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<h3>Job Description</h3>
Job DescriptionJob Title: Quality Assurance Technician Job Description
As a Quality Assurance Technician, you will be responsible for reviewing compliance documentation related to raw materials, in-process samples, and finished product analyses. You will monitor adherence to current Good Laboratory Practices (cGLP) by laboratory personnel during routine operations to ensure procedural compliance. Additionally, you will verify that laboratory chemicals, reagents, and standards are properly labeled in accordance with standard operating procedures (SOPs).
Responsibilities
<ul>
<li>Review laboratory audit trails during data assessments to ensure alignment with SOPs.</li>
<li>Coordinate with Analytical Laboratory Teams to compile and provide necessary documentation to cross-functional teams.</li>
<li>Manage incoming documentation, including tracking, recording, storing, and archiving in an organized manner.</li>
<li>Identify system gaps during routine monitoring and notify supervisors of areas requiring improvement.</li>
<li>Understand laboratory equipment operation, qualification, and calibrations, including their software audit trail reviews.</li>
<li>Actively participate in the review of data related to laboratory investigations and incidents to ensure regulatory compliance.</li>
<li>Support departmental and cross-functional initiatives and complete assignments as directed by the manager or supervisor.</li>
</ul>
Essential Skills
<ul>
<li>Strong documentation and technical writing skills, with the ability to apply relevant scientific principles and practices.</li>
<li>Ability to work under minimal supervision, independently, and in a team environment.</li>
<li>Proficiency in computer skills and software applications such as Microsoft Office tools and Quality applications and software programs.</li>
<li>Experience in analytical quality assurance with a focus on inhalation products (MDI) is a plus.</li>
<li>Effective interpersonal relationship skills and the ability to work in a team environment.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Possess a minimum bachelor's degree in Chemistry, Pharmaceutical Sciences, or related field from an accredited institution. A master's degree is preferred.</li>
<li>A minimum of 1-3 years of experience in analytical quality assurance.</li>
<li>Proficiently speak English as a first or second language and ability to read, write, and communicate effectively.</li>
<li>Self-starter with the initiative to seek additional training or direction as needed.</li>
<li>Knowledge and experience with analytical laboratory activities in areas such as active pharmaceutical ingredients (API), drug products, analytical development, Quality Control (QC), Good Laboratory Practices (GLP)/Good Manufacturing Practices (GMP)/Good documentation Practices (GDP).</li>
<li>Willingness to work any assigned shift ranging from first or second shift; work schedules may be Monday to Friday.</li>
</ul>
Work Environment
Work primarily during the first shift from 8:30 AM to 5:00 PM, Monday to Friday. You will be part of a supportive team of 15-20 people, collaborating with the manufacturing team. Reporting directly to the QA Manager, you will be required to stand or walk unassisted for 75% or more of an 8-hour period and may need to lift up to 10 kg unassisted. Appropriate personal protective equipment must be worn when required. You will spend considerable time sitting at a desk and working at a computer or other screens.
Pay and Benefits
The pay range for this position is $62000.00 - $75000.00/yr.
Health, Vision, Dental, 401K
Workplace Type
This is a fully onsite position in Fall River,MA.
Application Deadline
This position is anticipated to close on Jul 30, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email <a href="mailto:actalentaccommodation@actalentservices.com" target="_blank">actalentaccommodation@actalentservices.com</a> for other accommodation options.

