Document Coordinator for Biologics Process Validation

R&D Partners
California, CA
Full-time

R&D Partners is seeking to hire a Document Coordinator for Biologics Process Validation in Foster City, CA.

Your main responsibilities as a Document Coordinator for Biologics Process Validation :

Create, revise, and implement procedures, best practices, and business processes for the Biologics Process Validation program

Act as a Project Manager to track and monitor Process Validation progress and deliverables

Coordinate Process Validation documentation : Prepare, edit, proofread, coordinate and adjudicate reviewer comments with author and subject matter experts

Perform Data Verification of completed Process Validation studies and reports

Create study templates to drive alignment

What we are looking for in a Document Coordinator for Biologics Process Validation :

Bachelor's degree in life sciences or related field

Minimum of four years experience in biotechnology, process validation, Quality, or a related area

Must have understanding and application of GMP principles, concepts, and practices

Knowledge of biochemical manufacturing process and terminology

Knowledge and experience in process validation in highly regulated manufacturing environments

Why Choose R&D Partners ?

As an employee, you have access to a comprehensive benefits package including :

Medical insurance PPO, HMO & HSA

Dental & Vision insurance

401k plan

Employee Assistance Program

Long-term disability

Weekly payroll

Expense reimbursement

Online timecard approval

Pay Scale :

$82,534 $103,168 (Dependent on Experience)

R&D Partners is a global functional service provider and strategic staffing resource specializing in scientific, clinical research & engineering.

We provide job opportunities within major pharmaceutical, biopharmaceutical, biotechnology, and medical device companies.

R&D Partners is an equal-opportunity employer.

17 days ago
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