GxP Data Integrity guidance's, and is undertaken in accordance with applicable procedures (e.g., SOP's, Protocols, etc). Requirements Experience working in a Pharmaceutical/Biotech QC function within a sterile manufacturing site. Proven track record of managing a team within a cGMP QC analytical environment. Degree in a more »
or an MBA. 5+ Years' experience in Strategy, Management Consulting or Industry; with a dedicated focus and background on Healthcare and Life Sciences; (i.e., Pharma, Biopharma, Biotech and Medical Device). Proficiency with Microsoft Office, including Word, Excel, and PowerPoint; (experience in computer programming software (e.g., VBA) or other role more »
Stevenage, England, United Kingdom Hybrid / WFH Options
Workday
planning, time management and organizational skills. Experience demonstrating knowledge of essential regulatory guidelines world-wide. Awareness of or experience in clinical space in a pharmaceutical or biotech R&D environment or leading academic research center. Strong written/verbal communication skills and the demonstrated ability to work in a matrix more »
and use of clinical data Experience leading projects with multiple stakeholders Experience of the use and management of Information within the NHS, academic or pharmaceutical community Extensive experience with Microsoft Word, Excel, PowerPoint, and Outlook Experience of documenting results for publication Experience of successfully managing a number of equally important more »
role: Masters or PhD education (Life Sciences, Biochemistry, Biotechnology or similar) Previous experience in process development and tech transfers of biologics (ATMPs preferred) Prior pharmaceutical GMP experience Cell Culture | Upstream | Specialist | MSAT | CMC | Cell Therapy | Technical Operations | Scientist| Downstream | Tech Transfer | MS&T | Technical Transfer | Process Development | GMP | good manufacturing more »
RPi)To support the Head of Quality in ensuring the provisions of the licences are observed. Company Overview: Our client is a rapidly growing pharmaceutical wholesaling company involved in the procurement and supply of unlicensed medicines into the NHS and Private Hospital sector in the UK. They aim to deliver more »
wider business. Flexibility to work across multiple sites in London Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies. Proclinical Staffing is an equal opportunity employer. more »
programme | Recognition awards | Free Parking Bespak Holmes Chapel is an Investors in People silver award winner who employs over 300 people and are a pharmaceutical Contract Development and Manufacturing Organization (CDMO) that offers development and manufacturing solutions for a variety of medical products. Our products include medical devices such as more »
Ariba and S/4HANA implementations. Experience Record to Report, I2P, RPM/PPM, SOA Manager, ABAP and WebMethods is a plus. Experience in Pharmaceutical Industry, is a plus. Demonstrated technical leadership experience. Understanding of Procurement business processes and Supplier master data. Knowledge of integration of S/4HANA Procurement more »
moments and recognising their potential. Join us on our journey of building a new kind of organisation to reset expectations of what a bio-pharmaceutical company can be. This means we’re opening new ways to work, pioneering cutting edge methods and bringing unexpected teams together. Interested? Come and join more »
UK, please find the below job description: 8+ years of strong and hands-on experience in Data Management and Migration, Data Governance Expertise in Pharma domain, its source systems like SAP ERP, SAP BW, SAP HANA, Marketo, Salesforce etc. Proven expertise in gathering requirements from business users and converting it more »
Oxfordshire, South East, United Kingdom Hybrid / WFH Options
Hays
scientific or laboratory setting.Other key deliverables include: A proven track record of successfully designing and implementing a QMS within a Life Science Research environment, pharma or biotech. The ability to be adaptable to new challenges and changes within a company bringing a flexible approach to day-to-day operations. Strong more »
level in science or equivalent experience. Minimum 5- 7 years of experience in the Regulatory Affairs regulatory experience with new product introduction within the pharmaceutical industry covering both UK National and European regulations Strong communication and project management skills Proficiency in the use of MS Office suite (Excel, PowerPoint) Ability more »
As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 15,000 staff more »
Slough, England, United Kingdom Hybrid / WFH Options
Parkside Recruitment
is a home-based role offering a fantastic package including generous salary, incentive bonus, home based allowance plus much more. My client a Global pharmaceutical company are seeking an experienced Senior Manager, Global Quality Operations to manage and perform audits with focus on Pharmacovigilance audits. Responsibilities include Continuous improvement of more »
to project delivery. What experience you'll need to apply: You will be required to have a good knowledge of biotechnology and/or pharma to deliver new and existing projects for the BioPharma team. Ideally, the candidate will also have experience and interest in physical sciences to support project more »
Bachelor's degree in Data Management, Information Systems, or a related field Two years of experience in master data management, preferably within the healthcare, pharmaceutical, or consumer goods industry Basic understanding of supply chain operations and related data requirements Detail-oriented with a focus on data accuracy, integrity, and industry more »
leads and inspires colleagues. Strong influencing and leadership skills. Understands influencing, stakeholder management and negotiation strategies. The Client is ideally seeking someone from a Pharmaceutical or Bio Science background and who understands how to work with the government and government funding. This position will manage 15 people within the IT more »
or equivalent work experience supporting pharmacovigilance activities Proven experience as an IT Product Manager, preferably in an R&D or technology-driven environment or pharmaceutical industry Strong understanding of software development processes, agile methodologies, and IT project management. Excellent analytical and problem-solving skills, with the ability to translate R more »
experience to support our R&D business. Proven experience as an IT Product Manager, preferably in an R&D or technology-driven environment or pharmaceutical industry Strong understanding of software development processes, agile methodologies, and IT project management. Excellent analytical and problem-solving skills, with the ability to translate R more »
software, data analytics tools, process mapping software). Ability to leverage technology solutions to streamline processes, enhance efficiency, and drive innovation. Experience in PV pharma or Life Sciences industry-specific processes and best practices. Awareness of operating frameworks such as, Lean Six Sigma, ITIL V4, GDPR, ISO27000, ISO27001. Cyber Essentials more »
A working knowledge of UK regulations is preferred. The candidate will be a convincing communicator with strong interpersonal skills. Previous experience working within the pharmaceutical sector will be advantageous. more »
Cardiff, South Glamorgan, Wales, United Kingdom Hybrid / WFH Options
Gyrus Medical Ltd An ATL Technology Company
/Engineering/Quality orientated qualification Minimum of 3 years experience working in a QA/QS environment, preferably within the medical device or pharmaceutical industry. Knowledge of ISO13485:2003 and Medical Device Directive MDD 93/42/EEC Knowledge of FDA QSR Part 820 Computer literate to include more »
get stuff done” without an overreliance on process A self-starter with high levels of drive, energy, resilience Desirable Skills/Experience: Involvement in pharma IT and/or R&D/Commercial/Operations networks and organisations Experience of working with onshore and offshore suppliers Demonstrated understanding of quality more »
