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Biological Senior Production Technician

Consult

Guildford

On-site

GBP 30,000 - 60,000

Full time

5 days ago
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Job summary

An established industry player is seeking a Virus Production Senior Technician to join their Virus Production department. This pivotal role involves leading teams in the bulk production of inactivated viral antigens, ensuring strict adherence to biosafety, EHS, and GMP standards. The position offers a fantastic opportunity to enhance your skills in a regulated environment while contributing to global vaccine production. With a focus on team leadership and operational excellence, this role is ideal for those looking to make a significant impact in the pharmaceutical manufacturing sector. Join a forward-thinking company where your expertise will be valued and rewarded.

Qualifications

  • Experience in industrial pharmaceutical production in a regulated environment.
  • Proficiency in IT, preferably with SAP/GBS experience.

Responsibilities

  • Lead teams of operators in the production of activated virus antigens.
  • Maintain compliance with biosafety and GMP standards.

Skills

Organizational Skills
Leadership Skills
Problem-Solving Abilities
Methodical Work Approach

Education

Experience in Industrial Pharmaceutical Production
Proficiency in IT (SAP/GBS)

Tools

SAP

Job description

Consult Pirbright, England, United Kingdom

Location: Pirbright, UK

Type: Full-time, site-based

Openings: Two permanent positions

A key role is available within our Virus Production department for a Virus Production Senior Technician. This position is at the forefront of practical manufacturing operations, aseptic processes, team leadership, and investigative tasks. It offers an excellent opportunity to develop skills in biosafety, EHS, and GMP standards while contributing to the production of inactivated viral antigens used in vaccines worldwide.

Key Responsibilities:
  • Collaborate with the area Supervisor to lead two teams of operators.
  • Participate in the bulk production of activated virus antigens, ensuring compliance with UK and company biosafety, EHS, and GMP standards.
  • Perform cleaning, decontamination, and steam sterilization of vessels and plant according to SOPs.
  • Maintain accurate and compliant batch record documentation.
  • Report and investigate any EHS and quality discrepancies.
  • Operate within Grade A/B clean rooms, ensuring strict adherence to aseptic manufacturing procedures.
What We’re Looking For:
  • Strong organizational and leadership skills.
  • Ability to work methodically and carefully within tight timelines.
  • Excellent problem-solving abilities.
  • Experience in industrial pharmaceutical production in a regulated environment.
  • Proficiency in IT, preferably with SAP/GBS experience.
  • Experience working in graded GMP environments.
  • Work Schedule: 11-hour shifts with a rotating pattern (5 days on, 5 days off, followed by 2 days on, 2 days off), with work on every other weekend (either Monday/Tuesday or Wednesday/Thursday, depending on shifts).
  • Biosafety Requirements: Work is conducted in a restricted area with live FMD, requiring adherence to strict biosafety protocols. Note that showering is required only when leaving the facility.
Seniority level

Mid-Senior level

Employment type

Full-time

Job function

Science and Manufacturing

Industries

Pharmaceutical Manufacturing

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