Senior QC Analyst

BioSpear Consulting Group; Colorado; On-site; USD 70,000 - 85,000; Full time

Job summary

A leading company in pharmaceutical manufacturing seeks a Senior QC Analyst for a full-time, onsite role in Colorado. This position is pivotal in ensuring quality assurance through advanced analytical methods and mentoring junior staff, contributing to a collaborative environment focused on continuous improvement. The ideal candidate will have over six years of experience in quality control and possess a strong educational background in Chemistry or Biochemistry.

Qualifications

• 6+ years of hands-on QC experience in pharma, biotech, or a regulated lab.
• Experience mentoring junior analysts.
• Deep knowledge of compendial methods and analytical chemistry.

Responsibilities

• Perform advanced testing on raw materials and finished goods.
• Mentor junior analysts and provide technical leadership.
• Maintain compliance with GMP, GLP, and internal quality standards.

Skills

Analytical Chemistry

Technical Leadership

GMP Compliance

Troubleshooting

Data Integrity

Education

Bachelor's in Chemistry

Bachelor's in Biochemistry

Tools

HPLC

FTIR

GPC

GC

UV-Vis

Job description

BioSpear is partnering with a growing pharmaceutical manufacturer to find a Senior QC Analyst for a full-time, onsite role in Colorado. If you're an experienced quality professional with a passion for advanced analytical methods and mentorship, this is your chance to make a meaningful impact.

This is a direct-hire opportunity with a client committed to quality, innovation, and continuous improvement. You'll be part of a collaborative team supporting end-to-end manufacturing and QC operations, with the tools, tech, and autonomy to do your best work.

What you'll do:

• Perform advanced testing using HPLC, FTIR, GPC, GC, UV-Vis on raw materials, finished goods, and stability samples
• Mentor junior analysts and provide technical leadership across lab operations
• Troubleshoot instrumentation, support method transfers, and drive continuous improvement
• Maintain rigorous compliance with GMP, GLP, ICH, and internal quality standards

What you bring:

• 6+ years of hands-on QC experience in pharma, biotech, or a regulated lab
• Bachelor's in Chemistry, Biochemistry, or related field
• Deep knowledge of compendial methods and analytical chemistry
• Experience mentoring team members and reviewing technical documentation
• Strong understanding of lab instrumentation and data integrity standards

If you're looking for a high-impact role with room to lead and grow, we'd love to connect.

Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Full-time

Job function

• Job function

  Quality Assurance

• Industries

  Pharmaceutical Manufacturing

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