Home › Companies › Centogene › Quality Manger (Rostock)
Quality Manger (Rostock)
Centogene · Germany - Rostock · Remote · Active · Personio
Job facts
| Field | Value |
|---|---|
| Company | Centogene |
| Title | Quality Manger (Rostock) |
| Normalized title | - |
| Department / team | Quality and Regulatory |
| Location | Germany - Rostock |
| Work model | Remote / Remote |
| Employment type | Full Time |
| Salary | - |
| Status | active |
| ATS provider | Personio |
| Posted / first seen | 2026-05-19 / 2026-05-30 |
| Changed / last seen | 2026-05-30 / 2026-06-06 |
Related slices
| Page | What it contains | Open |
|---|---|---|
| Company jobs | Active postings from Centogene. | Open |
| Company breakdowns | Role, location, ATS, and work model facets for this company. | Open |
| ATS provider jobs | Active postings observed through Personio. | Open |
| Provider filtered search | The same provider as a filtered job collection. | Open |
| Department jobs | Active postings in Quality and Regulatory. | Open |
| Work model jobs | Active Remote postings. | Open |
| Lifecycle events | Open, update, close, and reopen events for this posting. | Open |
| Original posting | Canonical source or apply URL captured from the ATS. | Open |
Linked records
| Company | Centogene |
| Source | 9947623c-4675-437a-9d57-b249b50e3bcf |
| ATS provider | Personio |
Description
Your Responsibilities
Your core responsibilities will include, but are not limited to:
· Support continuous improvement and maintenance of the QMS in compliance with:
ISO 13485
ISO 15189
Global regulatory requirements (e.g., MDSAP)
· Ensure compliance with international quality standards and regulatory requirements
· Participation in regulatory inspections and external audits; support the planning and execution of internal audits
· Manage and oversee:
Change control processes
Non-conformities (NCs)
CAPA processes
SCARs
· Support with document control activities, including updates and maintenance in the eDMS
· Perform Quality Control activities
· Contribute to risk assessment processes
Your profile
Education:
· Degree in life sciences or a related scientific discipline
· Additional qualification in Quality Management is considered a plus
Knowledge and Skills:
· Background in the life sciences sector; experience in the biotechnology or pharmaceutical industry will be highly valued
· Proven experience with of ISO 15189, ISO 13485 and ISO14971 standards
· Knowledge of MDR, IVDR, FDA QMSR
· CLIA, CAP and GMP awareness is a plus
· Strong understanding of quality methods and problem-solving tools (e.g., FMEA, 5 Whys, Ishikawa)
· Strong analytical, structured, and solution-oriented working style
· Strong communication skills and confidence working with cross-functional teams
· Ability to work in a structured, detail-oriented and compliant manner
· Proficiency in Microsoft Word, Excel and electronic document management systems (eDMS)
· Fluent in English (written and spoken)
Why us?
What we offer
· Exciting International and diverse team which stands for integrity, involvement and innovation within the life sciences sector
· Training & development opportunities
· Company benefits such as company health insurance and company discounts
· Primarily on-site role with some remote work flexibility
· Permanent contract
About us
With employees from over 50 nations, CENTOGENE is a truly international company with offices is in Rostock, Berlin, Delhi, Boston, Valencia, Belgrade, and São Paulo. We were born to help diagnostic patients with rare disease and today we evolved to help patients of all clinical specialties to make bold progress with guided solutions for physicians, their patients and pharma partners.
Our Values
We Care: A culture of empathy and understanding for each other, our customers, and our patients, constantly driving our mission forward
We Innovate: A culture of big ideas, being bold, and taking calculated risks to develop never-before-seen solutions
We Act With Integrity: A culture of keeping to our principles with self-awareness, intellectual honesty, and speaking up
If you are interested, we look forward to receiving your application, including your CV, motivation letter, earliest possible start date, and salary expectations.
