Senior Officer, Quality Con-ARPL-QFSA AR

You will be responsible for performing and reporting the analysis of In-Process samples, finished products, Stability samples, and Cleaning Validation. Your key responsibilities will include: - Ensuring timely completion of analysis and data completion for the same. - Being responsible for all activities in the Quality Control Laboratory, including cGLP, documentation, and implementation of departmental quality systems. - Performing the in-process/finish product/stability testing of laboratory Batches, Commercial batches, other stability samples, and Cleaning validation. - Preparing Stability Trend Reports for Laboratory samples. - Collecting and maintaining various laboratory samples. - Generating and maintaining records related to laboratory samples. - Working as a member of a team to achieve all outcomes. - Performing all work in accordance with all established regulatory and compliance and safety requirements. - Demonstrating Behaviors that exhibit organizational Values: Collaboration, Courage, Perseverance, and Passion. - Assisting the Senior Analyst / Team Leader/Group Leader in the day-to-day functioning of the Quality Control Laboratory. - Ensuring 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. - Performing any other duties as assigned. Qualifications required for this role are: - Education: M.Sc\BPham or any equivalent degree - Knowledge, Skills, and Abilities: - Effective command over verbal and written communication with good interpersonal skills. - Command on Microsoft-Office (Word, Excel). - Able to prioritize tasks and effectively plan work activities to meet deadlines. - Experience: Minimum 2 to 4 years of experience in GMP regulated pharmaceutical industry.,