Exciting Science Graduate Opportunity –… at Alvotech · Reykjavik

Íslenska:

Vilt þú verða hluti af Drug Substance Operations teyminu hjá Alvotech í Reykjavík og starfa í öflugu og faglegu umhverfi þar sem nákvæmni, gæði og samvinna skipta máli?

Við leitum að jákvæðum og lausnamiðuðum einstaklingum sem eru tilbúnir að takast á spennandi áskoranir. Við bjóðum upp á vandaða þjálfun, góða handleiðslu og tækifæri til að vaxa í starfi.

EnglishOverview of role:

Join the Drug Substance Operations Team at Alvotech in Reykjavik and be a part of a dynamic, highly regulated environment where attention to detail and thoroughness are key. We're seeking individuals who are proactive, embrace challenges and have a positive mindset. The role requires extensive training, and Alvotech prioritizes teaching, mentoring, and guiding its technicians. Working in day/evening/night shifts is required.

Key Responsibilities:

• Perform all activities in full compliance with current Good Manufacturing Practices (cGMP) and Environment, Health & Safety (EHS) standards, ensuring work is executed in a safe and compliant manner. Demonstrate willingness to take on additional tasks under appropriate supervision.
• Execute cGMP manufacturing activities within Grade CNC, D, and C classified areas, adhering strictly to aseptic and containment requirements.
• Aseptically culture mammalian cells in shake flasks through the completion of the production process using single-use bioreactor systems, in accordance with approved protocols.
• Prepare media and buffers to defined specifications following approved standard operating procedures and batch documentation.
• Proactively maintain the USP manufacturing suite and associated equipment in a perpetual state of inspection readiness, ensuring compliance with regulatory and internal quality standards.
• Actively participate as a reviewer of cGMP documentation within the individual’s area of expertise.
• Support the execution of technical studies and validation activities, including process and equipment qualification, under approved protocols.
• Support successful regulatory inspections, including Pre-Approval Inspections (PAIs), and routine audits.
• Demonstrate a strong commitment to operational excellence, continuous improvement, and right-first-time execution within the assigned functional area.

Qualifications:

• Bachelor’s or technical degree in biotechnology, chemistry, biochemistry, biochemical engineering, or science related fields (desirable)
• No prior experience required, but laboratory experience is a plus
• Proficiency in Microsoft Office programs (Word, Excel)
• Excellent command of English language
• Ability to multitask and work both independently and as part of a team

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 wellbeing 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.