Full job record
| Job ID | 18231448c9a04cbda8349cc36df3828af694293a |
| Org ID | 3ac0b1f7-957c-4f65-8495-5611a8991c47 |
| Source ID | 9947623c-4675-437a-9d57-b249b50e3bcf |
| Board ID | 9947623c-4675-437a-9d57-b249b50e3bcf |
| Provider | personio |
| Provider Job Key | 2641775 |
| Title | Quality Manger (Rostock) |
| Normalized Title | — |
| Status | active |
| Active | yes |
| Location Text | Germany - Rostock |
| Department | Quality and Regulatory |
| Team | — |
| Employment Type | full_time |
| Workplace Type | remote |
| Remote Policy | remote |
| Country | Germany - Rostock |
| Region | — |
| City | — |
| Salary Raw | — |
| Salary Min | — |
| Salary Max | — |
| Salary Currency | — |
| Salary Period | — |
| Source URL | https://centogene.jobs.personio.de/job/2641775?language=en |
| Apply URL | https://centogene.jobs.personio.de/job/2641775?language=en |
| First Seen At | 2026-05-30 06:01:12Z |
| Last Seen At | 2026-06-06 07:47:01Z |
| Last Checked At | 2026-06-06 07:47:01Z |
| Last Changed At | 2026-05-30 06:01:12Z |
| Inactive At | — |
| Source Posted At | 2026-05-19 17:20:33Z |
| Source Updated At | — |
| Raw Payload Uri | s3://job-postings-prod-raw-590183727216/raw/provider=personio/board=centogene.de/date=2026-06-06/2026-06-06T07-47-00-830Z-5fb5f5a2eea91dbe8a8f75951baabf93e7303c9feaea0e4e9e0b30390e7ea765.json |
Event Fields
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{
"name": "Your Responsibilities",
"value": "<p style=\"color:rgb(0,0,0);font-family:'Times New Roman';font-size:medium;font-style:normal;font-weight:400;text-transform:none;\"><span style=\"color:rgb(0,0,0);font-family:Arial, Helvetica, sans-serif;\">Your core responsibilities will include, but are not limited to:</span></p><p style=\"color:rgb(0,0,0);font-family:'Times New Roman';font-size:medium;font-style:normal;font-weight:400;text-transform:none;\"><span style=\"color:rgb(0,0,0);font-family:Arial, Helvetica, sans-serif;\">· Support continuous improvement and maintenance of the QMS in compliance with:</span></p><ul style=\"list-style-type:disc;\"><li><p style=\"color:rgb(0,0,0);font-family:'Times New Roman';font-size:medium;font-style:normal;font-weight:400;text-transform:none;\"><span style=\"color:rgb(0,0,0);font-family:Arial, Helvetica, sans-serif;\">ISO 13485</span></p></li><li><p style=\"color:rgb(0,0,0);font-family:'Times New Roman';font-size:medium;font-style:normal;font-weight:400;text-transform:none;\"><span style=\"color:rgb(0,0,0);font-family:Arial, Helvetica, sans-serif;\">ISO 15189</span></p></li><li><p style=\"color:rgb(0,0,0);font-family:'Times New Roman';font-size:medium;font-style:normal;font-weight:400;text-transform:none;\"><span style=\"color:rgb(0,0,0);font-family:Arial, Helvetica, sans-serif;\">Global regulatory requirements (e.g., MDSAP)</span></p></li></ul><p style=\"color:rgb(0,0,0);font-family:'Times New Roman';font-size:medium;font-style:normal;font-weight:400;text-transform:none;\"><span style=\"color:rgb(0,0,0);font-family:Arial, Helvetica, sans-serif;\">· Ensure compliance with international quality standards and regulatory requirements</span></p><p style=\"color:rgb(0,0,0);font-family:'Times New Roman';font-size:medium;font-style:normal;font-weight:400;text-transform:none;\"><span style=\"color:rgb(0,0,0);font-family:Arial, Helvetica, sans-serif;\">· Participation in regulatory inspections and external audits; support the planning and execution of internal audits</span></p><p style=\"color:rgb(0,0,0);font-family:'Times New Roman';font-size:medium;font-style:normal;font-weight:400;text-transform:none;\"><span style=\"color:rgb(0,0,0);font-family:Arial, Helvetica, sans-serif;\">· Manage and oversee:</span></p><ul><li><p style=\"color:rgb(0,0,0);font-family:'Times New Roman';font-size:medium;font-style:normal;font-weight:400;text-transform:none;\"><span style=\"color:rgb(0,0,0);font-family:Arial, Helvetica, sans-serif;\">Change control processes</span></p></li><li><p style=\"color:rgb(0,0,0);font-family:'Times New Roman';font-size:medium;font-style:normal;font-weight:400;text-transform:none;\"><span style=\"color:rgb(0,0,0);font-family:Arial, Helvetica, sans-serif;\">Non-conformities (NCs)</span></p></li><li><p style=\"color:rgb(0,0,0);font-family:'Times New Roman';font-size:medium;font-style:normal;font-weight:400;text-transform:none;\"><span style=\"color:rgb(0,0,0);font-family:Arial, Helvetica, sans-serif;\">CAPA processes</span></p></li><li><p style=\"color:rgb(0,0,0);font-family:'Times New Roman';font-size:medium;font-style:normal;font-weight:400;text-transform:none;\"><span