Quality Control Technician

About Us

Purity One, a subsidiary of Fluid Flow Products, is the premier cleanroom‑certified, single‑use source for the biopharmaceutical market and life science industry. Established in 2019, Purity One provides top‑notch assemblies, quality individual tubing, hoses and fittings, and unmatched levels of customer service. Our state‑of‑the‑art hose assembly and testing facility enables us to deliver a comprehensive set of biopharmaceutical production solutions that meet strict standards for purity, certification and compliance.

As a problem‑solving partner, our experts connect life sciences, biopharmaceutical and pharmaceutical solutions providers with the products that meet their specific process and exacting quality assurance requirements. With shorter lead times and best‑in‑class traceability, we deliver a level of service and quality assurance that is unparalleled in the biopharmaceutical market.

Purity One

• Inspect and test incoming materials, in‑process components, and final assemblies for conformance to specifications (e.g., dimensions, appearance, performance).
• Review lot travelers for completeness and accuracy prior to product release.
• Create and issue Certificates of Conformance (C of
  
  C) for customer shipments.
• Maintain accurate records and inventory of inspected materials and components.
• Document and communicate inspection results, support trending and reporting activities within the QC database.
• Assist with nonconforming material investigations and related documentation.
• Support internal, customer, and regulatory (ISO) audits through record review and data collection.
• Coordinate sample management, including submission to external laboratories and follow‑up on test results.
• Collaborate with Production, Engineering, and Supply Chain to resolve quality issues in real time.
• Demonstrate strong organizational, communication, and time‑management skills to manage multiple priorities effectively.
• Maintain compliance with Good Documentation Practices (GDP) and cleanroom standards.

• High school diploma required;
  Associate degree in Engineering, Chemistry, Life Sciences, or a related field preferred.
• 1–3 years of experience in a regulated manufacturing or laboratory environment preferred.
• Experience with single‑use systems or biopharmaceutical manufacturing components is desirable.

• Excellent attention to detail and accuracy in inspection and documentation.
• Strong analytical and problem‑solving abilities.
• Working knowledge of manufacturing and assembly processes for single‑use bioprocess components is preferred.
• Cleanroom experience (ISO 7 or similar) is highly desirable.
• Proficiency in Microsoft Office (Excel, Word, Outlook, Teams).
• Ability to follow procedures precisely, identify deviations, and recommend or support corrective actions.
• Demonstrated commitment to quality, safety, and continuous improvement.

Everyone’s an owner of the company: because every team member contributes to Flow Control Group’s success, everyone has the benefits of ownership! Flow Control Group has a broad‑based employee ownership program extended to every employee within our portfolio companies.

Competitive benefits: enjoy an attractive benefits package that includes Medical, Dental and Vision insurance, competitive 401(k) matching program, career growth opportunities, employee referral program, paid time off and holidays, as well as parental leave.

Training: FCG University learning and training platform available to all employees offering over 80,000 courses.

Career growth opportunities:
At Flow Control Group, we are committed to your professional development. With a vast network of over 100 brands across North America, we provide unparalleled opportunities for growth and advancement. Whether you’re just starting your career or looking to take it to the next level, we offer custom training programs, mentorship, and a supportive environment to help you achieve your goals.

Flow Control Group is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or any other legally protected characteristics.