Instrument Qualification Expert

Job content

Proclinical are recruiting an Instrument Qualification Expert for a manufacturing establishment. This role is on a contract basis and is located in Visp. The client is focused on empowering a healthier society.

Responsibilities

• Guarantee compliance of laboratory systems rendering to cGMP, following pertinent SOPs, present best practices and global procedures and existing documents practices.
• When needed, evaluate and consent to laboratory systems associated documents, following valid SOPs and all present documentation practices.
• You will install, qualify, and sustain instruments for DP Physico-Chemical QC in line with present best practices and guidelines.
• Progress and transcribe IQ/OQ and PQ papers, validation designs/documents and any other prerequisite pertinent documents.
• The ideal candidate will warrant proper preservation of equipment, safety and health protection, following lab and safety protocols and all cGMP guidelines.
  

Skills & Requirements

• Past involvement in instrument qualification and/or computer system validation of analytical instruments and related applications in a pharmaceutical establishment.
• Know-how of regulatory needs such as 21 CFR Part 11, GAMP5, etc.
• Pertinent knowledge of analytical techniques and accessible apparatus as well as GMP compliant document knowledge.
• Comprehension and reporting of outcomes and a comprehension of pertinent guidelines and document needs.
• Fluency in the English language.
  

If you are having difficulty in applying or if you have any questions, please contact Sasha Botha at +41 61 568 79 88.

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

Proclinical Staffing is an equal opportunity employer.

#QACompliance