Quality Compliance Auditor

Location UK / Northern Ireland

Job Type Permanent full-time, TemporaryContract

Salary Not disclosed

Updated 6 days ago

Reference 1391910

 Job Description

You will support the Almac Clinical Services Qualified Persons (UK and IE) in assuring that the Drug Substance and Drug Product manufacture has been performed in accordance with GMP and any regulatory submissions.

Quality Compliance Auditor

Hours: 40 hours per week
Salary: Competitive
Ref No: HRJOB4670
Business Unit: Clinical Services
Location: Craigavon
Open To: Internal & External Candidates

 
The Company

Almac is an exceptional, award winning, drug development solutions provider at the forefront of the pharmaceutical industry.  We are a privately owned organisation that has organically grown over 50 years and now employs in excess of 5,000 highly skilled personnel worldwide.  Our Global headquarters is located in Craigavon, Northern Ireland with additional operations throughout Europe (UK, Ireland), across the US (Pennsylvania, North Carolina and California) and in Asia (Singapore and Japan). 
Our drive and passion for the values championed by our Founder, and enshrined in the ethos of Almac, ensures that ‘Partnering to Advance Human Health’ is more than just a strapline – it is our way of life.
Advancing human health requires exceptional people – your talent, experience and passion will be the perfect match.  Together we will make an exceptional difference to the health of countless patients all over the world ………and this is just the beginning. 

The Role

Working as part of the Quality team based in our global headquarters in Craigavon, you will support the Almac Clinical Services Qualified Persons (UK and IE) in assuring that the Drug Substance and Drug Product manufacture has been performed in accordance with GMP and any regulatory submissions.  In doing so they will perform these activities in line with internal timelines and customer / regulatory expectations.

As part of a busy team within a rapidly growing organisation, operating within a challenging industry you will benefit from the numerous personal and professional developmental opportunities available throughout the Almac group.

Essential Criteria

  • Bachelor’s degree in a scientific (Chemistry, Biology or Pharmacy) or related (or equivalent)
  • Knowledge of the manufacture of pharmaceutical dosage forms e.g. tablets, sterile injectable products, biological products
  • Proven ability to organise, plan and prioritise multiple concurrent tasks whilst maintaining a high level of accuracy in all work produced
  • Experience in processing a high volume of technical information to condense into simplified elements
  • Experience in the use of Microsoft Office Packages (to include Word, Excel, Outlook and PowerPoint)

 
Desirable Criteria
(The following criteria may be applied if a large pool of applicants exist)

  •  Bachelor’s degree (or equivalent) 2.2 or above
  • Experience in a Quality, Regulatory or Manufacturing related role within the pharmaceutical industry
  • Experience in the generation or review of manufacturing batch records, change controls and or deviations
  • Experience in a customer facing role

 
 
Reward

  •  Competitive salary
  • Family friendly flexible working
  • Learning and development opportunities and support
  • Health promotions
  • Enhanced pension contribution
  • Long service awards
  • 34 days annual leave allowance
  • Marriage leave
  • Free car parking
  • Moving house leave
  • Subsidised restaurant
  • Paid medical appointments
  • Occupational sick pay
  • Enhanced maternity pay
  • On site physiotherapist
  • Critical illness policy
  • Perks discount scheme
  • Death in service benefit
  • Westfield health benefit

(Full detail including eligibility criteria is outlined in the company handbook)

To Apply
Apply online at www.almacgroup.com/careers

Closing Date
25th February 2019 at 17.00 hours