style=\"color:rgb(0,0,0);font-family:Arial, Helvetica, sans-serif;\">SCARs</span></p></li></ul><p style=\"color:rgb(0,0,0);font-family:'Times New Roman';font-size:medium;font-style:normal;font-weight:400;text-transform:none;\"><span style=\"color:rgb(0,0,0);font-family:Arial, Helvetica, sans-serif;\">· Support with document control activities, including updates and maintenance in the eDMS</span></p><p style=\"color:rgb(0,0,0);font-family:'Times New Roman';font-size:medium;font-style:normal;font-weight:400;text-transform:none;\"><span style=\"color:rgb(0,0,0);font-family:Arial, Helvetica, sans-serif;\">· Perform Quality Control activities</span></p><p style=\"color:rgb(0,0,0);font-family:'Times New Roman';font-size:medium;font-style:normal;font-weight:400;text-transform:none;\"><span style=\"color:rgb(0,0,0);font-family:Arial, Helvetica, sans-serif;\">· Contribute to risk assessment processes</span></p>"
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{
"name": "Your profile",
"value": "<p style=\"color:rgb(0,0,0);font-family:'Times New Roman';font-size:medium;font-style:normal;font-weight:400;text-transform:none;\"><span style=\"font-family:Arial, Helvetica, sans-serif;\">Education:</span></p><p style=\"color:rgb(0,0,0);font-family:'Times New Roman';font-size:medium;font-style:normal;font-weight:400;text-transform:none;\"><span style=\"font-family:Arial, Helvetica, sans-serif;\">· Degree in life sciences or a related scientific discipline</span></p><p style=\"color:rgb(0,0,0);font-family:'Times New Roman';font-size:medium;font-style:normal;font-weight:400;text-transform:none;\"><span style=\"font-family:Arial, Helvetica, sans-serif;\">· Additional qualification in Quality Management is considered a plus</span></p><p style=\"color:rgb(0,0,0);font-family:'Times New Roman';font-size:medium;font-style:normal;font-weight:400;text-transform:none;\"><span style=\"font-family:Arial, Helvetica, sans-serif;\">Knowledge and Skills:</span></p><p style=\"color:rgb(0,0,0);font-family:'Times New Roman';font-size:medium;font-style:normal;font-weight:400;text-transform:none;\"><span style=\"font-family:Arial, Helvetica, sans-serif;\">· Background in the life sciences sector; experience in the biotechnology or pharmaceutical industry will be highly valued</span></p><p style=\"color:rgb(0,0,0);font-family:'Times New Roman';font-size:medium;font-style:normal;font-weight:400;text-transform:none;\"><span style=\"font-family:Arial, Helvetica, sans-serif;\">· Proven experience with of ISO 15189, ISO 13485 and ISO14971 standards</span></p><p style=\"color:rgb(0,0,0);font-family:'Times New Roman';font-size:medium;font-style:normal;font-weight:400;text-transform:none;\"><span style=\"font-family:Arial, Helvetica, sans-serif;\">· Knowledge of MDR, IVDR, FDA QMSR</span></p><p style=\"color:rgb(0,0,0);font-family:'Times New Roman';font-size:medium;font-style:normal;font-weight:400;text-transform:none;\"><span style=\"font-family:Arial, Helvetica, sans-serif;\">· CLIA, CAP and GMP awareness is a plus</span></p><p style=\"color:rgb(0,0,0);font-family:'Times New Roman';font-size:medium;font-style:normal;font-weight:400;text-transform:none;\"><span style=\"font-family:Arial, Helvetica, sans-serif;\">· Strong understanding of quality methods and problem-solving tools (e.g., FMEA, 5 Whys, Ishikawa)</span></p><p style=\"color:rgb(0,0,0);font-family:'Times New Roman';font-size:medium;font-style:normal;font-weight:400;text-transform:none;\"><span style=\"font-family:Arial, Helvetica, sans-serif;\">· Strong analytical, structured, and solution-oriented working style</span></p><p style=\"color:rgb(0,0,0);font-family:'Times New Roman';font-size:medium;font-style:normal;font-weight:400;text-transform:none;\"><span style=\"font-family:Arial, Helvetica, sans-serif;\">· Strong communication skills and confidence working with cross-functional teams</span></p><p style=\"color:rgb(0,0,0);font-family:'Times New Roman';font-size:medium;font-style:normal;font-weight:400;text-transform:none;\"><span style=\"font-family:Arial, Helvetica, sans-serif;\">· Ability to work in a structured, detail-oriented and compliant manner</span></p><p style=\"color:rgb(0,0,0);font-family:'Times New Roman';font-size:medium;font-style:normal;font-weight:400;text-transform:none;\"><span style=\"font-family:Arial, Helvetica, sans-serif;\">· Proficiency in Microsoft Word, Excel and electronic document management systems (eDMS)</span></p><p style=\"color:rgb(0,0,0);font-family:'Times New Roman';font-size:medium;font-style:normal;font-weight:400;text-transform:none;\"><span style=\"font-family:Arial, Helvetica, sans-serif;\">· Fluent in English (written and spoken)</span></p>"
