Looking for an opportunity in biopharmaceutical Quality Assurance? Whether you’re already in QA or would like to take on a new challenge from pharmaceutical manufacturing or quality control, this week’s job of the week could be what you’re looking for. Our client, a growing biopharmaceutical CDMO, are expanding across departments and taking on talent in all areas of the business. With focus on vector development, joining this organisation will allow you to operate at the cutting edge of science and work with experts in the field.
Amongst these opportunities, multiple vacancies in the contracts QA team have arisen for candidates with a sound working knowledge of cGMP and good attention to detail. This role will be split across facility/line inspection and batch record reviewal, so an adaptable individual with previous experience in the pharmaceutical cleanroom environment would be ideal. The most important aspect of the role will be technical document creation and review, so previous experience in this area as well as a understanding of the broader quality function will be necessary for success in the role.
Training will be available to supplement your experience, so if the next step in your career development is a move into QA, or you’re looking to accelerate your QA career within biopharmaceuticals, follow the link to find out more…