Biotechnology Jobs

• USA - Pennsylvania - Upper Providence
• Senior

End-to-end technical accountability for a product across bulk API manufacturing, formulation and packing, acting as MSAT's single-point decision maker for the Product Control Strategy. Leads Product Technical Lifecycle Teams, technology transfer and regulatory submission reviews, driving continuous verification and improvement plans across the supply chain.

MHRA · FDA · GxP +4

• Barnard Castle
• On-site
• Shift work

Carries out planned preventative maintenance, fault finding and repairs on manufacturing, packaging and utility equipment in a sterile pharmaceutical plant, responding to breakdowns to minimise downtime. Works within a shift-based cross-functional team, using SAP CMMS and GMP documentation, and supports root cause investigations, CAPAs and continuous improvement.

SAP · CMMS

• Bath
• Mid-level

Conducts site qualification, initiation, monitoring and close-out visits for a CRO embedded within pharmaceutical sponsor teams, ensuring GCP compliance, patient safety and data integrity. Manages site relationships, recruitment strategies, TMF/ISF documentation and risk escalation, with mentoring of junior staff and up to 40-60% regional travel.

Investigator Site Files · Trial Master Files

• Livingston
• Mid-level

Conducts site qualification, initiation, monitoring and close-out visits for a dedicated clinical trial program, ensuring GCP compliance, patient safety and data integrity. Builds relationships with investigators, resolves data queries, mentors junior staff and travels up to 40-60% within the region.

Investigator Site Files · Trial Master Files

• London
• Hybrid
• £47,540 – £88,289 pa
• Mid-level

Manage regulatory activities for clinical trial applications across an assigned portfolio, working with study teams, country leads and cross-functional partners. Anticipate regulatory risks, coordinate responses to Health Authority queries and maintain product information in compliance systems, while contributing to automation and simplification initiatives.

• Home Worker
• Remote
• £67,900 – £126,100 pa
• Senior

Lead the authoring of high-complexity regulatory documents and act as Program Writer for complex programmes, overseeing writing strategy, coordination, planning and resourcing. Provide expert guidance to clinical trial and submission teams, shape data analysis planning, and champion best practices, new technologies and AI tools to improve writing quality and efficiency.

Artificial Intelligence

• Macclesfield
• Permanent

Provide analytical support for drug substance manufacturing and method development, running project analysis, forced degradation studies and proof-of-concept validation. Author and review Analytical Testing Plans, method protocols and validation protocols, using HPLC and GC within a GMP-regulated lab. Work independently and in a multidisciplinary team, communicating findings to internal and external stakeholders.

HPLC · GC · NMR +4

• Macclesfield
• On-site
• Permanent

Perform structural elucidation and impurity characterisation of small molecule APIs using advanced mass spectrometry, supporting regulatory submissions and control strategies. Develop Eurofins' MS capabilities, collaborate with cross-functional teams, and work to GLP, cGMP and SHE standards at a client pharmaceutical facility.

• US - East Coast
• Hybrid
• Director

Oversees an outsourced global data management vendor across CAR T and autoimmune clinical trials, from protocol development through regulatory submission. Manages eCRF standards, data review and QC plans, database release and lock, and inspection readiness, acting as the main liaison between study teams, vendors and functional partners. Based hybrid in the UK or remote on the US East Coast.

eTMF · eCRF · SAS +2

• United Kingdom
• Remote
• Director · manages people

Senior medical leadership role within a clinical research organisation, acting as a cardiovascular subject matter expert supporting proposals, bid defences and client engagement. Responsibilities span RFP input, protocol and regulatory strategy, internal therapeutic training, and mentoring clinical scientists, with peer-level interaction with pharma medical leadership.

PPD

• Swindon
• On-site
• Shift work

Operate aseptic filling lines and manufacture pharmaceuticals to SOPs and Batch Manufacturing Records, performing filling, packaging, in-process checks, line changeovers and cleaning. Work in cleanrooms on Double Days, 24/7 or Night shifts, using HMI-controlled CIP/SIP systems, autoclaves and SAP, and support validation and new product introduction.

SAP · HMI · CIP +2

• Horsham
• On-site
• £13 – £16 ph
• Mid-level

Day-to-day you will pick and pack client orders, receive courier deliveries into correct storage, follow production orders for packaging and clean down rooms and equipment, and complete GMP paperwork, inventories and waste disposal. The role sits in an Operations team handling ambient, cold and frozen products, working to cGMP and safety standards with continuous improvement via the PPI Lean Process.

PPE

• Macclesfield
• On-site
• Senior
• Permanent

Lead the design, engineering, expression, purification and characterisation of complex biologic therapeutics including monoclonal, bispecific and multispecific antibodies. Acts as biologics scientific lead on client-facing drug discovery programmes, mentoring junior scientists and shaping project strategy within a multidisciplinary Protein Sciences team.

Structural Modelling · AI-enabled Protein Engineering

• Abingdon
• Director · manages people
• Permanent

Leads Evotec's consolidated AI Accelerator, owning machine learning, generative and agentic AI, and therapeutic hypothesis groups. Sets the AI vision and roadmap, makes build/buy/partner decisions for the AI stack, and turns proprietary multi-omics and experimental data into predictive models and reusable IP. Acts as the senior external technical voice for AI in drug discovery.

• Oxford
• Hybrid · 3–4 days in office
• Senior
• Permanent

Develops, validates and runs ligand-binding and cell-based bioanalytical assays generating pharmacodynamic and immunogenicity data for clinical mRNA programmes. Works in a GcLP-regulated lab using Thermo Watson LIMS and electronic notebooks, handling clinical samples, critical reagents, SOPs and validation reports while partnering with Clinical Operations and Sample Management.

Thermo Watson LIMS · Watson LIMS · LabVantage eLBN +1