for adhering to all health and safety guidance, provided by the Company. EXPERIENCE WE ARE LOOKING FOR:- Experience from a directly relevant biotechnology or pharmaceutical industry Experience of working in a busy laboratory environment D or MD/Ph.D in relevant scientific discipline, Master’s degree or native equivalent with more »
regulatory requirements and market dynamics is not necessary but a strong advantage •Proven experience within a CDMO or a similar commercial role within biotechnology, pharmaceutical and life-science consulting industry is advantageous •Excellent written and verbal communication skills, with the ability to present findings and recommendations in a clear and more »
Risk Management 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 more »
Chronicle Lead 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 more »
media and telcosConsumer Business; ranging from automotives to consumer goods and retail companies as well as travel, hospitality and services;Life Sciences; from global pharmaceutical organisations to MedTech startups, where we help organisations transform their operations to succeed against a radically changing backdrop of the future of health, andEnergy, Resources more »
working with minimum supervision under pressure to tight deadlines with customer focus. Requirements : Bachelors degree in applicable field (e.g Science, Engineering) or equivalent (e.g Pharma, Biopharm, Life Science, Biotech) Good Experience in Quality Assurance; Problem Solving, Analytical and Continual Improvements. Certified Lead Auditor in ISO 9001:2015 or more »
ensuring equipment performance? We are seeking a highly motivated Equipment Validation Specialist to play a vital role in maintaining the integrity and efficiency of pharma manufacturing processes. In this role, you will be responsible for: Defining and executing equipment validation activities , ensuring all equipment meets the required standards. Coordinating and more »
support for the company’s initiatives. Requirements: Bachelor's degree in a relevant field (think: Business, Life Sciences, Engineering). Strong experience in the pharmaceutical realm, where you've honed your project management skills. A deep-seated understanding of GMP and GDP guidelines. A proven track record of launching products 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 »
Weybridge, England, United Kingdom Hybrid / WFH Options
Clinigen
Clinigen is a rapidly growing global specialty pharmaceutical and services company with a unique combination of businesses. Our divisions operate in a complex global regulatory environment and ensure that vital medicines are delivered securely on time and wherever they are needed in the world. We are currently 1,100 people 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 »
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 »
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 »
the Supply Chain process areaSAP system design, build and deployment experience – 4 full lifecycle implementations preferredExperience of SAP in Manufacturing industries, Consumer Packaging Goods, Pharmaceutical, Oil and Gas, or Retail Experience of facilitating a design workshop and then translating the requirements into designAbility to build strong client relationships based on more »
unsupervised. Good knowledge of the principals and guidelines for GDP as set out in the Green Guide Experience of working a medical device or pharmaceutical quality function Qualified Internal Auditor Desirable: Good knowledge of the requirements of the MDD/MDR as well as ISO13485 & ISO9001 Ability to work in more »
Title: Automation Project Manager - Global Pharma Location: Near Watford Company Summary My client is a leading research based pharmaceutical organisation with an extensive portfolio across the Oncology, Neurology and Pain therapy areas. By joining my client, you will be working for an organisation with a human healthcare philosophy, which means … Desirable - Practical experience working on manufacturing execution systems (MES) OT Cybersecurity knowledge Experience working with edge computing/IIoT Practical experience working within the pharmaceutical industry Experience of serialisation/vision systems and interfaces to enterprise systems Practical experience working with Siemens PLCs and HMI software Experience of working with … pharma.co.uk If this role isn’t suitable for you, please let us know if you can refer anyone – any recommendations are much appreciated! Planet Pharma offers a competitive referral scheme so you will be rewarded for your help! ABOUT PLANET PHARMA Planet Pharma is an American parented Employment Business/ 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 »
Stevenage, Hertfordshire, South East, United Kingdom
CMR & Life Sciences
Project Controls Manager Pharmaceutical, Automation Stevenage, Luton, St Albans, Harlow Permanent Position £65000 to £75000 Position Overview: We are seeking a highly skilled and experienced Project Controls Manager to join our dynamic team. The successful candidate will be responsible for the planning, scheduling, cost management, and overall project controls for more »
Loughborough, Leicestershire, East Midlands, United Kingdom
Almac Group (Uk) Ltd
Analyst Hours : 37.5 hours per week Salary : Competitive Ref No : HRJOB9604 Business Unit : Pharma Services Location : Loughborough, Leicestershire Open To : Internal and external candidates About The Role As an Analyst within the Analytical Support team based in our Charnwood site in Loughborough, you will be responsible for conducting chemical testing more »
documented accurately. Ensure all equipment is suitable for use. The ideal candidate will have the following: A relevant BSc degree, eg Chemistry, Analytical Chemistry, Pharmaceutical Sciences, Forensics, or equivalent. Be computer literate, with good working knowledge of MS Office. Experienced in QC testing of API, including HPLC and GC. Other more »
and presentation at DRB. CAPEX project submissions and management. Invalid reporting. Maintenance of QC metrics. PPS problem-solving. Must haves: cGMP background in the Pharmaceutical industry Experience of Quality Control/Microbiological testing techniques and industry practices Knowledge and understanding of Lean Lab principles. Good understanding of the QC labs more »
Cambridge, Trumpington, Cambridgeshire, United Kingdom
Vector Recruitment
new array of cell culture and cell therapies instrumentation. Their technology is set to revolutionise the manufacturing and process automation for the Healthcare/Pharmaceutical/Biotechnology market. With a queue of clients and ‘off-plan’ pre-orders for the systems, this technology and company is set to evolve rapidly. more »
