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Qc analyst (stability)

Falkirk
Piramal Pharma Ltd
Qc analyst
Posted: 27 October
Offer description

About the Role


Weโ€™re looking for a QC Analyst to join our Quality Control team! Youโ€™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, youโ€™ll help deliver safe and effective medicines to patients worldwide



๐Ÿ”‘ Key Responsibilities


* ๐Ÿงพ Perform batch disposition and stability activities, including QC testing and reporting of raw materials, in-process, bulk drug substances, and finished products.
* ๐Ÿ“ฆ Manage stability study programmes, sample storage, and retention sample management.
* โš™๏ธ Act as system owner for QC equipment, overseeing calibration, periodic reviews, and maintenance.
* ๐Ÿ“ Take ownership of deviations, investigations, and lab incidents with timely documentation.
* ๐Ÿ“š Prepare, review, and update SOPs, protocols, and other QC documentation in line with Data Integrity standards.
* ๐Ÿ” Contribute to audit readiness and continuous improvement initiatives.
* ๐Ÿงช Calibrate equipment and escalate issues when necessary.
* ๐Ÿ’ป Maintain QC information systems and ensure accurate records.
* ๐Ÿ“– Stay updated on GMP, safety, and environmental regulations.
* ๐Ÿค Support investigations, problem-solving forums, and QMS documentation.
* ๐ŸŽค Represent QC in technical meetings and conferences when required.
* ๐Ÿงน Ensure housekeeping and proper maintenance of laboratories and equipment.
* ๐Ÿ”„ Provide support to other departments when needed.

๐Ÿ’ก Key Competencies

* ๐Ÿ”Ž Attention to detail
* โฑ๏ธ Reliability
* ๐Ÿ’ฌ Strong communication skills
* ๐Ÿงฌ Solid understanding of scientific and technical processes



๐ŸŽ“ Qualifications & Experience



Essential:

* ๐ŸŽ“ Degree in a Science discipline (or equivalent).
* ๐Ÿงช Experience in a QC laboratory working under GMP conditions.
* ๐Ÿ“‘ Experience writing, reviewing, and working to SOPs.
* ๐Ÿ“– Knowledge of GMP guidelines and regulatory bodies.


๐ŸŒ About Us


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.



๐Ÿค Equal Opportunities


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 ๐ŸŒˆ

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