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Senior Quality Control Analyst Jobs (NOW HIRING)

RoslinCT US

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 ...

ProKidney

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 ...

ProKidney

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 ...

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 ...

20BLOC

Quality Control Analyst

Thousand Oaks, CA · On-site

$74K/yr

The QC Analyst also plays a key role in maintaining lab compliance by authoring and reviewing SOPs, and controlled forms. This is a full-time position on site in Thousand Oaks, CA. Key ...

20BLOC

Quality Control Analyst

Thousand Oaks, CA · On-site

$74K/yr

The QC Analyst also plays a key role in maintaining lab compliance by authoring and reviewing SOPs, and controlled forms. This is a full-time position on site in Thousand Oaks, CA. Key ...

Kelly Services

QC Analyst Contract

Winston Salem, NC

$28 - $35/hr

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 ...

Matthey

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 ...

Johnson Matthey

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 ...

Buckeye Global IT Inc

Be Seen First

Quality Control Analyst

Memphis, TN · On-site

$20.13 - $21.13/hr

The Quality Control Analyst I for the QC Microbiology Department will be responsible for performing processing of routine environmental monitoring samples, product-release testing, and raw material ...

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

As of Sep 5, 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 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.

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 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 is the role of a senior quality control analyst?

A senior quality control analyst is responsible for inspecting and testing products or materials to ensure they meet quality standards and regulatory requirements. They analyze data, identify issues, and collaborate with production teams to improve processes, often using tools like laboratory equipment and quality management systems. This role typically requires experience, attention to detail, and knowledge of industry-specific regulations.
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Senior Quality Control Analyst jobs near you
Infographic showing various Senior Quality Control Analyst job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 81% Full Time, 13% Part Time, 4% Contract, and 1% Nights. Highlights an 84% Physical, 1% Hybrid, and 15% Remote job distribution, with an average salary of $100,916 per year, or $48.5 per hour.

Senior QC Analyst - Environmental Monitoring

Lonza

Portsmouth, NH • On-site

Full-time

Medical, Dental, Vision, Retirement

Re-posted 12 days ago

Lonza rating

8.3

Company rating: 8.3 out of 10

Based on 42 frontline employees who took The Breakroom Quiz

24th of 86 rated pharmaceutical

Job description

Senior QC Analyst - Environmental Monitoring
Location: Portsmouth, NH, USA
Schedule: Day Shift, Monday - Friday, 8:00 AM - 5:00 PM
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.
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.
o Deep understanding of global regulatory requirements (FDA, EMA, ICH) for environmental and utility monitoring.
o 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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About Lonza

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Industry

Biotechnology research and development and pharmaceutical and medicine manufacturing

Company size

10,000+ Employees

Headquarters location

Bern, KS, US

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