Entrust Resource Solutions

We are seeking an enthusiastic, resourceful and proactive Business Development Executive to join our growing team. This is an exceptional opportunity for a graduate, postgraduate or early-career professional looking to transition into a commercial role within the pharmaceutical industry. No previous business development experience is required. We provide comprehensive training, mentorship from experienced commercial leaders and exposure to cutting-edge pharmaceutical technologies and global client relationships. This role offers an ideal foundation for someone looking to build a long-term career in pharmaceutical business development, strategic partnerships and commercial leadership. The Opportunity As a Business Development Executive, you will support the identification and development of new client relationships across the pharmaceutical, biotech and investment communities. You will work closely with senior colleagues to understand market opportunities, communicate technical solutions and contribute to the company's continued growth. You will gain exposure to: Pharmaceutical business development and strategic partnerships Client relationship management Commercial research and market mapping Marketing and communications activities International conferences and industry events Pharmaceutical product development and innovation Investment and corporate growth initiatives Key Responsibilities Support the Business Development team in identifying and developing new client relationships. Research and engage prospective pharmaceutical, biotech and investment partners. Understand client development challenges and help align suitable technical solutions. Support outreach activities and new business initiatives. Assist with marketing campaigns, communications and content creation. Prepare for international conferences, meetings and industry events. Conduct commercial research, competitor analysis and market mapping. Collaborate with colleagues across the UK and wider organisation. Learn and communicate complex pharmaceutical technologies in a clear, professional and commercially relevant manner. About You We are looking for an ambitious and motivated individual who is eager to develop a career on the commercial side of life sciences. You will ideally have: A degree in Life Sciences, Pharmaceutical Sciences, Chemistry, Biology or a related scientific discipline. Excellent written and verbal communication skills. A genuine interest in human health, medicines and pharmaceutical innovation. The ability to quickly learn technical concepts and translate them into commercial value. Strong organisational skills and a proactive approach to your work. Natural relationship-building ability and a professional, personable manner. Energy, curiosity and a positive, can-do attitude. Flexibility to support wider commercial, marketing and operational activities. Evidence of achievement through academic, professional or extracurricular activities.

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.