qa tech

McLane Classic Foods

<div><p>Employee will be responsible for verifying/auditing completed products/documentation from each department.
</p><ul><li>Pre-op/ Changeover inspection including swabbing before or after sanitation.
</li><li>Complete and submit micro and swab forms to the lab.
</li><li>Conduct, assemble and report data for product testing requirements.
</li><li>Perform HACCP/Quality checks as required and document results.
</li><li>Ensure plant personnel are following GMP/HACCP/ Food Safety Programs/Allergen and other pre-requisite programs in accordance to internal, regulatory and BRC requirements.</li><li>
Collect product samples for further analysis or submittal to the lab.
</li><li>Calibrate lab equipment (thermometers, pH meter, salt titrator, brix, hygiena machine, etc.).
</li><li>Complete necessary documentation for QA functions.
</li><li>Enter data accurately into computer database.
</li><li>Place any non-conforming product under QA hold as needed or directed.
</li><li>Work closely with production and maintenance employees as needed to ensure Food Safety and Quality is maintained.
</li><li>Perform weekly and monthly facility inspections.
</li><li>Collect water monthly samples.
</li><li>Communicate information and escalate concerns adequately to QA Coordinator and Manager.
</li><li>Adhere to plant GMPs and safety guidelines.</li></ul><ul><li>
Be able to stand, bend and lift for extended periods of time.
</li><li>Must be able to work in a cool to cold environment (-10&deg;F to 40&deg;F) during an 8&ndash;10-hour shift.</li><li>
Must be able to periodically lift up to 50lbs. from ground level to height of 4&rsquo;.</li><li>
Intermediate math, literacy and computer skills required (English).</li><li>
Allergen &amp; HACCP training required. (Chemical training required if handling sanitation chemicals)</li></ul><p><b>
Additional Notes
</b></p><p><i>May be required to stay past end of shift to assist with daily activities depending on production flow.</i></p></div>

QA Tech I

Specialty Foods Group LLC.

<div><p><b>QA Tech - S</b><b>pecialty Foods Group, LLC Owensboro, KY</b></p><p><br>
In October of 2018, Specialty Food Groups was acquired by Indiana Packers Corporation (IPC) which greatly expanded the market presence. IPC, based out of Delphi, Indiana is a fully integrated retail, foodservice and private label producer of fresh and processed meats company. Since the start of operations in 1991, IPC has experienced rapid growth from a single pork processing company into a multi-plant diversified producer of fresh and processed meats, with locations throughout America's Heartland. Employing more than 3,100 hundred team members, IPC has processing facilities in Frankfort, Indiana, Holland, Michigan, as well as the Owensboro, Kentucky facility. With more than $1.5B in annual sales, we're a big company with a small company culture.</p><p>
Specialty Foods Group, makers of the &quot;Kentucky Legend ham, and part of Indiana Packers Corporation is accepting applications for an experienced Quality Assurance Technician. Specialty Foods Group (SFG) is a leading producer of premium-branded and private label processed meat products in the United States. Our diverse products, including hams, turkey, hot dogs, bacon, and lunch meats are beloved by millions of families across the country. SFG was recently voted the <b><i>&quot;Kentucky Manufacturer of the year for 2020&quot;!</i></b></p><p>
We have an immediate opening for a <i>Quality Assurance Technician</i><b>. </b>This Full-Time (40 hours a week) position will include duties that range from food safety verifications to process capability studies. This chosen candidate must be committed to completing tasks on time and working overtime as be needed to reach goals. Individuals must be able to assure pertinent, accurate and timely collection of data from all processes in the plant to aid operations in decision making, as well as, be continuously striving for improvement.</p><p><b>
Responsibilities:</b></p><ul><li>
Communicate and document process and product requirements, including development and maintenance work of instructions and finished product specifications.
</li><li>Provide quality related training to co-workers and production personnel.
</li><li>Perform job specific work instructions, updates procedures and forms according to document control policies.
</li><li>Perform product and process audits, report status and monitor through resolution.</li><li>
Maintain equipment and in sanitary manner and in accordance with applicable guidelines.
</li><li>Assure label approvals, verifications, and compliance.
</li><li>Assure communication, resolution and documentation of process and procedural deviations in a timely manner.
</li><li>Assure compliance with regulatory requirements and plant policies, including HACCP related activities, GMP and SSOP's.
</li><li>Perform product attribute and sensory evaluations according to finished product specifications.
</li><li>Monitor and resolve product and process deviations related to SSOP's, NR's, Product Complaints, and Non-conforming product</li></ul><p><b>
Supervisory Responsibilities:</b> This position has no supervisory responsibilities</p><p><b>
Qualifications:</b></p><p>
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.</p><p><b>
Education and/or Experience:</b></p><ul><li>
Associates Degree in related field plus two (2) years' related experience, or</li><li>
Four (4) years' experience in related field</li><li>
Demonstrated strong attention to detail</li><li>
Demonstrated objectivity and openness to others' views, receiving and providing feedback in a positive manner.</li><li>
Demonstrated contribution to building a positive team spirit and putting the success of the team above own interests.</li></ul><p>
Specialty Foods Group is an Equal Opportunity Employer (EOE) and values diversity. Our EOE policy not only prohibits discrimination on the basis of race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, veteran status, genetic information, or any protected category under state, local or federal law, but also reflects our commitment to making all employment decisions without regard to an individual's membership in a protected class. This policy relates to all phases of employment, including, but not limited to, recruiting, employment, placement, promotion, transfer, demotion, termination, rates of pay and other forms of compensation, selection for training, the use of all facilities, and participation in company-sponsored employee activities. As part of its equal opportunity policy, we also take affirmative action in accordance with applicable laws to ensure that women, minorities, protected veterans and individuals with disabilities have opportunities to join and progress within the Company.</p><p>
If you require reasonable accommodation in the application process, call SFG Human Resources. All other applications must be submitted online.</p></div>

