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Senior Quality Control Analyst Jobs (NOW HIRING)

Sr. QC Analyst

Raritan, NJ

$24.50 - $33/hr

Legend Biotech is seeking a Sr. QC Analyst as part of the Quality team based in Raritan, NJ . Role Overview The Sr. QC Analyst is an exempt level position with responsibilities for performing QC ...

Sr. QC Analyst

Raritan, NJ · On-site

$24.50 - $33/hr

Role Overview The Sr. QC Analyst is an exempt level position with responsibilities for performing QC testing related to the manufacturing of cell therapy products for clinical trials and commercial ...

$24.50 - $33/hr

Role OverviewThe Sr. QC Analyst is an exempt level position with responsibilities for performing QC testing related to the manufacturing of cell therapy products for clinical trials and commercial ...

Run routine and advanced analysis on non-routine samples. Work with the Process Chemists and QC Chemists to reach solutions to unresolved problems and train new technicians * Perform equipment ...

Independently create, maintain, analyze and/or update QC data following established methods and relevant specifications. * Contribute to Continuous Improvement in the optimization of test methods and ...

Independently create, maintain, analyze and/or update QC data following established methods and relevant specifications. * Contribute to Continuous Improvement in the optimization of test methods and ...

Title: Sr. Quality Control Associate (Contract) Location: Alameda County, CA Schedule & Contract ... Hours: 40 hours per week Job Duties We are seeking a Quality Control Analyst to support analytical ...

Other duties as directed by Team Leader or Sr. QC Analyst. * Maintains samples in accordance with established procedures. * Maintains statistical process control charts and other tracking reports ...

Other duties as directed by Team Leader or Sr. QC Analyst. * Maintains samples in accordance with established procedures. * Maintains statistical process control charts and other tracking reports ...

QC Analyst II

Orangeburg, NY · On-site

$24 - $29/hr

Other duties as directed by Team Leader or Sr. QC Analyst. * Maintains samples in accordance with established procedures. * Maintains statistical process control charts and other tracking reports ...

QC Analyst II

Orangeburg, NY · On-site

$24 - $29/hr

Other duties as directed by Team Leader or Sr. QC Analyst. * Maintains samples in accordance with established procedures. * Maintains statistical process control charts and other tracking reports ...

QC Analyst II

Orangeburg, NY · On-site

$24 - $29/hr

Other duties as directed by Team Leader or Sr. QC Analyst. * Maintains samples in accordance with established procedures. * Maintains statistical process control charts and other tracking reports ...

May interpret analytical data to guide formulation and process development decisions. NOTE: This is an EVERGREEN posting where we are collecting candidates for a future role Compensation: $35.00 - 50 ...

May interpret analytical data to guide formulation and process development decisions. NOTE: This is an EVERGREEN posting where we are collecting candidates for a future role Compensation: $35.00 - 50 ...

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How much do senior quality control analyst jobs pay per hour?

As of Jun 8, 2026, the average hourly pay for senior quality control analyst in the United States is $48.52, according to ZipRecruiter salary data. Most workers in this role earn between $42.31 and $54.33 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Senior Quality Control Analyst, and why are they important?

To thrive as a Senior Quality Control Analyst, you need expertise in laboratory testing, analytical methods, and a strong understanding of regulatory standards, often supported by a degree in chemistry, biology, or a related field. Familiarity with laboratory information management systems (LIMS), chromatography software, and relevant certifications such as GMP training are typically required. Attention to detail, strong problem-solving abilities, and effective communication skills distinguish top performers in this role. These competencies ensure accurate quality assessments, compliance with regulations, and efficient collaboration across teams to maintain product integrity.

What are some common challenges faced by Senior Quality Control Analysts, and how are they typically addressed?

Senior Quality Control Analysts often encounter challenges such as managing tight deadlines while maintaining high accuracy, adapting to evolving regulatory standards, and troubleshooting unexpected deviations in product quality. These challenges are typically addressed through effective collaboration with cross-functional teams, ongoing professional development to stay updated with industry regulations, and implementing robust standard operating procedures. Additionally, strong analytical and communication skills help in swiftly resolving issues and ensuring continuous improvement within the quality control process.

