CMC Project Manager

CMC are looking to hire a Project Manager for 6 months for the implementation of the Digital Operational Resiliency Act (DORA), with an implementation date of 1st January 2025. This is a onsite role based near London Liverpool Street. Work alongside the Global Head of Delivery, Heads of Business Functions, Business Analysts and Project Managers to deliver...

CMC are looking to hire a Project Manager for 6 months for the implementation of the Digital Operational Resiliency Act (DORA), with an implementation date of 1st January 2025. This is a onsite role based near London Liverpool Street. Work alongside the Global Head of Delivery, Heads of Business Functions, Business Analysts and Project Managers to deliver...

Regulatory Affairs Manager CMC Duration: 6 month Contract Inside IR35 Location: Uxbridge, 3 days on-site per week Hourly Rate: £40-£55 per hour dependent on experience. This role focuses on the critical aspect of Chemistry, Manufacturing, and Controls (CMC) within regulatory affairs. Responsibilities include: Leading global regulatory strategies with...

Regulatory Affairs Manager CMC Duration: 6 month Contract Inside IR35 Location: Uxbridge, 3 days on-site per week Hourly Rate: £40-£55 per hour dependent on experience. This role focuses on the critical aspect of Chemistry, Manufacturing, and Controls (CMC) within regulatory affairs. Responsibilities include: Leading global regulatory strategies with...

Job Description Regulatory CMC Consultant Join an unprecedented team, supporting a range of different projects. In this role, you will be driving a number of projects, including developing the eCTD for BLA filngs of Biologicals. Responsibilities: Represents the department on multi-functional project development teams to support regulatory filings...

Our client, a global pharmaceutical company, is currently looking for a CMC Regulatory Affairs Manager to join their team in Uxbridge on a temporary contract. 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 science....

Vacancy for (Senior) Director Regulatory Affairs CMC Location: United Kingdom Job Summary Role Summary An exciting opportunity has arisen for an experienced CMC Regulatory Affairs Sr. Director to join the Autolus team to take a leadership role for developing global CMC regulatory strategies and content plans for products across Autolus’ cell and gene...

Vacancy for (Senior) Director Regulatory Affairs CMC Location: United Kingdom Job Summary Role Summary An exciting opportunity has arisen for an experienced CMC Regulatory Affairs Sr. Director to join the Autolus team to take a leadership role for developing global CMC regulatory strategies and content plans for products across Autolus’ cell and gene...

Our client, a global pharmaceutical company, is currently looking for a CMC Regulatory Affairs Manager to join their team in Uxbridge on a temporary contract. 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 science....

CMC Project Manager Remote £Viral respiratory tract infections make up a huge percentage of reported illnesses in the UK. In a recent study conducted by ONS, 1 in 6 people surveyed had a viral respiratory tract infection! A rare opportunity has arisen to join a biotech start-up, who are developing a new intranasal spray to treat VRI's. As a CMC...

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,...

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,...

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,...

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,...

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,...

BioTalent are pleased to be supporting a longstanding client, a mid-sized biopharmaceutical business with offices across Europe, in their search for a Senior Manager Regulatory CMC, responsible for Dossier Management. The client would like to speak to candidates with experience in: Development activities for Biologics in the EU and US. ...

BioTalent are pleased to be supporting a longstanding client, a mid-sized biopharmaceutical business with offices across Europe, in their search for a Senior Manager Regulatory CMC, responsible for Dossier Management. The client would like to speak to candidates with experience in: Development activities for Biologics in the EU and US. Post-approval ...

BioTalent are pleased to be supporting a longstanding client, a mid-sized biopharmaceutical business with offices across Europe, in their search for a Senior Manager Regulatory CMC, responsible for Dossier Management.The client would like to speak to candidates with experience in:Development activities for Biologics in the EU and US.Post-approval activities...

BioTalent are pleased to be supporting a longstanding client, a mid-sized biopharmaceutical business with offices across Europe, in their search for a Senior Manager Regulatory CMC, responsible for Dossier Management.The client would like to speak to candidates with experience in:Development activities for Biologics in the EU and US.Post-approval activities...

BioTalent are pleased to be supporting a longstanding client, a mid-sized biopharmaceutical business with offices across Europe, in their search for a Senior Manager Regulatory CMC, responsible for Dossier Management. The client would like to speak to candidates with experience in: Development activities for Biologics in the EU and US. ...