QA Tech - 1st Shift

EK Machine

<div><div>SUMMARY<br>
<b>Summary:</b><br>
Tests and inspects products at various stages of production process and compiles and evaluates statistical data to determine and maintain quality and reliability of products by performing the following duties.</div>
<div></div><div><b>Essential Responsibilities and Duties:</b></div>
<ul><li>Interprets engineering drawings, schematic diagrams, or formulas and confers with management or engineering staff to determine quality and reliability standards.</li>
<li>Selects products for tests at specified stages in production process and tests products for variety of qualities such as dimensions, performance, and mechanical, electrical, or chemical characteristics.</li>
<li>Creates quality plans based on engineering drawings and specifications.</li>
<li>Selects and uses metrology equipment, including CMM&rsquo;s.</li>
<li>Records test data, applying statistical quality control procedures.</li>
<li>Evaluates data and writes reports to validate or indicate deviations from existing standards.</li>
<li>Recommends modifications of existing quality or production standards to achieve optimum quality within limits of equipment capability.</li>
<li>Prepares customer required quality documentation.</li>
<li>Sets up and performs destructive and nondestructive tests on materials, parts, or products to measure performance, life, or material characteristics.</li>
<li>Prepares graphs or charts of data or enters data into computer for analysis.</li>
<li>Other responsibilities assigned from the Quality Manager</li>
</ul>
<div><br>
<b>Qualifications:</b></div>
<ul><li>High school diploma or GED required.</li>
<li>Detailed orientated</li>
<li>Experience working in Manufacturing (Preferred)</li>
<li>1&ndash;3 months of related experience or training preferred.</li>
<li>Ability to read and understand work instructions, memos, and operating procedures.</li>
<li>Ability to write simple correspondence.</li>
<li>Comfortable communicating one-on-one with team members.</li>
<li>Basic math skills, including addition, subtraction, multiplication, and division using whole numbers, fractions, and decimals.</li>
</ul>
<div><br>
<b>What We Offer:</b></div>
<ul><li>Competitive pay and benefits</li>
<li>Opportunities for training and growth</li>
<li>A supportive, team-focused work environment</li>
<li>Consistent hours and stable workload</li></ul></div>

