Bio-Process Technician (24/7 Shift)

AstraZeneca
Ireland
Workplace: OnsiteFull timeFunction: Field Service, Maintenance & Skilled TradesSkills: ["Documentation","Mentoring","Problem-solving","Cross-functional collaboration","Continuous improvement"]

Operate and execute core biologics manufacturing tasks across cell culture, media preparation, purification, buffer preparation, and equipment preparation to deliver consistent, compliant batches. Perform cGMP work with accurate SOP and batch record documentation, investigate deviations via QTS, and lead change controls when needed. Develop subject-matter expertise, mentor colleagues, coordinate shift handovers, and collaborate with Technical Services, QA, Automation, and engineering to support validation, start-up, and continuous improvement in a Lean mindset.

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FursaFursa
AstraZeneca
AstraZeneca
5 hours ago

Bio-Process Technician (24/7 Shift)

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Canonical indexed version, validated from employer's careers page.

Source: Company careers pageValidated by: Fursa AI
Last checked: 5 hours agoStatus: Live
Reposted: similar role first listed 6 months ago

Job Summary

Operate and execute core biologics manufacturing tasks across cell culture, media preparation, purification, buffer preparation, and equipment preparation to deliver consistent, compliant batches. Perform cGMP work with accurate SOP and batch record documentation, investigate deviations via QTS, and lead change controls when needed. Develop subject-matter expertise, mentor colleagues, coordinate shift handovers, and collaborate with Technical Services, QA, Automation, and engineering to support validation, start-up, and continuous improvement in a Lean mindset.
Location: Ireland
Workplace: Onsite
Employment Type: Full time
Job Function: Field Service, Maintenance & Skilled Trades

Key Responsibilities

  • •Independently perform cell culture, media preparation, purification, buffer preparation, and equipment preparation to deliver consistent compliant batches.
  • •Execute cGMP tasks with full attention to SOPs and batch record documentation to safeguard product quality and patient safety.
  • •Develop subject-matter expertise in an operational area and lead improvements and excellence within the shift team.
  • •Assist with investigations of operational deviations through QTS and lead/own change controls when required to prevent recurrence.
  • •Mentor colleagues on SOPs and process execution, act as designee for shift handovers, and collaborate with Technical Services, QA, and Automation to resolve issues.

Key Requirements

  • •Be trained and competent to independently perform core production tasks including cell culture, media preparation, purification, buffer preparation, and equipment preparation.
  • •Execute all tasks according to SOPs and batch records in a cGMP environment with excellent documentation and attention to detail.
  • •Develop and apply high-level SME knowledge in at least one operational area and lead improvements within the shift team.
  • •Anticipate and troubleshoot operational issues and interface effectively with MCS.
  • •Serve as a mentor and designee for shift handovers, including reporting out to leadership, technical services, and engineering stakeholders.
Experience:BiologicsManufacturingCGMP
Skills:DocumentationMentoringProblem-solvingCross-functional collaborationContinuous improvement
Tech Stack:CGMPSOPsBatch recordsQTSMCSLeanRoot cause analysis

Company Brief

AstraZeneca
Global biopharmaceutical company discovering, developing and commercializing prescription medicines across oncology, cardiovascular, renal & metabolism, respiratory, and immunology, focused on innovative therapies and vaccines to improve patient outcomes worldwide.
Industry: Pharmaceuticals
Company Size: Enterprise (1,001+ employees)
Revenue: USD 1B+
Growth: Public Company
Valuation: Public Company (Market Cap in USD)
Funding: IPO / Publicly Listed
Headquarters: Cambridge, United Kingdom
Founded: 1999
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