Company

Operations

GMPOperationsCoordinator

$95–115k Redwood City, California, United States FULL TIME
Market Sentiment
HIGH DEMAND

Neural analysis suggests this role is
optimal for Mid candidates.

The Brief

“GMP Operations Coordinator. Skills: GMP operations, Inventory management, Cross-functional coordination, Troubleshooting. Support day-to-day GMP operations. Maintain GMP storage rooms”

Industry & Context.

Operations
Problems you'll solve

Dynamic troubleshooting; Proactively address issues; Troubleshooting logistics; Troubleshooting issues; Scrappy problem-solving

Eligibility Requirements

On-call responder for facility emergencies, Rotating team responsibility includes nights, weekends, and holidays, Physically comfortable in an active role, Able to safely lift and handle materials and supplies (up to 50 lbs), Willing to occasionally work outside regular hours

What They're Looking For.

Must Have

2+ years of experience working in GMP operations, quality assurance, or another highly regulated biotech environment, Hands-on and technically adept in cleanroom environments, Practical knowledge of electronic quality management or manufacturing execution systems, Organized and precise, Communicate clearly and confidently, Embrace technology and organization, Familiar with digital tools such as Google Workspace, Asana, and Notion, Confident in picking up new systems like MasterControl, Enjoy diving into complex problems and proactively troubleshooting issues, Physically comfortable in an active role, Able to safely lift and handle materials and supplies (up to 50 lbs)

Nice to Have

Directly supported cell therapy manufacturing, Know your way around environmental monitoring equipment, Understand contamination control practices, Feel at ease maintaining meticulous documentation, Enjoy optimizing how things are tracked, stored, and managed, Take pride in maintaining clear, detailed documentation, Intuitive feel for regulatory requirements and standards, Providing updates to colleagues in non-technical roles, Track tasks and document work, Not one to wait for instructions when you spot a potential improvement or an operational snag, Using appropriate support and equipment, Flexible and willing to occasionally work outside regular hours to address critical GMP activities, emergencies, or maintenance needs, Experience with Cell therapy or biologics manufacturing, Inventory and material handling systems (Quartzy, ERP systems, etc.), Equipment qualification (IQ/OQ/PQ) support, Startup or early-stage biotech environments, Comfortable with rapid change and scrappy problem-solving, Environmental monitoring program execution

What You'll Do.

Support day-to-day GMP operations

Maintain GMP storage rooms

Monitor inventory levels and reorder points

Manage warehouse organization and material segregation

Prepare for manufacturing runs

Serve as second SciOps team member

Support electronic batch record execution

Execute routine environmental monitoring sampling

Assist with equipment performance qualification documentation

Assist with deviation and CAPA investigation logistics

Assist with training record coordination

Support vendor coordination

Provide hands-on support to SciOps team

Serve as key on-call responder

How You'll Work.

Team & Collaboration

Collaborating cross-functionally; Providing updates to colleagues

Communication Scope

Communicate clearly and confidently

Process & Methodology

Improvement projects

Full Job Description

## 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’re hands-on, proactive, and take pride in keeping things stocked, staged, and ready so manufacturing can run smoothly. 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 Support day-to-day GMP operations including material ordering, receiving, inspection, logging, and distribution of consumables, PPE, and cleaning supplies across the manufacturing facility Maintain GMP storage rooms, monitor inventory levels and reorder points, and manage warehouse organization and material segregation to ensure cleanroom supplies are always available Prepare for manufacturing runs - scheduling support, pre-run checklists, reagent and consumable staging, and cleanroom setup Serve as the second SciOps team member on the manufacturing floor during production runs, supporting operators, troubleshooting logistics in real time, and assisting with environmental monitoring Support electronic batch record execution and real-time data entry in MasterControl Mx during manufacturing campaigns Execute routine environmental monitoring sampling during and between runs, and document results per established procedures Assist with equipment performance qualification documentation, deviation and CAPA investigation logistics, and training record coordination Support vendor coordination - assisting the GMP Operations Lead with purchase orders, vendor scheduling, and receipt documentation Provide hands-on support to the broader SciOps 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

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