QA Tech - 3rd Shift

Alvogen

<p></p><div><div><p><b>SUMMARY OF POSITION</b></p></div><p><br>
The QRM (Quality Relationship Manager) Technical Services is a member of the US Quality department. In this position, the QRM will be interacting primarily with Alvogen&rsquo;s external business partners/CMOs. The incumbent will have responsibility for mainly managing products from development to product launch and commercial phase as assigned. QRM is responsible for supporting the technical aspects of the products as well as the adherence to Alvogen&rsquo;s Quality Management System. The position will require in depth knowledge of Quality Systems including activities such as development, validation, troubleshooting/ investigation support, complaint handling, change control, product release, inspection support, etc. The individual will also support the technical transfer of products to/from various CMO&rsquo;s. The individual serves as a critical link to Alvogen&rsquo;s external partners. Being able to effectively communicate and transmit information to/from partners is essential to ensure compliance and optimal performance.</p><p></p><p><b><br>
ORGANIZATION STRUCTURE</b></p><p><br>
The QRM Tech. Services reports directly to the Director Quality, Commercial and Technical Services, Third Party Quality US. There are no reports.</p><p></p><p><b><br>
RESPONSIBILITIES</b></p><p>
Primary responsibilities of this role include, but are not limited to, the following:</p><br>
<p></p><ul><li>
Documentation Review &amp; Approval:</li><li>
Review and approve documentation such as Method Validations, Manufacturing Records, SOPs, Investigations, Change Controls, Validation Reports, Technical reports required for regulatory filing, including but not limited to Extractables/ Leachable studies, Nitrosamine Reports etc, Equipment Qualifications and similar documents as directed by Quality Management.</li><li>
Inspections and Audits:</li></ul><ul><li>
Prepare / Support preparation activities for regulatory inspections</li><li>
Evaluate regulatory agency findings from inspections conducted at CMOs/CPOs/analytical Laboratories, etc.</li></ul><ul><li>
Support the design and implementation of system / process improvements where opportunities are identified (Commercial &amp; Development), including associated CAPA&rsquo;s.</li><li>
Support technical transfer / validation activities with external business partners / CMOs.</li><li>
Manage the Finished Product / Bulk Drug Product ANDA/NDA, Launch Release System:</li></ul><ul><li>
Execute the Alvogen Inc. and Almatica Pharma Inc. material release procedure(s). Manage ANDA/NDA, launch release priorities per business deadlines. Work directly with CMOs and partners to resolve related questions/issues.</li><li>
File, retrieve, and maintain organized records</li></ul><br>
<p></p><ul><li>
Communicate with external business partners / CMOs regarding quality related issues and Quality Agreements.</li><li>
Provide investigation/trouble-shooting support as needed. Review and approve investigations, unexplained discrepancies, failures, and out-of-specification results. Evaluate if there is any quality impact to process/product and take appropriate action.</li><li>
Track metrics for external business partners / CMOs on change controls, deviations, complaints, audits, product releases and rejections and other Third-Party Quality Key Performance Indicators.</li><li>
Change Management Program:</li></ul><ul><li>
Process change controls for all systems requiring change control support (e.g. specifications for raw materials, drug product intermediates and finished drug products, validation protocols and reports, master production and packaging records, cleaning records, and analytical methods).</li><li>
Maintain change control electronic records in EQMS.</li><li>
Review, assess, and approve change controls as required by SOP&rsquo;s.</li><li>
Support training of company personnel on change control system.</li></ul><ul><li>
Support the corporate Training Program, when / if needed.</li><li>
Support the corporate audit program as needed / required.</li><li>
Keeps abreast of industry regulations and cGMP trends. Stays informed of FDA and ICH Guidelines related to GMP (Commercial &amp; Development).</li></ul><p></p><div><p><b><br>
QUALIFICATIONS</b></p></div><p><br>
Position requires the following education and qualification prerequisites:</p><br>
<p></p><ul><li>
Good leadership skills in all areas of communication, influencing, collaboration and decision-making.</li><li>
BS in Pharmacy, Chemistry, Microbiology or Biology with a minimum of 10 years&rsquo; experience in the Pharmaceutical Industry preferred. Other degrees will be considered based on extensive industry experience.</li><li>
Experience in GxP laboratory practices.</li><li>
Release of materials and products supporting both development and commercial activities.</li><li>
Has knowledge of GxP quality systems, US FDA regulations and ICH guidance documents.</li><li>
Experience with various manufacturing / filling processes associated with &lsquo;non-sterile&rsquo; drug products.</li><li>
Demonstrated experience supporting deviations, investigations especially, OOS investigations. Experience in conducting, writing/reviewing deviations and investigations, root cause analyses, and identifying corrective actions. Must have strong technical knowledge of FDA and other regulatory guidance and be able to critically review complex investigations, interpret results and able to evaluate technical input against compliance requirements in line with CFR requirements and other regulatory requirements and Alvogen procedures/policies.</li><li>
Must hold strong interpersonal and communication skills. Must have the ability to work well with diverse groups including the ability to work in a team environment. Must also display strong organizational skills with the ability to lead team meetings and to manage multiple projects at one time.</li><li>
Strong technical writing and computer skills are also required.</li><li>
Must display the ability to work independently with little or no supervision and plan and accomplish set goals.</li></ul><p></p><p><br>
Physical Demand Factors</p><br>
<p></p><ul><li>
While performing the duties of this job, the QRM Tech. Services is required to sit and work at a computer for extended periods of time.</li></ul><br>
<p></p><ul><li>
Is regularly required to talk, listen, and attend meetings / teleconference calls.</li><li>
Approximately 20% business travel required to external Contract Manufacturing Organization (CMO) / Business Partner sites, or to attend professional development training seminars &ndash; as needed / directed.</li></ul><p></p><p><b><br>
GMP DECISION-MAKING AUTHORITY</b></p><p><br>
Independent decision-making activities will be performed by the QRM Tech. Services for all the quality management system elements outlined in the Responsibilities section of this Job Description.</p><p></p><p><i><br>
The anticipated base salary range for this position is $100,000-$135,000. This position is eligible for Alvogen&rsquo;s annual discretionary bonus and comprehensive benefits package, consisting of medical and prescription drug coverage (two PPO plans and an HDHP with Health Savings Account and employer contribution), dental, vision, flexible spending accounts. Alvogen&rsquo;s benefits package also includes a retirement savings program, long-term care coverage, paid time off (176 hours per year, prorated to hire date) inclusive of sick time, disability benefits, life insurance, a wellness program, and 13 company recognized paid holidays per year. We anticipate this position will be posted on March 19, 2026 and remain open for at least 30 days. To apply, select the apply button and submit your application.</i></p><p></p><p><b><br>
An Equal Opportunity Employer, including disability/vets.</b></p></div><p></p>

