Associate Quality Manager job in Basel, Switzerland

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First Name*

Last Name*

Email*

Phone Number*

Country*

Are you an employer or a jobseeker?*

Message

First Name*

Last Name*

Email*

Phone Number*

Country*

Are you an employer or a jobseeker?*

Message

First Name*

Last Name*

Email*

Phone Number*

Country*

Are you an employer or a jobseeker?*

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Job type: Contract

Discipline: Senior/Director & VP

Location: Switzerland

This vacancy has now expired. Please see similar roles below...

A pharmaceutical company is looking for an Associate Quality Manager to join their team in Basel. This is an amazing opportunity to bring your experience and talent to an established Pharmaceutical organisation.

Job Responsibilities

Perform review of GMP relevant documents for compliance with SOPs across several customer groups
Negotiate deficiencies in GMP documents with the line unit
Recognize complex deficiencies in GMP documents, report them to supervisor, suggest actions and supervise agreed follow-up.
Act as contact person for QA questions of quality relevant electronic systems
Write and complete GMP relevant documents in own area of responsibility
Perform statistical interpretation of trending data collected by QA.
Collaborate with other associates to support the service function of QA
Participate in knowledge exchange within and outside of TRD.
Participate in training and coaching of new and temporary employees in QA and from associated line functions.

Skills and Requirements

Basic degree in science, laboratory, manufacturing or relevant discipline
At least 5 years of experience in a corresponding line unit function (e.g. laboratory, manufacture, packaging, IT)
Negotiation and communication skills to address GMP related questions with the line unit experts, in order to maintain GMP records in a compliant status.
Sound scientific, technical and regulatory knowledge in a specific area.
Detailed knowledge of relevant GMPs, working knowledge of safety and environmental regulations and guidelines.
Good knowledge of drug development
Proven ability to analyze and evaluate GMP compliance
Knowledge and flexibility to work with relevant IT systems

To Apply

Please click on the Apply button. Please include a short note outlining why you are interested in the role and why you think you are suitable.

In case you have difficulty in applying or if you have any questions, please contact Caleb Mensah at +44 203 854 1080 or upload your CV on our website - www.proclinical.com/send-cv

A full job description is available on request.

Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies

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