8 jobs found in Tonbridge

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 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...

ob Advertisement: Research Associate (Analytical Chemistry) Location: Cambridge Contract Type: Temporary Contract Length: 12 months Daily Rate: TBC Inside IR35 Are you passionate about advancing pharmaceutical research? Do you thrive in a dynamic laboratory environment? If so, we have an exciting opportunity for you! Our client is seeking a motivated Research Associate to join their department and contribute to innovative Discovery Projects. What You'll Do: As a Research Associate, you will play a pivotal role in supporting analytical chemistry operations. Your responsibilities will include: Providing practical LCMS support to enhance project outcomes. Collaborating closely with Chemistry and Biology teams to drive research initiatives. Ensuring the effective operation of four LCMS instruments, requiring your expert handling. Communicating with instrument and service providers, including consumables procurement. Engaging with the Operations Group to optimize project...

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 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...

CK Group are recruiting for a QC Microbiology Technician to join a global healthcare provider to hospitals, clinics and homes on a contract basis for 12 months. This is a shift role working Tuesdays to Saturdays inclusive. There are two potential shift, either 0700 – 1500 or 0800 – 1600. Salary: Paying up to £13.58 per hour PAYE  QC Microbiology Technician Role: Monitor and maintain laboratory stock, order new stock when necessary. Keep glassware clean and ready for use. Keep records of work in accordance with internal SOPs and external GLP standards. Routine maintenance and testing of lab equipment. Rotation of stock inventory on a weekly basis.Your Background: Hold a scientific qualification in science (A Levels, BTEC etc) Have a passion for science Excellent communication skills An eye for detailCompany: Our client is the global leader in enabling pharma, biotech, and consumer health partners to optimize product development, launch, and full life-cycle supply for...