Document Coordinator for Biologics Process Validation
Job Description
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.