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About the Role 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 🔑 Key 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., • 🔎 Attention to detail, • ⏱️ Reliability, • 💬 Strong communication skills, • 🧬 Solid understanding of scientific and technical processes 🎓 Qualifications & Experience Essential: • 🎓 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 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. 🤝 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 🌈

At Piramal Pharma Solutions, we are driven by a purpose: to help patients around the world live healthier, longer lives. As part of our continued growth, we’re seeking an Analytical Development Scientist to support and lead method development, validation, and technical transfer activities in a dynamic, GMP-compliant environment. Your Role You will be at the heart of our analytical development efforts, playing a key role in supporting new drug development, scale-up, and commercial manufacturing. You’ll lead and contribute to technical projects that directly impact quality, efficiency, and regulatory compliance. Key Responsibilities Project Leadership & Delivery • Develop, validate, and transfer robust analytical methods for raw materials, intermediates, and finished products., • Drive timely and compliant execution of project deliverables, ensuring alignment with client expectations., • Collaborate cross-functionally to plan, schedule, and manage project work across QC, production, and stability teams., • Participate in client communications and technical discussions, providing expert input and updates as needed. Technical & Operational Excellence • Conduct method development and troubleshooting using state-of-the-art instrumentation (e.g., HPLC, GC, UV, etc.)., • Author and review technical documentation including protocols, reports, and SOPs in accordance with cGMP standards., • Provide analytical expertise during technology transfer to QC and production environments., • Support analytical training and mentoring for junior staff and cross-functional teams. Compliance & Continuous Improvement • Maintain meticulous laboratory records and ensure all work complies with GMP, safety, and data integrity standards., • Actively contribute to investigations, deviation reports, and change controls., • Identify opportunities for process optimization, cost reduction, and waste minimisation. What We’re Looking For • A degree (BSc/MSc/PhD) in Analytical Chemistry, Pharmaceutical Sciences, or a related discipline., • Solid experience in analytical method development and validation in a GMP-regulated environment., • Strong understanding of ICH guidelines and regulatory requirements., • Hands-on experience with a range of analytical techniques and instrumentation., • Excellent problem-solving, communication, and project management skills. Why • Be part of a global CDMO with a strong reputation in delivering high-quality, end-to-end pharmaceutical solutions., • Collaborate with passionate scientists and professionals in a supportive, innovation-focused culture., • Access ongoing training, development, and career advancement opportunities., • Make a real-world impact in the life sciences industry

Piramal Pharma is a world-leading developer and manufacturer of high-quality biological reagents and is seeking a Quality Assurance officer to join their growing team in our QA department in Grangemouth. The Quality Assurance officer will act as the Quality Assurance representative for campaign projects, ensuring accuracy and compliance of procedures, quality management system records, manufacturing batch records and associated testing. Be the QA representative for new products and for change projects, dealing with aspects including review/approval of process instructions, change controls, deviations, investigations, validation, customer audits/quality requests, and material and product disposition. The QA officer is expected to identify, escalate and work to address any GMP/GxP issues with potential impact to product quality or quality compliance. Together we offer fantastic opportunities for committed employees to learn and develop their career with us. At Piramal , we research, develop, and supply Biopharma products and services that impact the lives of millions of people each day to make life better, and keep us safer. Your health and well-being matters to us and that’s why we offer you the flexibility to do what’s important to you whether that’s the ability to flex your start and finish times. Where possible, we support a working pattern that suits your lifestyle and helps you reach your ambitions. Key Roles/Responsibilities • QA primary point of contact (internal and external) for designated projects., • Collaborate with internal and external stakeholders to ensure quality of all product related activities., • Provide QA input to project activities including review and approval of change requests, specifications, Standard Operating Procedures, Manufacturing Procedures, Analytical Procedures and associated documentation., • Participate in quality related investigations, assist in the development, approval and implementation of effective CAPA in order to resolve production, audit and customer issues., • Participate in validation activities including approval of protocols and reports for analytical methods, manufacturing processes, analytical / production / packaging equipment and cleaning procedures, • Participate in the audits of suppliers and self-inspection of internal production and support functions as required, • Be involved in preparation for and successful completion of MHRA/FDA and other regulatory body audits., • Coordinate quality disposition activities associated with designated materials and products., • Verify manufacturing, laboratory and associated documentation prior to performing the relevant disposition of products. Where potential issues exist, these are to be highlighted to the QA manager., • Promote and work to ensure compliance with all relevant GMP/GxP requirements., • Support and lead as required, quality process improvements and quality management system improvements within the department and on site., • Escalate any identified GMP/GxP areas of concern to Quality Management and QP.Warehouse on call team.

About the Role 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 🔑 Key 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., • 🔎 Attention to detail, • ⏱️ Reliability, • 💬 Strong communication skills, • 🧬 Solid understanding of scientific and technical processes 🎓 Qualifications & Experience Essential: • 🎓 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 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. 🤝 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 🌈

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Experience in a QC laboratory working under GMP conditions.

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