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For our client, an international pharma company in Basel, we are looking for a motivated Quality Assurance Manager.

General Information:

Tasks & Responsibilities:

End-to-end quality oversight on the qualified state of all assets in your assigned area.
Provide fit for purpose quality support for all the activities related to qualification & CSV, calibration, maintenance & reliability engineering.
Review and approve GMP records that cover technical change management, deviation management & CAPAs, risk assessments and SOPs.
Coordinate and facilitate complex investigations, root cause analyses, technical risk assessments, and continuous improvement projects.
With your operations partner you present topics during health authority inspections and internal audits.

Must Haves:

University degree in science or engineering
Min. 3 years demonstrated experience in Quality Assurance at a pharmaceutical manufacturing site
Practical experience in commissioning & qualification projects in highly automated GMP production facilities
Well established confidence in setting precise guidance for QA compliance in technical changes, deviations and CAPAs
Your collaboration with partners is characterized by outstanding communication and team work.
You manage to drive quality awareness with operations partners at all levels by integrating regulatory requirements, analytical problem solving and scientific rationale.
Excellent German and English language skills, both written and spoken.

For our client, an international pharma company in Basel, we are looking for a motivated Quality Assurance Manager.

General Information:

Tasks & Responsibilities:

End-to-end quality oversight on the qualified state of all assets in your assigned area.
Provide fit for purpose quality support for all the activities related to qualification & CSV, calibration, maintenance & reliability engineering.
Review and approve GMP records that cover technical change management, deviation management & CAPAs, risk assessments and SOPs.
Coordinate and facilitate complex investigations, root cause analyses, technical risk assessments, and continuous improvement projects.
With your operations partner you present topics during health authority inspections and internal audits.

Must Haves:

University degree in science or engineering
Min. 3 years demonstrated experience in Quality Assurance at a pharmaceutical manufacturing site
Practical experience in commissioning & qualification projects in highly automated GMP production facilities
Well established confidence in setting precise guidance for QA compliance in technical changes, deviations and CAPAs
Your collaboration with partners is characterized by outstanding communication and team work.
You manage to drive quality awareness with operations partners at all levels by integrating regulatory requirements, analytical problem solving and scientific rationale.
Excellent German and English language skills, both written and spoken.

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Quality Assurance Manager (m/f/d).

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