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                    Principal consultant regulatory jobs in the R&D & Science category

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                    Senior Regulatory Consultant, Foods Ref: 19799 Our client provides expertise and support to the global food and beverage sector. They provide practical solutions that cover all stages of a product’s life cycle from consumer insight, ingredient innovation and sensory testing to food safety consultancy and global regulatory advice. The Regulatory Group provides members and clients with a global food...
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                    Food Regulatory Consultant, Dutch Speaking Ref: 19798 Our client provides expertise and support to the global food and beverage sector. They provide practical solutions that cover all stages of a product’s life cycle from consumer insight, ingredient innovation and sensory testing to food safety consultancy and global regulatory advice. The Regulatory Group provides members and clients with a glob...
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                    Regulatory Consultant Food and Beverage, Multilingual Ref: 19842 Role: Permanent Salary: Attractive + Benefits Location: South East England Our client is a leader in providing expertise and support to the global food and beverage sector and is a prestigious name in its sector. They provide practical solutions that cover all stages of a product’s life cycle from consumer insight, ingredient innovat...
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                    Principal Quality (QA) specialist I am recruiting for a Principal Quality specialist within a Pharmaceutical manufacturing business. This is an excellent opportunity to join a well established and growing organisation and will suit a confident professional with positive attitude to customer service with pharmaceutical GMP manufacture and release. The position will be working as part of the Quality...
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                    Pharmacogenomics Principal Scientist / Team Leader – Biomarker Discovery Ref: 19890 An exciting opportunity within a renowned gene expression laboratory to manage a team of PhD, MSc and BSc scientists delivering fee for service research and study partnerships to Biotech and Pharma groups. The team apply molecular profiling technologies to target biomarker discovery and validation, specifically in ...
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                    Are you looking for a step up into a Managerial position? Our Pharmaceutical client is looking for a Regulatory Affairs Compliance Manager to work for them on a permanent basis. This role will focus on assisting the Senior Regulatory Manager and Regulatory Global Director in the registration and re-registration of products globally. Key Responsibilities Management of Export Compliance Executive En...
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                    Regulatory Affairs Specialist, Biocides Ref: 19857 Role: Permanent Location: Flexible Salary: Flexible depending on experience Our Client is an independent advisory and advanced product development services Company focused on science and technology initiatives. They work closely with their clients to advise on technology, R&D and regulatory issues. They are seeking a Regulatory Affairs Specialist ...
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                    Senior Regulatory Chemist Ref: 19858 Role: Permanent Location: Flexible Salary: Negotiable depending on experience Our Client is an independent advisory and advanced product development services Company focused on science and technology initiatives. They work closely with their clients to advise on technology, R&D and regulatory issues. They are seeking a Senior Regulatory Chemist with extensive t...
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                    Regulatory Compliance Team Leader Ref: 19878 Role: Permanent Location: East Anglia Salary: Negotiable on experience Our Client is a Leader is a trusted ingredients manufacturer and solutions provider to the global flavour, fragrance and consumer goods markets from their bases in the UK, the US, China and Kenya. They pride themselves on making the world taste better since 1800s. Committed to contin...
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                    Jade Mosley is recruiting for a contract Regulatory CMC Associate to join a UK headquartered pharmaceutical development and manufacturing organisation located in Macclesfield on an initial 12 month contract. As a Regulatory CMC Associate, you will produce and support the production of Chemistry, Manufacturing and Control (CMC) documentation for designated commercial products at various stages of p...
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                    Regulatory Technical Information Officer Ref: 19908 Our south based client are actively looking for a Regulatory Technical Information Officer Duties for this role will include:- Controlling regulatory / technical documentation activities relating to formulated products including cosmetics and Raw materials Liaising with key departments to ensure accuracy of information Supporting the creation of ...
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                    PURPOSE Direct, oversee and manage complex regulatory projects, ensuring quality deliverables on time and within budget. Ensure that all project work is completed in accordance with SOPs, policies and practices. RESPONSIBILITIESMay act as a Project Manager for a large stand-alone programme, involving several regulatory or technical deliverablesand/or region, and/or operation. Undertakes risk analy...
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                    PURPOSE Prepares and/or reviews regulatory submissions to support clinical trial and marketing authorisation activities for either internal and/or external clients. With guidance from senior staff, provides regulatory support for more complex projects. RESPONSIBILITIES Acts as a Regulatory Team Leader on more complex projects, which may include technical writing. Prepares and/or reviews regulatory...
