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Biotech Quality Control Jobs (NOW HIRING)

Cellectis

Director, Quality Control

Raleigh, NC

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 ...

BioPhase Solutions

QC Inspector

San Diego, CA · On-site

$18 - $19.80/hr

Quality Control Inspector Are you passionate about ensuring the highest quality standards in the biotech industry? We are seeking a skilled and detail-oriented Quality Control Technician to join our ...

Astrix Inc

QC Lab Associate

Newark, CA · On-site

$28 - $31/hr

Our client, a clinical-stage biotechnology company focused on innovative cell therapy development, is seeking a QC Lab Associate to support essential laboratory operations. This is a great ...

TekWissen LLC

Quality Control Specialist

Vacaville, CA · On-site

$20 - $26/hr

Our client is a leading biotechnology company that combines technological insight with world-class ... Job Title: QC Specialist II Location: Vacaville, CA, 95688 Duration: 6 Months Job Type: Temporary ...

Adecco

Quality Control Analyst

Plainville, MA · On-site

$23.50 - $31.50/hr

Adecco Healthcare & Life Sciences is hiring for a leading global pharmaceutical and biotechnology ... QC Microbiology Analyst I Location: Onsite Schedule: Sunday - Wednesday | 11:00 AM - 9:30 PM (30 ...

TekWissen LLC

Quality Control Scientist

Vacaville, CA · On-site

$20 - $25/hr

Our client is a leading biotechnology company that combines technological insight with world-class ... Job Title: QC Associate I / Quality Control Scientist Location: Vacaville, CA - 95688 Duration: 6 ...

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Biotech Quality Control information

See salary details

$30.5K

$81.3K

$129.5K

How much do biotech quality control jobs pay per year?

As of Jul 10, 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.

Does QA or QC pay more?

In biotech quality control, Quality Assurance (QA) roles typically pay slightly more than Quality Control (QC) positions due to their broader responsibilities in process oversight and compliance. Both roles require attention to detail and knowledge of industry regulations, but QA positions often involve more strategic planning and documentation, which can influence salary differences.

What are the typical daily responsibilities of someone working in Biotech Quality Control?

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.

How to become a biotech quality control specialist?

To become a biotech quality control specialist, candidates typically need a bachelor's degree in biology, chemistry, or a related field. Relevant skills include knowledge of laboratory techniques, quality assurance processes, and familiarity with regulatory standards like GMP. Certifications such as ASQ CQE or training in laboratory management can enhance job prospects.

What is the highest paying job in biotech?

In biotech quality control, senior roles such as Director of Quality Assurance or Vice President of Quality typically have the highest salaries, often exceeding six figures. These positions require extensive experience, leadership skills, and knowledge of regulatory standards like GMP and ISO.

What is a Biotech Quality Control job?

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 are the key skills and qualifications needed to thrive in the Biotech Quality Control position, and why are they important?

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.

What does quality control do in biotech?

In biotech, quality control (QC) involves testing and inspecting products, raw materials, and processes to ensure they meet safety, efficacy, and quality standards. QC teams use analytical techniques and documentation to identify deviations and maintain compliance with regulatory requirements such as GMP. This role is essential for ensuring product consistency and regulatory approval.
More about Biotech Quality Control jobs
What cities are hiring for Biotech Quality Control jobs? Cities with the most 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 Biotech Quality Control jobs? States with the most job openings for Biotech Quality Control jobs include:
What job categories do people searching Biotech Quality Control jobs look for? The top searched job categories for Biotech Quality Control jobs are:
Biotech Quality Control jobs near you
Infographic showing various Biotech Quality Control job openings in the United States as of July 2026, with employment types broken down into 1% Locum Tenens, 1% As Needed, 91% Full Time, 1% Part Time, 1% Temporary, and 5% Contract. Highlights an 82% Physical, 2% Hybrid, and 16% Remote job distribution, with an average salary of $81,324 per year, or $39.1 per hour.
QC Lead/Manager

