9 jobs found in Maldon

Freelance Digital Designer Outside IR35 | Fully Remote | Healthcare & Pharma Standard 8 is partnering with a global digital agency, with offices in London and the USA, delivering healthcare and pharmaceutical campaigns for major international brands. They’re looking for an experienced freelance Digital Designer to support a busy pipeline of Veeva led projects. This is fully remote and outside IR35. The Role You’ll be designing digital assets for regulated healthcare and pharma clients, working within structured approval environments. The work sits heavily across Veeva platforms, so hands on experience is essential, not just awareness. Essential Experience • Proven design background within healthcare, pharma or life sciences • Comfortable working within regulated design projects • Strong Adobe Creative Suite skills, InDesign • High attention to detail around compliance and version control Desirable • Experience using Veeva PromoMats and Vault • CLM project experience Contract...

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...

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...

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...

Talentmark are recruiting for a Mechanical Laboratory Assistant to join a resin and composites company at their site based in Heanor, Derbyshire, on a contract basis for 6 months.  Salary: £13.00 per hour PAYE Mechanical Laboratory Assistant Role: Perform cleaning and maintenance tasks to ensure a safe and organized laboratory environment. Support the testing process by preparing materials and equipment. Maintain accurate records of tasks performed and materials used. Follow standard operating procedures and safety guidelines. Assist with basic technical tasks under the supervision of senior staff.Your Background: 5 relevant GCSE passes and 2-5 years relevant experience, or 3 A levels, or 4-6 years relevant experience. Relevant experience comprising familiarity with mechanical testing techniquesCompany: Our client is an advanced materials and speciality chemical company focused on the manufacture of resins. Location: This Mechanical Laboratory Assistant role will be...

Laboratory Technician based in Middlewich. 3-6 Month Contract position Key Responsibilities Working as part of a team of a dedicated lab team, you will be: Collecting samples from sample points located within chemical process plant areas. Conducting analysis and interpretation of results. Undertaking analysis and investigations on non-routine samples. Managing the laboratory calibration schedule and stocks of laboratory consumables including reagents. Providing support and guidance to the Process Operations team. Skills, Knowledge & Expertise Ideally you will have a background in chemical plant analysis and laboratory work. You are likely to have an A Level in Chemistry and/or hold or be working towards NVQ level III Laboratory and Associated Technical Activities. You must be computer literate to enable data input, interpretation and report writing. Technical problem-solving capability. Previous experience in a GMP environment would be...