Biotechnology Jobs

• Baar Onyx
• US$188,100 – US$313,500 pa
• Director

Leads end-to-end Model-Informed Drug Development and clinical pharmacology strategy across the drug development lifecycle, from first-in-human studies through filing and lifecycle management. Sits in the Clinical Pharmacology and Quantitative Medicine organisation, partnering with digital medicine, translational imaging, modelling and biostatistics teams, and drafting regulatory content for FDA, EMA and ICH submissions.

MIDD · QSP · AI/ML

• USA - Pennsylvania - Upper Providence
• US$188,100 – US$313,500 pa
• Director

Leads end-to-end Model-Informed Drug Development and clinical pharmacology strategy across the drug development lifecycle, from first-in-human studies through filing and lifecycle management. Designs MIDD and ClinPharm evidence strategies, drafts regulatory content for FDA, EMA, CDE, PMDA and ICH, and partners with digital medicine, translational imaging, modelling and data science teams. Sits in the newly formed Clinical Pharmacology and Quantitative Medicine organisation.

MIDD · QSP · AI/ML

• London
• Hybrid · 3 days in office
• Lead

Lead medicinal chemistry strategy across drug discovery programmes, from hit identification through lead optimisation to candidate nomination, while working hands-on as an individual contributor. Partner closely with AI/ML platform teams to shape predictive models, manage CRO resources and KPIs, and represent the company externally with collaborators.

AlphaFold

• London
• Hybrid · 3 days in office
• Lead

Lead formulation strategy for small molecules across drug discovery and preclinical development, designing technologies such as solid dispersions and co-crystals to improve solubility, stability and manufacturability. Work within an interdisciplinary team alongside AI/ML drug design platform groups, managing external CRO resources and authoring regulatory submissions.

ASAP

• Norwich
• On-site
• £21,805 pa
• Entry level
• Contract

Investigates how G-quadruplex DNA and RNA structures regulate metabolic changes during fungal spore germination, using Aspergillus fumigatus as a model. The student will map G4 formation genome-wide, engineer mutants via CRISPR-Cas9, and apply NMR metabolomics and microscopy to study cell-wall remodelling and antifungal susceptibility within an interdisciplinary research environment.

CRISPR-Cas9 · NMR Spectroscopy

• Wrexham
• Hybrid
• Lead
• Permanent

Leads Cell Line Development and Upstream Process Development strategies for biologic products, from candidate selection through commercial manufacturing. Acts as subject matter expert within cross-functional CMC teams, managing CDMO partnerships, supporting regulatory submissions and technology transfer, and mentoring junior scientists.

CHO

• IM92AP
• On-site
• £29,000 – £32,000 pa
• Mid-level
• Permanent

The QC Analyst role involves performing quality control testing of raw materials, intermediates, and finished products in a regulated manufacturing environment. Responsibilities include analytical testing, environmental monitoring, and maintaining compliance with GMP standards. The role offers exposure to a variety of analytical techniques and technologies, supporting continuous improvement initiatives.

• Cambridge
• On-site
• £45,000 – £50,000 pa
• Senior
• Permanent

Design and build large-scale synthetic gene loci and transgenic platforms for antibody discovery, using CRISPR/Cas9, RMCE and site-specific integrases. Hands-on molecular biology including PCR, NGS, plasmid construction and flow-cytometric immunophenotyping, within a small multidisciplinary team working from dry-lab design to wet-lab validation.

CRISPR/Cas9 · Recombinase-Mediated Cassette Exchange · Bxb1 +3

• Haywards Heath
• Hybrid · 3 days in office
• Director · manages people

Leads a global team of development and regulatory project managers overseeing complex R&D programs across a therapeutic area, including new product development and lifecycle management. Acts as strategic partner to TA and R&D leadership, driving portfolio planning, agile delivery, risk removal and cross-functional alignment as part of the Portfolio & Operations Excellence leadership team.

Microsoft Project · Planview · Smartsheet +1

• Stevenage
• Remote

Serves as the primary point of contact for Advanced Therapy Treatment Centres across South UK, driving appropriate utilisation of CAR T therapies and coordinating site qualification, setup and patient treatment logistics. Works cross-functionally with Marketing, Medical Affairs and Market Access, and is 80% field based with UK travel.

• Oxford
• On-site
• Temporary

Serve as engineering owner for GMP manufacturing equipment at Moderna's Harwell facility, supporting the Norwood (MA) network. Provide hands-on floor support, troubleshoot complex mechanical and process issues, lead CAPAs and change controls, and drive continuous improvement and tech transfer for mRNA production. Requires close cross-functional work with equipment SMEs and end users.

TMIX · Single Use Mixers · Buffer Prep Vessels +4

• Cambridge
• Hybrid · 3 days in office
• Director · manages people

Owns International regulatory strategy for complex cell therapy programs, embedding regional requirements into evidence generation, submissions and labeling. Leads BLA/MAA planning, Health Authority engagements and labeling negotiations, integrating clinical, CMC, safety and commercial input. Also leads a matrix regulatory team, coaching colleagues and shaping policy and process improvements.

BLA · MAA · IND +2

• United Kingdom
• Remote

Field-based commercial role owning relationships with Advanced Therapy Treatment Centres across the South UK, acting as the primary point of contact for CAR T therapy accounts. Responsibilities span site onboarding and qualification, coordinating patient treatment logistics and chain of identity, compliance audits, and strategic account planning with Marketing, Medical Affairs and Market Access. Requires deep haematology/oncology and cell therapy expertise, with around 80% travel.

• Abingdon
• On-site
• Director · manages people
• Permanent

Owns Evotec's in silico therapeutics design capability, uniting computational chemistry, generative and modality design (small molecules, peptides, protein engineering, degraders, molecular glues) and predictive ADMET/safety under one mandate. A newly created unit within the In Silico & AI group with an explicit build mandate: set technical vision, grow a multi-site team, and industrialise repeatable, benchmarked methods across partner programmes.

RDKit · Python · AlphaFold

• London
• Remote
• Mid-level
• Permanent

Lead site performance and compliance for assigned clinical protocols across the South East, acting as primary site contact through all study phases. Conduct remote and on-site monitoring to ICH/GCP standards, manage regulatory documentation in CTMS and eTMF, and mentor junior CRAs. Involves roughly 65-75% domestic and international travel.

CTMS · eTMF · MS Office