Job Opportunities in United Kingdom

Key Roles/Responsibilities:-

• QA primary point of contact (internal and external) for designated projects.
• Collaborate with internal and external stakeholders to ensure quality of all product related activities.
• Provide QA input to project activities including review and approval of change requests, specifications, Standard Operating Procedures, Manufacturing Procedures, Analytical Procedures and associated documentation.
• Participate in quality related investigations, assist in the development, approval and implementation of effective CAPA in order to resolve production, audit and customer issues.
• Participate in validation activities including approval of protocols and reports for analytical methods, manufacturing processes, analytical / production / packaging equipment and cleaning procedures
• Participate in the audits of suppliers and self-inspection of internal production and support functions as required.
• Be involved in preparation for and successful completion of MHRA/FDA and other regulatory body audits.
• Coordinate quality disposition activities associated with designated materials and products.
• Verify manufacturing, laboratory and associated documentation prior to performing the relevant disposition of products. Where potential issues exist, these are to be highlighted to the QA manager.
• Promote and work to ensure compliance with all relevant GMP/Gx P requirements.
• Support and lead as required, quality process improvements and quality management system improvements within the department and on site.
• Escalate any identified GMP/Gx P areas of concern to Quality Management and QP.

Key Competencies:-

• Attention to detail
• Good communication skills, both verbal and written
• Good organisation skills
• Ability to work effectively individually and as part of a team
• Ability to analyse data and information to make considered decisions
• The ability to identify root cause of problems to determine appropriate solutions
• Ability to prioritise workload to ensure timelines are met

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.