Senior Quality & Compliance Manager in Manufacturing (a), 100% — Bachem AG
- Location
- Bubendorf
- Contract
- full-time
- Posted
- Yesterday
Role overview
In order to drive our continuous organic growth, we are constantly looking for highly qualified professionals.
To strengthen our team in Manufacturing Coordination, we are looking for a dedicated Senior Qualitiy & Compliance Manager in Manufacturing (a), 100% You have a central role in dealing with more complex quality & compliance issues and report directly to the Senior Director Manufacturing Coordination in this responsible role. Their tasks:
Perform complex investigations in the company according to Quality Events in Manufacturing
- In order to drive our continuous organic growth, we are constantly looking for highly qualified professionals.
- To strengthen our team in Manufacturing Coordination, we are looking for a dedicated Senior Qualitiy & Compliance Manager in Manufacturing (a), 100% You have a central role in dealing with more complex quality & compliance issues and report directly to the Senior Director Manufacturing Coordination in this responsible role. Their tasks:
- Master in Natural Sciences (Chemistry, Pharmacy, Chemical Engineering) with doctorate
- At least 7 years of professional experience in a relevant industry (pharmaceutical industry/ C(D)MO in the field of drug substance manufacturing beneficial), of which several years with QA responsibility for their own area/department
Key requirements
- Master in Natural Sciences (Chemistry, Pharmacy, Chemical Engineering) with doctorate
- At least 7 years of professional experience in a relevant industry (pharmaceutical industry/ C(D)MO in the field of drug substance manufacturing beneficial), of which several years with QA responsibility for their own area/department
- At least 5 years of experience in the functional leadership of interdisciplinary teams in complex environments with multiple interfaces
- At least 5 years of experience in project management, managing interdisciplinary project teams and dealing with customers, authorities and internal stakeholders
- Experience in creating concepts for compliance with current GMP regulations, with a focus on cGMP rules for active ingredients of CH, EU and USA
- Good knowledge in the field of analytical processes and organic synthesis chemistry (peptide preparation and analysis advantageous) Appreciative, rousing leadership style; Example of teamwork; Bridge builders
- Strong communication and presentation skills, decision-making skills
- Business acumen with an eye for the big picture as well as for the relevant detail Experience in Change Management
- Negotiable knowledge of English and German in word and writing Our offer:
- A dynamic and rapidly growing working environment with internal development and further education opportunities
- Flexible working hours with the option of home office and the option to purchase additional holidays with reduced workload
- Company-internal KITA on the Bachem Campus Bubendorf
Application process
- Then we look forward to your complete application documents via our application portal.
- Learn more about the Bachem Group and be inspired by our inspiring working environment at our location in Bubendorf!
Company and context
- Formulating the associated Deviation Records together with QA and the relevant organizational units
- Derivation of purposeful, including cross-divisional, CAPAs in coordination with the organisational units concerned
- Ensuring deadline compliance in the processing of all quality events in the field of manufacturing
- Creation of quality metric dashboards for department management and presentation of quality topics at team meetings
- Continuous improvement of quality culture in manufacturing in accordance with cGMP guidelines and company requirements.
- Representation of the area in customer audits and inspections of the health authorities (e.g.
- Swissmedic, FDA, etc.) including preparation and follow-up
- Management / control of strategic projects in your own area as well as active participation in cross-divisional initiatives
Additional details
- To strengthen our team in Manufacturing Coordination, we are looking for a dedicated Senior Qualitiy & Compliance Manager in Manufacturing (a), 100% You have a central role in dealing with more complex quality & compliance issues and report directly to the Senior Director Manufacturing Coordination in this responsible role.
- Good knowledge in the field of analytical processes and organic synthesis chemistry (peptide preparation and analysis advantageous) Appreciative, rousing leadership style; Example of teamwork;
- Business acumen with an eye for the big picture as well as for the relevant detail Experience in Change Management
- Negotiable knowledge of English and German in word and writing
Notes and original content
- Their tasks:
- Your profile:
- Good knowledge in the field of analytical processes and organic synthesis chemistry (peptide preparation and analysis advantageous)
- Appreciative, rousing leadership style;
- Example of teamwork;
- Bridge builders
- Business acumen with an eye for the big picture as well as for the relevant detail
- Experience in Change Management
Questions about this listing
What salary does Bachem AG offer for this role?
Bachem AG lists CHF 99'500 - 151'000 gross per year for this position in Bubendorf. This is the salary published in the original listing (or, when the employer omits a figure, a realistic estimate for the role and sector) — the calculator on this site converts it to your actual net take-home once cross-border tax and social contributions are applied.
Is this a full-time role, and what type of contract does Bachem AG offer?
This listing is a full-time position. The contract type shown here comes directly from the employer's original posting; always confirm exact hours, notice period and probation length with Bachem AG during the application process, since these details can vary by role even within the same contract category.
Do I need a cross-border work permit for a role in Basel?
EU/EFTA residents living in the border zone of the country adjoining Canton Basel can apply for a G permit; the Swiss employer files it with that canton's migration office after the contract is signed. Border-zone rules and processing times vary by neighbouring country and canton, so confirm the specifics with Basel's cantonal migration office or with HR during the application.
How do I apply for this position at Bachem AG?
Use the "Apply now" button on this page — it links directly to Bachem AG's original listing at careers.bachem.com, so your application goes straight to the employer's own applicant-tracking system. Frontaliere Ticino does not collect or forward applications itself.
