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Document Coordinator for Biologics Process Validation

companyR&D Partners
locationLos Angeles, CA, USA
PublishedPublished: 6/14/2022
Full Time

R&D Partners

Document Coordinator for Biologics Process Validation

Location: Foster City, CA

Job Type: Scientific

Job Number: JN -082024-32754

Job Description:

R&D Partners is seeking to hire a Document Coordinator for Biologics Process Validation .

Your main responsibilities:

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:

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.

R&D Partners is an equal-opportunity employer.

Apply Now:
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