QAV Engineer

IE  ‐ Onsite
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Description

Our global biopharmaceutical organisation requires a QAV Specialist to join them on an initial 12 month contract.
Duties:
  • Reporting to the QA Manager.
  • Change control assessment and review for all laboratory equipment.
  • Review and approval of all laboratory equipment documentation.
  • Authoring, review and approval of appropriate Validation related procedures and philosophy documents.
Skills/Experience required:
  • A clear understanding of cGMP requirements of laboratory equipment and qualification.
  • A knowledge of ICH guidelines, FDA regulations and a working knowledge of GAMP guidelines would prove advantageous.
  • The successful candidate will hold a BSc in Biochemistry (or science related discipline), or a BEng.
  • Previous experience in a pharmaceutical environment within a Validation role.
  • A strong working knowledge of US and EU GMP regulations, and the principles of qualification and validation would be beneficial, but not essential.
  • The successful candidate must be able to demonstrate excellent time management and organisational skills along with a proven ability to multi-task.
  • The QAV Specialist will be required to work on his/her own initiative as much as working as part of a team.
  • As such excellent interaction, communication and presentation skills are necessary to be successful in the role.
If this is you please apply today
Start date
ASAP
Duration
12 months
From
Quanta Consultancy Services
Published at
12.05.2017
Project ID:
1342348
Contract type
Freelance
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