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 nicole.cooper@nextphaserecruitment