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Biotech Quality Control Jobs (NOW HIRING)

Stark Pharma Solutions Inc

QC Scientist

Irvine, CA · On-site

... Medical Device, Biotech, and IT industries across the USA, Canada, and India. We provide ... Position: QC Scientist Location: California Duration: Long Term Job Overview We are seeking a Mid ...

Alliance Biotech Solutions LLC

QC Microbiologist

Raleigh, NC · On-site

$22 - $28.75/hr

Alliance Biotech Solutions is seeking a dedicated QC Microbiologist to support Environmental Monitoring (EM) and microbiological testing activities within a GMP manufacturing environment. This role ...

KORE1 Technologies

Quality Control Inspector

Irvine, CA · On-site

$26 - $28/hr

The QC Inspector examines items for defects in materials, work, and damage. The Inspector is ... pharma/biotech quality management system (i.e., ISO 13485, ISO 14971, FDA 21 CFR Part 820) is ...

Cellectis

Director, Quality Control

Raleigh, NC · On-site

Minimum 12 years of experience in pharmaceutical or biotechnology QC, with. 8 years in leadership roles. * Strong leadership skills with experience building and leading high-performing technical ...

Cellectis Group

Director, Quality Control

Raleigh, NC · On-site

$125 - $150/hr

Minimum 12 years of experience in pharmaceutical or biotechnology QC, with. 8 years in leadership roles. * Strong leadership skills with experience building and leading high-performing technical ...

Cellectis

Director, Quality Control

Raleigh, NC · On-site

Minimum 12 years of experience in pharmaceutical or biotechnology QC, with. 8 years in leadership roles. * Strong leadership skills with experience building and leading high-performing technical ...

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Biotech Quality Control information

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$30.5K

$81.3K

$129.5K

How much do biotech quality control jobs pay per year?

As of Sep 9, 2026, the average yearly pay for biotech quality control in the United States is $81,324.00, according to ZipRecruiter salary data. Most workers in this role earn between $60,500.00 and $100,000.00 per year, depending on experience, location, and employer.

What is a biotech quality control?

A Biotech Quality Control (QC) job involves ensuring that biological products, processes, and facilities meet regulatory and quality standards. QC professionals conduct testing, analyze data, and document results to verify product safety and efficacy. They work with laboratory techniques such as PCR, HPLC, and microbiological testing. The role is critical in maintaining compliance with industry regulations like GMP and FDA guidelines.

What does a biotech quality control do?

On a daily basis, a Biotech Quality Control professional performs routine testing and analysis of raw materials, intermediates, and finished products to ensure they meet established specifications. This involves preparing samples, operating analytical equipment, maintaining accurate records, and documenting results in compliance with regulatory guidelines. Quality Control staff also collaborate closely with production, quality assurance, and research teams to troubleshoot issues and support process improvements. Regular internal audits and participation in team meetings are common, making communication and teamwork key parts of the job.

What are the key skills and qualifications needed to thrive in biotech quality control?

To excel in Biotech Quality Control, candidates typically need a background in biology, chemistry, or related sciences, with strong knowledge of laboratory techniques and regulatory requirements. Familiarity with laboratory information management systems (LIMS), Good Manufacturing Practices (GMP), and common analytical instruments such as HPLC or PCR is highly valued. Attention to detail, problem-solving abilities, and effective communication are crucial soft skills for this role. These competencies are vital for ensuring that biotech products consistently meet quality and compliance standards essential for patient safety and regulatory approval.

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What are the most commonly searched types of Biotech Quality Control jobs?

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Biotech Quality Control jobs near you
Infographic showing various Biotech Quality Control job openings in the United States as of September 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $81,324 per year, or $39.1 per hour.

QC Scientist

Irvine, CA • On-site

Stark Pharma Solutions Inc
See more jobs at Stark Pharma Solutions Incexternal

Contractor

Posted 12 days ago

Job description

About the Company

Stark Pharma Solutions Inc. is a global consulting and staffing partner established in 2014, serving the Pharmaceutical, Medical Device, Biotech, and IT industries across the USA, Canada, and India.

We provide specialized consulting and staffing solutions across Quality & Validation, Regulatory Affairs, R&D, Manufacturing, Supply Chain, Project Management, and IT, with a focus on delivering tailored solutions that drive growth, operational excellence, and long-term client success.

Position: QC Scientist
Location: California
Duration: Long Term

Job Overview

We are seeking a Mid-Level QC Scientist with strong hands-on analytical testing experience to support quality control laboratory operations within a GMP-regulated pharmaceutical/biotech environment.

Key Responsibilities

• Perform hands-on HPLC and dissolution testing for drug substance and related samples.
• Review and evaluate analytical data for accuracy, completeness, and compliance.
• Ensure laboratory activities follow GMP, SOPs, and data integrity requirements.
• Document test results, laboratory activities, and investigations accurately.
• Support analytical troubleshooting, deviations, and laboratory investigations.
• Collaborate with QC and cross-functional teams to maintain laboratory compliance.

Required Qualifications

• Bachelor’s degree in Chemistry, Pharmaceutical Sciences, or a related scientific field.
• 5+ years of pharmaceutical or biotech QC laboratory experience.
• Strong hands-on experience with HPLC testing.
• Experience with drug substance and dissolution testing.
• Strong analytical data review experience.
• Knowledge of GMP, SOPs, data integrity, and laboratory documentation.
• Experience supporting analytical investigations and troubleshooting.

How to Apply

Apply Now: Submit your updated resume to Stark Pharma Solutions Inc. for consideration.

Stark Pharma is an Equal Opportunity Employer and welcomes qualified candidates from diverse backgrounds.