Quality Relationship Manager, QA Tech Service

WESTROCK COFFEE

<div><div>We are currently seeking a <b>Quality Assurance Technician</b> for our QA Deprtament.
</div><ul><li>Inspect the set-up of all packing lines and grinders at the beginning of the day, verifying the readings and recording the results</li>
<li>Verify, inspect and record all grinder/dump executions and packing line changes during the course of a day</li>
<li>Perform quality checks (roast color, % moisture, grind analysis, dust content, weights, etc.) of product soon after a grinder/packing line has undergone an item change</li>
<li>Document results of quality checks</li>
<li>Identify and segregate nonconforming goods for proper disposition and notify QA Supervisor or Lead QA Technician</li>
<li>Visually inspect returned goods delivered by warehouse and, if necessary, perform analysis on goods and record results</li>
<li>Determine disposition of returned goods</li>
<li>Receive and analyze certain customer complaints</li>
<li>Retrieve production samples (after deemed acceptable) of each blend and forward to Cupping Lab for sensory analysis</li>
<li>Log blend change samples and quality issues for ISO purposes</li>
<li>Ensure physical blend &quot;target&quot; samples are properly maintained and updated</li>
<li>Perform general daily housekeeping in work area to maintain a quality/safe working environment</li>
<li>Collect, organize and set up product samples for sensory cupping</li>
</ul>Requirements:
<ul><li>Computer Skills including Word, Excel, Outlook etc.</li>
<li>Excellent oral and written communication skills</li>
<li>Sound Math skills e.g. Percent Calculations, averages, means, Standard deviation etc.</li>
<li>Able to lift 50 lbs</li>
<li>Proven reliability and responsibility</li>
</ul><div>Equal Opportunity Employer / Vets / Disabled</div></div>

