9 Jobs für Drug Regulation
Stellenangebote Drug Regulation Jobs
Neu Job vor 3 Std. bei Mindmatch.ai gefunden
Fresenius Kabi Austria
• AT- 6 Graz
Homeoffice möglich
Jobticket
Maintain an up-to-date knowledge of c Gx P
regulation and applicable standards (especially in the US and EU) and implement requirements into locally applicable procedures (SOPs, Guiding Documents, Working Instructions, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] etc) Manage a GMP compliant transition of Programs from development to commercial Manage GMP compliance during Tech Transfer of manufacturing activities of Combination Product Manage internal and external Change Controls, Deviations, Events, CAPAs, etc. , related to Drug Substance, Drug Product and Combination Products Contribute to QM programs and GMP/ GDP/ MDR compliance activities as appropriate Manage GMP/ GDP/ MDR quality oversight (qualification, approval, monitoring) of C (D) MOs, Testing Labs, Medical Devices suppliers, packagers and carriers A BA/ BS, MA/ MS or Ph D in a technical or [. .. ]
Job am 14.08.2026 bei Mindmatch.ai gefunden
Sandoz International GmbH
• AT- 7 Kundl
Sandoz International Gmb H seeks a Regulatory Affairs Device Manager to deliver global compliance for medical devices and
drug-device combinations. You will drive regulatory strategy, manage interactions with Notified Bodies [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and regulators, and lead the creation of compliant technical documentation for successful registrations. The role requires 5+ years in device regulation, MDR/ UK/ EU experience, and leadership in a matrix environment. J-18808-Ljbffr 01216257 [. .. ]
Neu Job vor 3 Std. bei Jobleads gefunden
Senior Manager Quality Operations (m/f/d)
• Graz, Steiermark
Homeoffice möglich
Jobticket
Maintain an up-to-date knowledge of c Gx P
regulation and applicable standards (especially in the US and EU) and implement requirements into locally applicable procedures (SOPs, Guiding Documents, Working Instructions, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] etc) Manage a GMP compliant transition of Programs from development to commercial Manage GMP compliance during Tech Transfer of manufacturing activities of Combination Product Manage internal and external Change Controls, Deviations, Events, CAPAs, etc. , related to Drug Substance, Drug Product and Combination Products Contribute to QM programs and GMP/ GDP/ MDR compliance activities as appropriate Manage GMP/ GDP/ MDR quality oversight (qualification, approval, monitoring) of C (D) MOs, Testing Labs, Medical Devices suppliers, packagers and carriers A BA/ BS, MA/ MS or Ph D in a technical or [. .. ]
Job vor 6 Tagen bei Jobleads gefunden
Führungs-/ Leitungspositionen
[. .. ] prioritize complex information from diverse sources Manage, track, and present assigned work; compile and report performance metrics Manage plainlanguage synopses, summaries, and clinicaldocument redactions under FDA, EMA, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] EU Clinical Trial Regulation, Health Canada PRCI, and other global requirements Educate the company on transparency/ disclosure regulations, industry trends, layperson summaries, and clinical study diversity planning Coordinate crossfunctional teams and liaise between vendors and internal teams for documents and postings Collaborate on diversity action plans in accordance with FDA guidance Coordinate multiple projects [. .. ] vendor oversight a plus Experience authoring clinical study reports, protocols, protocol amendments, and Investigators Brochures Experience authoring briefing books and Module 2 clinical summaries is a plus Solid understanding of drug development, clinical research, data analysis, CTD, ICH guidelines, Gx P, regulatory interactions, and relevant regulations and guidance Ability to manage competing priorities in a fastpaced environment Excellent problemsolving, organizational, analytical, and criticalthinking skills Excellent written and verbal communication skills Strong attention to detail regarding consistency, grammar, syntax, and formatting Familiarity with [. .. ]
Job vor 7 Tagen bei Jobleads gefunden
• Allschwil, Basel- Landschaft
[. .. ] hybrid role and will be located in Allschwil, Switzerland. The Principal Scientist, CMC Regulatory Affairs-Combination Products role will provide CMC (Chemistry, Manufacturing, and Controls) regulatory subject matter [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] expertise for drug-device combination products and related device constituent parts involved in the preparation or administration of drugs. This role may support pre-approval and post-approval programs, synthetic or biologic products, and products in any therapeutic area. The Principal Scientist will develop and execute regulatory strategies for assigned combination product programs, [. .. ] and frameworks applicable to drug-device combination products and medical devices, including FDA combination product regulations and guidance documents (e. g. , 21 CFR Part 4) , Quality Management System Regulation (QMSR) , EU Medical Device Regulation (EU MDR) , and related global guidance documents. Understanding of how device and combination product requirements are integrated into pharmaceutical or biologic product development, regulatory submissions, and lifecycle management activities. Ability to interpret and apply regulatory requirements to support scientifically sound, risk-based regulatory [. .. ]
