Continuous Improvement & Quality Lead at Extracellular
Bristol BS2 0JZ, , United Kingdom -
Full Time


Start Date

Immediate

Expiry Date

01 Oct, 25

Salary

45000.0

Posted On

02 Jul, 25

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Data Quality, It

Industry

Pharmaceuticals

Description

Are you a driven foods professional looking for a new challenge?
Extracellular is a Bristol based start-up aiming to be a global leader in sustainable biotechnology. We’re channelling expertise in biology, digitalisation and biomanufacturing to accelerate novel foods as a sustainable, ethical source of protein.
We provide development and manufacturing services to other companies developing ingredients like chocolate, coffee, meat and seafood, but using processes that more closely resemble brewing beer. We have built world-class development and scale-up capabilities, which we are using to help companies hit their development targets and bring product to market.
Extracellular is looking for a highly motivated and detail-oriented Continuous Improvement and Quality Lead to join our growing team. As an early-stage company, we’re looking for an individual to own and administer our QMS and to help improve upon what we have as we expand into key international markets.

CANDIDATE REQUIREMENTS

  • A passion for continuously finding and implementing opportunities for improvement, no matter how big or small.
  • A degree in Science/Food Science or related field would be desirable with 5+ years’ experience in QA within the food manufacturing industry.
  • Knowledge of food safety legislation, good manufacturing practice, and HACCP Level 3 certification.
  • Experience creating documents and their management and control including Policies, SOPs, Risk Assessments etc
  • A genuine team-player who asks for help when it’s needed and offers help when it isn’t.
  • Excellent organisational skills and a great attention to detail with a focus on data quality and integrity.
  • Comfortable with ambiguity, shifting priorities and responsibilities and being proactive in finding innovative ways to move work forward. You’ll see failure as a learning opportunity.
  • Experience with working within the US market and knowledge of FDA/USDA requirements is advantageous but not essential.
Responsibilities
  • Quality oversight of manufacturing and laboratory operations. This will include reviewing batch records, deviations, change controls, and CAPAs to ensure compliance.
  • Documentation: Manage and review SOPs, protocols, and quality documentation.
  • Drive a culture of quality and continuous improvement in everything we do. This will include supporting investigations into non-conformances and implementation of corrective actions.
  • Audit Support: Assist in regulatory and client audits, as well as internal quality audits.
  • Support the operations team to ensure smooth functioning of the business. This may include supporting areas such as procurement, maintenance and logistics.
  • This is a full-time role on site at our UK facility in Bristol.
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