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Senior Qc Analyst Jobs (NOW HIRING)

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 ...

QC Analyst Contractor

Winston Salem, NC

$22.25 - $29.75/hr

Supports Senior QC Analysts, as required. * Provides process development support, as needed. * Collects and compiles data from QC testing and Environmental Monitoring activities. * Procures dry ice ...

Sr. QC Analyst, Microbiology

Hopkinton, MA · On-site

$26.25 - $35.50/hr

... QC Technical Services, Quality Assurance, and Program Management. * Ability to prepare technical data and present to senior leadership. WHAT YOU WILL BRING * Bachelor's degree in Biology ...

QC Analyst Contractor

Winston Salem, NC

$22.25 - $29.75/hr

Supports Senior QC Analysts, as required.Provides process development support, as needed.Collects and compiles data from QC testing and Environmental Monitoring activities.Procures dry ice for ...

Quality Control Analyst

Charlotte, NC

$22.50 - $30/hr

Quality Control Analyst Candidates shall work to support requirements for PR0001 Program Support and will review and analyze the curriculum and substance of in-person, Webinar, and small group ...

QC Analyst Contractor

Winston Salem, NC · On-site

$22.25 - $29.75/hr

Supports Senior QC Analysts, as required. * Provides process development support, as needed. * Collects and compiles data from QC testing and Environmental Monitoring activities. * Procures dry ice ...

Quality Control Analyst

Smithfield, PA · On-site

$24.50 - $32.75/hr

Quality Control Analyst Location: Smithfield, PA At Johnson Matthey, your work will matter. As a Quality Control Analyst,you'lljoin a world leader in platinum group metals with over 200 years of ...

Work closely with Quality Assurance and Senior QC Analysts * Recognize and appropriately report deviations from established procedures * Procure and coordinate dry ice for clinical sample shipments ...

Quality Control Analyst

Smithfield, PA · On-site

$24.50 - $32.75/hr

Quality Control Analyst Job title: Quality Control Analyst Location: Smithfield, PA At Johnson Matthey, your work will matter. As a Quality Control Analyst, you'll join a world leader in platinum ...

Showing results 21-40

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 Sep 3, 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 is a senior QC analyst?

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 are the key skills and qualifications needed to thrive as a senior QC analyst?

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.

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.

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:

Infographic showing various Senior Qc Analyst job openings in the United States as of August 2026, with employment types broken down into 89% Full Time, 6% Part Time, and 5% Contract. Highlights an 82% Physical, 7% Hybrid, and 11% Remote job distribution, with an average salary of $109,846 per year, or $52.8 per hour.

Senior QC Analyst (2nd Shift; Tues - Sat)

Tolmar

Fort Collins, CO • On-site

$65 - $69/hr

Other

Re-posted 24 days ago


Tolmar rating

9.8

Company rating: 9.8 out of 10

Based on 6 frontline employees who took The Breakroom Quiz

1st of 86 rated pharmaceutical


Job description

Senior QC Analyst (2nd Shift; Tues - Sat)

Job Category: Quality Control

Requisition Number: SENIO005727

  • Full-Time
  • On-site
Locations

Showing 1 location

Description

Core Hours

Tuesday - Saturday, 3:00 pm - 11:30 pm

- Training hours may vary

Purpose and Scope

Performs complex testing of raw materials, bulk intermediate and finished products, and stability samples, according to established regulatory protocols and procedures, in support of manufacturing.

