Position title : ESO QA Specialist
- University degree in Pharmacy, Chemistry, Biology, or relevant Life Science
- Minimum of 5 years in a similar role or equivalent experience in a GMP-related environment
Job location - Ankleshwar, Gujarat, India
MISSION STATEMENT
To ensure the quality lifecycle management for dedicated, subcontracted, product portfolio. Qualified auditor.
MAIN ACCOUNTABILITIES AND DUTIES
Operational skills
Operational quality management of a dedicated product portfolio which includes :
Quality management of deviation and complaint records and their related CAPAsAssessment and management of change controlsEdition of QA Agreements with Zentiva third parties and subcontractorsCollection and evaluation of PQRs and stability dataCompliance evaluation of Third Parties and productsMaintenance of product databaseCollection and review of CoA / CoCQA support of product launches and transfersGMP, GDP, MDR, HACCP, Food Supplements and Cosmetics regulations and legislationsAuditing
Prepare audit and audit plansConduct and participate to external auditsEvaluation of audit reportsParticipate to internal audits and inspectionsKPI monitoring and reporting
Other tasks may be performed under the direction of the Manager within the agreed-upon type and scope of work.
REQUIRED QUALIFICATIONS, EXPERIENCE & SKILLS
University degree in Pharmacy, Chemistry, Biology, or relevant Life ScienceMinimum of 5 years in a similar role or equivalent experience in a GMP-related environmentThorough knowledge of GMP requirements as well as knowledge of ICH and pharmaceutical regulatory requirementsManagement of subcontractors is an advantageProven track record of project management skillsStrong communication skills and negotiation strengthProactive attitudeProblem-solving skillsHands-on attitude, flexible and open-mindedCollaborative and team-spiritedKnowledge of IT toolsLanguage - English : Advanced level