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W3Global

Quality Control Associate

W3Global, Boulder, Colorado, United States, 80301

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W3Global Get AI-powered advice on this job and more exclusive features. Company Description

This is a new company built on Ginkgo Bioworks' biotechnology platform with the goal of improving overall human health through probiotics ("biotic") technology that provide consumers with an Company Description

This is a new company built on Ginkgo Bioworks' biotechnology platform with the goal of improving overall human health through probiotics ("biotic") technology that provide consumers with an

"I feel the effect"

experience. We target specific health and wellness conditions and develop "biotic" solutions that have a clear "mechanism-of-action." We are building a passionate team of health and wellness experts and are seeking a Quality Control Associate.

Job Description

As a Quality Control Associate, you will play a vital role in ensuring the safety, quality, and efficacy of our biotic products. You will be responsible for conducting analytical testing, monitoring compliance with industry regulations, and maintaining accurate documentation to support our commitment to high-quality standards. This role requires a detail-oriented individual with a passion for quality assurance and a background in microbiology, biotechnology, or related fields.

Key Responsibilities

Perform microbiological and chemical testing of raw materials, in-process samples, and finished biotic products. Conduct quality control checks to ensure products meet specifications and regulatory standards. Prepare and coordinate the shipment of product samples to customers and third-party laboratories. Maintain and calibrate laboratory equipment to ensure accurate test results. Document and analyze test results, identifying trends and deviations from quality standards. Assist in investigating quality issues, non-conformances, and implementing corrective actions. Collaborate with cross-functional teams, including R&D and supply chain, to ensure quality consistency. Maintain compliance with Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and other regulatory guidelines. Prepare and review Standard Operating Procedures (SOPs) and quality documentation. Support audits and inspections by regulatory agencies and customers. Stay updated on industry best practices and emerging trends in microbiome and biotic quality control.

Qualifications

Bachelor's degree in Microbiology, Biotechnology, Biochemistry, Food Science, or a related field. 1-3 years of experience in a quality control or laboratory environment, preferably in biotics, probiotics, or fermentation-based industries. Familiarity with microbiological and analytical techniques, such as Bacterial Plate Count methods, enumeration and PCR, . Experience with flow cytometry a plus. Understanding of regulatory requirements such as FDA, cGMP, ISO, or HACCP. Knowledge of GFSI Certification programs and implementation (SQF, BRC, etc.) Proficiency in data analysis and interpretation Strong analytical skills with attention to detail, accuracy, and consistency. Ability to work independently and collaboratively in a fast-paced environment. Excellent organizational and documentation skills. Strong problem-solving abilities and a proactive mindset.

Our Core Values

We make products that work and improve lives We collaborate to make smart, resourceful decisions and get stuff done We are fun a bit geeky and always respectful

It is the policy to provide equal employment opportunities to all employees and employment applicants.

Seniority level

Seniority level Entry level Employment type

Employment type Full-time Job function

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