senior quality assurance associate in baar

posted
job type
temporary
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job details

posted
location
baar, zug
job category
Life Sciences
job type
temporary
reference number
13490
phone
058 201 55 50

job description

Randstad Professionals is currently looking for a Quality Assurance Associate who will be assigned an interesting challenge for a major client based close to Zug in Central Switzerland.

This contract is a great opportunity to join a global group in the Biotech sector. The initial assignment will start immediately and will last until June 2020.

 

Contract details:

Start Date:   ASAP

Requisition End Date:   June 2020

 

Assignment overview

The main purpose of this job is to manage own assignments (i.e. Finished Good GCCs related to new items, specifications artwork and Product Life Cycle) as well as to coordinate and to ensure accurate prioritization among all GEQ Int QA contacts who are supposed to take action on their Finished Googs GCC assignments. 

Manage the QA interface with all Logistics service providers and warehouses under the oversight of our client.

 

Responsibilities:

  • Managing the QA interface with manufacturing partners for commercial small molecules (oral solid dosages) finished good products by ensuring quality of product / process transfers, validations, investigations, tracking and resolution of issues in a timely manner as well as process improvements

  • Evaluation of the general performance of contractors and the identification, negotiation, implementation and follow-up of process and systems improvements, as well as the organization and conduct of quality management review with contract manufacturing organizations.

  • Continuous Improvement Lead for Global External Quality International (focusing on Quality Engineering and Release related projects).

 

Requirements: 

  • A minimum of 5  years of experience in similar position in pharmaceutical or biotechnology industries

  • Relevant experience in either manufacturing, development, quality or regulatory;

  • Understanding of cGXPs, quality systems and regulations (FDA and EU, knowledge of Japanese or other geographies’ regulations is a plus);

  • Knowledge of medical device regulations and manufacturing is a plus

 

If you are interested to learn more about this great opportunity, don’t hesitate to get in touch with me. Feel free to send me your CV at following email

 

olivier.worch@randstad.ch

I am looking forward to receiving your applications

 

Olivier Worch