QA/QC Biotech Manager

We have an exclusive 6 month contract role available to work onsite with a renowned Pharmaceutical company in Brussels, Belgium. This is an opportunity to provide QA support to analytical method life cycle management projects (incl. method validation) for QC. QA/QC Biotech Manager (Project manager) will maintain compliance level of method validation and associated quality life cycle elements with regulatory and internal standards and ensure the implementation of CAPA.

Please see general requirements for the application below:

- Experience of at least 2 years in a QA function supporting a Laboratory Quality Management
- System in a Bio/pharmaceutical industry
- Experience of at least 2 years in QC release and stability testing (analyst and supervisor), test method development, validation, comparison and batch overview testing to support existing and justify revised specifications
- University Scientific Degree (Master) in a general Science or Life Science Degree (Pharmacy,
- Chemistry, Bio Engineer, Biology, Biomedical Sciences).
- Good knowledge of current good manufacturing practices in biopharmaceuticals and analytical method validation within a analytical quality life cycle management framework
- Good manufacturing and laboratory operations knowledge (method validation included)
- Excellent French and good knowledge of English (written and spoken)

We welcome applications of consultants' who match most of the above requirements and are available on a short notice. There is a competitive Hourly rate available for the contract, alternative market rates are also welcome. Please note there is a job description available on request and there is a likelihood of the contract extending into 2016.

We hope the role will be of interest to you and understand that further information may be required before making an application to the end client, please feel free to send either your full name, contact details or a complete CV via this email and I will endeavour to get back to you with further information on the role and answer any questions you may have.

Kind regards,

Neha Sharma

MBA Michael Bailey Associates

Job Code: 106373

Keywords: Pharmaceutical, QC, Quality control, Biopharmaceutical, Biotech, Biochemistry, Quality check, GMP, ICH, GCP, CTA, clinical trials, clinical project management, pharmacology, clinical research, French, English, clinical reports, statistical, regulatory constraints, Re-Validation Assessment, RVA, CAPA, validation method, validation, stability testing, laboratory quality management system, QMS, SOP Michael Bailey International is acting as an Employment Business in relation to this vacancy.