Job Summary

The QA Technician at Piramal Healthcare UK Limited will be responsible for performing quality control activities to ensure the manufacturing process and final products meet established quality standards and regulatory requirements. This role involves in-process checks, product testing, and documentation to maintain a high level of product quality and safety.

• Provide QA support to GMP manufacturing, testing, and support activities in line with approved procedures.
• Review and approve master/executed batch records, validation and other documentation, and associated GMP records to ensure accuracy, completeness, and compliance.
• Support deviation management, including initiation, investigation support, assessment/ review and closure.
• Review and approve QMS records in accordance with authorised roles, including deviations, change controls, CAPAs, and risk assessments.
• Support material status control and batch lifecycle activities, including readiness for batch disposition.
• Ensure adherence to data integrity principles and GMP requirements across all assigned activities.
• Support regulatory inspections, client audits, and internal audits through preparation and review of QA documentation.
• Collaborate with Operations, QC, MSAT, Supply Chain, and Regulatory functions to resolve quality issues efficiently and compliantly.
• Promote a strong quality culture and continuous improvement mindset across the site.

Job Qualifications

• Bachelor's degree in a scientific discipline (e.g., Chemistry, Biochemistry, Pharmacy, Microbiology) or equivalent relevant experience.
• Previous experience (1-3 years) in a quality control or quality assurance role within the pharmaceutical, healthcare, or a regulated manufacturing industry.
• Familiarity with GMP (Good Manufacturing Practices) and other relevant regulatory guidelines (e.g., MHRA, FDA).
• Proficiency in performing laboratory tests and using analytical equipment (e.g., HPLC, GC, UV-Vis, pH meters).
• Strong attention to detail and accuracy in documentation and data recording.
• Excellent communication skills, both written and verbal, with the ability to clearly articulate technical information.
• Ability to work independently and as part of a team in a fast-paced environment.
• Proficient in Microsoft Office Suite (Word, Excel, PowerPoint).
• Knowledge of quality management systems (e.g., LIMS, TrackWise) is an advantage.

cGMP Regulations, Good Documentation Practices, Procedural Documentation, QC Microbiology