Quality & Compliance Team Lead - GMP & Audits

Piramal Pharma Limited; Riverview, Northern (FL, KY); Hybrid; USD 130,000 - 160,000; Full time

Job summary

Piramal Pharma Solutions is seeking a Team Lead, Quality & Compliance in Riverview, FL to supervise QA activities ensuring cGMP adherence and regulatory readiness. The role involves batch-record reviews, audits, and data integrity emphasis.

The incumbent will lead a QA team, coordinate with production and regulatory affairs, and drive continual improvement in quality systems and documentation integrity.

Qualifications

• Bachelor’s degree in physical/biological sciences or engineering; chemistry/chemical engineering preferred.
• 8+ years in pharmaceutical operations, regulated life sciences, or quality assurance; 2–5 years supervisory experience.
• Knowledge of GMP requirements (21CFR Parts 11, 210, 211, Annex 11 and ICH Q7/Q9/Q10).

Responsibilities

• Supervise the Quality & Compliance Team to ensure QA activities meet cGMP and regulatory requirements.
• Review and approve batch records, investigations, and change controls; support audits and regulatory inspections.
• Lead data integrity initiatives and maintain documentation/control systems; support management reviews.

Skills

GMP knowledge

MS Office

Relational Databases

Analytical skills

Communication

Planning

Education

Bachelor’s degree in physical or biological sciences or engineering (Chemistry/Chemical Engineering preferred)

Tools

TrackWise

SAP

Master Control

Job description

Piramal Pharma Solutions is seeking a Team Lead, Quality & Compliance in Riverview, FL to supervise QA activities ensuring cGMP adherence and regulatory readiness. The role involves batch-record reviews, audits, and data integrity emphasis.

The incumbent will lead a QA team, coordinate with production and regulatory affairs, and drive continual improvement in quality systems and documentation integrity.