QC Analyst - Shifts

Key Roles/Responsibilities:

• Perform batch disposition and stability activities in a proactive and timely manner which includes Quality Control testing and reporting of raw materials, in process, bulk drug substance, final products and
• stability products to GMP and in accordance with Annex 11 Computerized Systems and 21CFRpart11 Good
• Documentation Practices for Electronic Data.
• Perform stability study programme activities, storage of in process, and final products samples and retention sample management
• System owners of QC equipment, assisting in equipment periodic reviews, monitoring and maintaining calibration status of equipment within the Quality Control department.
• Ownership and accountability of deviations, investigations and laboratory investigations and timely completion of these documents
• Preparation and update of SOPs, instructions and protocols and other Quality Control documentation
• Checking and reviewing of data in compliance with Data Integrity requirements
• Actively contribute to department and site audit readiness requirements including any continuous improvement initiatives.
• Calibration of equipment and instruments used to perform QC testing and informing relevant personnel in a timely manner of any failure of calibration
• Maintain Quality Control information systems
• Maintain a technical ability, knowledge and understanding of relevant regulatory requirements for GMP, safety and environmental policies required in order to perform role as QC Analyst
• Assist in investigation of quality incidents and other problem solving forums and complete QMS documentation in a timely manner.
• Attend internal and external scientific and technical meetings and conferences where appropriate
• Carry out general maintenance and house keeping of equipment and laboratories
• Available to provide cover for other departments within the organization as required

Available to undertake any other duties as requested by the QC Manager in accordance with Company requirements

Piramal Pharma Solutions (PPS)is a Contract Development and Manufacturing Organization (CDMO) offering end-to-end development and manufacturing solutions across the drug life cycle. We serve our customers through a globally integrated network of facilities in North America, Europe, and Asia. This enables us to offer a comprehensive range of services including drug discovery solutions, process & pharmaceutical development services, clinical trial supplies, commercial supply of APIs, and finished dosage forms. We also offer specialized services such as the development and manufacture of highly potent APIs, antibody-drug conjugations, sterile fill/finish, peptide products & services, and potent solid oral drug products. PPS also offers development and manufacturing services for biologics including vaccines, gene therapies, and monoclonal antibodies, made possible through Piramal Pharma Limited’s investment in Yapan Bio Private Limited. Our track record as a trusted service provider with experience across varied technologies makes us a partner of choice for innovators and generic companies worldwide.