16 beste Stellen als regulatory affairs specialist in bayern – aktuell auf Personalsuche

Sr. Specialist - Regulatory Affairs - Operations 4C
Genpact Deutschland GmbH —München
- Vollzeit
- Englisch
- Master
- Künstliche Intelligenz
Direkt bewerben
12 Tage
Senior Regulatory Affairs Specialist (m/w/d)
Dornier MedTech Systems GmbH —Weßling
- Vollzeit
- Englisch
- Microsoft Office
- Zeitmanagement
- Flexible Arbeitszeiten
Direkt bewerben
Regulatory Affairs Specialist (m/w/d)
pates AG —Bayern
- Homeoffice-Möglichkeit
Specialist (m/f/d) Regulatory Affairs & Quality
Abbott Laboratories —München
- Vollzeit
5 Tage
(Junior) Manager Regulatory Affairs International (m/w/d)
HERMES ARZNEIMITTEL GmbH —Pullach im Isartal
- Vollzeit
- Laborerfahrung
- Englisch
- Microsoft Office
- Gleitzeit
- Flexible Arbeitszeiten
(Senior) Regulatory Affairs Specialist (m/w/d)
Ziehm Imaging GmbH —Nürnberg
- Englisch
- Künstliche Intelligenz
- Gleitzeit
- Weiterbildungsprogramme
Regulatory Affairs Specialist (m/w/d)
Unternehmensgruppe Theo Müller —Aretsried
- Englisch
- Analytik
- Flexible Arbeitszeiten
5 Tage
Post-Market Surveillance Manager / Regulatory Affairs Specialist (m/w/d)
GANSHORN Medizin Electronic GmbH —Bad Neustadt an der Saale
- Vollzeit
- Englisch
- Weiterbildungsprogramme
- Flexible Arbeitszeiten
4 Tage
Post-Market Surveillance Manager / Regulatory Affairs Specialist (m/w/d)
Ganshorn Medical Electronic GmbH —Bad Neustadt an der Saale
- Vollzeit
- Englisch
- Weiterbildungsprogramme
- Flexible Arbeitszeiten
4 Tage
Specialist Regulatory Affairs für Medizinprodukte (m/w/d)
TRB Chemedica AG —Feldkirchen
- Vollzeit
- Englisch
Direkt bewerben
Application Specialist für Brust-CT (m/w/d)
AB-CT - Advanced Breast-CT GmbH —Erlangen
- Per E-Mail
- Azure
- Englisch
- Mit Reiseanteil
- Kostenloser Parkplatz
- Homeoffice-Möglichkeit
Direkt bewerben
Brand Specialist – Germany
Pharmanovia —Fürth
- Hybrides Arbeiten
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Orthopedic Pre-Operative Planning Specialist, Arthroplasty (w/m/d)
Arthrex —Freiham
- CAD
- Englisch
- Microsoft Office
6 Tage
Senior Brand Manager Germany, Switzerland and Austria
Rhythm Pharmaceuticals —München
- Vollzeit
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Certification Specialist (m/f/d) - Quantum Frontline Industries
Quantum-Systems GmbH —Weßling
- Vollzeit
Direkt bewerben
Building Regulations & Permitting Specialist
Proxima Fusion —München
- Vollzeit
- Forschungserfahrung
9 Tage

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Senior Regulatory Affairs Specialist (m/w/d)
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Sr. Specialist - Regulatory Affairs - Operations 4C

Genpact Deutschland GmbH
München

Direkt bewerben

Details zur Stelle

Vollzeit
vor 12 Tagen

Qualifikationen

Englisch
Master
Pharmazie
Künstliche Intelligenz

Vollständige Stellenbeschreibung

Sr. Specialist - Regulatory Affairs - Operations

Ready to turn bold ideas into real-world impact?
At Genpact, we don’t just adapt to change, we lead it. AI and digital innovation are transforming the way businesses work, and we’re at the forefront of it. Genpact’s AI Gigafactory, our industry-first accelerator, exemplifies how we scale advanced technology solutions to help global enterprises work smarter, grow faster, and transform at scale. Whether tackling complex challenges through large-scale models or agentic AI, our breakthrough solutions tackle companies’ most complex challenges.

If you thrive in a fast-moving, innovation-driven environment, love building and deploying cutting-edge AI solutions, and want to push the boundaries of what’s possible, this is your moment.

Genpact (NYSE: G) is an agentic and advanced technology solutions company. We leverage process intelligence and artificial intelligence to deliver measurable outcomes. With a strong partner ecosystem and decades of client trust, we provide innovative solutions that transform how businesses run. Powered by a team with an active learning mindset and client centricity at its core, we deliver lasting value for the world’s leading enterprises.
Get to know us at genpact.com and on LinkedIn, YouTube, X, and Facebook.

