QC Team Leader (Technical Support)

Piramal Pharma Ltd; Grangemouth; On-site; GBP 55,000 - 75,000; Full time

Job summary

Piramal Pharma Solutions is seeking a QC Team Leader (Technical Support) to oversee analytical equipment within the Quality Control department. You will manage procurement, qualification, maintenance, calibration, and performance monitoring to ensure compliant operation supporting release testing of materials and products.

The role requires coordinating with QC, Manufacturing, QA, and external vendors, plus training QC staff and ensuring state-of-the-art practices and data integrity across the

Qualifications

• Broad experience in analytical equipment management within GMP environments.
• Strong understanding of laboratory equipment qualification and calibration.
• Knowledge of computerised systems and data integrity practices.

Responsibilities

• Be SME for all analytical equipment aligned to client projects.
• Lead management of QC activities and equipment-related projects.
• Manage procedures for testing and release of materials per SOPs and protocols.

Job description

Division

Piramal Pharma Solutions

Piramal Pharma Solutions is a contract development and manufacturing organization (CDMO), offering end-to-end development and manufacturing solutions across the drug life cycle. We serve our clients 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 like development and manufacture of Highly Potent APIs and Antibody Drug Conjugation.

Our capability as an integrated service provider & experience with various technologies enables us to serve Innovator and Generic companies worldwide.

For more details, please visit : www.piramalpharmasolutions.com

Job Title

QC Team Leader (Technical Support)

Job Description

The QC Equipment Team Leader is responsible for leading and coordinating the management of analytical equipment within the Quality Control department, ensuring that instrumentation required for the release testing of raw materials, in-process products, bulk drug substance, and finished products is maintained in a compliant, qualified, and operational state. The role has responsibility for the full equipment lifecycle, including procurement, qualification, maintenance, calibration, repair, and ongoing performance monitoring, ensuring equipment availability supports business and regulatory requirements. The ideal candidate will possess broad experience in analytical equipment management, including the qualification of laboratory equipment and computerised systems within a GMP-regulated environment.

Working closely with QC operations, Manufacturing, Quality Assurance, Engineering, and external vendors, the successful candidate will act as a key point of contact for equipment-related activities and client projects. The role requires effective planning and prioritisation to balance equipment compliance and reliability with laboratory testing demands, ensuring testing schedules, project milestones, and manufacturing timelines are achieved with minimal disruption while meeting client expectations and quality standards

• Be the Subject Matter Expert (SME) for all Analytical Equipment aligned to client projects
• Be the Subject Matter Expert (SME) for all QC activities aligned to client projects
• Manage analytical procedures, for testing of raw materials, in process products, bulk drug substance, final products and stability products according to defined by SOP´s, and protocols and ensure that the QC team is in compliance with the same.
• Apply best cGMP work-practices and techniques to manage the testing and release raw materials, in process products, bulk drug substance, final products and stability products within specification and in accordance with Data Integrity requirements, Annex 11 Computerised Systems and 21CFRpart11 Good Documentation Practices for Electronic Data
• Ensure that all QC Analysts, QC Technicians are appropriately trained and competent in the procedures they are conducting, and are in compliance with best cGMP working practices at all times.
• Ensure subcontract of QC testing and dispatching to approved suppliers is performed according to defined procedures and in compliance with GMP.
• Manage on-time reporting according to the defined and trained document management standards including review and verification of analytical data provided by the Senior QC Analysts and QC Analysts
• Immediately escape and report any deviations to materials, facilities, processes or procedures to the QC Manager
• Be accountable for the analytical laboratories being clean, tidy and well organized and in a state of continuous inspection readiness.
• Conduct all activities in the most careful and safe manner and in full compliance with ESH requirements
• Ensure that at any time equipment, facilities and materials used in the area of responsibility comply with defined standards.
• Issue, manage and close-out deviations, change controls, OOS or SST investigations and CAPA´s in a timely fashion
• Identify areas for continuous improvement and elevate those to the QC Manager.
• Actively contribute to the development and maintenance of an enthusiastic, supportive and collaborative environment within the team-setting.
• To undertake any other duties as requested by the line manager in accordance with company requirements.