Job Title
We are seeking a highly skilled Quality Assurance Specialist to join our Laboratory Team.
The ideal candidate will possess strong analytical and problem-solving skills, with the ability to prioritize multiple tasks and work under pressure to meet deadlines.
Key Responsibilities :
- 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.
- Participate in external audits to CMOs related to own release products, with execution of audit, review and evaluation of audit reports, CAPA plan evaluation and follow-up.
- Periodic follow-up of Customers for designed release products.
Requirements
GMP Knowledge :
Minimum 3-4 years' experience in GMP environment.Education :
Degree in life sciences, preferably in Pharmacy.Languages :
Excellent level of English and Spanish, spoken and written.Personal Qualities :
Motivated, disciplined, proactive, dynamic, methodical, organized and decisive.Self-sufficient.Strong analytical and problem-solving skills.Highly responsible and capable to work under pressure to meet deadlines.About Us
We're a company that values our employees and provides a supportive work environment. We believe in growth and development and offer opportunities for advancement.