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Regulatory Cmc Consultant

2 weeks ago

London, United Kingdom Proclinical Full time

Proclinical are recruiting a Regulatory CMC Consultant for a pharmaceutical organisation. This role is on a contract basis and is located in West London.

**Responsibilities**:

- Accountable for highlighting possible delaying factors promptly to line management as well as share knowledge of regulatory documentation and processes with others.
- You will pursue process improvement and share best practice.
- Precisely examine the chemistry, manufacturing and controls regulatory impact to suggested changes.
- Produce effective and solid tactic CMC lifecycle proposal plans and monitor the successful accomplishment of the committed plan.
- Communicate with any other staff to guarantee precision of records.
- You will operate to agreed deadlines and uphold records to reflecting project status.
- Other duties may be assigned to this role.

**Key Skills and Requirements**:

- At least 3 years of experience with CMC regulatory.
- Communication skills both verbally and in writing.
- A high attention to detail.
- Able to retain crucial information.
- Works well with others.
- A motivated individual with the ability to manage own time efficiently.
- Computer literacy.
- Capable of resolving issues.

Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

Proclinical Staffing is an equal opportunity employer.

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