Pharmaceutical industry jobs in Welwyn Garden CityCreate job alerts

CK Group are recruiting for a Senior Pharmacovigilance Scientist to join a company in the pharmaceutical industry on an outside IR25 contract basis until the end of 2026. PAYE Senior Pharmacovigilance Scientist Role: Use your pharmacovigilance expertise, particularly individual case safety report (I

CK Group are recruiting for a Clinical Study Manager, to join a company in the Pharmaceutical industry, at their site based in Welwyn Garden City, on a contract

CK Group are recruiting for a Senior Pharmacovigilance Scientist to join a company in the pharmaceutical industry on an outside IR25 contract basis until the end of 2026.Salary: £40 - £48 per hour UMB / LTD or £29.PAYE Senior Pharmacovigilance Scientist Role: Use your pharm

Report on regulatory progress and issues for new products or LCM activities at all project team and Project Review Meetings, and to Senior Management as required. Experience in CMC Regulatory within the pharmaceutical or biotechnology industry. Experience interacting with EU regulatory authorities &

Contract Clinical Operations Lead.Summary:Join our client, a leading organisation in the pharmaceutical industry, as a Contract Clinical Operations Lead in! This is an exciting opportunity for a passionate professional looking to make a difference in clinical trial delivery.Enjoy a competitive daily

Your Background: Hold a university degree or equivalent years of experience (preferred focus in life sciences) Have demonstrated strong and consistent performance as a Study Manager n the pharmaceutical and/or healthcare industry and drug development experience Experience in delivery and execution

CK Group are recruiting for a Clinical Study Manager, to join a company in the Pharmaceutical industry, at their site based in Welwyn Garden City, on a contract basis for 6 months. If this position isn't suitable but you are looking for a new role, or if you are interested in seeing what opportuniti

Job Title: Packaging Operator Location: Hatfield, UK Company: Leading Global CDMO We are connecting with a leading Contract Development and Manufacturing Organisation (CDMO) dedicated to supporting the pharmaceutical and biotechnology industries. Their Hatfield facility plays a key role in delivering high-quality products that improve patient lives worldwide. The Role As a Package Operator, you will be responsible for the efficient and compliant operation of packaging equipment, ensuring products are packaged to the highest quality standards. This is a hands-on role in a fast-paced GMP-regulated environment, offering the opportunity to develop your skills within a global pharmaceutical organisation. Key Responsibilities • Operate, monitor, and maintain packaging equipment in line with SOPs and GMP requirements., • Carry out line clearance, changeovers, and equipment cleaning to ensure smooth production flow., • Complete accurate documentation of all packaging activities., • Support quality checks to ensure compliance with company and regulatory standards., • Contribute to a safe and clean working environment, reporting any issues promptly., • Collaborate with colleagues across Production and Quality to meet output targets. Requirements • Previous experience in pharmaceutical, biotech, or FMCG packaging operations preferred (training will be provided)., • Understanding of GMP and health & safety standards (advantageous)., • Strong attention to detail and ability to follow procedures precisely., • Good communication and teamwork skills., • Flexibility to work shifts if required. What We Offer • Competitive salary and benefits package., • Training and career development opportunities within a global organisation., • A supportive, collaborative, and safety-focused workplace., • The chance to contribute to life-changing medicines. How to Apply If you are looking to take the next step in your career with a company that makes a real difference in global healthcare, we’d love to hear from you. Please submit your CV and a short cover letter via the application link. 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 recognised 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.

