Quality Manager

Posted 3 Hours Ago
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Saint Helens, St. Helens, England, GBR
In-Office
Mid level
Logistics • Transportation
The Role
Manage the site's Compliance and Health & Safety department while ensuring compliance with MHRA GDP guidelines and relevant legislation. Serve as the Responsible Person for WDA(H) and Controlled Drug licences, maintain the Quality Management System, oversee audits, CAPA, deviations, validation, recalls, risk assessments, change control, product release, training, temperature excursions, and quality reporting. Lead regulatory and client audits and manage a team of three.
Summary Generated by Built In
Company Description

IPS (Part of the Culina Group) works with some of the best known brands and provides cost effective and innovative co-packing, co-filling and co-manufacturing solutions within the UK.

At Culina we have a winning culture, we believe that our culture is one of the reasons our company continues to thrive… A place where you're valued, challenged, and inspired!

Job Description

As a Quality Manager you will be responsible for managing the Compliance and H&S department and ensuring the overall GDP compliance of the site.

You will have a key responsibility in maintaining and developing all aspects of compliance management and Health & Safety profile of the site.  Carry out all duties in such a way as to ensure that the wholesale distributor can demonstrate compliance with EU Guidelines on Good Distribution Practice of Medicinal Products for Human Use (2013/C 343/01) and all relevant legislations (COMAH, EU Medical Devices Directive 93 / 42 / EEC etc.)

  • Named as the primary Responsible Person on the WDA(H) and Controlled Drug licence
  • Maintain and continually improve the company’s Quality Management System in compliance with current MHRA GDP guidelines, applicable certifications and group policies and procedures.
  • Responsible for the generation, revision, approval of procedures and other GDP documents
  • Responsible for creation of annual audit programme, performance of RP audits and management of self-inspections.
  • Ensure that any subcontracted activities which may impact on GDP are approved
  • Act as the lead contact for MHRA, client and corporate audits
  • Responsible for creation and review of Technical Agreements
  • CAPA and NCR management. Responsible for management of the investigation and resolution of operational discrepancies and customer complaints having final approval of outcome.
  • Review and approve validation protocols and ensure that all systems are validated
  • Decide on the final disposition of returned, rejected or falsified products
  • Coordinate and promptly perform any product recall operations
  • Management of risk assessment programme and ensure that the mitigation strategies are defined and implemented
  • Responsible for change management. Ensure that change control process in place for documentation, processes and systems
  • Oversee sampling and quality assurance release of products
  • Ensure that initial and continuous training programmes are implemented and maintained
  • Review and sign off temperature records and handle all temperature excursions. Ensure timely notification to the relevant party for all relevant product temperature excursions
  • Host Quality Management Review meetings, collate monthly Quality stats and produce compliance reports.
  • Manage team of 3 (Compliance and H&S Manager and 2 QA Specialists)

Qualifications

  • You will ideally have a professional background and previous experience (minimum 3-5 years) as an RP in the medical/pharmaceutical industry with key accountabilities to self-manage all requirement of an RP
  • Quality Manager experience
  • Knowledge and experience of applying GDP guidelines and H&S
  • Experience in examining and reengineering procedures and developing and implementing new strategies and procedures
  • Effective time management
  • Strong attention to detail
  • Strong interpersonal and communication skills
  • Confidence and assertiveness
  • Excellent IT skills (including Microsoft Office packages)
  • Dynamic and self-motivated, keen to achieve excellence within the business

Additional Information

As part of our drive to make IPS a great place to work. We are proud to be an inclusive and diverse organisation where we are committed to employee development and recognising success for hard working performers.

Our dedicated learning and development programmes are open to every employee to give you the opportunity to shape your own future within logistics and continue to work in an environment where team culture thrives.

Our People are the driving force behind our success, which is why we offer a wide range of benefits which include:

  • Annual Leave – Competitive holiday entitlement of 25 days plus the normal bank holidays.
  • Company Bonus – We do our best work to succeed together. When we achieve our goals you'll be rewarded through our bonus scheme
  • Private Medical Cover – This gives you peace of mind, you have choice, flexibility and speed of access to the most clinically appropriate care via Bupa
  • Pension scheme – we want colleagues to enjoy a comfortable retirement so we offer a great contribution of 4% employee and 4% employer
  • Life Assurance -  4 x your annual salary
  • Wellness – Via our Employee Assistance Programme we offer immediate access to a confidential telephone counselling and legal information service that operates 24 hours a days, 365 days a year
  • Eye Care Vouchers – We can provide you with substantial savings with free eye tests and discounts on prescription glasses
  • Reward & Recognition – We recognise that employees have gone the extra mile via Employee of the month and year, special recognition and long service awards.
  • Everyday discounts - via our benefit platform you will have access to over 50 retailer discounts for everyday savings!

If you meet the requirements for the above role and are looking for your next career opportunity please apply now and become a part of our #WinningTeam

Skills Required

  • Minimum 3-5 years of experience as a Responsible Person in the medical or pharmaceutical industry
  • Experience as a Quality Manager
  • Knowledge and experience applying Good Distribution Practice guidelines and Health & Safety requirements
  • Experience examining and reengineering procedures and developing and implementing new strategies and procedures
  • Effective time management
  • Strong attention to detail
  • Strong interpersonal and communication skills
  • Confidence and assertiveness
  • Excellent IT skills, including Microsoft Office packages
  • Dynamic and self-motivated approach with a commitment to achieving excellence
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The Company
HQ: Drayton
1,363 Employees
Year Founded: 1994

What We Do

Culina Group is a market leading provider of high quality logistics services for food and drink companies in the UK and Ireland. We serve a sizeable portfolio of customers - ranging from niche operators to major multinational companies - across our vast depot network, comprised of over 100 strategically located sites. We work with over 22,000 fantastic people at peak and specialise in the development and implementation of total supply chain solutions for ambient and chilled brand manufacturers and distributors. We are totally customer focused and always seek to add real value to our clients, providing a holistic solution to meet the challenges faced by manufacturers and the changing demands of the retail sector.

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