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                    Quanta Consultancy Services - Hampshire, South East/Southern, Hampshire(4 days ago)
                    Our biotech client based in the of south of England is currently looking for a Project Manager to join their Technical Documentation and Regulatory Strategy Team. The successful candidate will be responsible for leading a Product Database project and overseeing the team implementing the database. Role: The Regulatory Dossier Project Manager will be responsible to track the execution of the Regulat...
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                    Dutch speaking Regulatory Advisor – Commercial Research A commercial research company based in Surrey are looking for a food science, nutrition or microbiology graduate to join their international team. Due to the technical requirements of the role the individual must speak totally fluent Dutch and hold at least 6 months’ work experience in a commercial research capacity. Key Responsibilities: Pro...
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                    CK Group - Redcar, Yorkshire (5 days ago)
                    Sarah Farrow is recruiting for a Regulatory Affairs Scientist for a leading provider of regulatory consultancy services, based at their site in Redcar on a permanent basis. Joining this multinational organisation you will be responsible for provision of regulatory and REACH compliance project support. This will include: - Advising clients on their regulatory obligations and compliance strategies i...
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                    CK Group - Leeds, Yorkshire (5 days ago)
                    CK Group is recruiting for a Regulatory Affairs Assistant to join a leading medical device company based in Leeds. This position is a contract role for the duration of 9 months initially. The Regulatory Affairs Assistant with support product registration activities and product registration submissions throughout the world, in order that registrations are achieved in a timely manner in accordance w...
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                    Medical device / ISO13485 / Herefordshire / Head of Regulatory Affairs / £80,000 - £100,000 A client of mine are looking for a Head of Regulatory Affairs to join their innovative organisation. This role will proactively develop, lead and drive the execution of global regulatory strategy where you will be managing the RA team. Responsibilities will include: • Senior Leadership, serve as a key and a...
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                    Quintiles - Reading, (46 days ago)
                    PURPOSE Direct, oversee and manage complex regulatory projects, ensuring quality deliverables on time and within budget. Ensure that all project work is completed in accordance with SOPs, policies and practices. RESPONSIBILITIESMay act as a Project Manager for a large stand-alone programme, involving several regulatory or technical deliverablesand/or region, and/or operation. Undertakes risk analy...
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                    PURPOSE IQVIA is committed to delivering a step change in strategy and operations within Regulatory, Safety, and Quality since the merger of Quintiles with imshealth. To do this, IQVIA has steadily invested in core capabilities to meet the needs of customers in a thoughtful and unique way. Furthermore, to achieve this vision, we are currently expanding our team and are looking for a highly motivat...
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                    Do you have specialist expertise in method development, validation of methods and could act as a lead scientist in Protein Chemistry/Biophysical analysis (Circular Dichroism, AUC, DSC, Western Blot, Capillary Electrophoresis)? Do you have experience of working in a Good Practice (GxP) regulatory laboratory within the chemical, pharmaceutical, biopharmaceutical industry? Do you want to be part of a...
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                    Catalent Pharma Solutions - Swindon, SN5 8RU(5 days ago)
                    The Principal Scientist is responsible for project management and execution of analytical activities. All work within the Analytical group is to be performed in accordance to cGXP requirements, including analytical investigations, adhering to project timelines and maintaining safe working conditions. Job Description Has extensive knowledge of use and operation of all commonly used laboratory equip...
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                    Are you a senior Quality Control or Quality Assurance (QA AC) professional working in Pharmaceutical Manufacture? Do you have an interest in Specials or IMPs? Are you interested in taking the helm of the Quality and Governance for a small / mid-sized leader in the pharmaceutical manufacturing sphere? Our client - a leader in pharmaceutical production across Primary and Secondary care - is looking ...
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                    Do you have specialist expertise in method development, validation of methods and could act as a lead scientist in Biological Chromatography (SEC, RP, IEX, HILIC) for peptides, glycoproteins, glycans? Do you have experience of working in a Good Practice (GxP) regulatory laboratory within the chemical, pharmaceutical, biopharmaceutical industry? Do you want to be part of a fast-growing, dynamic, su...
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                    Connect to great opportunity. Explore a career in epidemiology and outcomes at IQVIA. Do you love epidemiology? Do you really enjoy practical solutions? Do you worry about continued research funding? If you answer yes to all three questions, you need to check us out! We have a number of new and exciting Epidemiology opportunities within our fast growing and highly successful Real World & Late Phas...
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