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Role Overview You will create website and social media content to promote their solutions and services to Life Science Laboratories across Reading, Oxford and Cambridge. Company Information This company is positioned in a gap in the market and has ex...
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Summary Dechra Pharmaceuticals are looking for an experienced auditing professional to join our manufacturing division on a remote basis. Support the GxP and Regulatory compliance of Dechra Products by developing audit systems which will ensure proce...
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Walker Cole International are looking for a CMC Regulatory Affairs Director to join an established Pharmaceutical Business in the UK. In this role you will be responsible for the development and execution of CMC regulatory strategy for the business. ...
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Technical Help Desk Manager Basingstoke - commutable from Andover, Salisbury, Woking, Reading and Southampton 58k (neg dep exp) car / allowance generous benefits package Our globally renowned and respected client has been established for more than 60...
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Our client founded in 1889 grew into a global health and wellness company providing Pharmaceutical, OTC and medical device products to the market. A world leader in manufacturing and marketing of pharmaceuticals, cosmetics, skin care and health care ...
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Technical Helpdesk Manager Hampshire - commutable from Reading, Woking, Basingstoke and Southampton 58k (neg dep exp) car / allowance generous benefits package hybrid working Our globally renowned and respected client has been established for more th...
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A long term Medical Device client of ours based in West Yorkshire, are looking to add a Regulatory Specialist to their team to support their growing business. They are looking for an individual that is hard working and self-motivated to assist with a...
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UK Group Quality Director Pharmaceutical, Qualified Person/QP Type: Permanent Location: Onsite, 5 days a week - Cheshire based Our client, a multi sited pharmaceutical company is looking for an experienced QP /QM/QD to work onsite at their Cheshire s...
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Our Client is a Chemical Distributor. They are now seeking a Product Manager - Life Sciences . This is a full-time permanent position and will be office based near Doncaster. Key Responsibilities Meeting & exceeding the set budget for the role, and a...
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Quality Manager - Systems Swiss Precision Diagnostics (SPD) is a world leader in the research, design and supply of advanced consumer diagnostic products. SPD is a joint venture between Procter & Gamble (P&G) and Abbott ; and our brand Clearblue , is...
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Our Client is a Chemical Distributor. They are now seeking a Product Manager - Life Sciences . This is a full-time permanent position and will be office based near Oxford. Key Responsibilities Meeting & exceeding the set budget for the role, and asso...
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Our Client is a Chemical Distributor. They are now seeking a Product Manager - Life Sciences . This is a full-time permanent position and will be office based in London. Key Responsibilities Meeting & exceeding the set budget for the role, and associ...
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Quality Manager - Innovation Swiss Precision Diagnostics (SPD) is a world leader in the research, design and supply of advanced consumer diagnostic products. SPD is a joint venture between Procter & Gamble (P&G) and Abbott ; and our brand Clearblue, ...
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Our client, one of the worlds largest distributors of ingredients and a provider of integrated solutions such as nutrient premixes and particle management services is seeking a Quality Manager for their London office. The role will be responsible for...
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Group Leader Regulatory Affairs - Regulatory Affairs Manager Hybrid role - access to West London 2-3 days per week as needed. Product portfolio - A portfolio of branded generic pharmaceuticals within the respiratory space. The products have an excell...
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CSL Vifor is a world leading pharmaceutical company focused on Nephrology, Iron Deficiency and Cardio-Renal therapies. At this time we are seeking to add to our medical affairs leadership in the UK with a Head of Field Medical Affairs UK. In this pos...
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The Manager, Global Aggregate Reports Quality and Compliance is an integral member of the Global Aggregate Report office and PV Writing Organization. The position holder responsibility includes the entire CSL product portfolio and development pipelin...
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