Vacancy Description
Roles and responsibilities:
- Must-Have Skills & Experience.
- Strong experience in Large-Scale Equipment CQV.
- Mandatory IOQ experience with Filter Press or Centrifuge (one required).
- Hands-on execution of IQ, OQ, PQ for capital projects.
- Expertise in authoring CQV lifecycle documentation (Protocols & Reports).
- Biopharma industry experience (No CSV / No small-scale CQV).
- Ability to self-manage CQV projects independently end-to-end.
- Excellent written & verbal communication skills.
- Kneat experience is a strong plus.
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