Analysis of packing material, raw material samples as per method of analysis by adhering to the Regulatory Procedures.
Sampling and analysis of water as per the procedures defineded.
Works as a member of a team to achieve all outcomes.
Performs all work in accordance with all established regulatory and compliance and safety requirements.
Any other Responsibilities / Duties assigned by the Head of the Department / Designee as and when required.
Performs all work in support of our Corporate values of perseverance, passion, collaboration and courage.
Performs all work in accordance with all established regulatory and compliance and safety requirements.
Works in a safe manner collaborating as a team member to achieve all outcomes.
Demonstrate Behaviours that exhibit our organizational Values: Collaboration, Courage, Perseverance, and Passion.
Ensure personal adherence with all compliance programs including the Global Business Ethics and Compliance Program, Global Quality policies and procedures, Safety and Environment policies, and HR policies.
All other relevant duties as assigned.
Qualification & Experinece
Minimum Msc/Bpharm or any equivalent degree.
Knowledge, Skills Abilities
Effective command over verbal and written communication with good interpersonal skills
Command on Microsoft-office (Word, Excel)
Able to perform all the allocated tasks
Well expertised in cGDP and cGLP.
Best in effective planning of work activites to meet the time lines
Experience:
Minimum 3 to 6 years of experience in GMP regulated Pharmaceutical Industry