QC Lead/Manager

Neurona Therapeutics

South San Francisco, CA • On-site

Full-time

Re-posted 3 days ago

Job description

QC Lead / Manager
Location: South San Francisco, CA, 94080
About Neurona Therapeutics
Neurona Therapeutics is a clinical-stage biotechnology company based in South San Francisco focused on developing neuronal cell-based therapies for intractable neurological diseases. We are seeking an experienced and highly motivated leader to join our Quality Control team.
Our ideal candidate is a strong operational leader, highly organized, and brings deep technical expertise in QC laboratory environments. This individual thrives in a fast-paced, collaborative setting and is passionate about advancing high-quality cell therapy products.
Role Overview
The QC Lead / Manager will report directly to the Director, Assay Development & QC and provide operational and technical leadership for the Quality Control laboratory activities supporting Neurona's cell therapy programs. As an in-lab leader for Quality Control, this role will be responsible for scheduling all QC testing for lot release, stability plans and ad hoc test requests, in addition to managing test samples and reagent inventories, in accordance with cGMP and regulatory standards.
This role will also serve as a key liaison between QC, Manufacturing, and Quality Assurance teams to ensure product quality and operational excellence. In addition to leadership responsibilities, this individual will remain actively engaged at the bench, serving as a subject matter expert for Quality events and reviewing data to support critical QC deliverables.
Responsibilities
Operational Leadership
  • Coordinate scheduling and execution of QC assays for lot release, stability programs and ad hoc testing, ensuring timelines and quality standards are met.
  • Manage laboratory operations, including sample tracking, inventory control, and equipment readiness.
  • Review and approve data to ensure accuracy, completeness, and compliance.
  • Active involvement, including training and running QC tests, to support laboratory assay performance while maintaining testing throughput and timelines.
Compliance & Inspection Readiness
  • Ensure adherence to cGMP, GxP, and pharmacopeia standards across all QC activities.
  • Lead inspection readiness efforts and support internal and external audits.
  • Oversee and manage deviations, OOS/OOT investigations, and CAPAs, ensuring timely resolution and documentation.
  • Champion data integrity and documentation best practices within the QC laboratory.
Method Lifecycle Management
  • Oversee method transfer, qualification, validation, and lifecycle management within the QC lab.
  • Support assay optimization and troubleshooting to ensure robustness and reproducibility.
  • Partner with Assay Development and Process Sciences teams to implement new or improved methods.
Strategic Collaboration
  • Serve as a key liaison between QC and cross-functional stakeholders, including Manufacturing, CMC, and Site QA.
  • Support batch release activities and ensure alignment between QC deliverables and manufacturing timelines.
  • Collaborate with Quality and technical teams to resolve complex quality and process-related issues.
Continuous Improvement
  • Drive process improvements in laboratory workflows, efficiency, and throughput.
  • Identify and implement new technologies and automation to enhance QC capabilities.
  • Track and report key performance metrics to support operational excellence initiatives.
Education Requirements
  • Bachelor's degree in Biochemistry, Microbiology, Chemistry, or related scientific discipline (Master's degree a plus)
Experience Requirements
  • 5+ years of experience in a pharmaceutical or biotechnology QC laboratory environment.
  • Prior experience leading or mentoring teams in a QC or laboratory setting.
  • Demonstrated hands-on laboratory experience with a willingness to remain actively engaged in day-to-day operations.
  • Strong knowledge of cGMP regulations, pharmacopeia standards, and Quality Systems.
  • Demonstrated experience managing deviations, OOS investigations, and CAPAs.
  • Proven ability to lead method transfer, validation, and lifecycle management activities.
  • Strong technical writing and documentation skills.
  • Excellent organizational, communication, and cross-functional collaboration skills.

This job description is not exhaustive and not intended to cover all activities of the position. Duties, responsibilities and activities may change, or new ones may be assigned at any time with or without notice.
Neurona is proud to be an equal opportunity employer and will consider all qualified applicants for employment.
Recruitment Fraud Notice
We are aware of active recruitment scams using the Neurona name, where individuals pose as our recruiters or post fake remote job openings and make fraudulent job offers online. Please note, that we will never make an offer of employment without conducting multiple rounds of face-to-face interviews using secure video-conferencing technology. Additionally, we will never ask candidates to cash checks or make any payment to be considered for a position.
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