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Senior Quality Control Analyst Jobs in Nebraska (NOW HIRING)

Senior Quality Engineer

Omaha, NE ยท On-site

$85 - $120/hr

The Senior Quality Engineer will lead quality initiatives, drive root cause analysis, support new ... Develop control plans, PFMEA. Quality plans for legacy or new products or projects. * Manage ...

Senior Quality Engineer

Omaha, NE ยท On-site

$84K - $114K/yr

... Develop control plans, PFMEA. Quality plans for legacy or new products or projects. o Manage ... analysis and root cause investigation (3L5Ws, Fishbone, Fault Tree). o Strong experience in ...

Senior Quality Engineer

Omaha, NE ยท On-site

$84K - $114K/yr

... Develop control plans, PFMEA. Quality plans for legacy or new products or projects. o Manage ... analysis and root cause investigation (3L5Ws, Fishbone, Fault Tree). o Strong experience in ...

Senior Quality Engineer

Omaha, NE ยท On-site

$84K - $114K/yr

... Develop control plans, PFMEA. Quality plans for legacy or new products or projects. o Manage ... analysis and root cause investigation (3L5Ws, Fishbone, Fault Tree). o Strong experience in ...

Sr. Quality Analyst

Omaha, NE ยท On-site

$79.76 - $100.37/hr

... analysis techniques and best practices. Solve a wide range of difficult problems pertaining to system testing and quality assurance processes in imaginative and practical ways. Essential Functions

... analysis techniques and best practices. Solve a wide range of difficult problems pertaining to system testing and quality assurance processes in imaginative and practical ways. ESSENTIAL FUNCTIONS:

Quality Control

Bruning, NE ยท On-site

$21 - $27/hr

Quality Control Specialist Location: [Insert Location] Company: Metal-Tech Partners Metal-Tech ... Familiarity with root cause analysis methods (e.g., 5 Whys, Fishbone Diagram) * Previous experience ...

The Quality Control Scientist supports manufacturing by conducting analysis on raw and finished materials and maintains quality control and assurance of products and compliance within internal ...

The Quality Control Scientist supports manufacturing by conducting analysis on raw and finished materials and maintains quality control and assurance of products and compliance within internal ...

The Quality Control Manager works closely with stakeholders in key manufacturing and business ... Collect, analyze, and report data related to quality, such as costs of poor quality * Review ...

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Senior Quality Control Analyst information

See Nebraska salary details

$14

$46

$64

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

As of Aug 25, 2026, the average hourly pay for senior quality control analyst in Nebraska is $46.26, according to ZipRecruiter salary data. Most workers in this role earn between $40.34 and $51.78 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.

What are the most commonly searched types of Quality Control Analyst jobs in Nebraska?

The most popular types of Quality Control Analyst jobs in Nebraska are:

What are popular job titles related to Senior Quality Control Analyst jobs in Nebraska?

For Senior Quality Control Analyst jobs in Nebraska, the most frequently searched job titles are:

What cities in Nebraska are hiring for Senior Quality Control Analyst jobs?

Cities in Nebraska with the most Senior Quality Control Analyst job openings:

Infographic showing various Senior Quality Control Analyst job openings in Nebraska as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 17% Part Time, 3% Contract, and 1% Nights. Highlights an 84% Physical, 1% Hybrid, and 15% Remote job distribution, with an average salary of $96,218 per year, or $46.3 per hour.

Senior Quality Control Scientist

Omaha, NE โ€ข On-site

Full-time

Posted 29 days ago


Job description

Job Type
Full-time
Description
JOB SUMMARY:
The Senior Quality Control Scientist (SQCS) is the primary technical support contact for peers within the Pharmgate Quality Control Laboratories. The SQCS is also responsible for performing their own primary analytical duties, maintaining quality control and assurance of materials and instrumentation used in the laboratory. Additionally, the SQCS will help assure that daily, weekly, and/or monthly workflow tasks are completed to meet company and department goals. The position is key to supporting Laboratory management while independently applying advanced scientific knowledge to projects and assures adherence to Standard Operating Procedures(SOPs), Current Good Manufacturing Practices (cGMP) and other industry and company required standards and policies.
TECHNICAL WORKFLOW RESPONSIBILITIES:
1. Provide guidance on daily tasks for efficient workflow and assignments in the laboratory.
2. Oversee consistency in training across all areas of the laboratory.
3. Provide opportunities for on-the-job training and SOP review as necessary.
4. Troubleshoot and resolve work problems or assist workers in solving work problems.
5. Communicate difficulties, either production or personnel, with plans for resolution, to management for consultation and resolution approval.
INDIVIDUAL WORKFLOW DUTIES/RESPONSIBILIITIES:
1. Identify and recommend improvements to processes to maintain quality, cost- effectiveness, safety compliance, and other parameters.
2. Perform timely release testing on all incoming raw materials needed for manufacturing and finished goods.
3. Coordinate scheduling of all materials in order to meet company requirements.
4. Ensure that assigned products meet quality requirements for the customer and the company.
5. Draft written reports detailing results of testing analysis.
6. Approve release of raw materials and finished goods.
7. Proactively identify trends in laboratory analysis or functions and act to make improvements and/or communicate to management.
8. Perform operations for CMO support as necessary.
9. Operate and maintain laboratory equipment; identify problems when equipment fails and conduct or recommend repairs.
10. Perform maintenance and calibration of all equipment as needed.
11. Perform peer review of analytical results of peers.
12. Perform peer review of test methods and protocols.
13. Review and/or draft SOPs as needed to update to current procedures.
14. Author and execute written protocols and IQOQs as needed.
15. Cross train to be able to perform sample lab duties adequately and accurately.
16. Act as Quality Department Representative when necessary.
17. Perform other duties as assigned.
Requirements
REQUIRED SKILLS/ABILITIES:
1. Excellent organizational skills and attention to detail.
2. Thorough understanding of chemical tests and processes.
3. Understanding and proficiency in basic laboratory techniques and scientific instrumentation, including direct HPLC experience and troubleshooting.
4. Ability to follow Standard Operating Procedures (SOPs) and GMP guidelines. Ensure compliance with all NADAs/ANADAs.
5. Excellent time management skills with a proven ability to meet deadlines.
6. Strong verbal and written communication skills and the ability to work with all levels of personnel.
7. Strong analytical and problem-solving skills including the ability to read and understand instructions and materials in English; add, subtract, multiply, and divide in all units of measure, using whole numbers, common fractions, and decimals.
8. Ability to function well in a high-paced and at times stressful environment.
9. Thorough understanding of FDA and cGMP compliance regulations.
10. Proficient with Microsoft Office Suite, virtual meeting applications, SAP Business One, and other related software.
EDUCATION AND EXPERIENCE:
1. Bachelor of Science in Chemistry, Microbiology or Biology, required.
2. 3-5 years of experience in an FDA regulated pharmaceutical laboratory facility or other highly regulated industry, preferred.
PHYSICAL REQUIREMENTS:
1. Prolonged periods of standing and walking.
2. Exposure to various chemicals and compounds.
3. Prolonged periods of sitting at a desk working on computers.
4. Ability to occasionally lift 50 lbs. from floor to waist level.
5. Ability to occasionally climb stairs.