HireNow Staffing IncSanta Cruz (CA), 30 mi from San Jose
of Clinical Operations (MCO) or Physical Therapist (s)
Location (s): Santa Cruz, CA.
Salary Range: $ 90,000 $100,000
Direct Placement Requirement: Must guarantee work for 90 days
Job Summary:
Responsible for managing the clinical operations of multiple...
Riverside ResearchMountain View
RRI is seeking tech-savvy energy project managers to join our team of advisors supporting the Defense Innovation Unit (DIU). Participate in outreach, collaboration, and mentorship with commercial vendors, industry, academia, other non-traditional vendors, DoD entities, program offices, and recognize...
InsideHigherEdSan Jose
EXECUTIVE DIRECTOR, DISTRICT FOUNDATION. The Executive Director of District Foundation reports to the Chancellor at the District Office. Under the general direction of the Chancellor, the Executive Director plans, directs, and administers the business functions of a 501©3 Foundation, including fundr...
SoliantFremont
Inpatient Pharmacist OpeninginFremont, California - Contact: Megan. ...
SoliantSan Jose
Join CA Regional Hospital, located in the vibrant Santa Cruz, CA area, as an Interim Inpatient ClinicalPharmacist II for a 13-week assignment. CA Pharmacist license, active and in good standing. ...
Topography Health, Inc.San Jose
to change how research is conducted at the community level. We’re backed by Andreessen Horowitz, Bain Capital Ventures, and other great financial and strategic partners.
ABOUT THE ROLE
The Executive Director of Clinical Operations is critical...
BridgeBio PharmaSan Francisco, 40 mi from San Jose
applicable. Responsible for CRO oversight, training, vendor management, and review of agreements related to CRO clinical activities. Partner with internal and external stakeholders to ensure continuous harmonized operations of clinical operations activities...
EPM Scientific - Phaidon InternationalSan Francisco, 40 mi from San Jose
Salary: $185K-210K
Company Summary: A global immunology focused pharmaceutical group with an impressive track record is seeking an Associate Director of Clinical Operations for a hybrid role located in Palo Alto, CA. Their commercial supply...
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Reagent Manufacturing Associate
Guardant Health | Redwood City | www.resume-library.com |
Job Description
About the Role:
The Reagent Manufacturing Associate (RMA) I is responsible for manufacturing reagents, assembling kits, and qualification of assigned reagents following Good Manufacturing Practices and documenting events following current Good Documentation Practices.
Essential Duties and Responsibilities
Manufacture reagents, assemble kits, and qualify assigned reagents according to SOP;
Document reagent manufacturing activities following cGMP;
Perform equipment maintenance according to the laboratory’s standard operating procedures;
Maintain sufficient inventory of material, supplies and equipment in the laboratory for performance of duties;
Clean racks and other laboratory supplies;
Document all corrective actions taken when test systems deviate from the laboratory’s established performance specifications;
Perform clerical work and maintain Reagent Manufacturing and Quality Control documents as necessary;
Assist with managing and ensuring sufficient inventory of reagents in the laboratories of Clinical Operations;
Assist with troubleshooting of manufactured reagents;
Assist in the revision and development of reagent manufacturing SOPs and forms;
Participate in interdepartmental activities with Clinical Operations, Quality Assurance, Quality Control and Supply Chain Management to ensure qualified reagents are available for use at all times;
Assist in the inspection preparation activities as needed;
Perform other duties as assigned; and
Report all concerns of test quality and/or safety to the Laboratory Supervisor, Laboratory Director or Safety Officer.
About the Role:
The Reagent Manufacturing Associate (RMA) I is responsible for manufacturing reagents, assembling kits, and qualification of assigned reagents following Good Manufacturing Practices and documenting events following current Good Documentation Practices.
Essential Duties and Responsibilities
Manufacture reagents, assemble kits, and qualify assigned reagents according to SOP;
Document reagent manufacturing activities following cGMP;
Perform equipment maintenance according to the laboratory’s standard operating procedures;
Maintain sufficient inventory of material, supplies and equipment in the laboratory for performance of duties;
Clean racks and other laboratory supplies;
Document all corrective actions taken when test systems deviate from the laboratory’s established performance specifications;
Perform clerical work and maintain Reagent Manufacturing and Quality Control documents as necessary;
Assist with managing and ensuring sufficient inventory of reagents in the laboratories of Clinical Operations;
Assist with troubleshooting of manufactured reagents;
Assist in the revision and development of reagent manufacturing SOPs and forms;
Participate in interdepartmental activities with Clinical Operations, Quality Assurance, Quality Control and Supply Chain Management to ensure qualified reagents are available for use at all times;
Assist in the inspection preparation activities as needed;
Perform other duties as assigned; and
Report all concerns of test quality and/or safety to the Laboratory Supervisor, Laboratory Director or Safety Officer.
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