Release activities, by reviewing CoAs, Manufacturing & Packaging Records (BMR, BPR) and management of documentation related.
Proposal and management of corrective actions with focus on continuous improvement.
Support in the review of Quality Technical Agreements with customers and suppliers.
Management of deviations and customer/ suppliers claims.
Management of changes, incidences and nonconformities.
Keep updated on GMP regulations and evaluate the impact within our own Quality System and activities.
Previous experience required:
Minimum 3-4 years experience in GMP environment.
Minimum 2 years in QC/QA in a Pharmaceutical manufacturing site, preferably with Qualified Person (QP) release responsabilities.
Experience MS Office
Motivated, disciplined, proactive, dynamic, methodical, organized and decisive.
Strong analytical and problem solving skills.
Strong organizational, planning and time management skills, to achieve project timelines.
Highly responsible and capable to work under pressure to meet deadlines.
Ability to prioritize multiple tasks
Detail oriented and good communication and research skills.
Capable of working under your own initiative whilst being a good team player.
Degree in Pharmacy
Excellent level of English and Spanish, spoken and written.
Master’s degree in Pharmaceutical Industry.
Tagged as: QA Technician
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