CQV Technical Writer — GMP Validation Documents

A pharmaceutical solutions company is seeking a Technical Writer (CQV) to develop and manage commissioning, qualification, and validation documentation. The ideal candidate will have a degree in Engineering or Life Sciences, along with 3-5 years of relevant experience in a pharmaceutical or biotech setting. Responsibilities include authoring protocols, ensuring compliance with GMP standards, and collaborating with various teams. This role offers professional development opportunities and a supportive work environment. #J-18808-Ljbffr