QA Document Control Specialist I - San Francisco Bay Area, United States - Pacific BioLabs

Pacific BioLabs

Verified Company

San Francisco Bay Area, United States

3 weeks ago

Posted by:

Mark Lane

beBee recruiter

Description

:

PBL has immediate openings for full or part time Document Control Specialist I in the Quality Assurance Department.

The general responsibility of the QA Document Control Specialist I assisting Quality Management in administering the company's systems for document control.

A large part of the Document Control Specialist's job consists of maintaining the company's Operations Procedures and the company's Form/Worksheet Control System.

Overall, the Document Control Specialist role presents the employee with an opportunity to contribute substantially to the company's ongoing success as a quality testing laboratory.

PRIMARY RESPONSIBILITIES INCLUDE BUT ARE NOT LIMITED TO:

Under the direction of the Quality Management, maintain the company's Site Standard Operations Procedures. This includes word processing and other applicable software SOPs, routing SOPs for routine review, maintaining a current index for each section of the Manual, assigning numbers to new SOPs, publishing and approving SOPs into the appropriate department folders, routing SOPs, and assisting in archiving SOPs.
Assist Quality Management in maintaining the company's Form/Worksheet Control System. This includes assigning numbers to new forms/worksheets, assigning revision codes to revised forms/worksheets, and copying and filing forms/worksheets into the appropriate department folders.
Assist Quality Management in assigning, tracking, and bringing to closure Revision Requests.
Assist in managing and controlling Client methods.
Assist if needed in managing Quality Agreements and other legal documents including Nondisclosure and Service Agreements.
Compliance with GMP/GLP and ISO requirements as these pertain to document control.
Knowledge of and familiarity with all SOPs pertaining to the company's document control functions.
Other duties as needed.

Requirements:

QUALIFICATIONS:

High School Diploma or equivalent
Excellent organizational skills
Strong communication skills
Knowledge of pharmaceutical and/or medical device regulatory requirements expected (GLP, GMP, GCP) beneficial

Pacific BioLabs is an equal opportunity employer committed to diversity and inclusion.

We are pleased to consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, protected veteran status, or any other legally protected factors.