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Contractor 6
Pharmaceutical Braintree

6 jobs found in Braintree

CL
Mar 07, 2026  
Band 7 Pharmacist
Position: Band 7 Pharmacist Location: Welwyn Gardens Rate of pay: £32-£33 per hour Day Webster are currently recruiting a band 7 Pharmacist with hospital experience and clinical experience for a hospital based in Welwyn Gardens. Our client is looking for the ideal candidate to start as soon as possible for an ongoing duration. The shift pattern would be daily, although the service would consider other suitable work patterns for the right candidate.  If you would like to find out more about this band 7 Pharmacist starting as soon as possible paying a rewarding hourly rate of £32-£33 either on a full time or part-time basis,  What you need – Role requirements 1.       Hospital experience 2.       GPHC registered Day Webster Group currently have positions throughout the United Kingdon, Channel Islands, and Republic of Ireland for Pharmacy Professionals of all Bands between 3 – 8c; If this isn’t the right role for you and you would be eager to speak to a Specialist...
IR35 Status:
Unknown Status

CV-Library Welwyn Garden City, UK Contractor
CL
Feb 27, 2026  
Senior Regulatory Affairs Associate
Pharmaceuticals Regulatory Affairs Associate – Homebased and Office Opportunity: This is a great opportunity for a Regulatory Affairs (RA) Specialist to develop your career in regulatory affairs for drug products. Do you have experience in product labelling activities and regulatory drug submissions? Do you have experience of the Windsor Framework compliance? Have you compiled regulatory documents for submissions within the UK and Ireland? Looking for a contract role with an exciting global pharmaceutical company? If yes then this is the role for you. Your role as a Pharmaceuticals Regulatory Affairs Associate will involve supporting regulatory strategies for assigned product portfolios and performing life cycle management submissions for medicinal drug products. You will manage local Regulatory Affairs activities and help support business product launches and tender applications mainly for the UK and Irish markets. Duties and responsibilities include: * Supporting and...
IR35 Status:
Unknown Status

CV-Library RG1, Reading, Berkshire Contractor
CL
Feb 27, 2026  
Senior Regulatory Affairs Associate
Pharmaceuticals Regulatory Affairs Associate – Homebased and Office Opportunity: This is a great opportunity for a Regulatory Affairs (RA) Specialist to develop your career in regulatory affairs for drug products. Do you have experience in product labelling activities and regulatory drug submissions? Do you have experience of the Windsor Framework compliance? Have you compiled regulatory documents for submissions within the UK and Ireland? Looking for a contract role with an exciting global pharmaceutical company? If yes then this is the role for you. Your role as a Pharmaceuticals Regulatory Affairs Associate will involve supporting regulatory strategies for assigned product portfolios and performing life cycle management submissions for medicinal drug products. You will manage local Regulatory Affairs activities and help support business product launches and tender applications mainly for the UK and Irish markets. Duties and responsibilities include: * Supporting and...
IR35 Status:
Unknown Status

CV-Library RG30, Southcote, Reading Contractor
CL
Feb 27, 2026  
Senior Regulatory Affairs Associate
Pharmaceuticals Regulatory Affairs Associate – Homebased and Office Opportunity: This is a great opportunity for a Regulatory Affairs (RA) Specialist to develop your career in regulatory affairs for drug products. Do you have experience in product labelling activities and regulatory drug submissions? Do you have experience of the Windsor Framework compliance? Have you compiled regulatory documents for submissions within the UK and Ireland? Looking for a contract role with an exciting global pharmaceutical company? If yes then this is the role for you. Your role as a Pharmaceuticals Regulatory Affairs Associate will involve supporting regulatory strategies for assigned product portfolios and performing life cycle management submissions for medicinal drug products. You will manage local Regulatory Affairs activities and help support business product launches and tender applications mainly for the UK and Irish markets. Duties and responsibilities include: * Supporting and...
IR35 Status:
Unknown Status

CV-Library RG17, Kintbury, West Berkshire Contractor
CL
Mar 12, 2026  
Lab Assistant
Job Title: Laboratory Assistant Hours: Full Time, Monday to Friday, 8:00am - 5:00pm Location: Dukinfield Reports to: Laboratory Manager / Senior Technician Role Overview We are seeking a reliable and analytical Laboratory Assistant to support day-to-day laboratory operations. This role would suit a graduate (or equivalent) with a strong interest in science and laboratory work, or someone with relevant laboratory experience looking to develop their career further. The successful candidate will be detail-oriented, methodical, and comfortable working with data, samples, and testing procedures in a structured environment. Key Responsibilities * Comply with all safety protocols; * Ensure quality control of Raw Materials, Work in Progress Products and Finished-goods, performing necessary adjustments, according to existing Control Plans; * Investigate if results are outside control parameters; * Record all test results (relevant RM and In-Process testing) on appropriate database...
IR35 Status:
Unknown Status

CV-Library SK16, Dukinfield, Borough of Tameside Contractor
CL
Mar 07, 2026  
Clinical Supplies Project Coordinator
CK Group are recruiting for a Clinical Supplies Project Coordinator to join a global pharmaceutical company on a contract basis for 12 months. This role is hybrid with 50% home working and 50% site based Moreton, Wirral.  Salary: £20.18 per hour PAYE Clinical Supplies Project Coordinator  Role: Supports the delivery of clinical supplies through effective management of assigned projects. Generates, reviews and approves internal and external packaging and labelling production orders in accordance with the clinical trial design and product specifications. Reviews and approves vendor-generated production orders . Ensures CGMP compliance of activities in assigned areas of responsibility. Authors new and/or reviews existing procedural documents.Your Background: Hold a relevant degree in a scientific subject, or have equivalent working experience. Knowledge of and ability to understand/implement regulatory and CGMP principles. Knowledge of ERP/MRP systems and supply chain...
IR35 Status:
Unknown Status

CV-Library Wirral, UK Contractor
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