Neubourg GmbH & Co KG
Quality Management & Regulatory Affairs Manager – Medical Devices (m/f/d)
Wolfratshausen, Bayern, Germany
Get past the screening software and onto a recruiter's desk
hirly rewrites your resume for this job — matching the keywords and skills in the posting, moving your most relevant experience to the top, and writing a cover letter to fit. About 30 seconds.
- Keywords matched to this posting
- Fit score before you apply
- Cover letter included
Matched against 2.6M live jobs from 210,000+ employers in 200+ countries.
Tailor my resume for this job →Apply from your AI assistant
Connect hirly to Claude or ChatGPT and ask it to apply to this job. hirly tailors your resume, fills the employer’s form and asks before sending.
Some employer sites stop an application at a CAPTCHA or sign-in and hand it back with a link. Applying needs a paid plan. Works with any assistant that supports MCP.
hirly's read of this role
- Seniority
- Lead / management
- Country
- DE
- Work mode
- On-site / unstated
- First seen by hirly
- 26 Oct 2026
Derived automatically from the posting. Upload your resume above to see how the role scores against it.
the posting
As Quality Management & Regulatory Affairs Manager (m/f/d) , you ensure that our medical device portfolio meets the highest quality and regulatory standards. You are responsible for key QM processes for the companies of Avia Pharma Germany, keep us audit-ready at all times in line with ISO 13485 and MDR, and report directly to the Director of Scientific Affairs DACH. Your place of work is Wolfratshausen near Munich, full-time with the option to work remotely.
Your Responsibilities
- Operational management of change control, complaint handling and CAPA for the companies of Avia Pharma Germany
- Preparation and execution of internal audits and ensuring continuous audit readiness in line with ISO 13485 and MDR
- Maintenance and further development of the quality management system, including support for the migration to an eQMS
- Qualified regulatory support for our medical device portfolio
- Contribution to the maintenance and updating of technical documentation
- Support with ongoing vigilance activities
Your Profile
- University degree in a relevant scientific, technical, medical or pharmaceutical discipline
- At least one year of professional experience in regulatory affairs for medical devices
- At least one year of professional experience in quality management for medical devices, including experience in CAPA, change and complaint management
- Sound working knowledge of ISO 13485 and MDR
- Desirable: audit experience (internal/external), ideally with an auditor qualification, as well as experience with eQMS systems and RA databases
- An advantage: background in dermatology, medicinal products, cosmetics or food supplements
- Strong quality mindset, great attention to detail and an independent, structured way of working
- Reliability and assertiveness toward internal and external interfaces, as well as the willingness to take on broader regulatory responsibility over time
- Business-fluent German and English, both written and spoken
- Our Promise
- We offer you a responsible role in a dynamic working environment with challenging tasks and plenty of room for your own initiative, including the freedom to explore new paths. Short decision-making processes and flat hierarchies help us implement exciting ideas quickly and without red tape.
- On top of that, you can look forward to:
- First-name culture: We treat each other as equals – from apprentices to management
- Flexibility: Flexible working hours and a hybrid working model
- Fit & Active: eGym Wellpass membership and (e-)bike leasing
- Time off: 30 days of vacation per year
- Securing your future: Company pension scheme included
- Team spirit: Regular team events
- Little things that matter: Birthday gift, subsidy for computer glasses, plus fruit & drinks
Would you like to help shape our success story? Then we look forward to receiving your meaningful application, including your salary expectations.
Listed on hirly, a job board. hirly is not the employer: Neubourg GmbH & Co KG is hiring for this role.
Similar jobs
- Regulatory Affairs Manager (m/w/d) QRDPaul-Ehrlich-Institut Bundesinstitut für Impfstoffe u. biomedizin. Arzneimittel · Langen (Hessen), Hessen, GermanyFirst seen yesterday
- Regulatory Affairs Manager (f/m/d)Randstad Professional · Ludwigshafen am Rhein, Rheinland-Pfalz, GermanyFirst seen 7d ago
- Clinical Affairs Manager (m/w/d)Söring GmbH · Quickborn, Kreis Pinneberg, Schleswig-Holstein, GermanyFirst seen 9d ago
- Drug Regulatory Affairs Manager (m/w/d), NeumarktBIONORICA SE · Neumarkt in der Oberpfalz, Bayern, GermanyFirst seen 9d ago
- Regulatory Affairs Manager (m/w/d)ATMOS MedizinTechnik GmbH & Co. KG · Lenzkirch, Baden-Württemberg, GermanyFirst seen 9d ago
Want this one?
Upload your resume and hirly rewrites it for this job and writes the cover letter — in about thirty seconds, before you sign up.
Tailor my resume for this job