1 to 25 of 49 Contract Pharmaceutical Jobs

time, office based Benefits : Private medical insurance, Life insurance, Company pension, Additional leave, Flexitime, Free on-site parking, Referral programme and Wellness programme! BAP Pharma is the fastest-growing, independently owned pharmaceutical clinical trials supply organisation, with specialist divisions in Comparator Sourcing, Secondary Packaging & Labelling and Global Storage & Distribution. Our … or equivalent) 2 - 3 years proven experience in administrative role Good use of Microsoft Office (Word, Excel, PowerPoint) Strong interpersonal and organisational skills BAP Pharma is committed to enabling a supportive work environment, which is diverse and inclusive and based on mutual respect. We offer comprehensive training and development programmes … roles. We provide our team with a platform in which to continually progress and excel and deliver on our promises to our clients. BAP Pharma - Promise delivered. Our people are results driven, tenacious and customer focused. If you think you have what it takes to be part of a successful more »

management * Health and safety checks You * Ideally you'll have come from a safety critical/high pressure environment for example - Nuclear, Gas or Pharma * Ideally you'll have an engineering qualification * SC cleared or be eligible for security clearance Background This is an exciting opportunity to work for a more »

or Aerospace industry or similar. Proven experience working in a similar role within the defence sector: Candidates from other industries such as Automotive, Aerospace, Pharmaceutical, etc., with practical experience including Bill of Material Engineers, Material Requirements Planning Analysts, Engineering Change Engineers, Technical Data Managers, etc., will also be considered. Experience more »

We are recruiting Trainee Shift Process Technicians for INEOS Acetyls. INEOS Acetyls is a global chemicals business producing acetic acid and a range of derivatives across Europe, Asia and America. You will be based at the Hull site, which is more »

at Winsearch for more information) Winsearch acts as an employment agency for permanent staff. We recruit for roles based in Engineering & Manufacturing, Food & Drinks, Pharmaceutical, Supply Chain & Procurement and Professional Services. View our latest jobs today on our website and follow us on LinkedIn. FoodH Our clients and their customers more »

A dynamic supplier of Electronic Point of Sale (EPoS) and Patient Medication Record (PMR) Prescription and dispensing systems in the independent and corporate pharmacy sectors are seeking a Dispensing Software Trainer to join their team for an upcoming roll-out more »

A dynamic supplier of Electronic Point of Sale (EPoS) and Patient Medication Record (PMR) Prescription and dispensing systems in the independent and corporate pharmacy sectors are seeking a Dispensing Software Trainer to join their team for an upcoming roll-out more »

Job summary Clinical and Care Professional Leads support south east London-wide and borough programmes of work, therefore, there is an expectation that you currently work within south east London, and for borough based roles, within that borough. The Clinical more »

/4HANA Functional Consultant Tax £500.00 pd - Macclesfield, 6 months outside ir35 Skills and experience: Strong understanding of the indirect tax business process in pharmaceutical settings and tax touch points in E2E supply chain Analysis and interpretation of indirect tax (VAT,GST etc) requirements for domestic, free trade zones, exports more »

Functional Consultant Tax £500.00 pd - Luton/Macclesfield, 6 months outside ir35 Skills and experience: Strong understanding of the indirect tax business process in pharmaceutical settings and tax touch points in E2E supply chain Analysis and interpretation of indirect tax (VAT,GST etc) requirements for domestic, free trade zones, exports more »

/f/d) - GMP/Quality Risk Management/Qualification/Validation/Parentals/English & German Project: For our customer a big pharmaceutical company in Basel we are looking for a highly qualified QA Manager (m/f/d). Background: The IMP Quality Operations Unit Switzerland … in Global Technical Operations is the Quality partner for all Manufacturing Units and Clinical Packaging in Pharmaceutical Technical Development in Switzerland and responsible for the Quality, Quality Systems and GMP-compliance oversight of all Investigational Medicinal Products (IMPs) manufactured and packed for clinical studies in Switzerland. The Clinical Supply Centre … skills * Proficient contribution to health authority inspections and internal GMP audits Reference Nr.: 923408SDA Role: QA Manager (m/f/d) I ndustrie: Pharma Workplace: Basel Pensum: 100% Start: ASAP Duration: 12 Deadline: 07.05.2024 If you are interested in this position, please send us your complete dossier via the more »

Safety Case Subject Matter Experts and Technical Authorities Skills/Experience required: Design or operational experience in a regulated environment (Nuclear, Gas, Oil, Rail, Pharma) Experience of working in a highly regulated environment with responsibility for ensuring the quality and timely delivery of engineering design and outputs which underpins continuous more »

and co-ordinate multiple activities. This individual should be able to make competent scientific recommendations. Minimum of 5 years of industrial experience in the pharmaceutical or related industry, or an equivalent combination of education and experience with knowledge of pertinent Regulatory and Industry guidance's and regulations. Has demonstrated the … lifecycle strategies for the dosage forms manufactured by the site (solids, liquids, gels, terminal sterilisation) and a firm working knowledge of manufacturing platforms and pharmaceutical facility infrastructure. Understanding of the dosage form development process, along with some knowledge of process development techniques, cGMP regulations, FDA and EMA regulations, and recent … trends in product lifecycle concepts. 'Hands-on' knowledge of pharmaceutical manufacturing equipment, and ability to supervise bath manufacture and instruct production operators would be beneficial. Experience of the manufacture of potent products and associated containment systems. Supervisory experience would be beneficial as would step-in technical managers absence. more »

