Trainee, Quality Control-ARPL

Perform and report the analysis of In-Process samples, Cleaning Verification,Validation , Finished products, Stability and other samples.

• To ensure timely completion of analysis and data completion for the same.
• To be responsible for all activities in the Quality Control Laboratory, including cGLP, documentation and implementation of departmental quality systems.
• To perform the analysis of In-Process samples, Cleaning Verification,Validation , Finished products, Stability and other samples.
• To collect and maintain various laboratory samples.
• To generate and maintain records related to laboratory samples.
• 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.
• To assist the Senior Executive /Assistant Manager/Manager/Sr.Manager in the day-to-day functioning of the Quality Control Laboratory
• 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 activities as assigned.

• Education
  • Minimum MSc/B Pharma or any equivalent degree.
• Knowledge, Skills and Abilities
  • Data base Management system like Empower, LIMS.
  • Effective command over verbal and written communication with good interpersonal skills.
  • Maintaining Good interpersonal skills and communication skills.
  • Well expertised in cGDP and cGLP.
• Experience
  • Minimum 1 to 2 years of experience in GMP regulated Pharmaceutical Industry.