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We are hiring a new member of our Sci Ops team whose primary focus will be supporting the deployment and ongoing operation of our in-house GMP facility. Beyond that, you’ll work on improvement projects and daily tasks required for running Retro’s labs and facilities. You will be a part of the Science Operations team – a close-knit group of dedicated, resourceful humans, and you’ll report to their fearless leader.

About you:

You are detail-oriented, organized, and thrive in bringing structure among chaos. You enjoy both compliance-driven tasks and the challenge of dynamic troubleshooting. You proactively address issues, enjoy collaborating cross-functionally, and consistently demonstrate accountability and reliability. You’re comfortable in fast-paced environments and passionate about supporting groundbreaking science.

What you’ll do in this role:

  • Act as the point person for GMP-related daily GMP lab operations requests, material handling needs, troubleshooting, inventory management, and oversee stocking, ordering, shipping, and receiving activities
  • Perform routine cleanroom maintenance, coordinate vendor services, and handle operational tasks
  • Conduct environmental monitoring (temperature, humidity, particle counts, etc.) surveys and ensure the facility is within standards during operation
  • Collaborate with the R&D and Process Development teams to ensure smooth operational tech transfers to GMP.
  • Interface proactively with the Quality team, ensuring compliance with regulatory requirements and internal SOPs
  • Support documentation, validation, and calibration efforts for GMP instrumentation and facility equipment, including IQ/OQ/PQ activities under the guidance and final approval of the Quality team
  • Provide hands-on support to the broader Sci Ops team, including improvement projects and requests relating to general lab and facilities needs
  • Serve as a key on-call responder for facility emergencies and urgent issues (such as power failures, significant leaks, cold storage alarms, etc.) – a rotating team responsibility which includes some nights, weekends, and holidays

You might thrive in this role if:

  • Have 2-4 years of experience working in GMP operations, lab management, quality assurance, or another highly regulated biotech environment – bonus points if you’ve directly supported clinical manufacturing or equipment validation.
  • Are hands-on and technically adept in cleanroom environments – you know your way around environmental monitoring equipment, understand contamination control practices deeply, and feel at ease maintaining meticulous documentation
  • Have practical knowledge of instrument calibration, equipment qualification processes (IQ/OQ/PQ), and vendor management – you’re comfortable coordinating with external partners and internal teams to ensure smooth operations
  • Are naturally organized and precise – you take pride in maintaining clear, detailed documentation and have an intuitive feel for regulatory requirements and standards
  • Know inventory and material handling systems well (Quartzy, ERP systems, etc.) and enjoy optimizing how things are tracked, stored, and managed
  • Communicate clearly and confidently—whether you’re discussing detailed compliance procedures with the Quality team or providing updates to colleagues in non-technical roles
  • Embrace technology and organization – you’re familiar with digital tools such as Google
  • Workspace, Asana, and Notion to track tasks and document work, as well as confident in picking up new softwares or systems to monitor the facilities
  • Enjoy diving into complex problems and proactively troubleshooting issues – you’re not one to wait for instructions when you spot a potential improvement or an operational snag
  • Are physically comfortable in an active role – you’re able to safely lift and handle materials and supplies (up to 50 lbs), using appropriate support and equipment
  • Are flexible and willing to occasionally work outside regular hours to address critical GMP activities, emergencies, or maintenance needs

$70,000 – $90,000 a year
Total compensation also includes generous equity and benefits including:

– Medical, dental, and vision insurance for you and your family
– 401(k) plan with 4% matching
– Flexible time off and 10 company holidays per year
– Annual learning & development stipend
– Daily Retro-sponsored lunch and snacks

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Retro Biosciences

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