Entrust Resource Solutions

Regulatory Scientist Bracknell 12 month contract (initially) Are you passionate about ensuring patients get access to safe and effective medicines across the globe? Join Lilly as a Regional Regulatory Scientist , where you'll play a key role in supporting regulatory submissions, approvals, and product labeling across EMEA or the Americas. What You'll Do: Provide regional expertise to support global drug submissions and approvals Review and contribute to local labeling and packaging strategies Support interactions with regulatory authorities in your region Partner with cross-functional teams (clinical, medical, marketing, legal) Ensure compliance with regional regulations and internal standards Monitor regulatory changes and advise on impact to strategy Who You Are: Bachelor's degree in a scientific or health-related field A recent graduate Knowledge of regional regulatory procedures and the drug development process Excellent communication and teamwork skills Detail-oriented and able to manage tasks independently Bonus if You Have: Experience with US or EMEA regulatory bodies Knowledge of promotional material review (for US roles) Familiarity with local registration needs for clinical trials (for EMEA roles) What We Offer: A collaborative global team environment Opportunities to work on innovative medicines A culture that values inclusion, innovation, and leadership Ready to make a global impact? Apply now to help bring life-changing medicines to patients.

Medical Affairs Co-ordinator Basingstoke 12 months (initially) About the Role: We're looking for a proactive and detail-oriented Medical Affairs Coordinator to join our International Business Unit (IBU) . In this role, you'll be responsible for coordinating the IBU Investigator Initiated Research (IIR) program, ensuring effective execution, regulatory compliance, and seamless collaboration across functions and countries. Key Responsibilities: Serve as the primary point of contact for affiliates and cross-functional partners on ongoing externally sponsored research. Monitor and manage study performance, timelines, budgets, and risks using IIT tools and procedures. Oversee study contracts, amendments, and compliance tracking. Maintain inspection readiness across all platforms and documentation. Collaborate with investigators and internal teams to ensure timely milestone tracking, enrollment updates, finance support, and drug supply management. Lead site close-out activities and ensure final deliverables, reports, and publications are submitted and archived. Support regulatory readiness and documentation for Ethics Review Boards and authorities. What We're Looking For: Bachelor's degree (preferably in a scientific or health-related field) or 2+ years of clinical research experience. Strong experience in contract negotiation and project management. Excellent written and verbal communication skills. Experience working with cross-functional and cross-country teams. High attention to detail, with strong organizational and problem-solving skills. Ability to manage multiple studies and priorities simultaneously. Preferred Qualifications: Background in medical or clinical research. Knowledge of drug development processes, clinical research regulations, and medical terminology. Experience with finance processes (e.g., invoice processing, PO setup). Familiarity with project management tools like CTMS and Excel. Why Join Us? You'll be part of a collaborative and mission-driven team focused on advancing science through high-quality investigator-led research. This is an excellent opportunity to grow within a global organisation that values integrity, innovation, and patient-focused outcomes.

Supply Quality Officer Hours: Monday to Friday, 8.30am - 4.30pm (Some homeworking may be possible but will depend on business requirements) Salary: £30,000 - £35,000 DOE A fantastic opportunity has arisen for a Supply Quality Officer to join our award winning Global, Pharmaceutical and Biotechnology Company Role Responsibilities Ensure documentation from 3rd party suppliers are assembled and reviewed to ensure compliance to cGMP and associated relevant standards. This will require meticulous attention to detail and the ability to interrogate and challenge technical data and reports, and process documentation within our electronic documentation system. Review all quality related activities from 3rd party suppliers including technical information about the material or product, review of deviations, change notifications and change controls. Approval of master documentation in order to support the releasing QP in the process of batch certification of finished products. Qualification and routine evaluation of supplier's performance including auditing the relevant supplier and assisting and contributing to continuous improvements of the site quality system. Work closely with other departments including Supply Chain, Quality Control, Engineering, Warehousing and Development laboratories on-site in order to improve performance from our supplier base. Qualifications, Experience & Skills A relevant degree level qualification or equivalent in Chemistry, Pharmacy or Biology Good knowledge of EU GMP with internal/external auditing experience Excellent written and verbal communication skills Strong interpersonal skills and the ability to build relationships with both internal and external stakeholders A flexible approach to changing priorities and workloads The ability to work using your own initiative or as part of a team. Able to perform investigations including root cause analysis Able to manage multiple projects and tasks at one time Highly motivated with a drive to succeed If you have the skills and Experience APPLY NOW

