We deliver the right information, to the right person, at the right moment.
Product Quality Specialist
Location
United States
Posted
39 days ago
Salary
Not specified
Job Description
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.
Job Requirements
- Position Responsibilities:
- Product and raw material Release & Documentation:
- 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
- Quality Systems & SOP Support:
- 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
- Data Entry & Quality Records:
- 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
- Complaint Handling & Investigations:
- 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
- Co-Manufacturer & Supplier Quality Support:
- 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
- Compliance & Audit Support:
- 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
- Basic Qualifications and Skills:
- Experience & Background:
- 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
- Experience working with contract manufacturers and with manufacturing/packaging processes, strongly preferred
- Technical Knowledge:
- 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)
- Skills & Attributes:
- 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
- Education:
- Bachelor’s degree preferred in:
- Life Sciences, Food Science, Chemistry, Biology, or related field
- Equivalent experience considered in lieu of degree
Benefits
- Salary Range: $65-95k
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