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Full Time | Pay: €50,000/year

Regulatory Affairs Specialist Roles- Medical Devices Role Description: CPL is currently recruiting for several Medical Device companies based in Galway, Ireland. The Regulatory Affairs Specialist helps develop regulatory strategies, performs activities ass...

CPL Ireland

Galway, Ireland

Full Time

Als einer der „Hidden Champions des 21. Jahrhunderts' ist Jungbunzlauer ein erfolgreiches, verantwortungsbewusstes und nachhaltiges Familienunternehmen. Leidenschaft für unsere Produkte und ein sehr gutes Verständnis der Bedürfnisse unserer Kunden zeichnen...

Jungbunzlauer Ladenburg GmbH

Ladenburg, Germany

Full Time

Kennziffer JAF1723_jv.Über steht für Kompetenz und Leidenschaft in der Personaldienstleistung, ganz gleich ob Arbeitnehmerüberlassung oder Personalvermittlung. Vor 15 Jahren als interner Personaldienstleister von BAYER in Leverkusen ins Leben gerufen, sind...

GmbH

Darmstadt, Germany

Full Time

This position will be responsible for the preparation and submission of domestic regulatory applications for a class 3 PMA medical device including IDEs, PMAs, PMA Supplements, and Annual Reports. This position will be responsible for international regulat...

121 Gamma Dr, Pittsburgh, PA, USA

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Full Time

Our client, a fast growing food manufacturing company is seeking an experienced Food Regulatory Specialist to join their team. This is a cross functional position in a fast growing food environment, critical to the success and launch of new products....

Mississauga, ON, Canada

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Full Time | Pay: €60,000/year

CPL Galway is working on a number of regulatory affairs positions in the medical device industry. These openings range from a senior position in a start up working on class III devices, to one of the leading medical device companies in the world. If you wi...

CPL Ireland

Galway, Ireland

Full Time | Pay: $18 - $20/hour

Position Overview: The Regulatory Affairs Associate uses his or her scientific knowledge to support the research lab environment of this company. The Regulatory Affairs Associate ensures proper data organization, supplier communications, information aggreg...

Los Angeles, CA, USA

Full Time

? Der Bertrandt-Konzern bietet seit über 40 Jahren Entwicklungslösungen für die internationale Automobil- und Luftfahrtindustrie. Angefangen von der ersten Idee bis zur Serienbetreuung setzen wir Ideen in fertige Konzepte um. Unsere Tochtergesellschaft Ber...

Bertrandt AG

Wiesbaden, Germany

Full Time

Beachtung der Übereinstimmung der Kennzeichnung, der Packungsbeilage (Gebrauchsinformation), der Fachinformation und der Werbung mit dem Inhalt der Zulassung oder der Registrierung (bzw. der §§ 36 bzw. 39 Abs. 3 bei Freistellung von Zulassung oder Registri...

DIS | Life Science

Munich, Germany

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Full Time

Apex is an Equal Employment Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, age, sexual orientation, gender identity, national origin, disability, pro...

Glendora, CA, USA

Full Time | Pay: €100,000/year

Title: Regulatory Affairs Specialists Location: Galway Cpl Recruitment Ireland is currently working with a number of medical devices companies based in Galway, Ireland. Our clients are welcoming regulatory affairs specialists to join their quality departme...

CPL Ireland

Galway, Ireland

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Contractor

Looking for CMC experts specializing in regulatory affairs! We have an opportunity located in Switftwater, PA with a large pharmaceutical company to help contribute to their CMC authoring. This is an excellent opportunity for CMC specialists to showcase th...

Swiftwater, PA, USA

Full Time

Qualifications for the Regulatory Affairs Specialist: 2-3+ years' experience in Pharmaceutical Regulatory Affairs Pre and Post Regulatory Submission experience w/ ANDAs required Knowledge/Understanding of Drug Filing regulations (U.S. & Internation...

New Providence, NJ, USA

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Full Time

Joule is looking for a strong Quality Associate to add to their team! This position offers working within a great team and competitive pay. Send your updated resume to BAppel-Vazquez@jouleinc.com or call 610-915-2077....

Yardley, PA, USA

Full Time

Our people are everything. As a Best of Staffing ® Client and Talent leader, Aerotek ® Inc. has distinguished itself as a leader in recruiting and staffing services, by having a deep understanding of the intersection of talent and business. As a strategic...

Cll Manuel Colon, Florida, Puerto Rico

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Full Time

Responsible for supporting the implementation of Regulatory Affairs and Quality Assurance systems and procedures relating to Domestic and/or International regulatory requirements. Provides administrative support to a department or individual. Knowledge of...

Fremont, CA, USA

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Full Time

Advanced Clinical is an award-winning clinical development organization that provides global services including CRO, Functional Support, Quality & Validation, Patient Recruitment and Retention, and Strategic Talent Acquisition solutions for pharmaceuti...

North Chicago, IL, USA

Full Time

Our people are everything. As a Best of Staffing ® Client and Talent leader, Aerotek ® Inc. has distinguished itself as a leader in recruiting and staffing services, by having a deep understanding of the intersection of talent and business. As a strategic...

Gainesville, FL, USA

Full Time

As a member of the Miltenyi Biotec Regulatory Affairs Team, you will be responsible to support all company regulatory objectives to ensure that products meet worldwide regulatory requirements on all aspects of product approval and post-marketing compliance...

85 Hamilton St, Cambridge, MA, USA

Full Time

Our people are everything. As a Best of Staffing ® Client and Talent leader, Aerotek ® Inc. has distinguished itself as a leader in recruiting and staffing services, by having a deep understanding of the intersection of talent and business. As a strategic...

7077 Bonneval Rd #500, Jacksonville, FL, USA

CAREERBUILDER APPLY

Contractor

Participates in writing and filing appropriate FDA premarket submission to ensure devices are commercially available in the U.S. Supports the review of promotional material and device labeling for regulatory compliance. Participates in regulatory projects,...

Newark, DE, USA

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Full Time

Lead small group discussions to identify potential problems and to drive mitigation actions within timelines (Annual reports, Labels, Internal logs). B.S. in Chemistry 0-1 years of experience in pharmaceutical industry Microsoft office experience...

Morton Grove, IL, USA

Full Time

Our Paralegal, Regulatory Affairs assists in the regulatory compliance function. Performs research and supports activities relating to various legal and regulatory issues. Includes scope of practice issues, privacy laws (to include HIPAA, HITECH and state...

Nashville, TN, USA

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Full Time

Lab Support is an Equal Employment Opportunity/Affirmative Action Employer. We evaluate qualified applicants without regard to race, color, religion, sex, national origin, disability, veteran status, sexual orientation, gender identity, and other protected...

San Jose, CA, USA

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Full Time

We are proud to offer an exciting temp. opportunity to work as a Regulatory Affaris Consultant onsite at a Nutricuetical Company. 6+ Month Contract role as needed. SUMMARY: Contract engagement for Regulatory Affairs to lead strategy, submission and respons...

Santa Rosa, CA, USA

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