GMP Biomanufacturing Operator I (Mon-Thurs 3:30pm - 2:00am)

About the role

Bring more to life. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Aldevron, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact. You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas into impact – innovating at the speed of life. At Aldevron, we deliver world-class CDMO services that accelerate the development of groundbreaking therapies. Our mission is to be the engine of innovation for genomic medicine pioneers. As a member of our team, you’ll help bring life-changing innovations to life—impacting millions around the world. We bring together deep scientific expertise, an unwavering commitment to quality, and a collaborative spirit to drive progress. Whether you're launching your career or bringing years of experience, we value the unique perspective you bring. Join us and become part of a mission-driven team advancing science and unlocking human potential—one discovery at a time. Learn about the Danaher Business System which makes everything possible. The GMP Biomanufacturing Operator I is part of the GMP Manufacturing department located in Fargo, ND and will be onsite. At Aldevron, we combine best-in-class products and service with the ideal operating environment to lay the groundwork for vital new discoveries worldwide. You will be a part of the GMP Biomanufacturing Team and will be responsible for executing production events in a GMP manufacturing environment.

Responsibilities

• Execute manufacturing processes such as transformations, cell banking, fermentation, lysis, chromatography, diafiltration, and final fill to support pDNA, mRNA, and protein product types.
• Ensure a safety-first and audit-ready mindset and manage environment within manufacturing areas.
• Maintain a quality-first mindset and adhere to good manufacturing practices by following appropriate gowning protocols, standard operating procedures, good documentation practices, and regulatory expectations.

Requirements

• H.S. diploma or GED
• Ability to read, write, understand English, and apply basic math.
• Good communication skills as needed for reporting, documentation, and scheduling.
• Ability to use hands, stand and/or sit for extended periods of time, bend, and lift up to 50 lbs.
• Reasonable accommodations may be made to enable individuals with disabilities to perform essential functions of the position.

Qualifications

• Previous experience in a manufacturing or GMP biomanufacturing setting (preferred)
• Experience following standard operating procedures (preferred)

Benefits

• Comprehensive benefit programs including paid time off, medical/dental/vision insurance, and 401(k) for eligible employees.
• Eligible for bonus/incentive pay.

Pay

Eligible for bonus/incentive pay; compensation amounts are subject to company discretion and become wages only when earned, vested, and determinable.

Schedule

Schedule flexibility such as weekend work or extended/altered schedules may be required at times depending on production need.