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Biotech Quality Control Jobs (NOW HIRING)

Legend Biotech US

Sr. QC Analyst

Raritan, NJ · On-site

$24.50 - $33/hr

Legend Biotech entered into a global collaboration agreement with Janssen, one of the ... Role Overview The Sr. QC Analyst is an exempt level position with responsibilities for performing Q ...

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

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

$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 ...

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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 Jun 18, 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 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.

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.

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 June 2026, with employment types broken down into 4% Full Time, 92% Part Time, and 4% Nights. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution, with an average salary of $81,324 per year, or $39.1 per hour.
Manager Quality Control Analytical (Sunday-Wednesday)

Manager Quality Control Analytical (Sunday-Wednesday)

AstraZeneca

Rockville, MD

$112K - $168K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 13 days ago

AstraZeneca rating

8.6

Company rating: 8.6 out of 10

Based on 43 frontline employees who took The Breakroom Quiz

16th of 71 rated pharmaceutical

Job description

Manager, Quality Control Analytical, Cell Therapy

Sunday - Wednesday(4x 10 hour day shift)

Role Overview

TheManager, QCAnalytical, providesmanagerial,operationaland technical leadership for a cGMP Quality Control laboratory supporting cell therapy lot release and stabilitytesting. The role focuses onrightfirsttimeanalyticalassayexecution (e.g., flow cytometry, ELISA, PCR, automated cell counting, and othercellbasedassays)andendtoendlaboratory readiness,includingpeople andequipmentoversight.Responsibilities spanmanagement ofa routine testing team,testing execution,laboratory operations management,quality record management, and audit/inspection readiness. TheManagerpartners closely withother QC teams, MSAT/Analytical Development, Manufacturing, QA, and SupplyChainto ensure the laboperatessafely, compliantly, and efficiently to meet patient supply timelines.

This positionisfora4days per week, 10 hoursper day shift,Sunday through Wednesday.

Role Responsibilities

  • Laboratory operations oversight:Manage a QC laboratory team anddaytodaylab activities including sample intake, scheduling,testingflowand data review.

  • Analytical testing:Perform and oversee QC testing for cell therapy products (flow cytometry, ELISA, PCR,cell basedassays, cell count/viability) per approved methods, ensuring adherence to cGMP, GDP, and data integrity expectations (ALCOA+).

  • Documentation and compliance:Maintainaccurate, contemporaneous recordsin relevant electronic systems and forms; author/review SOPs, test methods, and certificates of analysis; ensure readiness for internal/external audits and regulatory inspections.

  • Training and mentoring:Train and coach junior team members on methods, cGMP/GDP, safety, and data integrity; support qualification of analysts and ongoingproficiencyassessments.

  • Planning and communication:Coordinate testing schedules, samplelogistics, and material controls; communicate status and risks; escalate issues proactively to meet lot release timelines.

  • Continuous improvement and LEAN: Drive 5S, visual management, standard work, and deviation trend reviews; improveflow andincreaserightfirsttimeperformance.

MinimumRequirements

  • Bachelor's degree in Biological Sciences, Chemistry, Biochemistry, or related discipline; advanced degree (MS/PhD) preferred.

  • At least 5 years' experience in pharmaceutical/biotech QC with emphasis on laboratory operations/management in a cGMP setting.

  • Demonstrated experienceoperatinga QC laboratory in a regulated environment with knowledge of cell therapy specific considerations (e.g., chain of identity/chain of custody, rapid turnaround for patient supply,phaseappropriatecontrols).

  • Proven ability to plan and coordinate laboratory operations, manage competing priorities, and communicate status, risks, and mitigations tocrossfunctionalstakeholders; experience presenting in audits/inspections.

  • Handsonexperience with qualification and maintenance of key QC instruments and with lab informatics (LIMS/ELN/LES, instrument data systems); strong command of data integrity controls and computerized systems compliance.

  • Ability to design and deliver effective training; mentor analysts on safe, compliant, and efficient lab practices; cultivate a culture of quality and continuous improvement.

  • Effectivecrossfunctionalpartner with Manufacturing, MSAT/AD, QA, Supply Chain, Facilities, and EHS; comfortable operating in afastchangingenvironment and adjusting plans to meetpatientcriticaltimelines.

  • Ability to work on-site in a lab-based rolefor the assigned shift.

The annual base pay (or hourly rate of compensation) for this position ranges from $112,604.80 - $168,907.20. Our positions offer eligibility for various incentives-an opportunity to receive short-term incentive bonuses, equity-based awards for salaried roles and commissions for sales roles. Benefits offered include qualified retirement programs, paid time off (i.e., vacation, holiday, and leaves), as well as health, dental, and vision coverage in accordance with the terms of the applicable plans.

Date Posted

05-Jun-2026

Closing Date

18-Jun-2026

Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and employees. In furtherance of that mission, we welcome and consider applications from all qualified candidates, regardless of their protected characteristics. If you have a disability or special need that requires accommodation, please complete the corresponding section in the application form.

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