QC Analyst

Piramal Pharma Limited; Falkirk; On-site; GBP 25,000 - 35,000; Full time

Job summary

A global pharmaceutical company is seeking a QC Analyst to join their Quality Control team in Falkirk, Scotland. The role is vital for ensuring that products meet high quality and compliance standards in a fast-paced, GMP-regulated environment. The ideal candidate will have a degree in a Science discipline and experience in a QC laboratory under GMP conditions, with responsibilities including QC testing, SOP management, and equipment oversight.

Qualifications

• Experience in a QC laboratory working under GMP conditions.
• Experience writing, reviewing, and working to SOPs.
• Knowledge of GMP guidelines and regulatory bodies.

Responsibilities

• Perform batch disposition and stability activities, including QC testing.
• Manage stability study programmes, sample storage, and management.
• Oversee calibration and maintenance of QC equipment.
• Prepare, review, and update SOPs and other documentation.
• Contribute to audit readiness and continuous improvement.

Skills

Attention to detail

Solid understanding of scientific and technical processes

Education

Degree in a Science discipline (or equivalent)

Job description

This range is provided by Piramal Pharma Ltd. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Base pay range

Overview

We’re looking for a QC Analyst to join our Quality Control team! You’ll play a vital role in ensuring our products meet the highest standards of quality and compliance. Working in a fast-paced, GMP-regulated environment, you’ll help deliver safe and effective medicines to patients worldwide.

Responsibilities

• Perform batch disposition and stability activities, including QC testing and reporting of raw materials, in-process, bulk drug substances, and finished products.
• Manage stability study programmes, sample storage, and retention sample management.
• Act as system owner for QC equipment, overseeing calibration, periodic reviews, and maintenance.
• Take ownership of deviations, investigations, and lab incidents with timely documentation.
• Prepare, review, and update SOPs, protocols, and other QC documentation in line with Data Integrity standards.
• Contribute to audit readiness and continuous improvement initiatives.
• Calibrate equipment and escalate issues when necessary.
• Maintain QC information systems and ensure accurate records.
• Stay updated on GMP, safety, and environmental regulations.
• Support investigations, problem-solving forums, and QMS documentation.
• Represent QC in technical meetings and conferences when required.
• Ensure housekeeping and proper maintenance of laboratories and equipment.
• Provide support to other departments when needed.
• Attention to detail
• Solid understanding of scientific and technical processes

Qualifications & Experience

• Degree in a Science discipline (or equivalent).
• Experience in a QC laboratory working under GMP conditions.
• Experience writing, reviewing, and working to SOPs.
• Knowledge of GMP guidelines and regulatory bodies.

About Piramal Group & Equal Opportunity

For over three decades, Piramal Group has grown into a global leader through innovation and collaboration. Guided by our core values, we are committed to delivering inclusive growth while maintaining the highest ethical standards.

Piramal Pharma Solutions (PPS) is a Contract Development and Manufacturing Organization (CDMO) with a globally integrated network across North America, Europe, and Asia. We offer end-to-end solutions across the drug lifecycle, from discovery and development to commercial supply, including specialized services in highly potent APIs, ADCs, biologics, gene therapies, and more.

Piramal Group is proud to be an Equal Employment Opportunity employer. We celebrate diversity and are committed to providing a fair, supportive, and inclusive workplace for all.