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Expired
  • Location: Worthing
  • Salary: Competitive Salary Plus Benefits
  • Job Type:Permanent

Posted almost 2 years ago

  • Sector: Quality
  • Contact: Adrienn Prezenszki
  • Contact Email: adrienn.prezenszki@nextphaserecruitment.com
  • Contact Phone: 01403 216216
  • Start Date: 2022-05-17
  • Job Ref: V-47309-1
Do you have strong experience in related to IT systems such as LIMS, eQMS etc. in a GxP environment? A brand-new role has been created for an IT Compliance Lead to join a pioneering Biopharmaceutical organisation in Worthing, West Sussex due to the growth of the company.

This is a permanent position, paying a competitive salary depending on your experience (around £60K - £70K plus benefits). The role will be hybrid, being on - site with opportunity to work remotely. You will be required to be intially be based on site 5 days a week for an idefinitie period due to paper based records and play a key part in driving the culture forward within Quality. They company has recently implemented an eQMS system. 

The Company
A pioneering Europe-based Pharmaceutical organisation specialising in the treatment and prevention of allergies. Their unique focus is on the vaccination and prevention of conditions such as hay fever and their products are fascinating, complex, and ever-changing. The company employs around 300 people in Worthing and has an excellent reputation for providing career development opportunities, challenging, and engaging work and a pleasant, vibrant working environment.

The Role
You will support the intergartion of a range of old and new legacy systems working with key stakeholders across the business to align all prcesses from a GxP perspective. You will be the System Owner/Administrator for IT systems such as LIMS, eQMS, and systems related to batch release and manufacturing processes to provide QA guidance and support impact assessment, validation to maintain compliance to GMP legislation. You will develop Quality System metrics and support Data Integrity compliance as per GxP legislation. You will provide QA expertise in Computer System Validation, and compliance processes related to backup & restore, data migration, software upgrades and audit trail checks. You will work closely with IT colleagues to oversee service providers associated with GxP IT systems. This role will focus on supporting quality systems including non – conformances, CAPA, QTAs.

 This is a great role if someone is looking for that next step up in leading various IT related projects from a QA perspective or if solely worked on IT projects within a GxP environment. 

Benefits
In addition to a competitive salary, the company offers excellent career development opportunities and the following benefits:


  • 25 days' holiday
  • Stakeholder pension plan
  • Private medical cover
  • Life insurance scheme
  • Non-contractual, discretionary annual bonus
  • Cycle to Work Scheme
  • Discounted GYM membership
 

Experience
The successful candidate will have a strong scientific/ technical background with previous experience gained in the Pharmaceutical industry working on projects related to IT Systems in a GxP environment. You were ideally involved in integrations to enable various IT systems to connect with each other. Familiarity with Trackwise, LIMS and other eQMS Systems would be advantageous. You will demonstrate the ability to multitask, use basic statistical tools and methods plus have proven abilities in Word, Excel and/or Access to process and display data graphically. In addition, you will need a strong and enthusiastic work ethic, excellent communication skills and attention to detail and enjoy a closely-knit team environment.