Job am 08.09.2026 bei Jobleads gefunden
[. .. ] the latest in a line of cuttingedge systems that have been helping customers and partners including Amazon Web Services, and Astra Zeneca achieve 20x performance results and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] accelerate innovation in drug discovery, materials science, financial modeling, logistics, cybersecurity, and defense. In 2025, the company achieved 99.99 twoqubit gate fidelity, setting a world record in quantum computing performance. Headquartered in College Park, Maryland, Ion Q has operations in California, Colorado, Massachusetts, Tennessee, Washington, Italy, South Korea, Sweden, Switzerland, Canada and the United [. .. ] real accountability for architecture decisions at scale. Familiarity with the security and compliance frameworks customers will map this work to: NIST CSF, CIS Benchmarks, ISO 27001, FISMA, Fed RAMP, or sectorspecific regulation. Publicsector, defense, financial services, or telecom experience, where highassurance and long dataconfidentiality horizons make this problem urgent today. Contributions to standards or the technical community: IETF, ETSI, national PQC migration working groups, published writing, or conference talks. Certifications that validate technical depth CISSP, CCIE/ JNCIE, CCNP Security, or equivalent. Comfort [. .. ]
Job am 22.08.2026 bei Jobleads gefunden
• Allschwil, Basel- Landschaft
[. .. ] hybrid role and will be located in Allschwil, Switzerland. The Principal Scientist, CMC Regulatory Affairs-Combination Products role will provide CMC (Chemistry, Manufacturing, and Controls) regulatory subject matter [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] expertise for drug-device combination products and related device constituent parts involved in the preparation or administration of drugs. This role may support pre-approval and post-approval programs, synthetic or biologic products, and products in any therapeutic area. The Principal Scientist will develop and execute regulatory strategies for assigned combination product programs, [. .. ] and frameworks applicable to drug-device combination products and medical devices, including FDA combination product regulations and guidance documents (e. g. , 21 CFR Part 4) , Quality Management System Regulation (QMSR) , EU Medical Device Regulation (EU MDR) , and related global guidance documents. Understanding of how device and combination product requirements are integrated into pharmaceutical or biologic product development, regulatory submissions, and lifecycle management activities. Ability to interpret and apply regulatory requirements to support scientifically sound, risk-based regulatory [. .. ]
Job am 18.08.2026 bei Jobleads gefunden
• Berlin
Führungs-/ Leitungspositionen
[. .. ] future of how AI is applied in pharmaceutical R D. We enable leading pharmaceutical teams to discover and develop drugs faster. We host the industrys largest federated [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] data networks for drug discovery AI, spanning co-folding, ADMET, and antibody development capability. Across these networks, models are trained on proprietary industry datasets to achieve higher performance and broader applicability while keeping data control and IP protected. We deliver these superior models through drug discovery applications that enable teams to run them at [. .. ] mindset that balances security, usability, and speed. Experience mentoring team members and helping them grow their security skills. Nice to have Experience acting as a Data Protection Officer or supporting regulation like GDPR. Experience leading and developing teams, with the ability to mentor others and scale a security function in a fastgrowing environment. Understanding of pharma deployment environments and integrations with common R D platforms (e. g. , Schrödinger Live Design, Benchling) . Experience working in B2B Saa S environments, particularly with [. .. ]
Job am 18.08.2026 bei Jobleads gefunden
• Köln, Nordrhein- Westfalen
[. .. ] CC. 120) and SCCM training certificate (EASA ORO. CC. 200) . Proven experience as a Senior Cabin Crew Member or comparable aviation leadership role. Valid medical certificate [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and current negative drug screening result. Valid hygiene training in line with EU Regulation 852/ 2004. Minimum age 21 and height 1.60m. Businessfluent English; German or other foreign languages are a strong plus. Ability to reach the assigned base within 90minutes when on call. Resilience under pressure, genuine service mindset and uncompromising commitment to safety. Solid IT skills and access to a tablet [. .. ]
Häufig gestellte Fragen
Wieviele offene Stellenangebote gibt es für Drug Regulation Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 9 offene Stellenanzeigen für Drug Regulation Jobs.
In welchen Bundesländern werden die meisten Drug Regulation Jobs angeboten?
Die meisten Stellenanzeigen für Drug Regulation Jobs werden derzeit in Niedersachsen (2 Jobs), Nordrhein-Westfalen (1 Jobs) und Berlin (1 Jobs) angeboten.
