Regulatory Affairs Specialist

An excellent opportunity to join a busy regulatory affairs department of a global chemicals company. The role will cover very diverse regulations including REACH, CLP, Food Contact legislation, heavy metals directive, medical device directive and cosmeticsregulations - we are looking for a chemistry (or similar) graduate with at least 2 years’ experience...

**Full Job Description** Inter Scientific is excited to offer the role of Regulatory Affairs Assistant (RAA) to join our growing team. As a small but rapidly growing entrepreneurial company, this role is ideally suited to individuals who are looking to learn a broad range of skills across several diverse industries. We are certified to ISO 9001, ISO 14001,...

Job Type: Contract Multi-National Pharmaceutical CPL Life Sciences are looking for a Labelling Specialist to support a Large Multi-National Pharma company on an initial Contract basis. The role will be working in combination with the QA and Regulatory teams ~ Project management ~

**An exciting opportunity has arisen for a Regulatory & Compliance Specialist to join our client, a leading global FMCG company with Brands such as Dove, Knorr, Persil & Magnum, to be based inKnowledge Quarter, 131 Mount Pleasant, Liverpool L3 5TF(will involve a mixture of home working 2 days per week and 3 days working on site, This is a full-time temporary...

**The Role** **Accountabilities** - Europe - USA (FDA) - Asia - Mercosur - Classification and labelling - REACh - BPD - Global chemical inventories - Overseeing document generation for customers: - MSDS - Declarations of compliance with food contact legislation, heavy metals legislation, absence of specific hazardous chemicals. - Dealing with non-routine...

**External Communications Specialist - Inside IR35** **Contract Term: 3 months with potential for extension** **Contracting Authority: Network Rail** **Location: Liverpool/Manchester with 2 days/week on site** **As an External Communications Specialist, your main responsibilities would be**: - Develop and implement communications strategy on projects...

ProPharma Group is the leading global, independent, single-source provider of regulatory, clinical, and compliance services serving pharmaceutical, biotechnology, and medical device companies. Our team of experts brings a comprehensive portfolio of regulatory sciences, clinical research solutions, life science consulting, R&D technology, pharmacovigilance,...

Who are Diligenta? Diligenta's vision is to be acknowledged as Best in-class Platform based Life and Pensions Administration Service provider. Customer service is at the heart of everything we do and our aim is to transform our clients' operations. A business that has been described as 'home' by existing employees, we drive a culture that is founded on...

**Salary**: From £29471-£36838 **Who are Diligenta?**: Diligenta's vision is to be acknowledged as Best in-class Platform based Life and Pensions Administration Service provider. Customer service is at the heart of everything we do and our aim is to transform our clients' operations. A business that has been described as 'home' by existing employees, we...

The Opportunity An exciting opportunity is available for a Data Protection Specialist to play a key role in ensuring Diligenta and the services we provide to our clients are compliant with the Data Protection Regulation. Within this role you will meet the demands of multiple clients where you will be developing and building relationships. You'll be:...

Information Assurance Specialist Fully Remote £400 - £500 - Outside IR35Summary: The Information Assurance Specialist plays a critical role in safeguarding the confidentiality, integrity, and availability of sensitive information and IT systems within the university environment. This role involves collaborating with various stakeholders to assess...

The CMO QA Specialist will be a member of the CMO QA team responsible for Quality Assurance oversight of a Contract Manufacturing Organizations (CMO) in Europe. The Specialist will be the Single Point of Contact (SPOC) for their CMO, providing strategic and technical expertise for all cGMP related matters, including assurance that all aspects comply with...

Client Money Reconciliations Specialist - Temporary assignment - Immediate start **About Our Client**: This business has been established for nearly 50 years with their heritage firmly rooted in managing investments and traditional stockbroking. This client money reconciliations specialist role will include but not be limited to the following: - To...

Client Money Reconciliations Specialist - Temporary assignment - Immediate start **About Our Client**: This business has been established for nearly 50 years with their heritage firmly rooted in managing investments and traditional stockbroking. This client money reconciliations specialist role will include but not be limited to the following: - To...

Responsibilities : Development/Improvement activities: Serve as SME to support Site/Global projects. Proactively identifies scope for improvement or development based on knowledge of short to mid-term business needs. Leads and develops a strategy, plans and manages projects for method development or improvement as identified. Makes data supported...

Director of Specialist Services Domestic Abuse Services, Recovery Services, Mental Health Services, Dutch Farm, Chaplaincy 5 Hours per week ( flexible working hours can be agreed) YMCA Together – Across Services 30 Days annual leave plus bank holidays ~ Company Pension Scheme 4% The Director of Specialist Services has oversight for the Domestic...

Director of Specialist Services Domestic Abuse Services, Recovery Services, Mental Health Services, Dutch Farm, Chaplaincy 5 Hours per week ( flexible working hours can be agreed) YMCA Together - Across Services 30 Days annual leave plus bank holidays ~ Company Pension Scheme 4% The Director of Specialist Services has oversight for...

Responsibilities:Development/Improvement activities:Scroll down to find the complete details of the job offer, including experience required and associated duties and tasks.Serve as SME to support Site/Global projects.Proactively identifies scope for improvement or development based on knowledge of short to mid-term business needs.Leads and develops a...

Reporting to the Senior Manager, Global Microbiology QC, and based at CSL-Seqirus Liverpool the role is accountable for Quality Control method validation lifecycle management and method standardisation of Microbiological methods. The Quality & Validation specialist is an SME in Microbiological testing methodology, able to troubleshoot technical issues,...

Oxford Global Resources is hiring a Clinical Study Lead (IVD experience is a must) for temporary maternity leave. As a Clinical Study Lead/Trial Manager you will be responsible for the development and execution of all study associated documentation including protocols, investigator brochure, informed consent, contracts, and reports, in compliance with...