ZipRecruiter

Log In

1

Assistant Biotech Quality Control Jobs (NOW HIRING)

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 ...

Legend Biotech US

QC, Analyst I

Raritan, NJ · On-site

$24.50 - $33/hr

Legend Biotech entered into a global collaboration agreement with Janssen, one of the ... Legend Biotech is seeking a QC Analyst I (IPL) as part of the Quality Operations team based in ...

Olympic Systems Corporation

Be Seen First

Quality Control Inspector

Winchester, MA · On-site

$22 - $25/hr

We are seeking a Quality Control Inspector/Assistant will be responsible for performing quality ... Biotechnology, Pharmaceutical, Medical, Food & Beverage, Semiconductor, and Fluid & Gas Processing.

Legend Biotech USA, Inc.

$24.50 - $33/hr

Legend Biotech entered into a global collaboration agreement with Janssen, one of the ... Legend Biotech is seeking a QC Analyst I (IPL) as part of the Quality Operations team based in ...

MSD

QC Instrument Specialist

Wilmington, DE

The Wilmington Biotech Campus will play a pivotal role in the manufacture of our company ... stakeholders * Assist with the development and execution of instrument commissioning and ...

Merck & Co.

At our Wilmington Biotech Campus, we are committed to keeping the patient at the very heart of all ... stakeholders - Assist with the development and execution of instrument commissioning and ...

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 ...

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 ... Responsibilities: * Assist in managing projects and technical activities associated with method ...

Peregrine Team

Quality Control Analyst

Seattle, WA · On-site

$27.25 - $36.75/hr

... and ensure product quality in a biotech environment. This role is essential to maintaining ... Support investigations and deviations * Assist with stability studies and data analysis ...

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 ... Perform trend analysis and assist in establishing limits * Identify discrepancies and support ...

next page

Showing results 1-20

All JobsBiotech Quality Control JobsAssistant Biotech Quality Control Jobs

Assistant Biotech Quality Control information

See salary details

$11

$22

$40

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

As of Jul 21, 2026, the average hourly pay for assistant biotech quality control in the United States is $22.84, according to ZipRecruiter salary data. Most workers in this role earn between $16.35 and $23.08 per hour, depending on experience, location, and employer.

What is the difference between Assistant Biotech Quality Control vs Laboratory Technician?

AspectAssistant Biotech Quality ControlLaboratory Technician
CredentialsAssociate degree or equivalent, relevant certificationsAssociate degree or diploma, technical training
Work EnvironmentBiotech labs, quality assurance settingsResearch labs, clinical or industrial labs
Employer & IndustryBiotech companies, pharmaceutical firmsResearch institutions, healthcare, manufacturing
Common TasksSample testing, data recording, quality checksSample preparation, equipment operation, data collection

Assistant Biotech Quality Control and Laboratory Technicians both work in laboratory settings, often with overlapping skills. However, quality control roles focus more on ensuring product standards and compliance, while laboratory technicians may be involved in broader research or testing tasks. Understanding these differences helps job seekers target the right roles in the biotech industry.

More about Assistant Biotech Quality Control jobs
What cities are hiring for Assistant Biotech Quality Control jobs? Cities with the most Assistant 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 Assistant Biotech Quality Control jobs? States with the most job openings for Assistant Biotech Quality Control jobs include:
What job categories do people searching Assistant Biotech Quality Control jobs look for? The top searched job categories for Assistant Biotech Quality Control jobs are:
Assistant Biotech Quality Control jobs near you
Infographic showing various Assistant Biotech Quality Control job openings in the United States as of July 2026, with employment types broken down into 1% As Needed, 76% Full Time, 20% Part Time, 1% Temporary, and 2% Contract. Highlights an 98% Physical, 1% Hybrid, and 1% Remote job distribution, with an average salary of $47,500 per year, or $22.8 per hour.

Director, Quality Control

Cellectis

Raleigh, NC • On-site

Full-time

Re-posted 16 days ago

Job description


POSITION SUMMARY
The Director, Quality Control provides strategic and operational leadership for all Quality Control (QC) activities supporting drug substance (DS) and dug product (DP) manufacturing at the site. This role is accountable for ensuing the generation of accurate, reliable, and compliant analytical data to support product release, stability, and lifecycle management in accordance with global GMP requirements.
The Director QC oversees all QC functions, including analytical, microbiological, and environmental monitoring programs, and ensures alignment with the overall control strategy. This role ensures inspection readiness data integrity, and continuous improvement of QC systems and processes. As a member of the site Quality Leadership Team, the Director partners cross-functionally with Manufacturing m QA, MSAT, AS&T, and Regulatory to support clinical and commercial manufacturing while advancing quality culture and operational excellence.
POSITION RESPONSIBILITIES
  • Provide strategic leadership and oversight of all QC activities supporting DS and DP manufacturing, including release testing, stability programs, and in-process testing.
  • Partner with AS&T to ensure the robustness and lifecycle management of the analytical control strategy including method qualification, validation, transfer, and performance monitoring.
  • Oversee analytical, microbiological, and environmental monitoring programs, ensuring compliance with GMP requirements and site contamination control strategy
  • Ensure data integrity, accuracy, and reliability of all QC data in accordance with regulatory expectations.
  • Establish and maintain inspection readiness, including hosting regulatory inspections and responding to health authority inquiries.
  • Drive timely and thorough investigations of OOS, OOT, and atypical results, ensuring appropriate root cause identification and effective CAPA implementation.
  • Ensure appropriate specifications, test methods, and acceptance criteria are established and maintained throughout the product lifecycle.
  • Oversee QC laboratory operations including resource planning, capacity management, and organizational capability development
  • Partner cross-functionally with Manufacturing, QA, MSAT, AS&T, and Regulatory Affairs to support batch release, process improvements, and regulatory submissions.
  • Lead continuous improvement initiatives to enhance laboratory efficiency, compliance, and right-first-time performance.
  • Develop and monitor QC performance metrics, identifying trends and driving actions to improve performance and compliance.
  • Build and develop a high performing QC organization, fostering a strong quality culture and technical excellence.
  • Participates in business sub-teams as a Subject Matter Expert (SME) to provide input on timeliness and to address analytical/microbiological related issues
  • Other responsibilities and duties as the company may from time-to-time assign

EDUCATION AND EXPERIENCE
  • Bachelor's degree in chemistry, Biology or related scientific discipline required, advanced degree preferred.
  • 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 teams.
  • Experience managing environmental monitoring and contamination control strategies in GMP manufacturing environments.
  • Experience supporting DS & DP manufacturing in GMP environments.
  • Proven track record of regulatory inspection success and audit management.
  • Proven experience with laboratory method lifecycle management.
  • Experience implementing or optimizing laboratory systems and processes preferred.

TECHNICAL SKILLS / CORE COMPETENCIES
  • Deep expertise in GMP regulations applicable to QC laboratories supporting ATMPs.
  • Strong knowledge of analytical techniques (e.g. q/rt/ddPCR, flow cytometry, ELISA, cell-based assays, microbiological methods) and their application tin DS/DP testing.
  • Strong understanding of data integrity principles and regulatory expectations (ALCOA+).
  • Ability to operate effectively in a matrixed, cross-functional environment.
  • Strong problem-solving skills with a risk-based and science-driven approach.
  • Excellent communication skills with the ability to influence at site and executive levels.
  • Strong project management skills.

Apply