Your new company My client is a global biopharmaceutical company with a goal of contributing to healthcare innovation and environmental sustainability. They are focused on improving people's quality of life, specialising in Oncology, neurology, rare diseases, ophthalmology and immunology. There is an opportunity for an Associate Director / Director Safety Scientist to join their team. Hybrid - Office 8 times in a month Your new role As a highly motivated individual, you will support early and late phase development activities as a member of the safety team, providing essential safety oversight and input into all aspects of study management across the entire development and marketed portfolio. In the post-market setting, this may include signal evaluation, safety-related activities associated with new drug applications/regulatory filings, benefit-risk assessment and safety risk management • Develop and maintain an understanding of the safety profile of their assigned product(s) or therapy areas, • Responsible for individual and aggregate case reporting activities including ICSR case management (medical review) and aggregate reporting (i.e. DSUR, PBRER), • Responsible for signal detection and management activities and contributing to the strategy and review of safety assessments and drug safety reports for signals or issues (inc, product quality) or in response to Regulatory Authority requests, • Contributing to risk management activities including preparation and maintenance of CCDS, labeling document maintenance, risk communications, RMP, REMS, • Contributing to study management from a safety perspective through SMT/PET and document review and maintenance across the development continuum (early phase to post-marketing studies), including PASS, • Contribute to regulatory authority submissions (Investigational New Drug/IND applications, New Drug Applications/NDAs, Marketing Authorisation Applications/MAAs, Variations, Renewals, etc.) by reviewing safety data and preparing relevant sections of the filing and submission packages in consultation with the team, • Establish and maintain collaborative working relationships with all key stakeholders, and internal and external customers and ensure the same across relevant teams, • Consistently comply with all governing laws, regulations, standard operating procedures (SOPs) and other guidelines What you'll need to succeed Primary life sciences degree and relevant postgraduate degree preferred Proven drug safety, clinical development experience in the pharmaceutical industry, ideally as a Safety Scientist - including signal evaluation, safety-related activities associated with new drug applications/regulatory filings, benefit-risk assessment, safety risk management and aggregate report writing. Understanding of GxP and regulated processes and end-to-end clinical trial lifecycleStrong orientation towards process improvement and cross-functional teamwork Excellent communication skills, both written and verbal Perform data analysis / statistical methods to evaluate, interpret and present scientific data with clarity Good presentation skills, effective at summarising and presenting the key considerations and decision points Understanding of project management methodology What you need to do now Before you apply for this position, it is vital that you are in possession of a UK passport or relevant visa to work without restrictions in the UK and residing in the UK. If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call Roberta Atkins on 03330106292

Jobstore are currently recruiting for a Field Service Engineer to join our clients state of the art operation and lead the maintenance, support and repair function for this organisation across the Home Counties,Hertfordshire, Cambridgeshire, and Oxfordshire areas. This is a leading and well established business who are seeking a Field Service Engineer to provide comprehensive service, maintenance, repair, commissioning, and validation services for a wide range of client equipment operating in hospitals, biotechnology, pharmaceutical, and industrial settings. This role involves working across a number of locations to ensure the best performance and functionality of their bespoke products, aligning with client requirements and specific industry standards. Ideally the right applicant will have prior field service experience in a relevant technical field and a flexible approach to travel, with a willingness to accommodate occasional customer visitsoutside of regular working hours (which will be compensated at an enhanced overtime rate) Experience in some or all of the following areas is highly desirable:ISO 9001 Quality systemsWorking under GMP conditionsMaintaining and certifying equipment to British, European, or International StandardsPLC-based control systemsIIE 18th EditionControl and Instrumentation systemsCalibration systemsLaboratory-type biomedical equipment The right applicant will have exceptional interpersonal and communication skills and long with the ability to work effectively under pressure, with strong self-management skills to achieve keytargets and goals. Any prior experience working with any of the following would be highly advantageous;Microbiological Safety Cabinets, Flow Cabinets, Powder Control Booths, Fume Cupboards, Clean Rooms, Sterile Suites or Operating Theatres. In return you will be provided with a company vehicle, door to door pay, generous overtime payments, company bonus scheme and extensive benefits scheme, along with a long term career with a highly successful and influential business. Please click to apply and send us your CV for an immediate review. Jobstore is an equal opportunities employer and we value diversity. JBRP1_UKTJ

Clinical Study Manager Role: - Drive Operational Excellence by developing operational plans, creating & managing clinical study budget & overseeing the consistency of operations. Job Description CK Group are recruiting for a Clinical Study Manager, to join a company in the Pharmaceutical industry,

CK Group are recruiting for a Clinical Study Manager to join a company in the Pharmaceutical industry, at their site based in Welwyn Garden City, on a contract basis for 6 months. Provide direction and leadership to the local study team, including Clinical Research Associates (CRAs) to ensure delive

Job Description CK Group are recruiting for a Senior Pharmacovigilance Scientist to join a company in the pharmaceutical industry on an outside IR25 contract basis until the end of 2026. Apply: For more information, or to apply for this Senior Pharmacovigilance Scientist role, please contact the Ke

Job Description CK Group are recruiting for a Senior Pharmacovigilance Scientist to join a company in the pharmaceutical industry on an outside IR25 contract basis until the end of 2026. Apply: For more information, or to apply for this Senior Pharmacovigilance Scientist role, please contact the Ke

Job Description CK Group are recruiting for a Senior Pharmacovigilance Scientist to join a company in the pharmaceutical industry on an outside IR25 contract basis until the end of 2026. PAYE Senior Pharmacovigilance Scientist Role: - Use your pharmacovigilance expertise, particularly individual