  • Expertise in performing analyses on a variety of samples using advanced preparation techniques and analysis methods. Expertise with basic and intermediate techniques and analysis methods.
  • Provide mentorship to QC analyst in all aspects of analyses performed within the QC chemistry laboratory including but not limited to documentation, procedures, and regulations.
  • Accountable for documenting all activities and maintaining records according to good documentation practices.
  • Accountable for proper use, care, maintenance, and troubleshooting of instrumentation.
  • Performs high-level method transfers. Guides the department in the evaluation and implementation of new technologies.
  • Provide detailed accounts of testing performed to investigators. Perform investigational testing as directed by a primary investigator.
  • Perform laboratory investigations with management assistance.
  • Make scientific recommendations to management/technical writers regarding QC procedures. Able to take recommendations and incorporate those recommendations into a document to ensure the appropriate changes are made.
  • Responsible for acting as a technical reviewer for document updates to ensure changes that are made are justified and scientifically sound.
  • Route documents in the electronic document control system to ensure document updates are routed promptly and correctly.
  • Act as a subject matter expert for the QC department.
  • Complete tasks on time and with minimal errors. Follow all procedures applicable to job functions to ensure high quality of work. Mentor others in the department to ensure department maintains high standards for quality of work.
  • Prioritize tasks and performs job duties with minimal guidance from management.
  • Contributes to a highly productive environment by avoiding distractions.
  • Responsible for ensuring that company and regulatory data integrity guidelines are consistently followed.
  • Participates in required monthly safety trainings and annual HAZ-COM, RCRA and API handling trainings. Hazardous waste involvement may include but is not limited to making waste determinations, generation, transportation, satellite accumulation, storage and disposal of multiple types of waste streams, and container management and inspections. Respond to spills per company procedures. Maintain compliance to all Tolmar health and safety policies, as well as OSHA standards.
  • Accountable for maintaining an atmosphere of teamwork, cordiality and respect towards co-workers. Exhibits a positive and understanding attitude at all times. Remembers to look at situations from all aspects. Assists co-workers with the completion of tasks. Able to identify areas of contention on the team and will work with QC management to correct.
  • Support adherence to department budget by identifying alternative cost-saving and compliant materials and equipment, where appropriate.
  • Represent the department by providing accounts and results of method transfer activities and assist with troubleshooting aberrant method transfer results, if necessary. May provide technical expertise to determine root cause of aberrant method transfer results.
  • Interact respectfully with all other employees both inside and outside of the department and members of management, and shows interest in others' input and reasoning. Appropriately resolves differences of opinion. Upon delegation may be responsible for representing the QC chemistry laboratory when communicating with outside departments and vendors.
  • A leader in compliance. Lead implementation of change and escalates issues as necessary. Demonstrate leadership aptitude in technical functions.
  • Identify issues and possible solutions and escalates those issues and solutions to the department senior leadership or management as appropriate.
  • Provide support to the department leadership with the implementation of new systems, and continuous improvement efforts. Generates new ideas to create efficiencies and improve processes; willingly supports new ideas and process enhancements.
  • Understand and process complex information and exercises sound judgment, considering the situation, the issues, the key players and the levels of authority involved. Propose courses of action that further the objectives, priorities, and vision of the organization; sees "big picture".
  • Perform additional duties as assigned.

Core Values

The Sr. QC Analyst is expected to operate within the framework of Tolmar’s Core Values:

  • Center on People: We commit to support the well-being of our patients. We are committed to treating our employees and those we serve as valued partners. By placing people at the heart of our actions, we actively engage, invigorate, acquire knowledge, and grow together.
  • Are Proactive & Agile: We embody a culture of engagement and action. With a hands-on approach, we fearlessly adapt to change. We anticipate, respond swiftly and efficiently to ignite a spirit that propels us towards extraordinary outcomes.
  • Act Ethically: We are committed to consistently conducting our business in an ethical, compliant, and socially aware manner, in line with our purpose of positively impacting lives. We actively cultivate diversity, equity,inclusion& sustainability in our workplace.
  • Constantly Improve: We are committed to a collaborative & proactive effort to improve our products, systems, processes, and services by reducing waste, increasing efficiency & improving quality.
  • Are Accountable: We think, act, and communicate with honesty, transparency, and clarity in alignment with our core values. We don't compromise our values for near term gain. We take accountability & ownership of our work, actions, successes, and setbacks. We strive to deliver our best as we shape the future.

Knowledge, Skills & Abilities

  • Advanced knowledge and application of government regulations for drugs or medical devices including GMP, GLP and ICH and their application to laboratory testing and review processes and procedures.
  • Advanced knowledge in the use of USP, NF and other compendia.
  • Highly proficient use of analytical laboratory instruments such as HPLC, FTIR, GPC, GC, and UV-Vis spectrophotometers.
  • Knowledge of computer systems for sample tracking, laboratory equipment, raw data handling and storage.
  • Effective written and oral communication skills.
  • Ability to interpret, understand and follow analytical procedures and calculations.
  • Demonstration of training and project leadership skills.
  • Ability to train analysts on complex methodology.
  • Expert knowledge in analytical testing of drug substances and formulations.

Education & Experience

  • Bachelor’s degree in scientific discipline, preferably in Chemistry or Biochemistry.
  • Six or more years of experience in an analytical laboratory position using advanced techniques and demonstrated proficiency with complex testing.

Working Conditions

  • Laboratory setting. Will be exposed to solvents, bio-hazardous materials, hazardous waste, and pharmaceuticals.
  • Must be adaptable to shifting priorities and operate with a sense of urgency while maintaining high quality in order to meet important timelines in a high throughput lab.
  • Business demands may present a need to work extended hours.

Compensation and Benefits

  • Pay: $47.00 - $50.00 depending on experience

Tolmar compensation programs are focused on equitable, fair pay practices including market-based base pay and a strong benefits package. The final compensation offered may vary from the posted range based on the selected candidates qualifications and experience.

Tolmar is an Equal Opportunity Employer. We do not discriminate on the basis age 40 and over, color, disability, gender identity, genetic information, military or veteran status, national origin, race, religion, sex, sexual orientation or any other applicable status protected by state or local law. It is our intention that all qualified applicants be given equal opportunity and that selection decisions are based on job-related factors.

Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities
This employer is required to notify all applicants of their rights pursuant to federal employment laws.For further information, please review the Know Your Rights notice from the Department of Labor.

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About Tolmar

Sourced by ZipRecruiter

Industry

Pharmaceutical and medicine manufacturing

Company size

1,001 - 5,000 Employees

Headquarters location

Fort Collins, CO, US

Year founded

2006