Talentmark

Purchasing & Office Manager Location: near Peterborough Job Type: Full-Time, Permanent Talentmark is partnering with an innovative and rapidly expanding bioscience organisation to recruit a Purchasing & Office Manager. This is an excellent opportunity for a procurement professional looking to join a growing business operating within a regulated scientific and manufacturing environment. The role will be responsible for managing purchasing activities, supplier relationships, logistics coordination and office operations, ensuring the business has the resources and services required to support its continued growth. Key Responsibilities Manage purchasing and procurement activities across multiple departments. Source, negotiate and maintain supplier relationships and agreements. Raise purchase orders, obtain quotations and monitor supplier performance. Coordinate imports, exports and logistics activities. Oversee inventory levels and support stock management processes. Manage equipment service and maintenance contracts. Support audits, inspections and quality compliance requirements. Work closely with Operations, Production, Engineering, Quality and Finance teams. Your Background: Previous experience within purchasing, procurement or supply chain. Experience with Sage accounting systems. Strong supplier management and negotiation skills. Experience handling logistics and import/export documentation. Excellent organisational skills and attention to detail. Proficient in Microsoft Office applications. Experience within GMP or regulated environments is advantageous. Full UK driving license - due to site location and lack of public transport in local area. Why Apply: Opportunity to join a growing, investment-backed organisation. Broad and varied role with significant responsibility. Collaborative and fast-paced working environment. Genuine opportunity to contribute to business growth and operational excellence. Apply: It is essential that applicants hold entitlement to work in the UK. Please quote job reference (Apply online only) in all correspondence.

Talentmark are recruiting for a Commercial Contracts Manager to join a company in the diagnostics industry on a contract basis for 12 months. Salary: (Apply online only) per day PAYE or .58 per day UMB/LTD (outside IR35) Commercial Contracts Manager role: Reviewing & managing contracts for large tender opportunities. Working closely with the tender team on bids - advising and drafting contract T's and C's. Reviewing, drafting, negotiating, and executing commercial contracts with customers. Ad hoc advice and guidance on public procurement legislation and contract queries. Your Background : Qualified commercial contracts lawyer / World Commerce and Contracting Association (IACCM) qualification Significant experience of commercial contract law, relating to complex service contracts (typically contracts 5M+ and long term). Understanding of public procurement contract regs (PCR2015/PA23) and healthcare sector would be beneficial but not essential. Acute business acumen and commercially minded. Experienced in negotiating at 121 level on contract terms. Experience of complex business operations - working in cross-functional environments. Company: Our client is one of the world's premier innovative biopharmaceutical companies, discovering, developing and providing over 160 different medicines, vaccines and consumer healthcare products to help improve the lives of millions of people in the UK and around the world every year. Location: This role allows hybrid working with 2 days per week based at our client's site in Burgess Hill. Apply: For more information, or to apply for this Commercial Contracts Manager please contact the Key Accounts Team on (phone number removed) or email (url removed). Please quote reference (Apply online only) . It is essential that applicants hold entitlement to work in the UK. Please note: This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check.

Talentmark is recruiting for a Training Specialist (blood glucose & ketone solutions) to join a company in the diagnostics industry on a contract basis for 12 months. Salary: Paying between 185 - 240 per day PAYE / 240- 300 per day UMB (inside IR35) Training Specialist Role: Deliver Expert Training : Provide and record product training for internal and external customers, ensuring compliance with our client's standards. Customer Support : Handle training-related inquiries, from product installation to ongoing contract support, offering occasional troubleshooting and technical assistance as needed. On-Site Activities : Support hardware/software implementations during product launches. Your Background : Demonstrates depth of scientific knowledge, both theoretical and practical, in a medical setting. Strong communication, time management, and decision-making skills. Proven ability to work collaboratively in a team environment and independently manage responsibilities. Full UK/EU (or equivalent) driving license. Passport for potential overseas training. Fluent in written and verbal English. Background in nursing, or training. Knowledge of Primary/Secondary Care organisations within the NHS, ideally in a hospital environment. Experience in designing and delivering high-quality, customised training programmes aligned with patient pathway strategies. Company: Our client is one of the world's premier innovative biopharmaceutical companies, discovering, developing and providing over 160 different medicines, vaccines and consumer healthcare products to help improve the lives of millions of people in the UK and around the world every year. Location: This role is field-based working across the territory of Scotland. There will be regular travel across the Scotland region, including overnight stays and occasional unsocial hours to meet business requirements and one role will be focussed on Glasgow and Tayside region. Apply: For more information, or to apply for this Training Specialist please contact the Key Accounts Team on (phone number removed) or email (url removed). Please quote reference (Apply online only) . It is essential that applicants hold entitlement to work in the UK Please note: This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check.