Role Profile After an incredible 12 months working towards US product approval and a recent site expansion, there are plenty of exciting projects planned across the business. As a Senior Scientist, you will lead on complex QC microbial projects and provide independant in-house and on-site expertise in Microbiology. Key Responsibilities : Perform and oversee advanced microbiological tests and experiments on sample, ensuring compliance to GLP Contribute to the efficient and effective day to day running of the microbiology laboratory such as prioritisation of testing workload, review and trending of data Update outdated test methods in accordance with regulatory standards to optimise efficiency within the microbiology laboratory Ensure current methods/ equipment are aligned with pharmacopoeia standard Support in technical discussions to support laboratory investigations and other problem-solving activities Support in the development of the Microbiology Staff Support the QC Manager in the development, collating and reporting of key business metrics to drive a quality culture Requirements: A Bachelors or Master s degree Microbiology At least 5 years of experience Experience of EU and cGMP requirements of the manufacturing and testing of medical device products in commercial environment Ability to troubleshoot complex technical problems Previous experience of hosting regulatory auditors

Job Title: Facilities Engineer Location: Dundee (Full-time onsite) Contract Type: 12-Month Contract Start Date: ASAP Pay Rate: £20 per hour Hours: 37.5 hours per week Additional Info: Flexibility required to cover occasional weekend shift work (paid as overtime) Role Overview: We are seeking a proactive and multiskilled Facilities Engineer to support the smooth operation of our site in Dundee. This is a hands-on role requiring a blend of mechanical, electrical, and IT skills to maintain and troubleshoot a range of automated systems and facilities infrastructure. Key Responsibilities: Conduct regular plant room readings and inspections Respond to breakdowns and faults on automated systems Monitor and manage building control software (e.g. temperature and vibration control systems) Write clear and concise reports on maintenance activities and system performance Perform general janitorial and facilities duties, including replacing lights, doors, and ceiling tiles Person Specification: Essential Skills & Experience: Strong IT and computer literacy Multiskilled in both electrical and mechanical disciplines Experience working with automation systems Proficient in report writing and documentation Familiarity with PLC software and control systems

Finishing Operator Process Location : Liverpool Are you passionate about manufacturing excellence and operational safety? Join our team as an Finishing Operator Process and play a key role in the production of high-quality products. Key Responsibilities As an Finishing Operator Technician, you ll be responsible for: Production Operations : Following SOPs and cGMP standards, conducting process testing, and ensuring water sampling schedules are met. Maintenance : Performing planned and reactive maintenance to ensure equipment reliability and process continuity. Problem Solving : Diagnosing equipment and process issues, identifying root causes, and implementing corrective actions. Documentation : Accurately completing batch production records, requisitions, and work requests. Continuous Improvement : Supporting equipment upgrades and contributing to the development of operating procedures. Safety & Compliance : Operating safely, reporting EHS incidents, and participating in investigations and proactive monitoring. IT Systems : Using process control systems and business tools such as CMMS, SAP, and Outlook Express. Training & Development : Managing your Individual Training Plan and sharing specialist knowledge with the team. Qualifications & Experience Minimum of 5 GCSEs (A C) including Maths and English. At least 2 years of experience in a manufacturing environment. Strong understanding of GMP and safety standards. Good problem-solving and diagnostic skills. Comfortable using IT systems and process control tools. Valid in date FLT licence

Manufacturing Operator Liverpool Initial 6-Month Contract (with potential extension) Industry: Pharmaceutical/Manufacturing (GMP Environment) Are you an experienced Manufacturing Operator looking for a new challenge? We are currently seeking a skilled and motivated Manufacturing Operator to join a leading team in Liverpool. This is an exciting opportunity to work in a GMP-regulated environment, with responsibilities that include ensuring production meets quality standards and adhering to Standard Operating Procedures (SOPs). Key Responsibilities: Operate and maintain manufacturing equipment in line with SOPs and GMP regulations. Monitor production processes to ensure adherence to quality and safety standards. Troubleshoot and resolve any operational issues to minimize downtime. Maintain accurate records of production data and quality checks. Collaborate with other team members to meet production goals. Essential Skills & Experience: Previous experience in a similar manufacturing role, ideally within a GMP environment. Strong understanding of Standard Operating Procedures (SOPs). Ability to work effectively within a team and independently. Flexible approach to shift work, including weekends and evenings if required. Strong attention to detail and problem-solving skills. Why Join Us? Initial 6-month contract with potential for extension. Competitive pay and shift allowances. Opportunity to work in a dynamic, fast-paced environment. Enhance your career with a leading company in the manufacturing industry. Please get in touch today, to find out more about this opportunity.