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Senior Qc Analyst Jobs (NOW HIRING)

ProSidian Consulting

Quality Control Analyst

Charlotte, NC · On-site

$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 ...

KBI Biopharma, Inc.

QC Analyst II

Durham, NC

$23.25 - $31.25/hr

Senior QC Analyst requires Bachelor' degree as described and 4+ years' experience or Master's Degree with 2+ years experience. * Strong ELISA and other plate-based assays experience preferred

KBI Biopharma, Inc.

QC Analyst II

Durham, NC · On-site

$23.25 - $31.25/hr

Senior QC Analyst requires Bachelor' degree as described and 4+ years' experience or Master's Degree with 2+ years experience. * Strong ELISA and other plate-based assays experience preferred

Pace

Sr. Quality Control Analyst (Pharma)

Waltham, MA · On-site

$90K - $110K/yr

Provides proper documentation of practices following GxP and QC procedures. * Provides complex to specialized analysis in support of various testing materials, products and/or devices utilizing ...

DISCGENICS INC

Quality Control Analyst

Salt Lake City, UT · On-site

$23 - $31/hr

The QC Analyst performs quality control analysis of raw material, and finished product using USP compendial tests or in-house developed analytical test methods and will play a role in transitioning ...

ResolveSoft Inc

Be Seen First

Senior QA/QC Analyst

Washington, DC · On-site

$90K - $105K/yr

ResolveSoft is seeking a highly motivated Senior QA/QC Analyst (Remote) to join our growing team. In this role, you will play a critical role in ensuring the quality and functionality of our software ...

ARUP Laboratories

Quality Control Analyst

South Jordan, UT

$22.75 - $30.50/hr

The Quality Control Analyst provides analytical expertise to the laboratories regarding the department Quality Control program. Evaluates and implements protocols and methods of quality control to ...

ARUP

Quality Control Analyst

South Jordan, UT

$22.75 - $30.50/hr

The Quality Control Analyst provides analytical expertise to the laboratories regarding the department Quality Control program. Evaluates and implements protocols and methods of quality control to ...

ARUP

Quality Control Analyst

Salt Lake City, UT · On-site

$23.25 - $31.25/hr

The Quality Control Analyst provides analytical expertise to the laboratories regarding the department Quality Control program. Evaluates and implements protocols and methods of quality control to ...

DISCGENICS INC

Quality Control Analyst

Salt Lake City, UT · On-site

$23 - $31/hr

The QC Analyst performs quality control analysis of raw material, and finished product using USP compendial tests or in-house developed analytical test methods and will play a role in transitioning ...

Intellectt INC

QC Analyst

Lebanon, IN · On-site

$23 - $31/hr

My name is Vyshu, and I'm reaching out from Intellectt Inc. regarding an exciting contract opportunity for a QC Analyst - Master Data (LI MS) based in Lebanon, IN with one of our prestigious clients.

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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.
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Senior Qc Analyst jobs near you

Senior QC Analyst - Environmental Monitoring

Lonza

Portsmouth, NH • On-site

Full-time

Medical, Dental, Vision, Retirement

Posted 17 days ago

Lonza rating

8.1

Company rating: 8.1 out of 10

Based on 40 frontline employees who took The Breakroom Quiz

31st of 71 rated pharmaceutical

Job description

Senior QC Analyst - Environmental Monitoring
Location: Portsmouth, NH, USA.
As a QC Analyst IV, you are a Subject Matter Expert (SME) and a primary technical lead for the Environmental Monitoring team. This senior role is critical for maintaining the microbial control strategy of our multi-modal facility. You will be responsible for leading complex investigations, driving continuous improvement projects, and ensuring our EM program remains in a permanent state of compliance with global regulatory standards.
Schedule: Day Shift, Monday - Friday, 8:00 AM - 5:00 PM
What You'll Get
  • Technical Leadership: Act as a lead for the EM department, influencing site-wide quality culture and operational strategy.
  • Audit Frontline: Represent the EM program as a Subject Matter Expert during internal and external regulatory inspections (FDA, EMA, etc.).
  • Advanced Project Ownership: Lead the implementation of new technologies, such as rapid microbiological methods or paperless data systems.
  • Comprehensive Benefits: Medical, dental, vision, 401(k), and performance-based incentives. Our full list of global benefits: lonza.com/careers/benefits.

What You'll Do
  • Technical SME Ownership: Serve as the technical lead for the site's EM and Utility monitoring programs. Provide high-level guidance on sampling plans, risk assessments, and the qualification of new cleanrooms.
  • Complex Investigations: Lead and author high-complexity environmental excursion investigations. Utilize root cause analysis (RCA) tools to identify systemic issues and implement effective CAPAs.
  • Data Trending & Strategy: Perform advanced analysis of environmental and utility data. Identify long-term trends and present findings to site leadership and the Quality Council to drive proactive contamination control.
  • Regulatory & Audit Excellence: Prepare, review, and defend EM data and procedures during regulatory audits. Ensure all department SOPs and sampling protocols meet current Annex 1 and global cGMP expectations.
  • Mentorship & Coaching: Provide advanced technical training and mentorship to Level I, II, and III analysts. Foster a culture of technical excellence and "Right First Time" performance.
  • Continuous Improvement: Identify and execute Lean Laboratory initiatives to increase efficiency, reduce lead times, and enhance data integrity across the EM program.
  • Review & Approval: Act as a final technical reviewer for complex laboratory records, validation protocols, and summary reports.

Who We're Looking For
  • Education: Bachelor's degree (BS) in a Life Sciences discipline (Microbiology, Biology, or related field) is required.
  • Experience: 5-10 years of advanced experience in Quality Control Microbiology or Environmental Monitoring within a cGMP manufacturing environment is required.
  • Technical Mastery: * Expert-level knowledge of cleanroom classifications (Grade A-D) and aseptic processing.
    • Deep understanding of global regulatory requirements (FDA, EMA, ICH) for environmental and utility monitoring.
    • Proficiency in utilizing Laboratory Information Management Systems (LIMS) and data trending software.
  • Leadership Attributes: A proven track record of leading projects, managing timelines, and influencing cross-functional teams without direct authority.
  • Communication: Exceptional technical writing skills and the ability to present complex scientific data clearly to senior management and auditors.

About Lonza
At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone's ideas, big or small, have the potential to improve millions of lives, and that's the kind of work we want you to be part of.
Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we offer equal employment opportunities to all qualified applicants regardless of race, religion, color, national origin, sex, sexual orientation, gender identity, age, disability, veteran status, or any other characteristic protected by law. If you're ready to help turn our customers' breakthrough ideas into viable therapies, we look forward to welcoming you on board.
Ready to lead the standard of excellence in QC? Apply now.

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