Talentmark are currently recruiting for a Refrigeration Design Engineer for an organisation based in Maldon, Essex. This role is on a permanent basis. Salary: Competitive (depending on experience) The Role: This position will focus on the design and development of ultra-low temperature refrigeration systems to meet customer and product requirements. Responsibilities: Use of specific numeric calculation methods to assure design performance. Create and review specifications of refrigeration systems and components. Meet regulatory compliance to ISO 9001, ISO 13485 and organisation requirements. Guide testing engineers on testing planning and execution. Feed the refrigeration technology roadmap pipeline by targeting new and feasible technologies. Provide support on manufacturing processes and methods to meet quality and safety standards of the product. Your Background: Relevant Mechanical Engineering qualification Proven track of record on product/ technologies development as a design engineer using thermodynamics and heat transfer. Experienced in mathematical modelling of technical problems in the field of refrigeration and heat transfer. Experience on Refprop, Flownex, SolidWorks (CAD), Agile Project Methodology within a regulated industry. F-Gas and Hydrocarbon conversion are a plus. Apply: It is essential all applicants hold entitlement to work in the UK. Please quote job reference (phone number removed) in all correspondence.

Talentmark are recruiting for a Protein Crystallographer to join a pharmaceutical company on a contract basis for 12-24 months . Salary : Paying between 28.54 and 38.01 per hour PAYE (Inside IR35). Protein Crystallographer Role: Support structural biology studies that help identify and optimise potential new medicines. Analyse and interpret protein crystal structure data generated from drug discovery programmes. Coordinate X-ray crystallography data collection activities using internal facilities and external research partners. Work closely with scientists across biology, chemistry and drug discovery teams to support research projects. Help develop and improve laboratory workflows and processes used in fragment-based drug discovery. Process, review and communicate structural data to support project decision-making. Your Background: PhD qualified in Structural Biology, Biochemistry, Chemistry, Chemical Biology or a related scientific discipline. Experience working with protein crystallography within an academic, biotechnology or pharmaceutical environment. Strong understanding of X-ray crystallography techniques and structural biology data analysis. Experience using crystallography software and data processing tools. Knowledge of fragment-based drug discovery or structure-guided drug design would be advantageous. Experience with automation, scripting or workflow improvement tools would be beneficial. Company: Our client is one of the largest pharmaceutical companies in the world. They focus on finding answers for some of the world's most urgent medical needs. Location: This role is based at our client's site in Bracknell , with 2 days per week onsite . Apply: For more information, or to apply for this Protein Crystallographer position please contact the Key Accounts Team on (phone number removed) or email (url removed) . Please quote reference (phone number removed) / 3338 . It is essential that applicants hold entitlement to work in the UK. Please note: This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check.

