Quality Control Manager

Zurich  ‐ Onsite
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Description

Quality Control Manager- Switzerland - 6 months

Our client, a Certified Contract Manufacturer in the pharmaceutical sector is currently seeking for a Quality Control Manager for a 6 month project in Zurich, Switzerland.

Responsibilities:
  • Lead the chemical-physical department at the site with the overall responsibility of the professional assessment for the analytical release of pharmaceutical semi-finished and finished products.
  • Participation in laboratory optimization projects (Laboratory Excellence)
  • Responsible for Raw Material Release, Finished Products Release, Validation / Product Transfer, QC-support (Stability and Packaging Release) and 1 Coordinator for analytical product transfers.
  • Responsible for the analytical release of raw materials, stability samples and finished products
  • Professional assessment and root cause analysis of analytical deviation reports, OOS examinations and the definition of corrective and preventive measures
  • Professional support in making changes, especially risk assessments
  • Ensuring the calibration, maintenance and qualification of analytical equipment
  • Professional and personnel overview of method transfer and validation activities
  • Knowledge of the most important pharmacopoeia book methods (Ph.EUR / USP / BP) and compliance with the most important regulatory requirements in the GMP environment
  • Support of customer projects in the analytical field
  • Ensuring the timely release of raw materials and finished products (OTIF)
  • Support in the preparation of Annual Product Quality Reviews
  • Evaluation of trends and collection of KPIs
  • Interdisciplinary cooperation with internal and external customers
  • Support for regulatory inspections and audits
  • Professional support of the HSE team


Requirements
  • Science degree (FH, Uni, ETH)
  • Knowledge of instrumental and classical chemical analysis
  • At least 7 years experience in pharmaceutical quality control
  • Sound GMP knowledge (EU, FDA), as well as ISO and ICH guidelines
  • Proficient in German and English
  • Knowledge of IT systems in the pharmaceutical environment
  • Assertiveness and good communication skills
  • Lean Six Sigma or statistical knowledge of advantage
  • Relevant working/residency permit or Swiss/EU-Citizenship required


I am a specialized recruiter, currently taking care of various projects within the Life Science area in Switzerland. If this role is of interest to you or to someone from your network, please send your CV in Word including your hourly rate expectation for immediate consideration.

You can reach me on or at (a.xenitidis'at'realstaffing.com)

Keywords: QC, Quality Control, validation, analytics, laboratory, contract, Switzerland, Zurich, German, English

Sthree Switzerland is acting as an Employment Business in relation to this vacancy.
Start date
02/2018
Duration
6 Months
From
Real Staffing
Published at
06.01.2018
Project ID:
1479410
Contract type
Freelance
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