Core Responsibilities:
Procedures / Governance:
Day to day assigned activities shall be conveyed to the reporting authority
Any requirement related to QA shall be conveyed to reporting authority
Draft quality assurance policies and procedures
Vendor Management Activities (Paper & Physical Onsite Audits)
Review Equipment Qualification Data
Performing issuance activity of all the departments
Review BMR and BPR
Arranging training as per the schedule
Maintain trackers for all QMS records
Batch release process
Follow GLP and GDP.
Testing sample for OOS, OOC, deviation and OOT.
Maintain stock for chemicals and glass wares.
Maintain control sample.
Responsible for discard expired and extra samples
Any job activity assigned by HOD.
Ensure to follow safety norms.
Ensure to wear PPE during analysis.
Training
Impart training on Safety to new recruits, employees, contractors, contract employees.
Periodically evaluate Training Effectiveness.
Maintain updated records for all the Training activities.
Qualified candidates will have:
Mandatory requirements:
Education requires, B.SC / M.SC Chemistry.
Minimum of 4-5 years of experience in a quality control laboratory, preferably in the
pharmaceutical industry / Chemical Industry.
Relevant Experience in Quality Laboratory in Pharma / Chemical Industry
English fluency, both written and spoken
Required behaviors and skills:
Meticulously checking every aspect of the product to ensure quality standards are met.
Ability to analyze complex problems and identify root causes.
Clear and effective communication with team members and stakeholders.
Taking initiative to identify potential issues before they become problems.
Flexibility to adjust to changing requirements and environments.
Working well within a team to achieve common goals.
Upholding ethical standards and honesty in all QA processes.