Associate Director, Toxicology Warrington Site-Based Talentmark is supporting a leading scientific services organisation in the search for an Associate Director, Toxicology to lead and develop a high-performing toxicology function within a highly regulated environment. This is a senior leadership opportunity for an experienced toxicology professional with a strong operational and strategic background. The successful candidate will support in the delivery of forensic toxicology services to the UK Criminal Justice System, and oversee toxicology operations, quality, R&D and continuous improvement initiatives, while helping shape the future direction of the function through innovation, automation and technology-driven efficiencies. Key responsibilities: Leading and developing multidisciplinary toxicology teams. Supporting strategic planning, operational delivery and business growth. Driving quality and compliance in line with international standards. Managing technical projects, budgets and performance KPIs. Building strong relationships with customers, regulatory bodies and external stakeholders. Supporting the implementation of new technologies and process improvements. Contributing to the delivery of high-quality forensic toxicology services in support of criminal investigations. Working closely with quality and compliance teams to maintain robust QA and QC systems. Representing the toxicology function at senior leadership and performance review meetings. Your Background: Significant experience and track record within a technical, highly regulated environment such as toxicology, pharmaceuticals, healthcare, clinical trials or scientific services. Strong leadership and people management experience. Degree in Toxicology or a related scientific discipline. Knowledge of international quality systems and regulatory standards. Excellent communication, organisational and stakeholder management skills. This is a full-time, site-based role in Warrington offering the opportunity to play a key role in a growing and impactful scientific organisation. Apply: It is essential that applicants hold entitlement to work in the UK. Please quote job reference (Apply online only) in all correspondence.

Talentmark are recruiting for a Quality Control Analyst to join a global healthcare provider to hospitals, clinics and homes on a contract basis for 10 months. This is a fully site-based role based in Dartford, Kent. Salary: 17.18 ph PAYE This is a shift-based role on a 3 weeks rotation: Early shift 6am - 2pm Monday-Friday Late shift 1:30pm - 10pm Monday-Thursday, 1:30pm - 7pm Friday Night shift 9pm - 7am Monday - Thursday Quality Control Analyst Role: To conduct Quality Control analysis in support of the smooth running of production by testing Perform analysis on analytical samples in accordance with defined analytical methods and Standard Operating Procedures Test particle size with a variety of analytical methods Prepare test methods for analytical testing and cleaning verification analysis Perform microbiological sampling, including generation of sample labels, organising sample collection and completing sample submission form Your Background : Hold a relevant scientific degree or have equivalent working experience Have experience with a range of analytical techniques, including HPLC, FTIR, Raman, Karl Fisher. microscopy etc Experience in preparing analytical test reports Previous experience with GMP environments Ability to work the above mentioned shifts Company: Our client is the global leader in enabling pharma, biotech, and consumer health partners to optimise product development, launch, and full life-cycle supply for patients around the world. They have the goal of putting patients first and to help people around the world live better and healthier lives. Apply: For more information, or to apply for this Quality Control Analyst please contact the Key Accounts Team on (phone number removed) or email (url removed). Please quote reference (Apply online only) . It is essential that applicants hold entitlement to work in the UK. Please note: This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check.

Talentmark are recruiting for a Technical Writer to join a leading pharmaceutical and healthcare organisation on a contract basis until 31st December 2026. Salary: 200 - 250 PAYE per day, or .10 per day LTD (Outside IR35) Technical Writer Role: Create and maintain technical and customer-facing documents. Prepare and distribute customer notifications and product communications. Work with teams across Regulatory Affairs, Marketing and Technical Services to ensure information is accurate and up to date. Review and update documentation as products, services and processes change. Track documentation activities and support continuous improvement initiatives. Maintain accurate customer and product information within company systems. Your Background: Degree in Biochemistry, Biomedical Science or a related Life Science subject. Experience writing technical, scientific or customer-facing documents. Strong written communication skills with the ability to explain complex information clearly. Experience within the pharmaceutical, healthcare, diagnostics or life sciences industry. Comfortable working with multiple stakeholders and managing information accurately. Experience using CRM systems or document management systems would be an advantage. Company: Our client is one of the world's premier innovative biopharmaceutical companies, discovering, developing and providing over 160 different medicines, vaccines and consumer healthcare products to help improve the lives of millions of people in the UK and around the world every year. Location: This role is based at our client's site in Burgess Hill, with hybrid working available (2-3 days on site). Apply: For more information, or to apply for this Technical Writer position, please contact the Key Accounts Team on (phone number removed) or email (url removed). Please quote reference (Apply online only) . It is essential that applicants hold entitlement to work in the UK. Please note: This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check. INDKA