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QA On The Floor Specialist

Alvotech · Reykjavik Headquarters

posted 27d ago, last live 13d ago

Key factors at a glance

Seniority
Mid
Experience
2+ years
Work mode
On-site
Salary
Not stated
Required working language
English

Must-haves

  • Bachelor’s degree in Life Sciences, Pharmacy, Biotechnology, or related field
  • Minimum 2 years of experience in GMP-regulated environment
  • Strong knowledge of GMP and quality systems
  • Ability to work rotational shifts
  • Excellent communication abilities
  • Attention to detail

Nice-to-haves

  • Experience supporting manufacturing operations
  • Problem-solving skills
  • Collaboration abilities

Company hiring signal

See whether Alvotech is scaling up or slowing down, from its posting history.

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Original posting

English

Join Alvotech’s Quality Assurance team and play a key role in supporting manufacturing operations while ensuring compliance with GMP requirements and quality standards. This hands-on position provides real-time QA support to manufacturing teams and contributes to the delivery of high-quality biopharmaceutical products. Please note that this is a rotational shift position, requiring flexibility to support manufacturing operations across designated shifts in a 24/7 production environment. Scope and Responsibilities: • Act as the primary QA contact for DPM and DSM operations during rotational shifts. • Provide QA support for batch-related and facility issues, including deviations and CAPAs. • Perform shop floor monitoring and ensure compliance with GMP, GDP, and ALCOA principles. • Review manufacturing documentation, alarm logs, and failure assessments. • Approve area release, line clearance, and other QA-controlled activities. • Support media fills, cell bank issuance, AQL sampling, and visual inspection activities. • Maintain QA documentation and support inspection readiness and audits. • Contribute to SOP updates and train new QA team members as needed. Job Requirements: • Bachelor’s degree in Life Sciences, Pharmacy, Biotechnology, or a related field. • Minimum 2 years of experience in a GMP-regulated pharmaceutical or biotechnology manufacturing environment. • Strong knowledge of GMP, quality systems, documentation practices, GDP, and ALCOA principles. • Experience supporting manufacturing operations and quality oversight activities. • Strong attention to detail and problem-solving skills. • Excellent communication and collaboration abilities. • Ability to work rotational shifts in a fast-paced manufacturing environment. • Proficient in written and spoken English. What we offer: • An inspiring challenge to work with great co-workers on ambitious projects that change people's lives. • The chance to be a part of a global and fast-growing company. • An international work culture that encourages diversity, collaboration, and inclusion. • Positive, flexible, and innovative work environment. • Support for personal growth and internal career development. • Company social events and milestone celebrations. • Excellent in-house canteen and coffee house. • Exercise and well-being support for full-time employees. • On-site shower facility. • Transportation grant towards eco-friendly modes of travel for full-time employees. • Internet at home for full-time employees.

Shown in its original English. To apply, continue to the company's own page.