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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 🌈

Are you a QC Analyst/Analytical Chemist based in Central Belt of Scotland looking for a new challenge? SRG are recruiting for several QC Analysts to for a leading life sciences company who are going through an exciting period of growth, offering excellent development opportunities. These are great opportunities with an excellent salary and benefits on offer including bonus scheme, healthcare and flexi-time. There are both standard day shift and 24 hour shift roles available. Main responsibilities: • Use a range of analytical chemistry techniques- predominantly HPLC Ensuring all analysis and documentation are conducted and recorded in compliance with GMP standards, • Working to set protocols within a busy environment Preparation and update of SOPs, instructions and protocols and other Quality Control documentation Checking and reviewing of data in compliance with Data Integrity requirements, • Assist in investigation of quality incidents and other problem solving forums and complete QMS documentation in a timely manner, • Perform stability study programme activities, storage of in process, and final products samples and retention sample management, • Supporting the team leader where required Skills/Experience Required: • Degree or equivalent in a relevant scientific discipline, • Experience in QC Analytical techniques such as UV, HPLC, FTIR Will be able to demonstrate previous effective experience in a similar environment is essential, • Prior experience working in a regulated GxP environment

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 🌈