Responsibilities also include documentation review, maintaining product quality, coordinating training, conducting initial incident investigations, and managing process orders.
This role is responsible for managing and overseeing critical aspects of the production process, ensuring adherence to quality standards and regulatory compliance.
Seeking a motivated PVQA professional who will own PV and QMS excellence, lead audits, ensure inspection readiness, and drive continuous improvement across the safety system.
Develop business plans and implement related activities like customer events, sales & marketing campaigns, sales presentations necessary to achieve agreed objectives.
SCIENCES OR PHARMACY GRADUATES (B.SC./M.SC./B. PHARM./M. PHARM.) WITH 0 TO 5 YEARS EXPERIENCES IN PARENTERAL MANUFACTURING (VIAL / AMPOULES / BOTTLES OF GLASS OR PLASTIC THROUGH
Minimum 2 years of experience in the medical writing industry; freshers with substantial knowledge of the publication landscape or clinical research are also eligible.
Bachelors degree required advanced degree preferred, scientific discipline preferred with at least 2 years of operational experience in pharmaceutical production, Supply Chain, Quality and/or clinical trials.