9 jobs found in Bristol

TalentMark is recruiting for a Cleaning Validation Analyst to join a global healthcare provider to hospitals, clinics, and homes, based in Swindon, on a contract basis for 12 months. This role is shift-based (4 days on/4 off, 12 hour shifts). Salary: PAYE £13.34 per hour. Cleaning Validation Analyst Role: Swabbing of production equipment and the analysis of samples. Working in line with GMP and GLP procedures. Performing analytical work with a high Right First Time rate. Identifying correct specifications and methods for testing, including validation protocols. Maintaining personal and communal laboratory areas in line with 5S principles. Full training will be given and the flexi cleaning validation analyst will be supporting and working with a trained scientist.Your Background: A working knowledge and be able to conduct Cleaning Validation analysis. Using techniques such as Balances, pH meter, HPLC. Working experience in an active pharmaceutical manufacturing environment...

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...

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...

Talentmark is recruiting for a Regulatory Affairs Specialist to join a company in the Pharmaceutical industry, at their site based in Reading, on a contract basis initially for 6 months. Salary: £63.52 per hour PAYE or £86.22 per hour Umbrella (inside IR35) Regulatory Affairs Specialist Role: Ensures the success of new product registrations, line extensions and new indications and claims in alignment with the business plan Manages the coordination, compilation, and submission of new drug applications and cosmetics to the regulatory agencies within their geographical and/or brand area of responsibility Maintains compliance for all products with local regulations and quality system requirementsYour Background: Relevant Bachelor's Degree or higher in Life Sciences, Chemistry, or Pharmacy Expertise across a broad spectrum of Regulatory classifications, but must have experience in cosmetics Oral care experience is preferred, but broader cosmetics will also be considered Strong...

TalentMark is recruiting for a Regulatory Affairs Specialist to join a company in the Pharmaceutical industry, at their site based in Reading, on a contract basis initially for 4 to 6 months. Salary: £50.75 per hour PAYE or £68.89 per hour Umbrella (inside IR35) Regulatory Affairs Specialist Role: Ensures the success of new product registrations, line extensions and new indications and claims in alignment with the business plan. Manages the coordination, compilation, submission of new drug applications, cosmetics, medical devices, and food supplements. Assesses the acceptability of quality, preclinical and clinical documentation for submission filing. Monitors the progress of the regulatory authority review process through appropriate communication with the Health Authority.Your Background: Hold a relevant scientific degree or have equivalent working experience. Experience with local UK/IE affiliates, Direct engagement with authority MHRA and HPRA. knowledge of OTC...

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...

Job summary We have an exciting opportunity for a Pharmacy Support Worker Aseptic to join the Pharmacy Cancer & Aseptic Unit at Stoke Mandeville Hospital, Buckinghamshire Healthcare NHS Trust. You will support the accurate preparation and dispensing of a wide range of aseptically prepared medicines to wards, outpatients, and the Cancer Day Unit, including cytotoxic chemotherapy, monoclonal antibodies, and other aseptic products, under the supervision of a pharmacist. You will assist with dispensing oral cytotoxic medicines and supportive treatments for cancer patients using the JAC computer system, participate in tray assembly of raw materials for aseptically prepared products, and help record patient and product details. You will also contribute to environmental monitoring and cleaning schedules within the aseptic unit, follow all legal and departmental practices including SOPs, GMP (Orange Guide), COSHH, and lifting and handling regulations, and support the development of...

Position: Locum ACT/MMT Pharmacy Technician Location: Shrewsbury Rate of pay: £23.29 - £26.78 Day Webster are currently recruiting an experienced Locum Aseptic Pharmacy Technician to provide full-time locum cover in Liverpool.  Starting ASAP full-time (37.5 hours pw) for 3 months initially. What you need – Role requirements GPhC Registration Aseptic experience in an NHS Hospital setting  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 Industry expert to discuss your personal requirements and further roles available, contact Jamie Dean on (phone number removed) or by email on (url removed) Why work for Day Webster Group? Daily payroll Access to some of the UK’s most sought-after roles Timesheet submissions via Mobile Specialist Industry expert as your dedicated...

Talentmark are recruiting for a Medical Advisor to join a global pharmaceutical company on a contract basis for 6 months. This role is hybrid, with 50% office working in Uxbridge and 50% home working.     Salary: £48 per hour PAYE Medical Advisor Role: Act as the primary Medical lead for Health Technology Assessments (HTAs) of relevant products Provide oversight of the portfolio and prioritise tasks appropriately based on the brand team/portfolio When applicable, act as a conduit between the brand team and the Field Medical and other Medical team members Provide medical expertise for New Product planning to assist in launch and commercialisation decisions Drive content and execute UK medical strategy and research plans in designated therapy areaYour Background: Hold an advanced scientific or clinical degree Medical Affairs experience in early, mid and late-stage product lifecycle management Product strategy development and product launch experience Deep scientific...