and problem solving skills Ability to collaborate effectively across global teams and communicate complex ideas in a simple manner Preferred Qualifications Financial Services or Pharmaceutical industry experience Experience in distributed system design Experience with Pure/Alloy Working knowledge of open-source tools such as AWS lambda, Prometheus Spark, Hadoop 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 »
maintaining the GMP facilities and equipment in accordance with maintenance and validation programmes. The successful applicant will operate within and contribute to a GMP Pharmaceutical Quality System including change control, preventive actions, deviation management and document control. Excellent interpersonal and communication skills are essential, as is the ability to work more »
challenges, with experience in quality management systems and tech transfer. 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 »
have any questions, please contact Ingrid Aymes at i.aymes@proclinical.com 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 »
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 »
Royston, Hertfordshire, South East, United Kingdom Hybrid / WFH Options
Sartorius Corporate Administration GmbH
Electrical Engineering You have experience in electrical product design and development with an understanding of the product life cycle ideally in laboratory automation, or pharmaceutical manufacturing environment following ISO/IEC and/or GMP standards though candidates from other industries will also be considered Hands on experience in electrical more »
SENIOR DATA SCIENTIST (FTC) HYBRID (London) £60,000 - £70,000 COMPANY: We are working with a consultancy, specialised in healthcare/pharma analytics. They are looking to bring in a Senior Data Scientist on an FTC to work with one of their biggest clients. ROLE: Work directly with a team more »
to influence peers and exec-level staff. Good knowledge of IBM Maximo is required along with hands on experience working in industries such as Pharmaceutical, Oil and Gas, Facilities Management, manufacturing or Travel and Transport. PLEASE NOTE that sponsorship is not available for overseas candidates. more »
support to internal teams and external partners. Requirements Bachelor's degree in a relevant scientific discipline. Experience in a quality assurance role within the pharmaceutical industry. Deep understanding of Good Clinical Practice guidelines, regulations, and standards. Relevant certifications such as RQAP-GLP, RQAP-GCP are desirable. Leadership experience along with 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 »
service cardiovascular contract research organisation (CRO) powered by an integrated Clinical Research Platform and a Global Site Network. We provide research solutions to our Pharma, Biotech and CRO partners via: CYTE Connect, our integrated clinical platform that allows seamless collaboration for sites, sponsors and CROs; CYTE Locate, our global site more »
Newport, Shropshire, West Midlands, United Kingdom
Omega Leeds
and efficiency projects within a quality driven manufacturing environment BSc/BEng in Process or Chemical Engineering or related Engineering Experience of Process/Pharmaceutical/FMCG or other regulated industry such as food and drink Operational knowledge of manufacturing equipment Track record of leading engineering projects in manufacturing processing more »
Role Provide technical engineering support to the Macclesfield Campus Teams Assisting in the management of Engineering, Safety Health & Environment, and Goods manufacturing compliance Supporting pharmaceutical operations such as HVAC, Purified Water systems, automated control systems Assisting with Site Asset Management Strategy and delivery of Asset Life Cycle activities Propose and more »
ourselves on being a leading provider of comprehensive engineering project delivery services across a wide range of industries, including food and drink, homecare, chemical, pharmaceutical, warehousing and even construction! From installing packaging lines to providing hygienic processing solutions you name it, we've already done it or we are currently more »
TGA and FDA regulations desirable Minimum of 7 years’ experience working as a GCP Quality professional in a management/leadership role within a Pharmaceutical/Biotechnology industry Experience at conducting service provider, site and internal audits highly desirable Experience of building and maintenance of Sponsor Oversight File (SOF) Experience more »
delivery Managing project teams including coordination of study design and protocol development where appropriate. We expect most projects would be for clients in the pharmaceutical sectors Being a Subject Matter Expert on projects and engagements across the breadth of the HEOR team and the client's wider services Driving the more »
technical files, and post-market surveillance. A minimum of 8 years post-qualification experience in regulatory affairs in the medical device and/or pharmaceutical industry in product registration, medical device file, and/or technical compliance activities. Due to the organisation's rapid growth, there is extensive opportunity to more »
enable our clients to meet the changing needs of the global landscape. Required Understanding of Supply chain planning domain, preferably in Life Science or Pharma Industry Have multiple cycles of leading implementation experience in complex supply-chain solution design, development, and testing. With at least, 1 full cycle Kinaxis implementation more »
Essex, England, United Kingdom Hybrid / WFH Options
Walker Hamill
listed organisations, private equity backed businesses and privately owned companies. We recruit across all sectors and have particularly strong client relationships in media, retail, pharma/biotech, technology, property/real estate, leisure and business services. Headquartered in London, we have additional offices in continental Europe. For more information, please more »
and gene synthesis applications. Yourgene also has a global laboratory service network equipped to be a full life-cycle partner for clinical, research and pharmaceutical organisations to support partners at the preclinical, clinical, and post market stage to develop, manufacture, obtain regulatory approval and commercialise new products and services. In more »
you are a Data Centre Mechanical Engineer or above or if you come from a mechanical engineering back ground within a critical environment albeit Pharmaceutical , Manufacturing, Production, x Forces then please read on and contact me directly Basic Salary @ £65,000 to £75,000 depending on Experience , Annual Bonus, Car more »
