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QC Manager - Biopharmaceutical (maternity cover)

QC Manager - Biopharmaceutical (maternity cover)

Job Title: QC Manager - Biopharmaceutical (maternity cover)
Contract Type: Permanent
Location: Worthing
Industry:
Salary: Very attractive pay rates
Start Date: 2020-03-11
Reference: V-46121
Contact Name: Steve Twinley
Contact Email: steve.twinley@nextphaserecruitment.com
Job Published: March 17, 2020 10:54

Job Description

A maternity cover contract position has arisen for an experienced QC Manager with a strong GMP background gained in a commercial Pharmaceutical or Biopharmaceutical production environment. We are looking for someone to start as soon as possible and will consider either a fixed-term appointment or engaging an experienced daily-rate contractor.
 
Based on the West Sussex Coast, this could be a great career move for someone looking to move to a beautiful part of the country and join an innovative, growing organisation. You will be paid a very generous salary / pay rate (depending on experience).
 
You will join a leading vaccine company, managing all aspects of a QC department, comprising 3 analytical labs (chemistry, biochemistry, microbiology) and supporting services. This is a genuinely exciting, varied opportunity for an ambitious individual with strong leadership skills and positive energy.
 
The Company
 
A pioneering UK-based Pharmaceutical company specialising in the development and production of injectable and oral dose vaccines and diagnostic kits for patients who suffer from allergies. They have developed an innovative approach to immunotherapy which will be of particular interest to someone with a passion for scientific innovation and GMP / sterile production. There are around 300 employees in Worthing and the company has an excellent reputation for its welcoming atmosphere, pioneering science and ongoing development opportunities.
 
The Role
 
This is a varied and highly rewarding position, based around the management of a QC department, comprising Chemistry, Microbiology and Biochemistry labs. You will have 4-5 direct reports and around 30 indirect reports, and will be picking things up on an interim basis to cover maternity leave.
 
The teams perform analytical testing of raw biological materials and vaccine / diagnostics products, using a range of state-of-the-art analysis techniques (e.g. HPLC, ELISA, SDS-PAGE and others). You will have a broad range of responsibilities including:
 

  • Managing programmes & projects to deliver significant improvements in QC and product sciences capabilities, efficiency, throughput and compliance.
  • Leading, organising and managing required Laboratory functions such as equipment, compliance investigation and personnel issues within the team including performance management, absence management and development.
  • Organising the management of QC work, both for short-term turnaround and ongoing projects
  • Representing the QC department at management meetings, collaborating with QA, Development, Production and other departments
  • Encouraging the teams to propose ideas and collaborate effectively
  • Ensuring laboratories work within current GXP
  • Making sure that analytical methods and procedures are in place and followed consistently
  • Hosting laboratory audits from QA and regulatory authorities
  • Conducting investigations to establish root cause and appropriate CAPAs
  • Maintaining Quality systems within the lab, including OOS, non-conformances, annual product reviews and change controls
  • Ensuring that equipment is maintained, validated, calibrated and serviced; and ensuring the lab equipment log book process is managed correctly
  • Maintaining QC budgets and department spend


This is a genuinely unique, busy and exciting role with many different aspects, presenting a real opportunity to progress to the next phase of your career. Full details, including a comprehensive job spec, will be provided on application.
 
Experience
 
The successful candidate will ideally have a degree (or higher) in Chemistry, Biochemistry or Microbiology, including a strong understanding of the commercial application of analytical techniques within a GMP / GLP Pharmaceutical or Biopharmaceutical setting. You will need to be able to demonstrate excellent leadership skills and experience, gained in a managerial capacity within a regulated, process-led environment. Experience as a QC Team Leader / Manager in a Biopharmaceutical environment would be a particular advantage. You must be able to demonstrate the ability to learn, listen actively to others, and build collaborative relationships.
 
 

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