Quality Control Analyst

Stellaromics Inc. • Boston, MA

4h • $60 - $90

About The Position

We are seeking an experienced Quality Control Analyst. This is a critical hands-on role for a scientist who thrives in a manufacturing but fast-paced startup environment. You will be the guardian of product quality, performing analytical testing on raw materials, intermediates, and finished reagents. Working closely with Manufacturing and R&D, you will execute rigorous inspections, maintain GMP compliance, and help scale our quality systems for high-impact product launches.

Requirements

• Bachelor’s degree in Chemistry, Biochemistry, Molecular Biology, or a related field.
• 2+ years of experience in quality control or analytical testing within the life sciences or diagnostics industry.
• Demonstrated familiarity with GMP, ISO 13485, and regulated manufacturing environments.
• Strong documentation, organizational, and communication skills.
• Demonstrated experience with optical microscopy (or confocal microscopy)
• Hand on experience with tissue-based assay, RNase- free workflows
• Ability to follow detailed procedures and maintain accurate records.
• Strong attention to detail and commitment to quality.

Nice To Haves

• Buffer preparation, enzyme handling, or antibody-based reagents.
• Familiarity with LIMS, ERP, or digital manufacturing tools and electronic notebooks
• Prior work in a startup or fast-paced, innovation-driven company.

Responsibilities

• Perform routine testing of raw materials, intermediates, and finished reagents using biochemical and analytical methods.
• Maintain control samples and reference standards.
• Monitor lab conditions including temperature, humidity, and particulate levels.
• Calibrate and maintain QC instruments and equipment.
• Work with Manufacturing and R&D to support product development and troubleshooting.
• Conduct regular production areas walkthroughs-line/area clearance
• Conduct visual inspections, functional assays, and documentation reviews.
• Record and analyze test results in accordance with GMP and ISO 13485 standards.
• Author and review QC protocols, test methods, and batch release documentation.
• Support investigations and CAPAs related to quality deviations.

Benefits

• Innovative Technology: Be part of a company at the cutting edge of spatial biology and genomics, revolutionizing the way researchers understand biology.
• Impactful Role: You will have a significant impact on the department and the future of the company.
• Collaborative Environment: Work with a talented, passionate team in a culture that values creativity, innovation, and teamwork.
• Career Growth: As a high-growth company, we offer significant opportunities for professional development and career advancement.
• An attractive compensation and benefits package based on market pay data will be commensurate with candidate skills, qualifications, and experience.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level