Quality Assurance & Quality Control Associate

Join Liquidyne Process Technologies, Inc., a leading distributor and fabricator of innovative fluid transfer, measurement, and control solutions. Since 1993, we’ve been serving Life Sciences, Food & Beverage, and Industrial markets, with a special focus on Biopharmaceutical, Pharmaceutical, Nutraceutical, Animal Health, and Cosmetics industries.

We are a dynamic, growing company in beautiful Golden, Colorado, seeking a talented Quality Assurance & Quality Control Associate to ensure excellence in product quality and compliance.

What You’ll Do

As a QA/QC Associate, you’ll play a critical role in upholding Liquidyne’s commitment to quality. Your key responsibilities will include:

Documentation & Inspection:

• Review and approve batch records, logs, and documentation supporting production activities.
• Conduct quality control checks on products, labels, and packaging to meet internal standards.
• Prepare and finalize Certificates of Conformity (CoC) for sterile single-use products, including gamma irradiation documentation.

Regulatory & Compliance Support:

• Collaborate with Operations & Engineering on new product requests and ensure regulatory compliance.
• Create, review, and approve changes to processes and documents, guiding teams on regulatory requirements.
• Provide guidance on cGMP principles and applicable FDA (21 CFR 820) and ISO 13485 regulations.

Audits & Investigations:

• Support internal and external audits for customers, suppliers, and internal processes.
• Lead root cause investigations and corrective action plans for identified quality issues.

Documentation & Vendor Management:

• Develop and maintain quality documentation, such as validation protocols, site master plans, and procedures.
• Oversee the vendor approval process, ensuring supplier compliance with quality standards.

Customer Interaction:

• Respond to customer requests, including surveys and evidence of quality systems, and support onboarding activities.

What We’re Looking For

We’re searching for a detail-oriented, collaborative professional who brings:

Education & Experience:

• Bachelor’s degree in a science-related field (e.g., biology, chemistry).
• 3-5 years of quality assurance experience, including 1-2 years in regulatory roles within cGMP manufacturing environments.

Skills & Expertise:

• Experience with audits (internal or external), cleanroom environments, and sterile/single-use assemblies.
• Familiarity with sterilization validation (ISO 11137), environmental monitoring, and ISO 9001/13485 standards.
• Strong problem-solving skills for root cause analysis and quality improvement.
• Excellent attention to detail, confidentiality, and professionalism in client and team interactions.

What We Offer

At Liquidyne, we believe in investing in our team. We offer:

Compensation: $75K–$88K annually

Benefits:

• Health, Dental & Vision Insurance
• 401(k) Plan with company contribution

Perks:

• Monthly team lunches & healthy snacks
• Quarterly team-building events
• Professional learning opportunities
• Bi-annual team volunteering and annual holiday parties

Time Off:

• 10 PTO days & 5 sick days per calendar year
• 9 paid company holidays

Why Join Liquidyne?

We’re a collaborative team passionate about delivering innovative solutions to our clients while fostering a supportive and inclusive workplace. Located in the vibrant Golden area, our office offers a fantastic environment for personal and professional growth.

Apply Today!

Be part of a company that values innovation, quality, and team success. Submit your resume and let’s make a difference together!