126 to 150 of 1,005 Pharmaceutical Jobs

PhD in Biology or a relevant field, ideally with a strong background in IO or Oncology. Minimum of 7 years relevant experience in the pharmaceutical industry with focus on discovery research/pre-clinical development. You are currently living in London or willing to travel frequently to London (Must be more »

Permanent Recruitment Consultant – Vacancies Across London Finance/Banking/Accountancy Tech - Data, Cloud, Cyber, Infrastructure Life Science/Pharma Technical/Engineering/White Collar Construction Permanent People are pleased to be working with an industry-leading recruitment agency who have an international presence. This forward-thinking business have more »

needs. Ideally degree qualified, you will have a wealth of experience in assessment, development and management of quality systems and ideally within Medical Device, Pharma and associated Life Sciences sectors. You will have first class communication skills, both verbal and written, and be well versed in developing highly effective client more »

Process Control technology, for the Heat Treatment Industry. With a focus on temperature control solutions and data acquisition our client offer innovative solutions to Pharmaceutical, Biotechnology and Healthcare organisations globally. A bit about the role: Our client is looking to hire a dedicated and results-oriented individual to join their 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 »

the business Requirements: Expert in GCP with working knowledge of GMP 5 years experience in a QA Manager role within a CRO, Biotech or Pharma company Contract: Hours: 3 days a week - can worked across 3-5 days Location: Wilmslow - hybrid working Length - 6 months IR35 - Outside Please hit APPLY more »

active attitude Team player work a strong work ethic For more information please call Chris on 0161 526 1898. Keywords: quality control, laboratory, lab, pharmaceutical, QC, analytical, sample, chemical, GMP, science, QC inspection, testing, materials, ingredients, analysis, GC, wet chemistry, titrate, titration, HPLC, raw materials, intermediates, in-process, finished products more »

An advanced degree and related accreditations a plus. • 7+ years of experience within IT, ITIL and Service Management • 3+ years of experience within the Pharma/Life Science industry preferable • 5+ years demonstrated experience managing IT services or delivering IT service improvement initiatives. This is a 6 month contract in more »

corresponding customs charges, and coordinate deliveries to site. The ideal Candidate: Previous experience in supply chain management, demand, procurement within the beauty, cosmetic, FMCG pharmaceutical, or chemical industry is essential. Essential experience in contract negotiation. A flexible approach, willing to tackle supply chain, logistics, quality control, and other areas as more »

Experience Required Minimum 3-5 years' previous experience in a similar role ideally within a fast paced multi-disciplinary environment Experience working in the Pharma industry Experience in the development, implementation & auditing of Safety management systems would be an advantage Proficient in the use of Microsoft Office Suite & phone based more »

ability to manage multiple projects and clients simultaneously Comfortable utilising technology as a key part of the sales process Mantell Associates is a specialist Pharmaceutical and Life Sciences headhunting firm. For more information on this role, please contact us at +44 (0)20 3854 7700. more »

SAFELINE X-RAY LIMITED Mettler Toledo Safeline Xray is considered the premier brand supplier of X-ray equipment for the protection of food and pharmaceutical products. One of the many things our systems are used for is product inspection, checking for contamination to minimize risk to the public and also more »

serialisation regulations, with a track record of installing, configuring, deploying, documenting, and testing SAP ATTP systems tailored to specific business needs Familiarity with global pharmaceutical industry standards and guidelines necessary for serialisation across manufacturing and logistics. Hands-on experience in configuring SAP ATTP to meet business requirements, including setting up more »

globally active technology leader in the field of high-quality chain system solutions and engineering services in a variety of industries including: automotive, agricultural, pharmaceutical, logistics and conveying, food, medical and many more. more »

required to lead and influence internal and external stakeholders in a matrix organisation in industries like FMCG/Food & Beverages/Consultancies, Healthcare/Pharma/Biotech/Nutraceuticals/Medical devices or key Packaging organisations. Commercially aware and able to manage cost and value of projects. Excellent inter-personal more »

database management systems and website authentication mechanisms. - Excellent problem-solving skills and ability to work effectively in a collaborative team environment. - Good to have pharmaceutical experience Working remotely 6 months + extension more »

the Basic and Detail design, FAT, installation, commissioning/SAT and qualification (PQ) Ensures implementation of divisional and corporate procedures and internal standards Qualifications Pharma and/or Biotech Experience Solid experience in a Sterile Manufacturing environment Solid experience within QA, Validation activities and Risk management Previous experience as a more »

Accountable for supplementing data or documents for any queries from authorities during submission procedures. Support CA function input for studies during audits e.g. BIMO, Pharma partner, FDA. Education: Bachelor’s degree in, life sciences, biomedical engineering or nursing 5-8 years working experience with in vitro diagnostic devices company. Minimum more »

coordinating cross cutting activities with internal stakeholders, regulatory authorities and project partners Experience we are looking for: Masters degree in Biochemical Engineering, Biological sciences, Pharmaceutical Sciences or an equivalent level of experience is essential. Preference will be given to candidates who hold a PhD. Extensive experience in biologics CMC development more »

changing the game in environmental science, drug discovery and analytical water testing. The company are dedicated to expanding their workload across different industries including pharma, biotech and forensics. This varied role will see you responsible for various aspects of the automation machinery in an attempt to increase efficiency, you will more »

international company. Fluent in English (ideally with business French). Nice to Haves Data Protection Officer certification. Knowledge of regulatory requirements specific to the pharmaceutical industry (e.g., FDA 21 CFR Part 11). Experience with Agile or Scrum Methodologies. Proficiency in Electronic Document Management Systems (EDMS) and other quality management more »

career in an impactful role at a tech company that provide cyber security products to a range of finance, government, defence, law enforcement and pharmaceutical companies. As a Senior SOC Analyst you'll play an integral role in ensuring the security and resilience of both internal and client based information more »

career in an impactful role at a tech company that provide cyber security products to a range of finance, government, defence, law enforcement and pharmaceutical companies. As a Senior SOC Analyst you'll play an integral role in ensuring the security and resilience of both internal and client based information more »

The successful candidate will have a strong background in the supply chain, with experience gained working in the following industries considered favourable, Automotive, Telecommunications, Pharmaceutical, or Aviation. You will be required to attend meetings with senior management, be comfortable with presenting information and supporting with the scheduling of the workload more »

knowledge of relevant quality standards; GMP, GLP, GCP and other analytical related quality standards Good working knowledge of Quality Assurance in the Chemical and Pharmaceutical Industry Quality Assurance background which includes some specialist knowledge within a defined area Good experience of auditing documents with technical support or guidance across multiple more »