🚀 Research & Development Scientist - Slough - Global CDMO

Research & Development Scientist - Slough - Global CDMO Location: Slough, and likely fully onsite Start date: ASAP Type of position: 12 months contract (Has to the view to be extended) Job Description Partnered with a global leader in multinational company that provides contract development and manufacturing services (CDMO) to the pharmaceutical, biotechnology, and nutrition industries. They help companies bring new therapies to market by offering everything from early-stage research support to large-scale production. Overview: This is a hands-on, lab-based scientific role focused on driving innovation in bioprocess sciences. The position supports the development and optimization of purification processes to meet evolving industry needs through technical experimentation and data-driven solutions. Role Purpose: Contribute to the design, planning, and execution of studies that support technology development and process improvement. Conduct experiments within defined scopes and timelines, and analyze results to guide next steps in development. Key Responsibilities: Support the interpretation of problem statements and study rationale to ensure alignment with project objectives Assist in developing and executing high-throughput (HTP) workflows for process studies under supervision Configure HTP equipment to enable reliable monitoring and data capture Identify potential risks to study execution and contribute to mitigation strategies Collaborate on study plans and documentation with senior team members Execute HTP studies according to protocols and timelines, and perform preliminary data analysis Contribute to improving HTP workflows for greater efficiency and integration into broader development pipelines Provide purification support during technology implementation in cross-functional settings Work Practices: Deliver experimental support for bioprocessing technology development and implementation Maintain accurate records in accordance with quality standards and project requirements Perform technical analyses and assist in preparing reports and presentations Participate in team planning by updating task progress and resource needs Follow good laboratory practices and support equipment maintenance and housekeeping Adhere to safety, health, and environmental guidelines, including participation in risk assessments Ensure compliance with data integrity, documentation, and training standards Candidate Profile: Bachelor’s or Master’s degree in Biochemistry, Biotechnology, Chemical Engineering, or related life sciences Hands-on experience with high-throughput purification workflows , chromatography, and filtration techniques Familiarity with bioprocessing equipment Understanding of process development , scale-up, and tech transfer If this role isn’t suitable for you, please let us know if you can refer anyone – any recommendations are much appreciated! Planet Pharma offers a competitive referral scheme so you will be rewarded for your help! About Planet Pharma Planet Pharma is an American parented Employment Business/Agency that provides global staffing services with its head-quarters in Chicago and our EMEA regional office located in Central London. We have invested significantly in creating a robust international platform that enables us to work compliantly in 30 countries with a current network of 2500 active contractors globally as well as a very strong permanent / direct hire recruitment offering. Our specialist knowledge and close relationships with our clients and the wider industry really makes us unique in our field. Just recently we were recognized by FORBES as the 17th best professional staffing firm, and have won multiple awards from industry accredited bodies for our commitment to excellence and service delivery. We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing. We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their race, sex, disability, religion/belief, sexual orientation or age.41bf1e1f-b16b-4260-a40a-17c77a06fd15