Curious about a career move that allows you to really use your training skills in a way that contributes to other’s career development and quality assurance?
GBI Biomanufacturing is expanding their QA team! GBI is a fantastic biologics CDMO focused on keeping the world healthy. This particular role will be responsible for coordinating, delivering, monitoring and improving training activities and systems that directly affect manufacturing and laboratory processes.
The QA Training Manager will assist with QA Systems Management and Document Control, and report to the Associate VP of Regulatory & Quality Assurance.
- Coordinate, schedule and deliver training, ensuring documentation is completed and filed, the Training System is updated, and resolve any training questions.
- Organize and facilitate New Hire Orientation, schedule and monitor the 90-day onboarding activities.
- Maintain SOPs, procedures, audit training documents, and other technical competencies to ensure effective training delivery. Participate in client and regulatory audits, and review the QMS to determine focussed training needs.
The ideal candidate will have a Bachelor’s degree in a Life Science, or related field. They will also have 7+ years experience of working in an FDA-regulated environment (Biologics/ Pharmaceuticals/ Medical Devices/ Tissues), along with at least 1 year experience working with electronic QMS (Master Control, Documentum, Trackwise).
Apply now or find out more about this role here: QA Training Manager – GBI.
Don’t meet all the requirements? Don’t sweat! We’re always looking for an excuse to discuss your next opportunity. You might just surprise yourself…
Lead Candidate wholeheartedly supports Equality and Diversity in employment and opposes all forms of unlawful or unfair discrimination on the grounds of age, disability, sex, gender reassignment, sexual orientation, pregnancy and maternity, race, religion or belief and marriage and civil partnerships.