Job Description

Data Remediation/Regulatory Master Data Management

Responsibilities

Data Analyst
- Handling of Master Data Entries in all relevant systems according to Data Governance Rules and Business needs
- Provides hands‑on data remediation expertise to correct, standardize, and stabilize regulatory
- Provides recommendations to align with the Veeva data model, including data definitions, structures, relationships, and dependencies.
- Performs detailed data analysis and validation, identifying data quality issues, root causes, and remediation actions.
- Applies strong knowledge of data governance principles, ensuring alignment to defined standards, controlled vocabularies, and business rules.
- Supports regulatory and RIM teams by translating business and compliance requirements into accurate data corrections.
- Works closely with RIM, Regulatory Operations, and Data Operations to execute remediation activities in a controlled and compliant manner.
- Demonstrates strong analytical capability using Excel and related tools to manage large datasets and remediation trackers.
- Operates in a hands‑on, execution‑focused role, ensuring timely and high‑quality remediation outcomes.
- Preparation of IDMP changes/entries in all relevant systems

PROJECT DELIVERABLES/SCOPE OF WORK

Ø Data Remediation/ Regulatory Master Data Management

- Regulatory Master Data Entries according to internal process including necessary investigations for correct and complete data entry and contact to data owner and business
- Remediated, high‑quality regulatory data aligned to Veeva data model standards and European regulatory requirements.
- Documented remediation actions and traceability, supporting audit and inspection readiness.
- Data quality reports and metrics highlighting issues resolved, remaining risks, and trends.
- Consistent application of data definitions and structures across impacted records and markets.
- Validated datasets ready for downstream regulatory processes, submissions, and reporting.
- Reduced data inconsistency and rework through accurate, first‑time remediation.
- Effective collaboration with cross‑functional teams to ensure clear handoffs and issue resolution.

Sustained data governance compliance, supporting long‑term data stability post‑remediation

Qualifications

Bachelors - Health Administration, Bachelors - Healthcare, Bachelors - Pharmacy, Masters - Public Health, Masters - Regulatory Affairs

Certifications

Certified Compliance Officer (CCO) - VskillsVskills, Certified Public Accountant (CPA) - Perfekt SzolnokPerfekt Szolnok, Certified Regulatory Compliance Manager (CRCM) - The International Association of Risk and Compliance Professionals (IARCP)The International Association of Risk and Compliance Professionals (IARCP)

Required Skills

Data Analytics

Language

English (Required)

Language Proficiency -

Proficient - C2

Additional Job Location -

Job Type

Fixed Term (Fixed Term)

Job End Date

2027-07-31

Master Skill List -

Regulatory Affairs - Operations

Remote Type -

Hybrid

Work Shift -

Standard (Germany)

Why join Genpact?

Lead AI-powered transformation – Drive innovation and solve real-world business challenges that matter
Make an impact – Help global enterprises solve business challenges that matter
Accelerate your career – Gain hands-on experience, mentorship, and world-class learning opportunities to stay ahead
Work with the best – Join 140,000+ bold thinkers and problem-solvers who push boundaries every day
Thrive in a values-driven culture – Our courage, curiosity, and incisiveness - built on a foundation of integrity and inclusion - allow your ideas to fuel progress

Come join the 140,000+ coders, tech shapers, and growth makers at Genpact and take your career in the only direction that matters: Up.
Let’s build tomorrow together.

Genpact is an Equal Opportunity Employer and considers applicants for all positions without regard to race, color, religion or belief, sex, age, national origin, citizenship status, marital status, military/veteran status, genetic information, sexual orientation, gender identity, physical or mental disability or any other characteristic protected by applicable laws. Genpact is committed to creating a dynamic work environment that values respect and integrity, customer focus, and innovation.
Furthermore, please do note that Genpact does not charge fees to process job applications and applicants are not required to pay to participate in our hiring process in any other way. Examples of such scams include purchasing a 'starter kit,' paying to apply, or purchasing equipment or training.

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regulatory affairs specialist Jobs in bayern

Sr. Specialist - Regulatory Affairs - Operations 4C

Senior Regulatory Affairs Specialist (m/w/d)

Regulatory Affairs Specialist (m/w/d)

Specialist (m/f/d) Regulatory Affairs & Quality

(Junior) Manager Regulatory Affairs International (m/w/d)

(Senior) Regulatory Affairs Specialist (m/w/d)

Regulatory Affairs Specialist (m/w/d)

Post-Market Surveillance Manager / Regulatory Affairs Specialist (m/w/d)

Post-Market Surveillance Manager / Regulatory Affairs Specialist (m/w/d)

Specialist Regulatory Affairs für Medizinprodukte (m/w/d)

Application Specialist für Brust-CT (m/w/d)

Brand Specialist – Germany

Orthopedic Pre-Operative Planning Specialist, Arthroplasty (w/m/d)

Senior Brand Manager Germany, Switzerland and Austria

Certification Specialist (m/f/d) - Quantum Frontline Industries

Building Regulations & Permitting Specialist

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