Key Roles/Responsibilities JOB DESCRIPTION Perform testing activities by following procedures and report results in timely manner of raw materials and in process samples and where assigned by the Team Leader, of bulk drug substances, final products and stability products applying cGMP and quality standards. Check and review data in compliance with Data Integrity requirement. Perform any stability study programme activities, storage of in process and final samples and retention samples management. Ensure that PPE, consumable and material are available by maintaining adequate stock control. Assist in coordination of incoming deliveries and dispatches. Arrange subcontract of QC testing and dispatches to approved suppliers as appropriate. Assist in document writing including procedure, investigation and deviation where training has been completed. Ensure that all laboratory areas and surrounding QC facilities are cleaned and maintained in accordance with housekeeping procedure and processes and remain at an inspection ready state. Ensure that all storage units, fridges, freezers and incubators are defrost and cleaned as defined per procedure and monitor and report any temperature excursion in a timely manner. Carry out general maintenance and calibration of equipment used to perform testing and inform relevant personnel in a timely manner of any failure of calibration. Actively contribute to department and site audit readiness requirements including any continuous improvement initiatives. 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 Technician. Be available to provide cover for other departments within the organisation as required. Be available to undertake any other duties as requested by the QC Manager in accordance with Company requirements. Key Competencies:- Attention to details Reliability and effective communication Ability to follow instructions accurately Qualifications Essential Experience Basic analytical techniques experience within a QC laboratory. Basic GMP knowledge. Ability to organise work within a dynamic and busy environment. Experience of working to SOP documentation. About Us In the three decades of its existence, Piramal Group has pursued a twin strategy of both organic and inorganic growth. Driven by its core values, Piramal Group steadfastly pursues inclusive growth, while adhering to ethical and values-driven practices. Equal employment opportunity Piramal Group is proud to be an Equal Employment Opportunity and Affirmative Action employer. We do not discriminate based upon race, ethnicity, religion, color, national origin, gender (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, gender expression, age, status as a protected veteran, status as an individual with a disability, genetics, or other applicable legally protected characteristics. We base our employment decisions on merit considering qualifications, skills, performance, and achievements. We endeavor to ensure that all applicants and employees receive equal opportunity in personnel matters, including recruitment, selection, training, placement, promotion, demotion, compensation and benefits, transfers, terminations, and working conditions, including reasonable accommodation for qualified individuals with disabilities as well as individuals with needs related to their religious observance or practice. About The Team 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.