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{
"name": "Why us?",
"value": "<p style=\"color:rgb(0,0,0);font-family:'Times New Roman';font-size:medium;font-style:normal;font-weight:400;text-transform:none;\"><span style=\"font-family:Arial, Helvetica, sans-serif;\">What we offer</span></p><p style=\"color:rgb(0,0,0);font-family:'Times New Roman';font-size:medium;font-style:normal;font-weight:400;text-transform:none;\"><span style=\"font-family:Arial, Helvetica, sans-serif;\">· Exciting International and diverse team which stands for integrity, involvement and innovation within the life sciences sector</span></p><p style=\"color:rgb(0,0,0);font-family:'Times New Roman';font-size:medium;font-style:normal;font-weight:400;text-transform:none;\"><span style=\"font-family:Arial, Helvetica, sans-serif;\">· Training & development opportunities</span></p><p style=\"color:rgb(0,0,0);font-family:'Times New Roman';font-size:medium;font-style:normal;font-weight:400;text-transform:none;\"><span style=\"font-family:Arial, Helvetica, sans-serif;\">· Company benefits such as company health insurance and company discounts</span></p><p style=\"color:rgb(0,0,0);font-family:'Times New Roman';font-size:medium;font-style:normal;font-weight:400;text-transform:none;\"><span style=\"font-family:Arial, Helvetica, sans-serif;\">· Primarily on-site role with some remote work flexibility</span></p><p style=\"color:rgb(0,0,0);font-family:'Times New Roman';font-size:medium;font-style:normal;font-weight:400;text-transform:none;\"><span style=\"font-family:Arial, Helvetica, sans-serif;\">· Permanent contract</span></p><p style=\"color:rgb(0,0,0);font-family:'Times New Roman';font-size:medium;font-style:normal;font-weight:400;text-transform:none;\"><span style=\"font-family:Arial, Helvetica, sans-serif;\"><br></span></p><p style=\"color:rgb(0,0,0);font-family:'Times New Roman';font-size:medium;font-style:normal;font-weight:400;text-transform:none;\"><span style=\"font-family:Arial, Helvetica, sans-serif;\">About us</span></p><p style=\"color:rgb(0,0,0);font-family:'Times New Roman';font-size:medium;font-style:normal;font-weight:400;text-transform:none;\"><span style=\"font-family:Arial, Helvetica, sans-serif;\">With employees from over 50 nations, CENTOGENE is a truly international company with offices is in Rostock, Berlin, Delhi, Boston, Valencia, Belgrade, and São Paulo. We were born to help diagnostic patients with rare disease and today we evolved to help patients of all clinical specialties to make bold progress with guided solutions for physicians, their patients and pharma partners.</span></p><p style=\"color:rgb(0,0,0);font-family:'Times New Roman';font-size:medium;font-style:normal;font-weight:400;text-transform:none;\"><span style=\"font-family:Arial, Helvetica, sans-serif;\">Our Values</span></p><p style=\"color:rgb(0,0,0);font-family:'Times New Roman';font-size:medium;font-style:normal;font-weight:400;text-transform:none;\"><span style=\"font-family:Arial, Helvetica, sans-serif;\">We Care: A culture of empathy and understanding for each other, our customers, and our patients, constantly driving our mission forward</span></p><p style=\"color:rgb(0,0,0);font-family:'Times New Roman';font-size:medium;font-style:normal;font-weight:400;text-transform:none;\"><span style=\"font-family:Arial, Helvetica, sans-serif;\">We Innovate: A culture of big ideas, being bold, and taking calculated risks to develop never-before-seen solutions</span></p><p style=\"color:rgb(0,0,0);font-family:'Times New Roman';font-size:medium;font-style:normal;font-weight:400;text-transform:none;\"><span style=\"font-family:Arial, Helvetica, sans-serif;\">We Act With Integrity: A culture of keeping to our principles with self-awareness, intellectual honesty, and speaking up</span></p><p style=\"color:rgb(0,0,0);font-family:'Times New Roman';font-size:medium;font-style:normal;font-weight:400;text-transform:none;\"><span style=\"font-family:Arial, Helvetica, sans-serif;\"><br></span></p><p style=\"color:rgb(0,0,0);font-family:'Times New Roman';font-size:medium;font-style:normal;font-weight:400;text-transform:none;\"><span style=\"font-family:Arial, Helvetica, sans-serif;\">If you are interested, we look forward to receiving your application, including your CV, motivation letter, earliest possible start date, and salary expectations.</span></p>"
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