Regulatory CMC Specialist
- Employer
- Actalent
- Location
- Reading
- Salary
- 40000.00 - 45000.00 GBP/Salary
- Start date
- 4 Jan 2022
- Closing date
- 18 Jan 2022
View more
- Discipline
- Regulatory Affairs, CMC, Regulatory Writing
- Hours
- Full Time
- Contract Type
- Permanent
- Experience Level
- Experienced (non-manager)
Job Details
Description:
This is an exciting opportunity to join a global leading Clinical Research organisation within their dynamic CMC team. The role will require you to provide CMC subject matter expertise to a leading pharmaceutical client giving you excellent career development opportunities including progression opportunities within the company.
In this role you will be required to:
• Acts as a Regulatory Team Leader on complex projects, which may include technical writing.
• Prepares and review regulatory documentation in area of expertise, as appropriate.
• Establishes relationships with many customers as well as working with cross functional teams and stakeholders
• Acts as a subject matter expert for Regulatory Chemistry, Manufacturing and Controls
We are looking to speak to candidates with:
• At least 3 years Regulatory CMC experience including post marketing submissions
• Experience reviewing and approving change request controls
• Experience taking ownership for assigned products
• A life science degree (Masters preferred)
• Experience working cross functionally and managing multiple stakeholders
This is an excellent opportunity to join a global leading company who make a positive impact on millions of people around the world.
This is a permanent role which will give you the chance to become a valued member of the team and eventually progress into a leadership position.
This role can be fully remote based from anywhere in Europe and is offering a competitive salary as well as an attractive benefits package.
We are looking for people to join immediately so apply today!
“Regulatory” “Regulatory Affairs” “CMC” “Regulatory CMC” “Regulatory" "Pharmaceutical" "CRO" "Clinical Research"
“Regulatory” “Regulatory Affairs” “CMC” “Regulatory CMC” “Regulatory" "Pharmaceutical" "CRO" "Clinical Research"
“Regulatory” “Regulatory Affairs” “CMC” “Regulatory CMC” “Regulatory" "Pharmaceutical" "CRO" "Clinical Research"
“Regulatory” “Regulatory Affairs” “CMC” “Regulatory CMC” “Regulatory" "Pharmaceutical" "CRO" "Clinical Research"
“Regulatory” “Regulatory Affairs” “CMC” “Regulatory CMC” “Regulatory" "Pharmaceutical" "CRO" "Clinical Research"
“Regulatory” “Regulatory Affairs” “CMC” “Regulatory CMC” “Regulatory" "Pharmaceutical" "CRO" "Clinical Research"
“Regulatory” “Regulatory Affairs” “CMC” “Regulatory CMC” “Regulatory" "Pharmaceutical" "CRO" "Clinical Research"
“Regulatory” “Regulatory Affairs” “CMC” “Regulatory CMC” “Regulatory" "Pharmaceutical" "CRO" "Clinical Research"
“Regulatory” “Regulatory Affairs” “CMC” “Regulatory CMC” “Regulatory" "Pharmaceutical" "CRO" "Clinical Research"
“Regulatory” “Regulatory Affairs” “CMC” “Regulatory CMC” “Regulatory" "Pharmaceutical" "CRO" "Clinical Research"
“Regulatory” “Regulatory Affairs” “CMC” “Regulatory CMC” “Regulatory" "Pharmaceutical" "CRO" "Clinical Research"
“Regulatory” “Regulatory Affairs” “CMC” “Regulatory CMC” “Regulatory" "Pharmaceutical" "CRO" "Clinical Research"
“Regulatory” “Regulatory Affairs” “CMC” “Regulatory CMC” “Regulatory" "Pharmaceutical" "CRO" "Clinical Research"
“Regulatory” “Regulatory Affairs” “CMC” “Regulatory CMC” “Regulatory" "Pharmaceutical" "CRO" "Clinical Research"
“Regulatory” “Regulatory Affairs” “CMC” “Regulatory CMC” “Regulatory" "Pharmaceutical" "CRO" "Clinical Research"
“Regulatory” “Regulatory Affairs” “CMC” “Regulatory CMC” “Regulatory" "Pharmaceutical" "CRO" "Clinical Research"
“Regulatory” “Regulatory Affairs” “CMC” “Regulatory CMC” “Regulatory" "Pharmaceutical" "CRO" "Clinical Research"