What does a Senior Quality Control Analyst do?

A Senior Quality Control Analyst is responsible for overseeing and ensuring the quality of products or processes within a company, typically in industries like pharmaceuticals, manufacturing, or food production. They design and implement testing procedures, analyze data, identify defects or inconsistencies, and ensure compliance with regulatory standards. Additionally, they mentor junior analysts, prepare reports, and collaborate with other departments to improve quality systems. Their expertise helps maintain product integrity and supports continuous improvement initiatives.
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$24.50 - $33/hr

Other

Posted 26 days ago


Job description

Legend Biotech is seeking a Sr. QC Analyst as part of the Quality team based in Raritan, NJ.

Role Overview

The Sr. QC Analyst is an exempt level position with responsibilities for performing QC testing related to the manufacturing of cell therapy products for clinical trials and commercial operations in a controlled GMP environment.

Key Responsibilities

  • Be responsible for the completion of QC testing related to the manufacturing of autologous CAR-T products for clinical trials and commercial operation in a controlled cGMP cleanroom environment.
  • Ensure testing is completed in compliance with all applicable procedures, standards and GMP regulations.
  • Conduct analytical testing of raw material/utility, in-process, or final product samples submitted to the QC laboratories.
  • Perform peer review/approval of laboratory data.
  • Utilize electronic systems (LIMS) for execution and documentation of testing.
  • Create, review and approve relevant QC documents, SOP's and WI's.
  • Perform tasks in a manner consistent with the safety policies, quality systems and cGMP requirements.
  • Work in a collaborative team setting with quality counterparts that include Quality Assurance, Manufacturing Operations, and Analytical/Process Development.
  • Job duties performed require routine exposure to and handling of biological materials and hazardous chemicals. 

Requirements

  • Bachelor's Degree in Science, Engineering or equivalent technical discipline is required.
  • Minimum of 1 year relevant work experience, preferably within a biological and/or pharmaceutical industry is required.
  • Experience in a Quality Control setting is preferred.
  • Experience with processing samples in biosafety cabinets utilizing aseptic technique is strongly preferred.
  • Knowledge of cGMP regulations and FDA/EU guidance related to manufacturing of cell-based products is strongly preferred.
  • Knowledge of Good Tissue Practices is required.
  • Knowledge of CAR-T QC test methods and related equipment is preferred.
  • Excellent written and oral communication skill are required.
  • Candidates must be able to accommodate shift schedule. Shifts include routine weekend and evening work as required by the manufacturing process.
  • Candidates must be able to accommodate unplanned overtime (including nights and weekends) on little to no prior notice.
  • The candidate must be highly organized and capable of working in a team environment with a positive attitude under some supervision.
  • Comfortable with speaking and interacting with regulatory inspectors.
  • This position may require occasional travel to partner sites in NJ or PA as business demands.
  • This position may require up to 5% domestic or international travel as business demands.
  • Takes responsibility for one's results and deliverables; sets and achieves goals to support organizational priorities.
  • Takes initiative; willing to take unpopular positions/actions when necessary; courageous and assertive.
  • Works effectively in the face of ambiguity, shifting priorities, and rapid change; maintains a positive outlook in difficult situations; a change agent.
  • Identifies and focuses on activities of highest value and impact; makes informed decisions quickly.
  • Results oriented; defines goals, metrics and actionable plans and manages work to deliver desired outcomes; has a sense of urgency.
  • Considers resources, alternatives, constraints and desired outcomes to make effective decisions.
  • Employs good project management principles to appropriately align time, resources, and budgets.
  • Appreciates diverse perspectives and is actively inclusive of others' input and ideas; treats others with respect.
  • Articulates ideas clearly and succinctly in a variety of settings and styles; can get messages across that have the desired effect.
  • Leverages personal credibility and interpersonal skills to help others make better decisions and positively impact outcomes; able to develop/maintain effective working relationships internally and externally.
  • Employs a global mindset in decision-making and errs on the side of over-communicating to create organizational transparency, trust and alignment.
  • Takes initiative, actively shares knowledge, builds skills, promotes new ideas and embraces change.
  • Generates new solutions to problems by challenging the status quo and conventional thinking. 

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