QA Technician

Crider Foods

<div><p><b>Position Summary</b></p>
<p>
The position will conduct inspections and record results on products and facilities.</p><br>
<p></p>
<p><b>
General Purpose</b></p>
<p>
Quality Assurance is a process which requires specific knowledge and skill. Quality Assurance Technicians work across all sectors of manufacturing and are responsible for carrying out checks on products and processes to ensure they meet predetermined quality standards.</p><br>
<p></p>
<p><b>
Position Responsibilities</b></p>
<ul><li>
Crider, Foods requires all employees to comply with and support all Food Safety and Quality policies, programs and procedures to ensure our products meet and exceed consumers&rsquo; expectations.</li><li>
Performing measurement and weight control checks.</li><li>
Performing equipment inspections</li><li>
Performing incoming raw material inspections</li><li>
Check instruments such as temperature gauges at regular intervals.</li><li>
Making sure that machines are always kept clean.</li><li>
Inspection of product labels, MSDS and safe use of chemicals.</li><li>
Recording and maintaining accurate and detailed records.</li><li>
Ensuring GMP&rsquo;s are being properly followed.</li><li>
All other duties as assigned.</li><li>
(In case of absence of key personnel, the job will be filled by a trained employee)</li></ul><br>
<p></p>
<p><b>
Essential Skills and Experience</b></p>
<ul><li>
Successfully passed QA Proficiency Exam.</li><li>
Must be able to read and write English.</li><li>
Maintain a good attendance and performance standard.</li><li>
Excellent communication skills both verbal and written.</li><li>
Optimal organizational skills with a systematic approach to work.</li><li>
Ability to prioritize workloads.</li><li>
Close attention to detail.</li><li>
Ability to work as part of a team.</li><li>
Ability to follow written instruction and to keep accurate records.</li><li>
Ability to act quickly when there is a problem.</li></ul><br>
<p></p>
<p><b>
Preferred Relevant Skills and Experience</b></p>
<ul><li>
College education preferred</li><li>
Minimum high school diploma or equivalent.</li></ul><br>
<p></p>
<p><b>
Positions reporting to this person</b></p>
<p>
None</p><br>
<p></p>
<p><b>
Physical Demands and Work Environment</b></p>
<ul><li>
Able to walk and stand, use arms and legs for long periods of time including wrist turning and finger manipulation.</li><li>
Employee stands frequently with tasks requiring consistent bending, stooping, kneeling, or crawling to complete; Lift, carry and push/pull occasionally of up to 50 pounds is required.</li><li>
While performing the duties of this job, the employee may be exposed to extreme temperature conditions.
</li><li>Job locations can be consistently 40 degrees or below.</li><li>
The noise levels at work are moderate to loud and hearing protection is required.</li></ul><br>
<p></p>
<p><b>
General Sign-Off:</b> The employee is expected to adhere to all company policies and to act as a role model in the adherence to policies. The company reserves the right to modify, interpret, or apply this job description in any way the company desires. This job description in no way implies that these are the only duties, including essential duties, to be performed by the employee occupying this position. This job description is not an employment contract, implied or otherwise. The employment relationship remains &ldquo;AT- WILL.&rdquo; Qualified employees who, because of a physical or mental impairment that significantly limits a major life activity, require a reasonable accommodation to perform the essential functions of this position should notify their Manager or Human Resources.</p><br>
<p></p>
<p><b>
Food Safety Sign-Off: </b>All team members at Crider Foods must adhere to our food safety requirements and must report food safety problems to management. All attempts should be made to ensure that the written and digital records are documented at the time the activity is performed, legible, clear, concise and suitably authorized (not falsified) by those undertaking monitoring (documented work tasks). This position may be responsible for the inspection and verification of records.</p><br>
<p></p>
<p>
&ldquo;<i>We are an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity or expression, pregnancy, age, national origin, disability status, genetic information, protected veteran status, or any other characteristic protected by law&rdquo;.</i></p></div>

