Assistant Manager Quality Control

Full time Full day
  • Testing of Finished products and stability
  • Testing of water and other utilities (as applicable) from all plants and GMP areas
  • In-house calibration of instruments (where required)
  • Perform and support/manage other testing's e.g. Cleaning verification, process validation, complaints samples & generics as and when required
  • Timely documentation of all testing and sampling and adherence of Data integrity principles
  • Maintain data management and other documentation of analyzed Finished Goods, Stability and Raw Material
  • Timely reporting of OOT & OOS results
  • Follow company policies and execute departmental procedures (SOP)
  • Follow and support company policies and site specific initiatives and standards to remain fully aligned with company’s objectives
  • Interactions and interpretations for better safety environment and quality of drugs
  • Ensure update of the logbooks of all instruments
  • Participate and ensure participation of the team in behavior observation program of site and drive the positive change in safety culture of the site through leading the safety champion’s nomination and the reward in the area
  • Monitor and ensure compliance of PASS achievement, Medical Screening and Surveillance and on floor safety training programs
  • Ensure compliance with Permit To Work, Lock Out/ Tag Out, Safe Work Practices and PPEs to drive health and hygiene program of the site, related to your area/function
  • Ensure on time CAPA closure for all HSE audits, inspection and incidents gaps and actions, relevant to your function
  • Ensure on time reporting of all incidents including near misses and environmental incidents, to the concerned person
  • Management of Glassware and chemical inventory
  • Management of reference standards
  • Management of raw data log books
  • Testing of semi-finished, stability and finished drug products
  • Sign off the QC Status labels (sample taken, release, hold and reject)
  • Revision and preparation of SOPs and methods
  • Trainings on different topics which are assigned by supervisor
  • Analytical method validation of non pharmacopeia
  • Analytical method verification of pharmacopeia products
  • Management of Specification

At Sanofi diversity and inclusion is foundational to how we operate and embedded in our Core Values. We recognize to truly tap into the richness diversity brings we must lead with inclusion and have a workplace where those differences can thrive and be leveraged to empower the lives of our colleagues, patients and customers. We respect and celebrate the diversity of our people, their backgrounds and experiences and provide equal opportunity for all.

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