Qualified Person at Alliance Medical Ltd
Sutton SM2 5PT, England, United Kingdom -
Full Time


Start Date

Immediate

Expiry Date

12 Jun, 25

Salary

0.0

Posted On

12 Mar, 25

Experience

3 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Regulatory Compliance, Medicine, Biology, Chemistry, Addition, Pharmaceutical Manufacturing

Industry

Pharmaceuticals

Description

SKILLS AND EXPERIENCE

The ideal candidate for this role will have a strong background in pharmaceutical manufacturing, quality assurance, and regulatory compliance, and have excellent attention to detail and problem-solving skills.
As a minimum you should hold a third level qualification in a scientific discipline – pharmacy, medicine, chemistry, pharmaceutical chemistry and biology.
In addition, must have fulfilled the education requirements for the role of the Qualified Person such as a diploma in Pharmaceutical Manufacturing Technology.
Previous Experience.
A minimum 3 years practical experience in activities of quantitative and qualitative analyses of active substances and of the necessary testing and checking to ensure the quality of medicinal products.

Responsibilities

We have an exciting opportunity for a Qualified Person to join us at Alliance Medical This is a full time role working 40 hours a week on a permanent basis.
We are ideally looking for an experienced Qualified Person, with management experience and responsbility for a Quality Management System. It is preferable that you have experience as a releasing QP within Radiopharmaceuticals/ steriles on a UK MHRA licence.
This role covers batch release of Radiopharmaceuticals for use in diagnostic PET scanning and contributing to the management of QMS.

Other key responsibilities of the role include:

  • Overseeing the release of medicinal products for distribution, ensuring compliance with all relevant regulations and guidelines
  • Reviewing and approving batch records, analytical data, and other documentation related to the manufacturing and testing of medicinal products
  • Investigating and resolving quality issues and deviations related to manufacturing processes and materials
  • Participating in internal and external audits of the manufacturing facilities and quality systems
  • Providing expertise and guidance on regulatory requirements and quality standards to internal teams

Please note that we will be interviewing throughout the duration of this advert. Therefore if you are interested in this role an early application is advised as we may close the advert prior to the advertised date.

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