QC Analyst – Standard BioTools
Would you like to be part of a bold, innovative team driving breakthroughs in human health? Standard BioTools is inviting passionate individuals to join as a QC Analyst I in Boulder, Colorado. This QC Role is a full-time, on-site position. Join the Quality Control Jobs that offer a dynamic opportunity to enhance your biology careers by working with cutting-edge technologies that empower discoveries in academic, clinical, pharmaceutical, and biotech research.
Job Details:
- Position Title: QC Analyst I
- Location: Boulder, Colorado, USA
- Work Type: Full-Time, On-Site
- Requisition ID: 2025-0126
- Salary Range: $54,200 โ $63,000 per year
About the Company:
Standard BioTools is a global leader in life sciences technology, empowering scientists and healthcare innovators to gain deeper insights into human health. The company focuses on developing advanced tools that accelerate research and innovation in proteomics, genomics, and precision medicine. At Standard BioTools, the team thrives on collaboration, accountability, and a shared vision to create transformative technologies that improve lives by providing various jobs that unleash your Biology Careers.
Core Values:
- Keep customers front and center in all work
- Be accountable and deliver on commitments
- Drive continuous improvement
- Foster collaboration and a culture of learning
Educational Requirements:
-
Bachelorโs Degree in Biology, or a related scientific field is required.
Key Responsibilities of the Quality Control Jobs:
- Perform analytical testing of raw materials, finished products, stability samples, and R&D materials.
- Ensure compliance with cGMPs, CLIA regulations, SOPs, and safety standards.
- Generate and maintain laboratory records following company policies.
- Conduct stability and functional testing of materials for identity, purity, and conformance.
- Perform ELISA, PCR, HPLC, MS, UV-Vis, and other analytical tests.
- Investigate out-of-specification (OOS) or out-of-trend (OOT) results.
- Participate in cross-departmental projects and process improvement initiatives.
- Support new method development and documentation improvements.
- Cross-train across departments to meet production timelines when required.
Skills Required for the Quality Control Jobs:
- 0โ5 years of Quality Control experience, preferably in pharmaceutical or medical device industries.
- Strong understanding of cGMP or ISO regulations.
- Experience with ELISA, PCR, HPLC, MS, UV-Vis, and microbiological testing.
- Excellent technical writing, documentation, and reporting skills.
- Strong problem-solving and time management abilities.
- Proficiency in Microsoft Office, especially Excel.
- Ability to communicate effectively and collaborate across teams.
How to Apply for the QC Role?
Interested candidates can apply directly through the Standard BioTools Careers Page. Stay updated on job alerts and future openings by subscribing to their career notification service on their official website.
