Research Associate 2, Critical Reagent Inventory Management (CRIM)

BioMarin Pharmaceutical•Novato, CA

14h•Onsite

About The Position

The AS S&O team is seeking a highly organized and proactive Research Associate 2 to own CRIM activities across AS. You will ensure critical reagents and reference standards (CR/RS) are available to support analytical testing throughout the product lifecycle — managing inventory, logistics, and storage on-site while supporting contract administration, documentation compliance, and operational planning. This position will also support general contract management for the AS department, including CRIM contract management, to ensure the supply and quality of materials. You will partner closely with AS laboratories, Supply Chain, Procurement, and external vendors to ensure material supply, replenishment, inventory management, and logistics keep CR/RS well supplied to AS testing labs in support of development programs. You will engage the Quality organization when CR/RS ownership transfers to Quality.

Requirements

Minimum of 3-5 years of industry experience (biotechnology, pharmaceutical, or laboratory environment), including experience in similar laboratory operations, inventory management, or CRIM-related role.
Experience in laboratory operations, inventory management, quality systems, or analytical sciences.
Good understanding of critical reagents and reference standards with the ability to serve as the single point of contact (SPOC) for CRIM.
Strong organizational and documentation skills with the ability to manage multiple priorities.
Ability to work on-site (5 days per week) to perform hands-on material handling and storage activities.
Ability to work independently, proactively identifying opportunities and taking action.
Proven flexibility and execution skills to deliver in a fast-paced, multi-tasking environment, with the ability to work with ambiguity and complexity.
Excellent communication skills, both written and verbal, with the ability to effectively communicate requirements and strategies to diverse audiences.
Bachelor’s degree in biology, chemistry, biochemistry, biotechnology, or a related scientific discipline, or equivalent experience.

Nice To Haves

5+ years of industry experience, including 2-3 years in a similar CRIM, laboratory operations, or inventory management role.
Experience with GMP, GLP, or other regulated environments.
Experience with Veeva, QMS records, or change control processes.
Experience supporting contract administration or vendor management.
Experience with inventory management systems and reagent/reference standard lifecycle management.
Experience in pharmaceutical or biotechnology development environments.
Bachelor’s degree in biology, chemistry, biochemistry, or biotechnology; additional training or certification in inventory/supply chain management and/or experience in GMP/GLP environments is a plus.

Responsibilities

Support replenishment planning to ensure availability of critical reagents through effective planning and forecasting.
Conduct risk assessments for critical reagents to ensure operational continuity.
Monitor urgent needs across AS and respond quickly to prevent testing interruptions.
Conduct freezer mapping, cataloging, and storage organization for optimized on-site storage.
Perform on-site receipt, handling, and movement of CR/RS and laboratory samples.
Register samples and inventory in the data management system (e.g., Benchling).
Coordinate and fulfill shipment requests for CR/RS, laboratory samples, and other laboratory materials, as requested.
Coordinate with laboratory teams, Supply Chain, and Procurement to keep materials flowing to testing groups.
Support the transfer of CR/RS to the Quality organization as programs progress.
Perform contract management for AS, including service contract discussions, contract initiation, drafting scopes of work (SOWs), and vendor administration.
Track contract status end-to-end and support business operations processes in partnership with the Project Management & Operations (PM&Op) function.
Maintain documentation and records associated with external vendors and service providers.
Draft CR/RS reports and supporting documentation, including change records, change actions, and follow-up activities.
Own Veeva and QMS documentation processes for CRIM, ensuring records are accurate, current, and compliant.
Ensure activities comply with applicable Good Manufacturing Practice (GMP), Good Laboratory Practice (GLP), and company procedures.
This is an individual contributor role with no direct reports. You will coordinate cross-functional activities and may guide or train colleagues on CRIM processes and documentation.
Responsibilities may evolve based on business needs; flexibility and adaptability to take on additional or shifting priorities are expected.