SRG - Qualified Person

Job Title:

Qualified Person

Category:

Technical roles

Closing Date:

01/05/2021

Job Title: Qualified Person (QP)

Location: Lancashire

Employment Term: Permanent

Salary: Up to £75,000 (+ benefits)

SRG are working with a leading supplier of FMCG products who specialise in the production of Personal care, cosmetic and pharmaceutical products. They are currently looking for a QP to become the site lead Qualified Person for their batch release. The main purpose of this role is to ensure all medicinal products produced on site are in total compliance with the MHRA.

This is a fantastic opportunity to join a successful company who are passionate and proud of the work they do. Set in an Idyllic surroundings, this position offers the opportunity to join a leading company who are have high values and an incredibly supportive culture.

Benefits: Bonus up to 10% of salary depending on company and personal objectives, flexible working hours and opportunity for remote working a couple days a week.

The role

• Ensure the site is operating within full compliance of their MHRA Manufacturers licence
• Ensure all GMP and regulatory updates appropriate to the medicinal products being produced at the site are implemented within the regulator’s published timeframe
• Undertake batch release of all medicinal products produced on site ensuring compliance with appropriate GMP standard and Marketing Authorisation
• Manage effectively the day-to-day activities of the Regulatory Compliance Officer
• Host site audits undertaken by regulatory bodies and customers of medicinal products in conjunction with the Quality Manager
• Provide guidance and technical assistance for new product introduction and technical transfer of medicinal products
• Ensure API and contract laboratory GMP compliance is maintained undertaking or supporting site audits where required.
• Assist the QA group with the supplier assurance audit programme for medicinal product excipients and components undertaking sites audits where required.

Requirements

• Educated to degree level in either a chemistry, biology or pharmacy based discipline
• Must be eligible to practise as a Qualified Person as defined within EU regulations
• Good working GMP experience of human non-sterile liquid medicinal product production, validation, qualification and QC testing techniques.
• Thorough understanding and working experience of GMP and Quality Management System implementation and development
• Experience of managing regulatory, customer and supplier meetings with a multi-discipline group of attendees
• Ability to handle multiple demands, to be self-managing and to work under pressure

If you would like to apply for this position, please use the link provided. Alternatively please email a copy of your CV to emma.white@srgtalent.com.  For more information regarding this position or any others, please call Emma on 0161 868 2222.

SRG is the UK’s number one recruitment company specialising in the scientific, engineering, clinical, pharmaceutical, food/FMCG, energy & renewables, biotech, chemical and medical device sectors.

As scientists ourselves, our specialist sector knowledge and our passion are second to none. It’s this combination that makes us different. We’re committed to providing outstanding temporary, contract and permanent career opportunities of all levels for our candidates and a comprehensive range of expert strategic recruitment services for our clients.

If you have a scientific background and this position is not relevant / suitable for you, please feel free to get in touch or visit www.srg.co.uk to view our other vacancies