Production Operator
R&D Partners, Los Angeles, CA, United States
Production Operator – Tarzana, CA
R&D Partners is seeking to hire a Production Operator in Tarzana, CA.
Responsibilities
Using general application of principles, support activities to ensure GMP readiness for clinical manufacturing, including but not limited to equipment procurement, installation and qualification, facility qualification, and technology transfer.
Perform operational tasks within a cleanroom environment in a manner consistent with safety policies, quality systems, and cGMP requirements.
Assist in developing Standard Operating Procedures (SOPs) and other documents for manufacturing processes.
Set up manufacturing areas and equipment, including complex automated cell processing equipment.
Follow all cleaning and gowning procedures for the facility.
Qualifications
Minimum of five (5) years of experience with a High School Diploma or a BS/BA in a relevant science or engineering discipline.
Understanding of cGMP process and knowledge of CMC regulatory framework for biologics.
Knowledge of aseptic techniques for primary human cell cultures and GMP manufacturing and supporting tech transfer and GMP clinical/commercial manufacturing operations.
Knowledge of industry practices, cell therapy manufacturing experience preferred.
Develop solutions to complex problems independently.
Benefits
Medical insurance – PPO, HMO &
Dental & Vision insurance
401k plan
Employee Assistance Program
Long-term disability
Weekly payroll
Expense reimbursementOnline timecard approval
Pay Scale
$38,421 - $48,027 (Dependent on Experience)
R&D Partners is an equal-opportunity employer.
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R&D Partners is seeking to hire a Production Operator in Tarzana, CA.
Responsibilities
Using general application of principles, support activities to ensure GMP readiness for clinical manufacturing, including but not limited to equipment procurement, installation and qualification, facility qualification, and technology transfer.
Perform operational tasks within a cleanroom environment in a manner consistent with safety policies, quality systems, and cGMP requirements.
Assist in developing Standard Operating Procedures (SOPs) and other documents for manufacturing processes.
Set up manufacturing areas and equipment, including complex automated cell processing equipment.
Follow all cleaning and gowning procedures for the facility.
Qualifications
Minimum of five (5) years of experience with a High School Diploma or a BS/BA in a relevant science or engineering discipline.
Understanding of cGMP process and knowledge of CMC regulatory framework for biologics.
Knowledge of aseptic techniques for primary human cell cultures and GMP manufacturing and supporting tech transfer and GMP clinical/commercial manufacturing operations.
Knowledge of industry practices, cell therapy manufacturing experience preferred.
Develop solutions to complex problems independently.
Benefits
Medical insurance – PPO, HMO &
Dental & Vision insurance
401k plan
Employee Assistance Program
Long-term disability
Weekly payroll
Expense reimbursementOnline timecard approval
Pay Scale
$38,421 - $48,027 (Dependent on Experience)
R&D Partners is an equal-opportunity employer.
#J-18808-Ljbffr