Product Quality Specialist

Blueprint

1d•$65 - $95

About The Position

Death is our only foe. Blueprint was founded by Bryan Johnson, who has the world’s best comprehensive biomarkers. He is quantitatively the healthiest person on the planet. Blueprint is methodically built on science. Bryan freely shares his protocol, learnings and data with everyone to use. Blueprint has also developed a family of nutritional products to make the benefits of the Blueprint protocol affordable and available to all. We’re a small, tight-knit team working to clean up the global food supply, provide healthy food to everyone, and build Don’t Die into the most influential ideology in the world. We move quickly, work efficiently, and enjoy an environment defined by competence. We are looking for our Product Quality Coordinator, that will support day-to-day quality operations across our dietary supplement product portfolio. This role plays a critical part in ensuring products are released compliantly, quality documentation is accurate and up to date, and quality issues are investigated and resolved efficiently.This is a hands-on role suited for a detail-oriented quality professional with experience in the dietary supplement or nutraceutical industry who is looking to broaden their exposure across product release, documentation, supplier communication, and quality investigations. The role works closely with internal teams and third-party manufacturing partners in a fast-paced, growth-oriented environment.

Requirements

Minimum 3 years of quality experience in: Dietary supplements, nutraceuticals, food, or regulated consumer products
Hands-on experience with: Batch release documentation
Material and Finish Product specifications
CoAs, Test methods and Laboratory reports
Complaints and investigations
SOP creation and maintenance
Working knowledge of: FDA cGMPs (21 CFR Part 111, 117)
Quality documentation and recordkeeping best practices
Familiarity with quality systems such as: Document control
Deviations / CAPAs
Complaint handling
Comfortable working with ERP, LIMS, or quality management systems (or equivalent tools)
Highly detail-oriented with strong organizational and cross functional skills
Clear written and verbal communicator
Able to manage multiple tasks and deadlines in a fast-paced environment
Practical, solutions-oriented mindset
Comfortable interacting with external partners and internal stakeholders
Strong sense of ownership and accountability
Bachelor’s degree preferred in: Life Sciences, Food Science, Chemistry, Biology, or related field
Equivalent experience considered in lieu of degree

Nice To Haves

Experience working with contract manufacturers and with manufacturing/packaging processes, strongly preferred

Responsibilities

Support product and raw materials release activities by compiling and reviewing required documentation
Verify completeness and accuracy of batch records, test results, and release checklists
Coordinate issuance and distribution of Certificates of Analysis (CoAs) to internal teams and customers
Maintain organized electronic quality records and databases
Draft, update, and maintain Standard Operating Procedures (SOPs), work instructions, and forms
Support document control processes including versioning, approvals, and archiving
Assist with quality system improvements and procedural consistency
Enter and maintain quality data within internal systems (LIMS, ERP, shared drives, or quality platforms)
Track deviations, complaints, investigations, and CAPAs
Generate basic quality reports and summaries as needed
Log, investigate, and document product complaints in accordance with SOPs
Support root cause analysis and corrective / preventive actions (CAPAs)
Assist in resolving product quality issues and coordinating follow-up actions
Support quality communications with contract manufacturers and key suppliers
Request, review, and archive quality documentation (CoAs, specifications, change notifications)
Participate in quality discussions related to deviations, non-conformances, and product issues
Support internal audits, third-party audits, and regulatory inspections as needed
Assist in preparing documentation for audits and responding to follow-up requests
Ensure quality activities align with cGMP requirements and company procedures