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Act as a lead writer across multiple projects, overseeing timelines, quality, and team resourcing. Coach and mentor junior writers, contributing to team knowledge sharing and best practice. Proven experience as lead writer across at least 3 document types (e.

This role offers the opportunity to work in a high-impact environment with a global client base, excellent support systems, and the ability to work remotely or flexibly.

Employment Solicitor - Remote | Flexible Hours Location: Fully Remote | Flexible Hours Salary: £40-70,000 Experience: NQ+ Full-time | Part-time This is a rare opportunity offering excellent work-life balance, with flexible working days and hours tailored to your lifestyle. ABOUT T...

We are recruiting on behalf of a well-established and highly respected firm, known for delivering exceptional conveyancing services with a strong reputation for quality and client care. Key Responsibilities: - Manage property transactions from instruction through to completion, ensuring a smo...

Executive Assistant to the Chief Executive Rochdale £38,500 per annum Permanent Full time, hours – 36.5 per week Our client is looking for an Assistant to the Chief Executive, to provide a confidential and high-level executive support role to the Chief Executive, and who will manage the E...

Location: North West England (Rochdale base, multi-site coverage) Job Title: Operations Manager / Responsible Individual Salary: Up to £70,000 + £5,000 performance-related bonuses Reporting to: Director Disclosure Level: Enhanced DBS Job Purpose This is a pivotal role providing strategic and oper...

Health and Safety Oldham up to £45,000 Manufacturing / FMCG Are you passionate about driving a proactive safety culture? Do you thrive on using digital tools to transform health and safety management? We're working on behalf of a leading manufacturing site in Oldham that is seeking a dynamic...

Quick Snapshot: Job Title: Registered Homecare Manager Location: Rochdale, Greater Manchester From £40,000 per annum plus bonus package Are you an experienced Registered Manager who thrives on making an impact? Do you take pride in being able to provide top-quality home care to p...

Role:Engineer Surveyor - Crane/Lift Location:Home based with daily travel to client sites and we aim to minimise travel where possible and offer localised geographical areas. Package:£42,148 - £45,232pa,Car Allowance of £5,000pa or Company Car, one-off retention payment of up to£2,500,Fuel Car...

JOB DESCRIPTION About the role We have an exciting opportunity for a Senior Internal Auditor to join the Guinness Partnership Team. This is a permanent, full-time vacancy based in our Oldham, Bower House office. We are currently working to a hybrid working style. The overall purpose of the role i...

Registered Manager Homecare Bury, Greater Manchester £38,000 - £40,000 per annum Full-time, permanent position TRC is working with a great, private business, one of the leading providers of home care in the North of England and has been for the last 20 years. We are working hand in hand to...

Project Manager – Investment Delivery Location: Oldham (hybrid) Salary: £54,475 per Annum. Job Type: Permanent Other requirements: Must hold a current valid driving license and have a car available for work at all times. To support the Head of Asset Investment Delivery to deliver FCHO’s i...

This is a fantastic opportunity to contribute to meaningful regulatory submissions across a variety of therapeutic areas, working with a highly collaborative and well-established team. This position involves the development of high-quality, accurate, and compliant documentation to support global ...

Your new role /n /nJoining a team that operates nationally, this regulatory/health and safety solicitor role will see you handle a range of contentious and non-contentious regulatory matters for clients across a number of sectors. Job Description /n/n Your new company /n /nThis Manchester law fir...

The Regulatory Labelling and Artwork Specialist role is part of a project with a leading biopharmaceutical company focused on developing innovative treatments for rare and ultra-rare genetic diseases.

Due to the development and expansion of the firm, they are now seeking to appoint an experienced Health & Safety Regulatory Solicitor to support the Partner, dealing with regulatory cases and inquest work. The firm is recognised for its outstanding client care and high-quality Crime and Regulator...

This well-known biotech is looking for an experienced Regulatory Affairs Manager to join their established EU Regulatory Affairs team. As EU Senior Regulatory Affairs Manager, you will support the creation of strategy and execution plans and manage regulatory submissions (e. As EU Senior Regulato...

About the Role: As a Senior Regulatory Medical Writer, you will independently lead the development of a wide range of core regulatory documents across various therapeutic areas. BSc or PhD in life sciences (PhD preferred) Strong understanding of ICH and regulatory authority requirements Experienc...

Advise on regulatory aspects of payment services for both bank and non-bank PSPs and e-money issuers. Minimum of 5 years PQE within a Financial Regulatory team, with strong knowledge of payment services and experience working with e-money businesses. Ability to draft regulatory provisions related...

About the Role: As a Senior Regulatory Medical Writer, you will independently lead the development of a wide range of core regulatory documents across various therapeutic areas. Senior Regulatory Medical Writer. This is a unique opportunity to join a high-performing regulatory writing team, with ...

Strong understanding of global regulatory requirements and submission standards. If you're looking for your next challenge in regulatory writing and want to be part of a high-performing, expert-led team, we’d love to hear from you. At Complete Regulatory, we offer.

The Regulatory Labelling and Artwork Specialist role is part of a project with a leading biopharmaceutical company focused on developing innovative treatments for rare and ultra-rare genetic diseases.

They are strengthening the team by hiring a Regulatory EU Lead, to be based in their offices in West London, hybrid working set-up.

The ideal candidate will be an experienced Regulatory Solicitor with a background in handling insurance-related claims and a proven track record in regulatory law. The firm is well known for delivering high-quality legal services to both individuals and businesses, with a strong reputation for ou...

