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# Technical Services Specialist

- **Company:** Berkeley Nutritional Manufacturing Corp.
- **Location:** Livermore, CA, United States
- **Experience:** Experienced
- **Salary:** $62,400.0 - $79,040.0
- **Contract:** Permanent contract
- **Skills:** Microsoft Word, Microsoft Excel, Microsoft Outlook, Microsoft Office
- **Published:** June 21, 2026
- **Apply:** https://www.indeed.com/viewjob?jk=a163c8a783e11b82

## About the Role

Do you have experience in Technical writing within manufacturing?, Do you have a Bachelor's degree?, * Bachelor's degree or equivalent professional experience

 * Proficiency in Microsoft Office (Word, Excel, Outlook), Project Mgmt and ERP software; ability to quickly master new platforms
 * Acute attention to detail with high accuracy in technical editing
 * Strong organizational and analytical problem-solving skills
 * Ability to manage shifting priorities in a fast-paced environment
 * Excellent written and verbal communication skills

Preferred:

 * 5+ years of experience in the nutritional/dietary supplement industry
 * Prior experience in nutritional and dietary supplement labels
 * Prior administrative, regulatory and/or quality control experience
 * Knowledge of manufacturing processes, GMPs, dietary supplement regulations, and product lifecycle, * Technical documentation: 2 years (Required)
 * Compliance management: 2 years (Preferred)

Language:

 * English (Required)

## Description

Are you passionate about quality, precision, and making an impact in the nutritional and dietary supplement industry? Protein Research is looking for a detail-oriented Technical Services Specialist to join our Quality Assurance team. In this dynamic, cross-functional role, you'll serve as the vital bridge between Quality, R&D, and Production - ensuring that every product we deliver meets the highest standards of compliance, accuracy, and operational excellence.

You'll take ownership of critical workflows - from Master Manufacturing Records and label compliance to third-party certifications and regulatory support - all while collaborating with talented teams across the organization. If you thrive in a fast-paced environment and love turning complexity into clarity, this is the role for you.

What You'll Do

 * Master Manufacturing Records: Compile, review, and route all Master Manufacturing Record (MMR) elements for approval.
 * Initiate and manage project tracking systems for MMR updates - including formulation changes, label updates, and specification revisions - driving them through to completion.
 * Documentation Management: Update and track approvals for Finished Product Specifications and MMRs for food and dietary supplement products, maintaining strict adherence to Good Documentation Practices.
 * Label Compliance: Review and approve product labels in collaboration with customers and R&D teams.
 * Facilitate necessary edits, track changes, and organize master copies to ensure full regulatory compliance.
 * Certification & Audit Support: Support the submission and maintenance of third-party certifications including Organic, NSF, GFCO (Gluten-Free), Non-GMO Project, Kosher, and Halal - and assist in their respective audits.
 * Regulatory Support: Provide technical and administrative support for regulatory inquiries and internal projects to meet customer and stakeholder needs.
 * Supplier Qualification: Assist in collecting supplier documentation and manage the qualification program.
 * Records Retention: Oversee the scanning, filing, and organization of documents to ensure audit readiness at all times., * Be part of a mission-driven team dedicated to quality and innovation in the nutritional supplement industry
 * Collaborate cross-functionally with R&D, Production, Supply Chain, and Customer Service teams
 * Grow your career in a role that blends technical expertise with project management and regulatory knowledge
 * Work in a supportive, fast-paced environment where your attention to detail truly makes a difference


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