Regulatory Affairs CMC Author – Post-Approval Biologics

Regulatory CMC Project Manager - Contract Partnering with an international pharmaceutical company focused on both in house product development and CDMO services, we are now supporting the appointment of a new Regulatory CMC Project Manager to oversee regulatory activities for a small molecule oncology product globally. This position will be a contract until...

Parexel, a leading Clinical Research Organization (CRO), is seeking a highly qualified Principal Regulatory Affairs Consultant (Associate Director level) with expertise in Chemistry, Manufacturing, and Controls (CMC) for small molecule. The ideal candidate will possess strong regulatory affairs experience, project management skills, and in-depth knowledge of...

Role: EMEA Regulatory Affairs ConsultantDuration: 5 MonthsLocation: High Wycombe, UK - Hybrid working (2 /3 days in High Wycombe office)KEY RESPONSIBILITIESManagement of post-approval activities for specified OTC products• Supports the EMEA Regulatory Affairs team for post-approval activities for MRP/DCP products across EEA and coordinate worksharing (WS)...

Title: Regulatory Affairs ManagerDuration: Till March 2024Location: Hybrid. 1 - 2 days in the office per week at High Wycombe HP12 4PTNotes: Inside IR35 - till March 2024 initially - OTC experience is essential.Job Description:EMEA REGULATORY AFFAIRS –REGULATORY CONSULTANTKEY RESPONSIBILITIESManagement of post-approval activities for specified OTC...

Director of Regulatory AffairsOur client, a global pharmaceutical company is seeking a Director of CMC Operations to lead and grow its CMC capabilities in Europe. This role will be pivotal in shaping early-stage drug development strategy, working across a diverse portfolio including small molecules, peptides, and macromolecules.About the Role:You will be...

An opportunity to join the Regulatory Affairs team at an R&D focussed global PPP company. You will:Manage a portfolio of plant protection products in specific geographical territoriesDevelop regulatory strategy Become the subject matter expert on the regulations/guidelines in your territory. As a regulatory Specialist, you will develop regulatory strategy...

We are looking for a Senior Regulatory Affairs Manager/Consultant with 10+ years of experience in regulatory affairs, including CMC expertise. This challenging role offers the opportunity to work on diverse projects, manage client relationships, and contribute to regulatory strategies in a global pharmaceutical environment.This is a client dedicated project,...

This job is with Autolus Therapeutics, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ+ business community. Please do not contact the recruiter directly. Role Summary With a significantly expanding regulatory team, an exciting opportunity has arisen for an experienced Director, Regulatory Affairs to...

Exciting opportunity to join the regulatory affairs team at an established and highly reputable chemical regulatory science consultancy. This is expansion to cover an increasing workload. The role is delivery focussed with no commercial or business development aspects. We are looking for a regulatory person for a purely regulatory delivery role. This role...

Company Overview:As a proud United Arab Emirates company based in Abu Dhabi, Medisal Pharma is dedicated to excellence in manufacturing high-quality pharmaceutical products. To support our expanding international operations, we are looking to hire a skilled Regulatory Manager to oversee our regulatory affairs and ensure compliance in the United Kingdom.Job...

We are seeking experienced Regulatory Affairs professionals to join our dynamic team in support of a global acceleration client initiative for late-stage phase III assets. This is an exciting opportunity to play a crucial role in accelerating time to filing and approval in Global Country Initiative (GCI), emerging markets, and non-EU markets.Our global...

This job is with Autolus Therapeutics, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ+ business community. Please do not contact the recruiter directly. Role Summary With a significantly expanding regulatory team, an exciting opportunity has arisen for an experienced Senior Manager, Regulatory...

Our client, a global pharmaceutical company which develops a portfolio of prescription generic and branded pharmaceuticals within the CNS, Neurology and respiratory areas. As Regulatory Affairs Manager, you will:Preparation, submission, and management of variation applications to agreed timelinesManage and submit Renewals and PSURs in line with specified...

Cure Talent are delighted to be working with a well-established Medical Device company that supply and distribute innovative Medical Devices. Due to their continued growth and success, we have an exciting opportunity for a Senior Regulatory Affairs Associate to join them in West Yorkshire.As the new Senior Regulatory Affairs Associate, you will be working...

Due to continued expansion we are currently seeking an additional Senior Regulatory Affairs Executive to join our team in a well-established Consultancy. You would have proven success in your current role and an ambition to continually develop together with commercial awareness, a drive to innovate and be a key part of a growing company in the pharmaceutical...

Our client, a global pharmaceutical company, is currently looking for a Senior Regulatory Affairs Associate to join their team in Cambridge or West London (Uxbridge). This is a great opportunity to work for a pharmaceutical company who have created a centre of excellence and constantly focus on driving innovation and using cutting edge techniques in their...

Job: Regional Regulatory Affairs Senior AssociateContract: 12 Month ContractLocation: Remote with occasional presence in Cambridge or UxbridgeCompany: A Global biopharmaceutical companyAbout the RoleJoin a dedicated team of regulatory professionals providing expert regional regulatory leadership and execution across Europe. This role focuses on the...

We have an opportunity for a Senior Scientific and Regulatory Affairs - UK/IRL Market Lead (known internally as - Program Manager SRA (Science & Regulatory Affairs) UK/IRL) to join us at Mars. You will lead a variety of regional regulatory activities related to raw materials, finished products, labelling, claims, packaging and supporting UK/IRL. In this...

Our client, a global pharmaceutical company is currently looking for a EU Regulatory Specialist to join their team based on the outskirts of London on a full time, 12-month temporary basis (35 hours per week).In this role, you’ll lead and manage the operational aspects of European regulatory filings, collaborating closely with European Regulatory groups...

We have been instructed to work on behalf of a key insurance client of ours on an exclusive basis, to help bolster their Delegated Authority team during a period of continued growth.One of the pivotal appointments is a Delegated Authority Oversight Manager. This is a rare and exiting opportunity, offering someone the ability to shape, develop and grow the...