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  • Location: Findon
  • Salary: £23255 per annum, Benefits: + Benefits package including life insurance and private healthcare
  • Job Type:Permanent

Posted 9 months ago

  • Sector: Scientific Development, Manufacturing
  • Contact: Bernie Collins
  • Contact Email:
  • Contact Phone: 01403 216216
  • Start Date: 2023-09-19
  • Job Ref: V-49545
Are you a dedicated and hard working individual who is ready to get stuck into producing life changing vaccines? Our client is a pioneering and unique biotechnology in West Sussex, tackling the root cause of allergies and producing unique and individual vaccines. As part of the Specifics Production team, you'll play a pivotal role, ensuring the highest standards of quality and safety. If you are a detail orientated, proactive and motivated individual, this could be a good fit for you. 

General Responsibilities
  • To comply with all Good Manufacturing Practice regulations and carry out all duties whilst maintaining good Health & Safety practices. 
  • To provide support to other departments and production teams as and when required
  • Read & follow Standard Operating Procedures (SOPs) 
  • To complete all necessary documentation to GMP standards 
Key Responsibilities:
  •  To perform specifics ‘set up’ in Grade C for all products
  •  To operate VHP for ‘set up’ vials and other components and materials into Grade B/A
  •  To manufacture all specific product types in Grade B/A and ensure manufacture within 5 days
  •  To manufacture all specific product types in Grade C
  •  To carry out clean down procedures prior and post manufacturing.
  •  To perform service function for team members when they are manufacturing in Grade A or Grade C.
  •  To deliver batches in line with daily production schedule.
  •  To transfer completed batches out of clean suites
  •  To perform work as directed accordingly by Supervisor/Manager.
  •  To carry out production activities in a compliant manner following batch records and SOPs
  •  To complete all necessary documentation to GMP standards: Batch records, log books
  •  Working areas to be kept clean and tidy at all times in line with GMP
  •  Knowledge and understanding of stock control
  •  To follow and complete batch records with no missing data
  •  To deliver environmental plates and samples to Quality Control (QC).
  •  To understand FMS system and follow signals
  •  To alert any problems to team, Supervisor/Manager or Quality Assurance (QA)
  •  To understand and ensure batch records are fully completed when work is finished
  •  Wear appropriate clothing in unclassified, Grade C and Grade A/B areas.
  •  Undergo environmental monitoring and gowning assessment
  •  To assist with stock checks and stock control
  •  Remove expired stock from clean suite in line with procedures
  •  To prepare components/sundry items for transfer from corridor into Grade C via transfer hatch in line with procedures
  •  Tropos check of batch records
  •  To train team members
What we need from you 
  • Previous experience of a production environment is desirable but further training will be given.
  • Previous experience of GMP desirable.
  • Scientific knowledge
  • Good standard of written and oral English and Maths 
  • Computer literate
  • Ability to work and perform in a team.
  • Flexible and proactive approach to task and duties.
  • Show initiative and self-motivation.
  • Customer focussed approach to work.
  • Willingness to take on extra responsibilities when required.
  • GMP focussed approach to production activities and be able to show meticulous attention to detail.
  • To be able to work and react to targets and deadlines.
  • Able to demonstrate good written and verbal communication skills, and good standard of numeracy
  • Work neatly and methodically
  • Demonstrate a ‘what’s next’ mentality

To discuss this role further, please apply or contact bernie.collins@nextphaserecruitment