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 »
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 »
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 »
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 »
PhD and/or MBA in the field of Biology, Biochemistry, or related Engineering is preferred.Advanced no of years of commercial experience in the Pharmaceutical, Biotech or CDMO space. Proven track record in delivering year on year financial and customer satisfaction targets. General understanding of drug development and commercialization pathways. more »
of software solutions. Manage the risk to avoid the need to test. Experience : Experience in quality assurance or software testing roles within the biopharmaceutical, pharmaceutical, or healthcare IT industry Profound understanding of software development lifecycle (SDLC) methodologies, quality assurance principles, and regulatory standards applicable to the biopharmaceutical sector. Proven expertise more »
Slough, Berkshire, South East, United Kingdom Hybrid / WFH Options
Ad Warrior
some of the worlds largest and most successful Brands and Agencies, delivering enterprise scale technology and marketing transformation programs across sectors such as, FMCG, Pharma, Telco, Retail, Travel, Financial Services, Insurance, Manufacturing, Automotive, Utilities, Public Sector, Marketing & Advertising Agencies and Technology Vendors. In the last few years, they have focused more »
in an operational Packaging Labelling Distribution (PLD) role within Clinical Trial Supplies. Knowledge of Clinical Trial Supply CMOs and their capabilities Knowledge of the pharmaceutical and clinical development processes and their relationship to the clinical supplies delivery processes; aware of clinical supply GMP requirements and standards. Lean Sigma training/ more »
successful leader will be a dynamic, experienced individual with a strong track record of team leadership experience across various settings and topics in the pharmaceutical or biopharmaceutical industry. They should have the proven ability to lead a teamand manage complex projects effectively, influence stakeholders without authority, effectively network across the more »
into manufacturing – not just been part of the process. Engage regularly with multi disciplined teams/training and mentoring. Worked within an Automotive/Pharmaceutical/Medical device/GMP environment. Bachelors degree or equivalent in Engineering. DMAIC (desirable). Lean/Six Sigma qualifications. Travel requirements; Travel between local 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)
changes to improve forecast accuracy over timeAbout you: 3 + years of experience in Demand Planning ideally within in Food & Bev/Cosmetics/Pharma SME or start up experience is essential Highly analytical, can build strong working relationships and has a genuine proactive and 'can do' attitude Excellent prioritization more »
Oxford, Oxfordshire, South East, United Kingdom Hybrid / WFH Options
Nurse Seekers
analyze data, and provide actionable insights to improve results Requirements: Proven experience as an SEO Specialist or similar role, preferably in the healthcare or pharmaceutical industry In-depth knowledge of SEO best practices, algorithms, and ranking factors Experience with SEO tools such as Google Analytics, Google Search Console, SEMrush, or more »
similar field. Demonstrated ability to work to set procedures and follow written instructions Desirable Previous experience in a similar role: a Clean room or pharmaceutical background Experience Essential Ability to work using own initiative and without supervision Clear literate handwriting and numeracy skills Good communication skills Good interpersonal skills and more »
What you have to offer: PhD or Masters in (Bio)Statistics, Mathematics or equivalent Minimum 15 years (18 years for masters) in the pharmaceutical industry and/or CRO At least 10 years of work/leadership experience, overseeing statistics staff (internal as well as outsourced) and in representing Biostatistics more »