Tetra Tech

<div><div><b>The Opportunity:</b></div><div>
Tetra Tech is adding a Senior Advisor &mdash; Nuclear Quality to lead program-level Quality Assurance and Quality Control (QA/QC) for construction, procurement, materials, and vendor management on nuclear, radiological, and industrial projects. The advisor will serve as the Quality Discipline Lead, elevating quality culture, directing audits and vendor surveillance, managing receipt inspection and materials logistics, and providing technical oversight for installations and construction activities.</div><div></div><div><b><br>
Why Tetra Tech:</b></div><div>
At Tetra Tech, we are <i>Leading with Science</i> to solve the world&rsquo;s most complex challenges. Our industry-leading experts in engineering and consulting are committed to driving positive change in communities around the world. For over 50 years, we have been at the forefront of innovation and sustainability. Today we stand as a market leader, offering cutting-edge solutions in water, environment, energy, and international development. Our work has improved more than 625 million lives around the world.</div><div></div><div><b><br>
Your Impact:</b></div><div>
Join Tetra Tech to make a real difference. Our work leverages cutting-edge technologies, advanced analytics, and the expertise of world-class scientists and engineers to create meaningful change around the world. Discover your full potential &ndash; join us to advance your career while leaving a lasting legacy.</div><div></div><div><b><br>
Essential Job Functions:</b></div><ul><li>
Serve as QA Discipline Lead: develop, implement, and maintain nuclear-quality programs, policies, and training to strengthen organizational quality culture.</li><li>
Plan and perform internal and external QA audits and assessments (including lead auditing activities) to ensure compliance with applicable codes, standards, and regulatory requirements.</li><li>
Oversee vendor qualification, vendor surveillance, and supplier assessments for procurement of components and spare parts; review and approve procurement and quality documentation.</li><li>
Manage QC activities during construction and installation projects (e.g., radiological monitoring equipment installation, wind turbine generator installation, landfill cover construction, remediation projects). Provide on-site inspections, nonconformance disposition, and corrective action oversight.</li><li>
Lead materials management tasks: receiving, inspection, storage, shipping, inventory control, export/logistics coordination for sensitive equipment.</li><li>
Develop and deliver QA/QC training (including nuclear-specific QA topics) to project and field staff.</li><li>
Prepare and maintain QA/QC procedures, inspection plans, and reports; interface with program/project management to integrate QA requirements into schedules and budgets.</li><li>
Act as construction QC manager when required: supervise contractors&rsquo; QC programs, conduct surveillance of fabrication and field work, and ensure compliance with contractual and regulatory requirements.</li><li>
Conduct activities in line with internal procedures, legislation, and industry standards.</li><li>
Pursue continuous professional development and maintain a high degree of discipline knowledge and awareness.</li><li>
Work in a safe manner at all times and report all health and safety incidents and concerns.</li><li>
Additional duties as required.</li></ul><div></div><div><b><br>
Required Qualifications:</b></div><ul><li>
Bachelor&rsquo;s degree in Engineering, Environmental Science, or related field</li><li>
15+ years of progressive experience in Quality Assurance/Quality Control, construction management, procurement, or materials management &mdash; preferably including nuclear industry experience.</li><li>
Demonstrated experience performing and leading QA program audits, vendor surveillance, and supplier qualification activities.</li><li>
Experience with receipt inspection, vendor surveillance, and materials/warehouse operations.</li><li>
Familiarity with nuclear-quality standards and regulatory requirements (e.g., 10 CFR 50 Appendix B, ANSI N45.x series).</li><li>
Proven ability to manage procurement documentation, review technical purchase orders, and support contract generation and budget analysis.</li><li>
Must possess a valid driver&rsquo;s license with a clean driving record without restrictions.</li></ul><div></div><div><b><br>
Preferred Qualifications / Certifications:</b></div><ul><li>
