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Job Details

Qualified Person, Solid & Liquid Dose - CDMO

Company: Skills Alliance
Location: Greater Manchester
Reference: SA/JG00112
Closing Date: 28 Nov 17
Type: Permanent
Salary (£): 60,000 - 80,000
Benefits: Bonus and comprehensive benefits package

Job Summary:

Qualified Person, Solid and Liquid Dose, CDMO, Greater ManchesterSkills Alliance have partnered with a rapidly-expanding, leading CDMO for the appointment of a Qualified Person...


Qualified Person, Solid and Liquid Dose, CDMO, Greater Manchester

Skills Alliance have partnered with a rapidly-expanding, leading CDMO for the appointment of a Qualified Person (QP) to be based on their manufacturing site in Greater Manchester, UK. Specialising in supporting some of the industry’s most reputable pharmaceutical and biotechnology companies in developing and manufacturing innovative new products, this company now have an excellent reputation for Quality due in no small part to the Quality Leadership function on this site. As QP, this person would form a significant part of this and will have a high-profile role across multiple functions on the site.

Role Overview

As QP you will be responsible for releasing Solid and Liquid dose products (Human and Veterinary) on this busy manufacturing site. You will also be responsible for implementing and leading ‘Continuous Improvement’ and ‘Right First Time’ initiatives across all aspects of the site. Hosting Customer audits and performing external and internal audits are an important function of the QP role and maintaining strong external relationships are key. This is a diverse, high profile role and as such will provide the successful candidate with the experience to progress into leadership (Head of Quality/Quality Director) quickly.

Required Skills/Experience

Degree in a Science-based subject is required, as is eligibility to act as a QP under permanent provisions. Ideally you will have released Solid and Liquid Dose products previously but experience across other dosage forms would also be beneficial. Background in QA/QC within the Pharmaceutical, Biotechnology or Medical Devices sectors and significant experience of leading both internal and external audits (certification preferred). Expert knowledge of and ability/experience of training in international GxP guidelines is also important.

This opportunity should appeal to a QP looking to build on existing experience or work with different dosage forms (specified above). Fantastic potential to gain the experience and exposure needed to develop into a position of leadership in the future.

If you would like to be considered for this opportunity, please click APPLY to send a copy of your CV. For further details and a full job description, please call Joshua Godden on +44 (0) 207 220 6224 or e-mail Joshua.Godden All inquiries are treated confidentially.

Apply for this job: Qualified Person, Solid & Liquid Dose - CDMO

Contact Information:

Address:  Head Office
10 Aldersgate Street, London
Tel:  +44 20 7220 6200
Fax:  +44 870 831 1705
Website:  Visit Our Web Site

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