Document Control Specialist for Product Development (Dietary Supplements)

Work Location: 784 W Channel Street San Pedro, Ca 90731

Hybrid Remote: Thursday Work From Home

Pay Grade: $26.00 - $29.00 Per Hour Depending on Experience

We have an opportunity for an experienced cGMP dietary supplement product development Document Control Specialist to join our amazing team here in our beautiful San Pedro, CA office (work from home Thursdays). This role is responsible for ensuring the document control system is managed in compliance with standard operating procedures (SOPs), quality systems and complies with our internal procedures, cGMPs, and 21 CFR FDA regulatory requirements. This role ensures traceability from product development through finished product production.

Sports Research is one of the largest privately held cGMP dietary supplement nutraceutical brands in the United States. Established in 1980 and made popular by our flagship product Sweet Sweat, Sports Research remains a family owned & operated company dedicated to providing the highest quality health & wellness products. We believe in our products because we use only the best raw materials, sourced from the finest suppliers. As a leader in this industry, we are searching for the right people to bring into the brand and be a part of The Sport Of Life!

https://www.sportsresearch.com/about-

Responsibilities Include, But Are Not Limited To:

• Serves as document control administrator from product development through finished product production of dietary supplements and health & wellness products.

• Supports review, update, filing and distribution of controlled documents, including but not limited to Request for Quotes, Formula Specifications, Packaging Specifications, and Component Technical Documents.

• Works independently to manage and administer effective document control systems. Ensures controlled documents conform with applicable procedures and are maintained to latest revisions, and reviews formats for consistency.

• Works with the manager to establish and execute document control procedures.

• Supports the creation and updates of SOPs related to document control/document management.

• Updates current or future project management systems accordingly.

• Performs proofreading, editing, word processing, and filing support.

• Creates and maintains filing systems (electronic and paper) for all controlled documents.

• Provides cross-functional support as needed.

• Other duties as needed/assigned.

Skills and Qualifications:

• Knowledge of cGMP regulations and industry standard guidelines for electronic records.

• Experience with 21 CFR Part 111 is preferred.

• 3 years’ experience in managing a cGMP document system.

• Experience in document control, change control, and quality systems.

• Strong technical computer skills using various computer programs and web-based applications, including Microsoft and Google Suite.

• Ability to work under pressure with tight deadlines.

• Ability to maintain confidentiality and work with sensitive documents.

• Interacts well with colleagues, leadership, and vendors.

• Strong organizational skills.

• Adapts to changing priorities effectively.

• Ability to work independently on assignments.

• Strong problem-solving skills.

• Team player committed to quality.

• Organized and detail oriented.

• Excellent written and oral communication skills

• Ability to manage multiple projects at one time.

* Sports Research is an equal opportunity employer committed to providing a diverse environment.

**For our Career Privacy Statement please visit https://www.sportsresearch.com/cpra