420 jobs for “Pharmaceutical Engineer-Ktp Associate-No”
Designs disease data information models for priority discovery areas, writing mapping rules to harmonise biomedical data and building quality checks that keep models trustworthy. Works hands-on in code and modelling tools, using AI assistants daily, and partners with research, ontology and data platform teams to get models adopted.
NCI Thesaurus · MONDO · EFO +6
Designs disease data information models for priority discovery areas, writing mapping rules to harmonise biomedical data and building quality checks to keep it trustworthy. Works hands-on in code and modelling tools, using AI assistants daily, and partners with research, ontology and data platform teams plus external partners.
NCI Thesaurus · MONDO · EFO +6
Fortrea
Technical lead for all data management activities on late phase (IIb-III) clinical trials, from start-up through completion. Develops Data Management and Quality Management Plans, designs CRF/eCRF and database structures, and coordinates edit checks and discrepancy management. Acts as client liaison, tracking cycle times and metrics while overseeing data review staff.
RAVE · EDC
Parexel
Manage worldwide post-approval regulatory activities for biological and plasma products, focusing on CMC variations, renewals, market expansions and annual reports. Assess change controls, review quality control and production study reports, and coordinate submission content with manufacturing, supply chain and QA teams. Client-dedicated role working in Regulatory Information Management systems such as Veeva Vault.
Veeva Vault · Word · PowerPoint +1
Parexel
Acts as principal labelling strategist within Global Regulatory Affairs, driving development and maintenance of dCCDS, CCDS, USPI and EU SmPC documents across an assigned product portfolio. Leads Global Labeling Committee reviews of proposed label exceptions and represents labelling on regulatory strategy teams, working with safety, clinical and commercial stakeholders. Home or office based across European locations.
Company Core Data Sheet (CCDS) · Development Company Core Data Sheet (dCCDS) · US Prescribing Information (USPI) +3
Platform Recruitment
Develops and optimises therapeutic delivery formulations, designing lab experiments to assess stability, physicochemical properties and in vitro performance. Works in a multidisciplinary biotech team, characterising formulations analytically and supporting scale-up and tech transfer towards manufacturing. Distinct for its blend of formulation science, experimental development and translational research.
Danaher
Provides medical and clinical leadership for the development of novel diagnostic and companion diagnostic assays and platforms supporting precision medicine. Acts as subject matter expert for R&D projects, clinical studies and regulatory submissions, and supports pharma partnerships and pathology education. Hybrid role based in Newcastle Upon Tyne with 30-40% international travel.
IVD · CDx · Digital Pathology
IQVIA
Provides strategic medical and scientific subject matter expertise in obesity, cardiology, endocrinology or nephrology, leading proposal development and bid defence meetings as a medical director. Acts as a consultant across the research and development lifecycle and clinical trials, formulating clinical development plans and leading the strategic direction of a Center of Excellence. Requires a terminal MD degree and board certification, with occasional national or international travel.
Thermo Fisher Scientific
Lead medical writer dedicated to a single client, authoring and reviewing clinical study reports, protocols, IBs, INDs and MAAs while advising on document strategy and regulatory requirements. Provides senior review, mentoring and training to junior writers and program managers, and leads process improvement initiatives. Therapeutic experience in neurology, immunology, oncology or vaccines is valued.
Thermo Fisher Scientific
Operates and sets up bulk formulation, filling, inspection and packing lines for sterile and non-sterile pharmaceuticals, following SOPs, BMRs and cGMP in a cleanroom environment. Performs CIP/SIP, autoclave and airlock operations, equipment monitoring and documentation, and provides team leadership on night shifts. Distinct for its aseptic manufacturing focus, hazardous materials handling and supervisory duties.
SAP · HMI · EDMS
ONI
Owns the full sales cycle for Nanoimager microscopy systems across the UK and Nordic territory, from lead generation and tender-portal prospecting to demos and closing deals with academia, pharma and biotech customers. Maintains Salesforce pipeline and forecasting, feeds market insight back to Marketing and Customer Success, and travels at least 50% to customer sites.
Salesforce · Nanoimager
Moderna · 1001–5000 people · Late stage
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
AstraZeneca · 10000+ people · Public
Provides medical and scientific leadership across late-stage respiratory and immunology clinical programs, from Phase IIb to Phase IV. Involves designing, executing and interpreting pivotal trials, medical monitoring, regulatory document input and building relationships with external scientific experts in an international team.
Hyper Recruitment Solutions
Designs, delivers and interprets complex molecular and cellular biology studies for drug discovery and translational research, combining hands-on lab work with technical direction across client programmes. Provides scientific leadership on multiple projects, evaluates new technologies and supports colleagues, working with mammalian cell cultures and advanced cellular systems.
Leads a global team of development and regulatory project managers overseeing complex R&D programs across a therapeutic area, including new product development and life cycle management. Drives portfolio planning, risk assessment, and cross-functional alignment as part of the Portfolio & Operations Excellence leadership team, with hands-on coaching and process improvement.
Microsoft Project · Planview · Smartsheet +1