ASME &amp; NQA-1 Lead Auditor Certification (or equivalent).</li><li>
Industry-specific certifications such as ANSI N45.2.6 Receipt Inspector or equivalent lead auditor credentials.</li><li>
Training in 10 CFR 50.59 evaluation process, construction quality management (NAVFAC/USACE), auditing methods, and hazmat/radiation worker training.</li><li>
HAZWOPR and DOT hazmat training; First Aid/CPR.</li></ul><div></div><div><b><br>
Experience Requirements (target):</b></div><ul><li>
Nuclear quality program management and nuclear vendor/supplier oversight.</li><li>
Project QC management for installations (electromechanical, radiological monitoring, environmental remediation).</li><li>
Materials logistics and export control coordination for sensitive equipment.</li><li>
Development and delivery of QA/QC training and procedures.</li></ul><div></div><div><b><br>
Core Competencies:</b></div><ul><li>
Leadership of QA teams and cross-functional project groups.</li><li>
Auditing and assessment expertise.</li><li>
Vendor management and supplier qualification.</li><li>
Inspection, testing, and nonconformance management.</li><li>
Strong written and verbal communication; technical report preparation.</li><li>
Safety and regulatory compliance mindset (radiological and hazardous materials awareness).</li></ul><div></div><div><b><br>
Working Conditions &amp; Travel</b></div><div>
Field inspections and periodic international/domestic travel to installation sites and vendor facilities may be required.</div><div></div><div><b><br>
Life at Tetra Tech:</b></div><div>
The perks of working at Tetra Tech include:</div><ul><li>
Comprehensive and market-competitive benefits.</li><li>
Medical benefits, workers compensation insurance, and 401(k) plan.</li><li>
Merit-based financial rewards.</li><li>
Flexibility and company-wide commitment to work/life balance.</li><li>
Collaborative team atmosphere that values the contributions of all employees.</li><li>
Learning and development opportunities for ongoing professional growth.</li></ul><div></div><div><br>
A pre-employment drug screen in compliance with federal regulations is required, along with a physical if needed.</div><div></div><div><b><br>
Compensation:</b></div><div>
Pay commensurate with experience.</div><div>
Pay Range: $72.14 &ndash; $86.57 hourly</div><div></div><div><br>
Pay Range - There are multiple factors that are considered in determining final pay for a position, including, but not limited to, relevant work experience and demonstrated work experience in the above role; skills, certifications, and competencies that align to the specified role; geographic location; and education, as well as contract provisions regarding labor categories that are specific to the position.</div><div></div><div><i><br>
At Tetra Tech, health and safety play a vital role in our success. Tetra Tech&rsquo;s employees work together to comply with all applicable health &amp; safety practices and protocols, including public health orders and regulations that are mandated by local, state, provincial, federal, international authorities, and clients.</i></div>
<div><div><b>About Tetra Tech:</b></div><div>
Tetra Tech is the leader in water, environment, and sustainable infrastructure, providing high-end consulting and engineering services for projects worldwide. With 30,000 employees working together, Tetra Tech provides clear solutions to complex problems by <i>Leading with Science</i><i>&reg;</i> to address the entire water cycle, protect and restore the environment, design sustainable and resilient infrastructure, and support the clean energy transition.</div><div></div><div><br>
Tetra Tech is proud to be an Equal Opportunity Employer. All qualified candidates will be considered without regard to race, color, religion, national origin, age, disability, sex, marital or familial status, status as a protected veteran, or any other characteristic protected by law. Tetra Tech is a VEVRAA federal contractor and we request priority referral of veterans.</div><div></div><div><br>
We invite applications from all interested parties.</div><div></div><div><br>
Explore our open positions at https://www.tetratech.com/careers. Follow us on social media to learn more about our people, culture, and opportunities:</div><div>
LinkedIn: @TetraTechCareers</div><div>
X (Twitter): @TetraTechJobs</div></div></div>

Senior Advisor – Nuclear Quality (Richland, WA)

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QA Technician

Senior Advisor – Nuclear Quality (Richland, WA)