Senior Virus Production Shift Technician

Boehringer Ingelheim GmbH; Guildford; On-site; GBP 30,000 - 45,000; Full time

Job summary

A leading biopharmaceutical company seeks a Virus Production Senior Technician at their Pirbright manufacturing site. This role involves team leadership and hands-on production of viral antigens for vaccines. Ideal candidates will have experience in industrial pharmaceutical production and skills in biosafety, GMP standards, and leadership to guide junior technicians effectively.

Qualifications

• Experience working in a regulated environment.
• Ability to work methodically within tight timelines.
• Previous experience in graded GMP environments.

Responsibilities

• Lead two teams of operators in virus antigen production.
• Ensure compliance with safety and quality standards.
• Perform cleaning and sterilization of equipment.

Skills

Organizational skills

Leadership skills

Problem-solving

IT proficiency

Education

Experience in industrial pharmaceutical production

Tools

SAP

Job description

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THE POSITION

We are looking for a passionate individual to join our Virus Production 2 (VP2) department at our manufacturing site in Pirbright. As a Virus Production Senior Technician, you'll be at the forefront of practical manufacturing operations, aseptic processes, team leadership, and investigative tasks. This role offers a fantastic opportunity to develop a wide range of skills in a dynamic and supportive environment.

WHY JOIN US?
• Impactful Work: Contribute to the manufacture of inactivated viral antigens used in vaccines distributed globally
• Skill Development: Enhance your expertise in biosafety, EHS, GMP standards, and more
• Team Leadership: Lead and inspire a team of shift technicians, ensuring smooth and efficient operations

KEY RESPONSIBILITIES
• Collaborate with the area Supervisor to lead two teams of three operators
• Participate in the bulk production of activated virus antigens, adhering to UK and company biosafety, EHS, and GMP standards
• Perform cleaning, decontamination, and steam sterilization of vessels and plant following SOPs
• Ensure accurate and compliant batch record documentation
• Raise reports for EHS and quality discrepancies, support, and conduct investigations
• Operate in Grade A/B clean rooms, performing aseptic manufacturing

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