ...technology. This Regulatory Affairs Manager position is an onsite... ....Experience with Class II and Class III medical devices....- Summary/Job Purpose The Contracts Manager II drafts, negotiates, and manages contracts supporting research, development, and supply chain functions. Responsibilities Draft, negotiate, and manage a wide range of contracts (e.g., NDAs, consulting/services agreements, materials...Contract workFlexible hours
- BRG is seeking a Workplace Project Manager to lead end-to-end office projects globally, from planning through occupancy. You will drive analyses in Excel, present executive updates in PowerPoint, review construction docs, and coordinate with architects, contractors, and...For contractorsWork at office
- Scorpion Therapeutics is seeking a Contracts Manager II to draft, negotiate, and manage contracts supporting R&D, manufacturing, and supply chain. You will partner with internal clients, identify risks, and advise on compliance, while assisting in-house attorneys. This...Contract work
- ...diagnostics, and interventional pain procedures. For more information please visit: and POSITION SUMMARY The Clinic Support Specialist II is responsible for greeting and checking in patients, verifying demographics, updating insurance information, collecting...Hourly payFull timeWork at office
- Are you an experienced Regulatory Affairs professional with a passion for biological crop protection... ...as Regional Regulatory Affairs Specialist Northern Europe at Koppert could be your... ...country teams, commercial stakeholders and Global Regulatory Affairs. You will develop...Full timeLocal areaRemote workWorldwideFlexible hours
- ...labor as a variable cost. Job Description Duties: This position will be responsible for supporting the maintenance of the Global Regulatory Affairs filing system and the Registration Tracking System (RTS) database. The position would also be responsible for Client's integration...Work at officeImmediate start
- Koppert seeks a Regulatory Affairs Specialist to secure and maintain market access for biological solutions across Northern Europe. You will work with Global Regulatory Affairs and country teams, develop strategies, manage registrations, and ensure compliance. This role...
- ...Position Details Job Code # JC-531982 Position #(s) (***) ***-****-XXX Working Title Program Budget Analyst Classification ANALYST II $6,031.00 - $7,775.00 New to State candidates will be hired into the minimum salary of the classification or minimum of alternate range...Permanent employmentFull timeRemote work
- ...MEG staff, ensure timely vigilance reporting, and coordinate with multiple groups to maintain compliant medical device reporting globally. The role requires a science/medical degree and 4+ years of relevant experience, with staff leadership a plus. Abbott offers comprehensive...
$148.7k - $297.3k
...Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies... ...scientists. The Opportunity This Associate Director Regulatory Affairs will work on-site out of our Alameda, CA location in the...WorldwideShift work
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