1

Senior Qc 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 ...

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 ...

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 ...

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 ...

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 ...

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 ...

next page

Showing results 1-20

Senior Qc Analyst information

See salary details

$53.5K

$109.8K

$142.5K

How much do senior qc analyst jobs pay per year?

As of Jun 12, 2026, the average yearly pay for senior qc analyst in the United States is $109,846.00, according to ZipRecruiter salary data. Most workers in this role earn between $90,500.00 and $137,000.00 per year, depending on experience, location, and employer.

What are Senior QC Analysts?

Senior QC (Quality Control) Analysts are experienced professionals responsible for overseeing and conducting quality control tests in laboratories, typically within the pharmaceutical, biotechnology, or manufacturing industries. They ensure that products meet required standards and specifications by performing analytical tests, reviewing data, and troubleshooting issues. Senior QC Analysts also mentor junior staff, help develop testing methods, and ensure compliance with regulatory guidelines such as GMP (Good Manufacturing Practices). Their role is crucial in maintaining product quality and safety before products reach consumers.

What is the difference between Senior Qc Analyst vs Quality Control Technician?

AspectSenior Qc AnalystQuality Control Technician
Required CredentialsBachelor's degree, often with certifications like CQEAssociate's or Bachelor's degree, sometimes with certifications
Work EnvironmentLaboratories, manufacturing plants, quality departmentsManufacturing sites, labs, production lines
Employer & Industry UsagePharmaceuticals, biotech, manufacturingManufacturing, food production, pharmaceuticals
Job ResponsibilitiesData analysis, process improvement, oversightTesting, sampling, data recording

The Senior Qc Analyst typically has more advanced responsibilities, including data analysis and process improvements, while the Quality Control Technician focuses on testing and sampling tasks. Both roles are essential in quality assurance within manufacturing and biotech industries.

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

To thrive as a Senior QC Analyst, you need a strong background in analytical chemistry or life sciences, experience with quality control procedures, and typically a bachelor's degree or higher in a related field. Familiarity with laboratory instrumentation (such as HPLC, GC, or FTIR), LIMS software, and regulatory requirements like GMP and FDA guidelines is essential. Attention to detail, problem-solving, and effective communication skills help you lead investigations and mentor junior staff. These skills are crucial for ensuring product quality, regulatory compliance, and efficient laboratory operations.

What are some common challenges faced by Senior QC Analysts, and how can they be addressed?

Senior QC Analysts often encounter challenges such as managing tight project deadlines, ensuring compliance with evolving regulatory standards, and troubleshooting unexpected laboratory issues. Successfully navigating these challenges requires strong organizational skills, up-to-date knowledge of industry regulations, and effective communication with cross-functional teams. Building robust documentation processes and fostering a culture of continuous improvement can also help Senior QC Analysts maintain high-quality results while adapting to changing project needs.
More about Senior Qc Analyst jobs
What cities are hiring for Senior Qc Analyst jobs? Cities with the most Senior Qc Analyst job openings:
What states have the most Senior Qc Analyst jobs? States with the most job openings for Senior Qc Analyst jobs include:

$24.50 - $33/hr

Other

Posted 13 hours 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. 

#Li-RP1

#Li-Onsite