Release Engineer 6 month contract up to £620pd INSIDE IR35 2 days per month in Surrey I am currently working with a leading Pharmaceutical manufacturing & distribution business who are looking for a Release Engineer. Note, this is not a Release Manager role, they are looking for someone to be proactive more »
understanding of GDP regulations and ISO 9001 and ISO 13485 standards. * Proven experience in a quality assurance role, preferably within the distribution, logistics, or pharmaceutical sector. * Exceptional attention to detail and problem-solving skills. * Strong communication and interpersonal skills. * Ability to work independently and as part of a team. * Flexibility more »
etc. Will have method development and validation experience with the above techniques. Will have previously worked to GMP. Will ideally have come from a pharmaceutical background, but other backgrounds will be considered if the above criteria is met. Strong IT literacy with good use of all Microsoft applications. Important Information more »
Pawl on +44 20 3319 3199 or J.pawl@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 »
objectives. REQUIREMENTS: PhD or Master's degree in a relevant field. Proficiency in handling behavioural data and modeling. Prior experience in the Health/Pharma industry or domain knowledge. Expertise in developing and deploying machine learning models. Proficiency in programming languages such as Python or R. Strong communication skills, capable more »
protocols and SOPs. Troubleshooting and maintenance of HPLC instrument. Your Background: PhD in Chemistry or related scientific discipline with significant experience working in a pharmaceutical or biotech environment. A background in polymer Chemistry combined with extensive expertise in Chromatography and spectroscopy to quantify genetic material loaded inside polymeric particles. Practical more »
This is a new role based in Cambridge, working for a specialist clinical laboratory within the sample management team. You will be supporting the Pharma Services projects for the business and taking a lead role in the accessioning of samples for the team. Role requirements: *Accessioning of specimens into the more »
Cheshire, Chester, North West Hybrid / WFH Options
Real Staffing
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 »
Systems and processes. - Proven experience in resource planning. - A background in natural/life sciences or relevant experience in a CRO/biotechnology/pharmaceutical company in a Clinical Data Management position. Interested or know someone who might be? Reach out to Heidi Hennigan using the following: ✉️ h.hennigan@proclinical.com 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 »
Hounslow, England, United Kingdom Hybrid / WFH Options
Swift Recruit
We require a VAT Specialist to start in Chiswick for a 12 month FTC working for a leading pharmaceutical business who are passionate about advancing healthcare. Brilliant opportunity to build a career with a very respected client, with an opportunity for career progression. Salary: £50,000- £65,000 per annum more »
Biological sciences, or Microbiology Bioengineering, Bioprocess engineering, Biochemical Engineering, Biotechnology. Lab experience is key, or industry in production environments such as brewing, food beverage, pharma anywhere it would be sterile. Experience in a similar role, including experience in implementing or managing/supervising ISO 9001:2015 systems and procedures. (Experience 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 »
Stevenage, Hertfordshire, South East, United Kingdom
Guidant Global
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 »
Employment Type: Contract
Rate: Up to £42 per hour + In IR35 (PAYE & Umbrella available)
City Of London, England, United Kingdom Hybrid / WFH Options
Proclinical Staffing
team to enhance the audit quality management system, actively participating in process improvements including QMS documentation updates. Maintain current awareness of the regulatory and pharmaceutical industry environment, influencing internal Business Partners and stakeholders on best quality & compliance. Act as Subject Matter Expert/Point of Contact to provide expertise and more »
you have any questions, please contactTom Russell at t.russell@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 »
Planet Pharma is currently recruiting for a Senior Research Associate to work within the Protein Sciences team of a leading clinical trials organisation. You will actively participate in developing and providing analytical support for our Antibody-based and mRNA delivery platforms. This includes necessary capabilities for primarily emphasizing analytical, formulation more »
St Neots, England, United Kingdom Hybrid / WFH Options
Ennov
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 »