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Displaying 1-12 of 12 jobs
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We found 12 jobs outside your search area.
Posted 2 days ago by Russell Taylor Group Ltd
Quality Assurance Assistant, Pharmaceutical (open to Science graduates. Location: Widnes, (this is an onsite role and duties cannot be performed from home). Type: Permanent. Hours: Working 9-17.30 Monday to Friday. Salary: £23,000 - £27000 depending on experience. Additional: 25 days +BH … more
Posted 10 hours ago by Atom Recruitment Ltd
Our Client is a very successful Pharmaceutical and Personal Care manufacturing company. They are now seeking a Formulation Chemist. This position will be Laboratory based on site near Bedford and is a full-time permanent role. Job Purpose. An opportunity has arisen to join the Formulation … more
Posted 6 days ago by CK Group- Science, Clinical and Technical
CK Group are recruiting for an Laboratory Validation Analyst to join a global pharmaceutical company, based in Runcorn on a contract basis initially for 12 months. Salary. Up to £26.43 per hour PAYE. Laboratory Validation Analyst Role. Author of qualification documents for Quality control … more
Posted 6 days ago by Leaders in Care
Registration with the General Pharmaceutical Council UK.If you've previously held or are interested in roles such as Hospital Pharmacist, Community Pharmacist, Pharmacy Consultant, Medication Management Pharmacist, or Pharmaceutical Care Specialist, this Clinical Pharmacist role … more
Posted 8 hours ago by CK Group- Science, Clinical and Technical
CK Group are recruiting for a Regulatory Affairs Consultant to join a company in the Pharmaceutical industry at their site based in High Wycombe, on a contract basis for 6 months. Salary. Up to £64.18 per hour PAYE or £86.00 per hour via umbrella. This role is inside IR35. Regulatory … more
Posted 4 days ago by CK Group- Science, Clinical and Technical
CK Group are recruiting for a Regulatory Affairs Manager to join a company in the Pharmaceutical industry at their site based in High Wycombe, on a contract basis for 6 months. Salary. Hourly rate up to £62.93 PAYE (inside IR35). Regulatory Affairs Manager Role. Management of a product or … more
Posted 5 days ago by CK Group- Science, Clinical and Technical
CK Group are recruiting for a Clinical Study Manager to join a company in the Pharmaceutical industry at their site based in Welwyn Garden City, on a contract basis for 6 months. Salary. Daily: £339.00- £376.97 PAYE or £450.00-£500.00 per day Umbrella. Clinical Study Manager Role. Lead or … more
Posted 5 days ago by CK Group- Science, Clinical and Technical
Experience in the design, execution, and analysis of epidemiology studies within Pharmaceutical or Public Health setting. Prior experience with large databases such as Marketscan or CPRD and experience in SAS, R or other statistical software is highly desired. Experience in working with … more
Posted yesterday by Gap Personnel
Knowledge of pharmaceutical working practices. Ability to work independently. If this role is permanent, gap personnel is operating as the employment agency. If this job is a temporary role, gap personnel is operating as the employment business. Gap personnel is committed to the selection, … more
Posted just now by Appoint Healthcare
Undertakes to assist in the clinical evaluations of new pharmaceutical products. Participate in risk management audits. Travel across different sites if required. Participate in on- call rota. Who we're looking for. Registered Pharmacist. Eligibility to live and work in the UK. GPHC … more
Posted 4 days ago by Blackstone Recruitment Limited
They will be in a patient-facing role, providing medication review services to patients, delivering pharmaceutical care plans that maximize cost effective prescribing and improve the quality of patient care. Benefits. CPPE Primary Care training and are fully supported in undertaking the … more
Posted a week ago by Clearline Recruitment Ltd
Strong regulatory knowledge and experience in the medical devices (and preferably pharmaceutical) industry to support foundation and squad work within a regulated environment. Possess broad regulatory expertise to contribute to foundation and squad tasks, help develop squad/chapter plans … more