CTD clinical summaries, investigator brochures) across multiple therapeutic areas Ensure all documents are clear, accurate, and aligned with relevant regulatory guidelines and client expectations Review and quality-check clinical documentation, data outputs, and other supporting materials Liaise ...

Significant hands-on registration experience associated with development, maintenance, and commercialization activities within Regulatory affairs. Understand regulatory implications of product strategy with regards to the product label & assessment. Ability to interpret and apply global and local...

Strong understanding of regulatory writing standards and processes (e. This is a fantastic opportunity to contribute to meaningful regulatory submissions across a variety of therapeutic areas, working with a highly collaborative and well-established team. This position involves the development of...

As EU Senior Regulatory Affairs Manager, you will support the creation of strategy and execution plans and manage regulatory submissions (e. As EU Senior Regulatory Affairs Manager, you will take the lead role in advising the Global Regulatory team on regional considerations in developing strateg...

Strong understanding of regulatory writing standards and processes (e. This is a fantastic opportunity to contribute to meaningful regulatory submissions across a variety of therapeutic areas, working with a highly collaborative and well-established team. This position involves the development of...

You will work closely with internal teams and external clients to ensure that deliverables meet both scientific and regulatory standards. Write and edit a variety of regulatory documents (e. Ensure all documents are clear, accurate, and aligned with relevant regulatory guidelines and client expec...

CTD clinical summaries, investigator brochures) across multiple therapeutic areas Ensure all documents are clear, accurate, and aligned with relevant regulatory guidelines and client expectations Review and quality-check clinical documentation, data outputs, and other supporting materials Liaise ...

Ensure all documents are clear, accurate, and aligned with relevant regulatory guidelines and client expectations. Conduct background research to confirm references and stay aligned with current regulatory requirements. Previous experience producing regulatory documentation within a medical commu...

Over years 5 years working on a range of Regulatory documents.

Senior Compliance Consultant – Financial Crime & Regulatory Compliance (Payment Services & E-Money). Audits (financial crime, regulatory, safeguarding). AML, sanctions, fraud & regulatory compliance.

As a Senior Regulatory Medical Writer, you will independently lead the development of a wide range of core regulatory documents across various therapeutic areas. Independently produce a range of high-quality regulatory documents (e. Minimum of 5 years' regulatory writing experience in a medical c...

Senior Regulatory Affairs Associate – Class III Devices | PMA Submissions | Remote + Monthly Onsite in Oxford | Equity + £100M Backed Start-up. Senior Regulatory Affairs Associate. Regulatory team and help take a breakthrough neuromodulation device through PMA submission and into the market.

Write and edit a variety of regulatory documents (e. Ensure all documents are clear, accurate, and aligned with relevant regulatory guidelines and client expectations. Conduct background research to confirm references and stay aligned with current regulatory requirements.

To support in this development we are seeking a satellite regulatory and licencing manager, who will focus on the management and meeting of our regulatory compliance obligations across the EU. Lead on the regulatory and licencing strategy for Europe, including ensuring that licences are applied f...

As a Senior Regulatory Medical Writer, you will independently lead the development of a wide range of core regulatory documents across various therapeutic areas. Independently produce a range of high-quality regulatory documents (e. Minimum of 5 years' regulatory writing experience in a medical c...

As a Senior Regulatory Medical Writer, you will independently lead the development of a wide range of core regulatory documents across various therapeutic areas. Minimum of 5 years' regulatory writing experience in a medical communications agency or pharma/biotech setting. Strong understanding of...

Professional growth and development: You’ll have the opportunity to work on a diverse range of projects, from writing and editing regulatory documents to providing oversight for outsourced deliverables to our clients. Our services include device development and CE/UKCA marking certification, glob...

Facilitate cross-functional and team awareness and understanding of regulatory issues as appropriate. Significant hands-on registration experience associated with development, maintenance, and commercialization activities within Regulatory affairs. Understand regulatory implications of product st...

Proven experience as a lead author on multiple regulatory documents, including at least 3 of the following: protocols, clinical study reports, clinical summaries, clinical overviews, investigator brochures, narratives, briefing documents, or regulatory response documents. Advise clients and colle...

Ability to draft regulatory provisions related to commercial contracts; experience in corporate transactions or commercial contracts is advantageous. Advise on regulatory aspects of payment services for both bank and non-bank PSPs and e-money issuers. Minimum of 5 years PQE within a Financial Reg...

Our work spans a wide range of high-quality clinical and regulatory documents, including:. Regulatory responses to health authorities. Write, edit, and review regulatory documents in accordance with guidelines and client requirements.

Healthcare Regulatory Partner | Manchester | up to £165k + Bonus + Excellent Benefits. A Tier 1 Legal 500 firm with a stellar reputation in healthcare law is looking to appoint a senior hire—Legal Director or Partner level—into its expanding Healthcare Regulatory team in Manchester. This is a r

As a Senior Regulatory Medical Writer, you will independently lead the development of a wide range of core regulatory documents across various therapeutic areas. This is a unique opportunity to join a high-performing regulatory writing team, with exposure to international projects, complex docume...

Ensure all documents are clear, accurate, and aligned with relevant regulatory guidelines and client expectations. Conduct background research to confirm references and stay aligned with current regulatory requirements. Previous experience producing regulatory documentation within a medical commu...