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Day Biotech Quality Control Jobs (NOW HIRING)

... 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 ...

... pharma/biotech quality management system (i.e., ISO 13485, ISO 14971, FDA 21 CFR Part 820) is ... We build deep relationships with leading companies, connecting them to exceptional talent every day.

... pharma/biotech quality management system (i.e., ISO 13485, ISO 14971, FDA 21 CFR Part 820) is ... We build deep relationships with leading companies, connecting them to exceptional talent every day.

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 ...

... pharma/biotech quality management system (i.e., ISO 13485, ISO 14971, FDA 21 CFR Part 820) is ... We build deep relationships with leading companies, connecting them to exceptional talent every day.

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 ...

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 ...

Director, Quality Control

Raleigh, NC · On-site

$120 - $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 ...

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Day Biotech Quality Control information

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How much do day biotech quality control jobs pay per hour?

As of Sep 7, 2026, the average hourly pay for day biotech quality control in the United States is $20.97, according to ZipRecruiter salary data. Most workers in this role earn between $18.03 and $23.08 per hour, depending on experience, location, and employer.

What is the difference between Day Biotech Quality Control vs Day Biotech Quality Assurance?

AspectDay Biotech Quality ControlDay Biotech Quality Assurance
Primary FocusTesting and inspecting products to ensure quality standards are met
ResponsibilitiesConducting lab tests, analyzing samples, documenting results
Work EnvironmentLaboratories, manufacturing facilities
CertificationsRelevant lab certifications, GMP training

Day Biotech Quality Control professionals focus on testing products to verify quality, while Day Biotech Quality Assurance staff develop and maintain processes to prevent defects. Both roles are essential in biotech manufacturing, often working closely but with distinct responsibilities.

What cities are hiring for Day Biotech Quality Control jobs?

Cities with the most Day Biotech Quality Control job openings:

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

The most popular types of Biotech Quality Control jobs are:

What states have the most Day Biotech Quality Control jobs?

States with the most job openings for Day Biotech Quality Control jobs include:

QC Scientist

Stark Pharma Solutions Inc

Irvine, CA • On-site

Contractor

Posted 9 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.