QA Officer Batch Release
Description✓QA Officer Batch Release
✓We are working exclusively with an award winning pharmaceutical company based in the East Midlands
✓This is a new hire for a QA Officer, which has come about as the current incumbent has been promoted.
✓This is a perfect opportunity for someone who is looking to take their first step into the quality assurance field from a GMP production or laboratory role
✓Equally, this could be an excellent fit for an established QA professional who would be keen on a new challenge in a dynamic and fast paced company.
✓Beyond experience, the most important qualities are enthusiasm, a willingness and ability to learn quickly and working as a team player.
✓Experience/ Requirements:
✓* 1-2 years’ working with pharmaceutical GMP standards
✓* Previous experience from either QA, laboratory or production job
✓* Some previous experience dealing with quality documentation
✓* Any relevant experience with batch documentation, CAPA, deviations would be an advantage
✓* IT literate [Excel, Word etc.]
✓* Team player and collaborative nature
✓* Quick learner
✓* Attention to detail
✓Key Words;
✓QA, quality, assurance, pharma, pharmaceuticals, 9001, GMP, ISO, audit, CAPA, document, documentation, investigation, complaint, deviation, supplier, external, QMS, manufacturing, SOP, process, change, controls, batch, release, administration, BSc, admin
✓Harris Lord is acting as a recruitment agency for this role Show more →
✓We are working exclusively with an award winning pharmaceutical company based in the East Midlands
✓This is a new hire for a QA Officer, which has come about as the current incumbent has been promoted.
✓This is a perfect opportunity for someone who is looking to take their first step into the quality assurance field from a GMP production or laboratory role
✓Equally, this could be an excellent fit for an established QA professional who would be keen on a new challenge in a dynamic and fast paced company.
✓Beyond experience, the most important qualities are enthusiasm, a willingness and ability to learn quickly and working as a team player.
✓Experience/ Requirements:
✓* 1-2 years’ working with pharmaceutical GMP standards
✓* Previous experience from either QA, laboratory or production job
✓* Some previous experience dealing with quality documentation
✓* Any relevant experience with batch documentation, CAPA, deviations would be an advantage
✓* IT literate [Excel, Word etc.]
✓* Team player and collaborative nature
✓* Quick learner
✓* Attention to detail
✓Key Words;
✓QA, quality, assurance, pharma, pharmaceuticals, 9001, GMP, ISO, audit, CAPA, document, documentation, investigation, complaint, deviation, supplier, external, QMS, manufacturing, SOP, process, change, controls, batch, release, administration, BSc, admin
✓Harris Lord is acting as a recruitment agency for this role Show more →