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QA Officer Liverpool United Kingdom

QA Officer

Wellington House, Physics Road | Liverpool | United Kingdom | L249HP

About us

Imperial Brands PLC is a dynamic FTSE100 FMCG company headquartered in Bristol with a global workforce of around 32,000 people. Borne out of a strong tobacco heritage, we have continually evolved to embrace changing market dynamics and our purpose is to create something better for the world’s smokers.  Our high-quality cigarette brands include Davidoff, Gauloises Blondes, JPS and West and we are increasingly focused on developing a leading portfolio of next generation products built around the vaping brand blu

Acquired by Imperial Brands Plc in 2017, Nerudia is a young and dynamic business which is wholly owned by Fontem Ventures, the NGP (Next Generation Products) arm of Imperial Brands.

The role

Liverpool
Permanent, Full time
Competitive Salary + Benefits

As QA Office you will provide direct support to the QA Manager (and/or deputy) in the management of the day to day aspects of the QA department (UK), including deviation close out and associated investigations, conducting self-inspections, supporting the Product Quality Review (PQR) and Change Control (CC) processes and participating in quality based projects. You'll ensure both ensure both QA regulatory and business requirements are met.  In addition you will work with other departments to ensure a strong QA culture throughout the business and provide guidance as required. Your main focus will be in Liverpool with a small percentage of the focus on global sites. 

Key accountabilities

  • Management of Batch Manufacturing record (BMR) updates and approval process. Perform training to end users, as required
    Review batch records and provide timely documented feedback for corrections / amendments to ensure any fixed product release dates are adhered
  • Co-ordinate the business document management system ensuring quality standards are maintained, documents are prepared, approved, revised, obsoleted and archived as required, & providing training as necessaryCo-ordinating the CAPA, Incidents and deviations system(s) to ensure root cause investigation and close out in a timely manner
  • Review batch/QC test records and release intermediate product for onward processing and final release of products to market both commercial
  • Carry out / participate in self-inspections (i.e. internal audits), as required
  • Support any site customer & regulatory audit(s)
  • Delivery of annual GxP/new starter training
  • Participate in the continual improvement of the site Quality systems and ensure ongoing compliance in-line with current regulatory requirements
  • Work closely with the Manufacturing/Warehouse/QC areas of the business to ensure Quality system(s) are maintained/compliant

Skills & experience

  • Substantial experience of working in a Quality Assurance related role in the Pharmaceutical  or similar industry
  • Demonstrated ability to implement procedures and processes which ensure compliance to GxP and other relevant regulatory standards specific to the Tobacco/Nicotine industry
  • Excellent oral and written communication skills for effectively interfacing with all levels of management and departments within the global business
  • Strong technical, analytical, and writing skills
  • Time management & able to work on own initiative
  • Good level of IT skills
  • Decisive thinker able to work within agreed timescales
  • Experience of conducting quality based investigations and root cause analysis
  • Working knowledge of GMP (Good Manufacturing Practice), GDocP (Good Documentation Practices) and PMTA (Pre-Market Tobacco Product Application) TPD (Tobacco Products Directive)

Qualifications:

  • At least 3 years’ experience in a quality, documentation, or project management role or combination thereof within a pharmaceutical or similar development setting required.
  • Higher National Certificate or degree in Biology, Chemistry, Pharmaceutical Sciences, or related scientific discipline is desirable
  • Area of expertise preferred:  Quality, GxP, Regulatory and/or Nicotine products

What we offer

Nerudia offers a competitive package of salary, pension and 25 days holiday, as well as onsite parking.

Next steps

Interested applicants should apply with their CV highlighting their suitability for the role. 

Opening date:16th April 2019
Closing date: 16th May 2019

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