Job summary An excellent opportunity has arisen within the Electronic Patient Record (EPR) Configuration Team for enthusiastic individuals to join the Willow team as Senior Application Coordinators/Analysts on a 12-month fixed term contract (1 fixed term, 2 more »

Control Systems Engineer West Yorkshire 3-6 month contract (likely longer)/Outside IR35 Rate £40.00 p/h (outside IR35) Water/Process/Coding/Testing/Allen Bradley/Commissioning I am currently recruiting on behalf of more »

specifications, user guides, and best practices. Qualifications: Proven experience as Business Analyst, SAP Global Key User or a related role within the biopharma or pharmaceutical industry. Proficiency in project management methodologies. Excellent communication and interpersonal skills. Ability to work collaboratively in cross-functional teams. Knowledge of SAP ECC Plant Maintenance more »

Postdoctoral Research Associate (Experimental Condensed Matter Physics) Salary: £39,375 to £43,313 per annum (dependent on skills and experience) Hours: Full time Contract Type: Fixed Term (36 months) Location: Science and Technology Facilities Council, Rutherford Appleton Laboratory Harwell, Oxfordshire more »

in a cGMP environment to ISO or FDA regulatory standards is desirable Experience in calibration and/or maintenance support is ideal for a pharmaceutical, medical device, or biotech manufacturing company, or equivalent, with demonstrated skills in writing complex calibration SOPs and technical operating procedures Good planning skills to produce more »

Control Systems Engineer West Yorkshire 3-6 month contract (likely longer)/Outside IR35 Rate £40.00 p/h (outside IR35) Water/Process/Coding/Testing/Allen Bradley/Commissioning I am currently recruiting on behalf of more »

all aspects of the HePMA implementation and dependent systems e.g. Welsh Clinical Portal/PMS. Ensure all medicines built in HePMA comply with relevant Pharmaceutical legislation to ensure patient safety is maintained Assist when required the set up new medicines, users, cost centres and consultants on the pharmacy stock management more »

Job summary 'This is an opportunity to cover for 9 months the band 4 officer in our high performing eRostering Team. Do you want to be part of a team that makes a difference by supporting managers to create the more »

for a global client. What we are looking for: Technical background or relevant background in working with SAP PM and SAP QM Experience within pharmaceutical production/QA working with SAP PM and SAP QM (still, if you have knowledge of SAP and interest in taking on this role, you more »

C (w/m/d) - GMP/cold room/management/SAP/English,German, French Project : For our customer a big pharmaceutical company in Visp we are looking for a highly qualified Global Category Specialist for Cleanroom and EI&C. Background : The Clean Room Solutions and EI … or FH) * Preferred area of study: Process engineering, chemical engineering, business management, project management, supply chain, electrical or Computer Engineering * At least 3 years pharma or biotech industry or similar environment with sterile environment (eg semiconductors for clean rooms) * At least 2 years' experience doing tendering of complex and large … and problem-solving skills * Initiative and resilience * Able to work under pressure Nice to Haves: * German language skills * Has experience working in Switzerland in Pharma or Capex * Has participate in at least one capex project from early engineering until MC or OQ/PQ. * Has experience with claims * Has experience more »

Qualification/Validation/CSV of Small Molecules/Data Integrity/GMP/IMP/English & German Project : For our customer a big pharmaceutical company in Basel we are looking for a highly qualified Technical QA Manager (m/f/d). Background : The IMP Quality Operations Unit … Switzerland in Global Technical Operations is the Quality partner for all Manufacturing Units and Clinical Packaging in Pharmaceutical Technical Development in Switzerland and responsible for the Quality and GMP-compliance oversight of all Investigational Medicinal Products (IMPs) manufactured and packed for clinical studies in Switzerland. The candidate supports the end … of new employees Must Haves: * Degree in Engineering, Chemistry, Life Science, Pharmacy or equivalent. * Min. 5 years of Quality Management related experience in the Pharmaceutical industry. * Experience in Qualification/Validation and CSV of Small Molecules, Analytics and/or Biologics * Sound understanding on current DI (Data Integrity) requirements * Experience more »

Lead to join their team on a contract basis. As the ideal candidate, you will have significant experience in implementing SAP ATTP within the Pharma industry, specifically in the area of Global Track and Trace Serialization system realization and deployments. Key Skills: - Extensive experience with SAP ATTP and SAP HANA... more »