“Regulatory” “Regulatory Affairs” “CMC” “Regulatory CMC” “Regulatory" "Pharmaceutical" "CRO" "Clinical Research"
“Regulatory” “Regulatory Affairs” “CMC” “Regulatory CMC” “Regulatory" "Pharmaceutical" "CRO" "Clinical Research"
“Regulatory” “Regulatory Affairs” “CMC” “Regulatory CMC” “Regulatory" "Pharmaceutical" "CRO" "Clinical Research"
“Regulatory” “Regulatory Affairs” “CMC” “Regulatory CMC” “Regulatory" "Pharmaceutical" "CRO" "Clinical Research"
Job Title: Regulatory CMC Specialist
Location: Reading, UK
Rate/Salary: 40000.00 - 45000.00 GBP Yearly
Job Type: Permanent
Trading as Aerotek. Allegis Group Limited, Maxis 2, Western Road, Bracknell, RG12 1RT, United Kingdom. No. 2876353. Allegis Group Limited operates as an Employment Business and Employment Agency as set out in the Conduct of Employment Agencies and Employment Businesses Regulations 2003. Aerotek is a company within the Allegis Group network of companies (collectively referred to as "Allegis Group"). Aerotek, Aston Carter, EASi, Talentis Solutions, TEKsystems, Stamford Consultants and The Stamford Group are Allegis Group brands. If you apply, your personal data will be processed as described in the Allegis Group Online Privacy Notice available at https://www.allegisgroup.com/en-gb/privacy-notices.
To access our Online Privacy Notice, which explains what information we may collect, use, share, and store about you, and describes your rights and choices about this, please go to https://www.allegisgroup.com/en-gb/privacy-notices.
We are part of a global network of companies and as a result, the personal data you provide will be shared within Allegis Group and transferred and processed outside the UK, Switzerland and European Economic Area subject to the protections described in the Allegis Group Online Privacy Notice. We store personal data in the UK, EEA, Switzerland and the USA. If you would like to exercise your privacy rights, please visit the "Contacting Us" section of our Online Privacy Notice at https://www.allegisgroup.com/en-gb/privacy-notices for details on how to contact us. To protect your privacy and security, we may take steps to verify your identity, such as a password and user ID if there is an account associated with your request, or identifying information such as your address or date of birth, before proceeding with your request. If you are resident in the UK, EEA or Switzerland, we will process any access request you make in accordance with our commitments under the UK Data Protection Act, EU-U.S. Privacy Shield or the Swiss-U.S. Privacy Shield
Company
About Actalent
Actalent connects passion with purpose. Our scalable services and talent solutions drive value and results and provide the expertise to help our customers achieve more. Every day, our experts around the globe are making an impact. We’re supporting critical initiatives in engineering and sciences that advance how companies serve the world.
Actalent’s global footprint and flexible delivery models ensure access to specialized talent where and when you need it. We promote consultant engagement through professional development and provide experiences to ensure continuous learning. Our people are the difference.
Our expertise spans capabilities in engineering including product and manufacturing, systems and software, construction management, environmental, architecture and civil; and power and utilities. We focus on sciences capabilities in laboratory sciences, healthcare, and clinical research.
Actalent is an operating company of Allegis Group, the global leader in talent solutions.
- Website
- https://www.actalentservices.com/en-gb
- Telephone
- +44 0 1344 383 100
- Location
-
Maxis 2 ,
Western Rd
Bracknell
Berkshire
RG12 1RT
GB
Get job alerts
Create a job alert and receive personalised job recommendations straight to your inbox.
Create alert