CMC Regulatory Consultant - 382 (3)
Posted 19 hours 10 minutes ago by New Scientist
Permanent
Not Specified
Other
Buckinghamshire, High Wycombe, United Kingdom, HP109
Job Description
CK Group are recruiting for a CMC Regulatory Affairs Consultant to join a company in the Pharmaceutical industry at their site based in High Wycombe on a on a contract basis for 6 months.
Salary:
£45-£62.93 per hour PAYE or £65-84.55 per hour Umbrella
CMC Regulatory Affairs Consultant Role:
- Responsible for the development of CMC/technical regulatory strategies across the EMEA
- Leads a Regulatory Affairs team ensuring the success of new product registrations, line extensions and new indications and claims
- Manages the global or regional regulatory deliverables for drugs, dietary supplements & medical devices as relevant
- Develops strong partnerships with Regulatory Affairs Franchise, R&D, Marketing, Supply Chain & local business representatives.
- Represents the Regulatory Affairs CMC function as appropriate in Self Care Franchise, functional & business Leadership teams
Your Background:
• Relevant Bachelor's Degree or equivalent work experience in pharmaceutical CMC regulatory affairs
• Expertise across a broad spectrum of Regulatory classifications including Drugs, Dietary Supplement and/or Medical Devices
• Knowledge of regulatory frameworks and external environments in the EU/ EMEA , & the ability to apply these to regulatory solutions throughout the product lifecycle.
• Solid understanding of regulatory CMC in the markets of relevance
• Strong project management skills.
Company:
Our client is the largest and most broadly-based healthcare company. They strive to improve access and affordability, create healthier communities, and put a healthy mind, body and environment within reach of everyone, everywhere.
Location:
This role is based at our clients site in High Wycombe. This is a hybrid role with 2-3 days expected on site.
Apply:
For more information, or to apply for this CMC Regulatory Affairs Consultant role please contact the Key Accounts Team on or email . Please quote reference .
It is essential that applicants hold entitlement to work in the UK
Please note: This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check.
Salary:
£45-£62.93 per hour PAYE or £65-84.55 per hour Umbrella
CMC Regulatory Affairs Consultant Role:
- Responsible for the development of CMC/technical regulatory strategies across the EMEA
- Leads a Regulatory Affairs team ensuring the success of new product registrations, line extensions and new indications and claims
- Manages the global or regional regulatory deliverables for drugs, dietary supplements & medical devices as relevant
- Develops strong partnerships with Regulatory Affairs Franchise, R&D, Marketing, Supply Chain & local business representatives.
- Represents the Regulatory Affairs CMC function as appropriate in Self Care Franchise, functional & business Leadership teams
Your Background:
• Relevant Bachelor's Degree or equivalent work experience in pharmaceutical CMC regulatory affairs
• Expertise across a broad spectrum of Regulatory classifications including Drugs, Dietary Supplement and/or Medical Devices
• Knowledge of regulatory frameworks and external environments in the EU/ EMEA , & the ability to apply these to regulatory solutions throughout the product lifecycle.
• Solid understanding of regulatory CMC in the markets of relevance
• Strong project management skills.
Company:
Our client is the largest and most broadly-based healthcare company. They strive to improve access and affordability, create healthier communities, and put a healthy mind, body and environment within reach of everyone, everywhere.
Location:
This role is based at our clients site in High Wycombe. This is a hybrid role with 2-3 days expected on site.
Apply:
For more information, or to apply for this CMC Regulatory Affairs Consultant role please contact the Key Accounts Team on or email . Please quote reference .
It is essential that applicants hold entitlement to work in the UK
Please note: This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check.