Quality & Compliance Team Lead — GMP & Audits

CamWebDir; Riverview; On-site; GBP 65,000 - 95,000; Full time

Job summary

Piramal Pharma Solutions in the UK division is seeking a Team Lead for Quality & Compliance to ensure GMP-compliant manufacturing, review batch records, and release products according to SOPs. The role emphasizes leading QA activities, audits, data integrity, and cross-functional collaboration with production, QA, and regulatory teams.

Bachelor's in sciences with 8+ years in pharma operations and supervisory experience is required; expertise in TrackWise, SAP, MasterControl is a plus.

Qualifications

• Bachelor's degree in physical or biological sciences or engineering.
• Minimum eight years' experience in pharmaceutical operations or quality assurance, with 2–5 years supervisory.
• GMP knowledge per 21 CFR Parts 11, 210, 211, Annex 11 and ICH Q7/Q9/Q10.
• Proficient with TrackWise, SAP and MasterControl; strong computer skills.

Responsibilities

• Review batch production records to ensure GMP compliance and release according to SOPs.
• Walk production areas to ensure current Good Manufacturing Practices are followed and address deviations in real time.
• Support QA administrative duties and document control activities.
• Assist internal and external audits and regulatory inspections; participate in audit responses.
• Prepare or review documents such as Analytical Methods Validation, Cleaning Validation, and Process Validation reports.
• Support data integrity and risk management programs within Production.

Skills

Attention to detail

Analytical skills

Strong communication

Leadership

Independent work

Education

Bachelor's degree in physical or biological sciences or engineering

Chemistry/Chemical Engineering preferred

Tools

MS Office

Relational Databases

TrackWise

SAP

MasterControl

Job description

Piramal Pharma Solutions in the UK division is seeking a Team Lead for Quality & Compliance to ensure GMP-compliant manufacturing, review batch records, and release products according to SOPs. The role emphasizes leading QA activities, audits, data integrity, and cross-functional collaboration with production, QA, and regulatory teams.

Bachelor's in sciences with 8+ years in pharma operations and supervisory experience is required; expertise in TrackWise, SAP, MasterControl is a plus.