Analytical Quality Assurance Associate

<h3>Job Description</h3>
Job DescriptionJob Title: Technical ManagerJob Description
The Experienced Technical Manager (Cell Lead) is responsible for driving results in a fast-paced environment by directing all product development team activities. This role involves coordinating the direction of the development program through development and production, including Chemistry, Analytics, Engineering, and Solid State Chemistry. The incumbent will play a key role in external communication with customers, supporting the Project Manager and ensuring the collaborative development and performance of the work cell team members.
Responsibilities
<ul>
<li>Lead the execution and supervision of process development and design to ensure an effective right-first-time control strategy in production.</li>
<li>Keep project documentation and deliverables up-to-date with relevant data pertaining to research and production.</li>
<li>Maintain responsibility for the scientific substance of projects, ensuring team accountability to functional standard work deliverables and their integration with other development functions.</li>
<li>Foster a culture of innovation to add value to the customer's program.</li>
<li>Coordinate the generation of updates, reports, protocols, and governance packages, ensuring scientific and executional accuracy.</li>
<li>Ensure appropriate technical and project escalation occurs when necessary.</li>
<li>Participate in meetings by telephone with the customer.</li>
<li>Ensure readiness of development outputs and drive deliverables with the team for manufacturing readiness.</li>
</ul>
Essential Skills
<ul>
<li>Proficiency in Analytical Chemistry, Chemistry, and Management.</li>
<li>Bachelor’s Degree in Chemistry, Pharmaceutical Sciences, or Chemical Engineering required; Master's or PhD preferred.</li>
<li>7-10 years of experience in a pharma, biotech, or regulated industry.</li>
<li>Experience in a Contract Development and Manufacturing Organization (CDMO) preferred.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Pharmaceutical industry experience, preferably in a smaller setting rather than a large corporation.</li>
</ul>
Work Environment
The Senior Technical Manager will work in various areas within the facility as needed, leading a team of approximately 10-11 people. The role offers a 5% bonus based on team success and a high opportunity for advancement into the executive team.
Pay and Benefits
The pay range for this position is $100000.00 - $130000.00/yr.
When hired they will receive a 5% bonus. They have PTO, holiday, health, dental vision and several other benefits.
Workplace Type
This is a fully onsite position in Germantown,WI.
Application Deadline
This position is anticipated to close on Aug 8, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email <a href="mailto:actalentaccommodation@actalentservices.com" target="_blank">actalentaccommodation@actalentservices.com</a> for other accommodation options.

Technical Manager

<h3>Job Description</h3>
Job DescriptionQuality Technician
Responsibilities 
<ul>
<li>Verify line clearance prior to startup.</li>
<li>Perform equipment swabbing after sanitation.</li>
<li>Conduct quality audits for each production line throughout the shift.</li>
<li>Document in-line process check results per pre-approved specifications.</li>
<li>Report any out-of-specification or non-conformance issues.</li>
<li>Ensure immediate corrective action is completed before startup for non-conformance.</li>
<li>Label and store non-compliant products following MRB process.</li>
<li>Conduct periodic quality and GMP audits of the production area.</li>
<li>Audit ingredients staged for manufacturing to ensure no expired materials are used.</li>
<li>Perform temperature audits of ingredients, WIP, and finished products.</li>
<li>Prepare shift report for next shift follow-up.</li>
<li>Conduct case count audits on all products.</li>
<li>Perform daily pre-operational inspections.</li>
<li>Assist in metal detector validations and line checks.</li>
<li>Ensure operators follow metal detector SOP.</li>
<li>Report any food safety risks to the supervisor.</li>
<li>Collect samples from raw materials, in-process, and finished products for lab testing.</li>
</ul>
Qualifications 
<ul>
<li>1 year of experience in food manufacturing quality.</li>
<li>Demonstrated GMP experience.</li>
<li>Ability to work cross-functionally with other departments and in a team setting. </li>
<li>Ability to work in a fast paced environment. </li>
</ul>
About Actalent
Actalent connects passion with purpose. We help visionary companies advance their engineering and science initiatives through access to specialized experts that drive scale, innovation, and speed to market. With a network of almost 30,000 engineering and sciences consultants and more than 4,500 clients across the U.S., Canada, Asia, and Europe, Actalent serves many of the Fortune 500. An operating company of Allegis Group, the global leader in talent solutions, Actalent launched as a new specialized engineering and sciences services and workforce solutions brand in 2021.
Diversity, Equity &amp; Inclusion
At Actalent, Diversity And Inclusion Are a Bridge Towards The Equity And Success Of Our People. DE&amp;I Are Embedded Into Our Culture Through:
<ul>
<li>Hiring diverse talent</li>
<li>Maintaining an inclusive environment through persistent self-reflection</li>
<li>Building a culture of care, engagement, and recognition with clear outcomes</li>
<li>Ensuring growth opportunities for our people</li>
</ul>
Pay and Benefits
The pay range for this position is $20.00 - $20.00/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
 • Medical, dental &amp; vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in Manteno,IL.
Application Deadline
This position is anticipated to close on Aug 7, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email <a href="mailto:actalentaccommodation@actalentservices.com" target="_blank">actalentaccommodation@actalentservices.com</a> for other accommodation options.

Quality Technician

<h3>Job Description</h3>
Job DescriptionJob Title: Test Technician Job Description
As a Technician I, you will be responsible for performing set-up, calibration, testing, and troubleshooting of circuits, components, instruments, and mechanical assemblies. You will engage in testing and troubleshooting assemblies and final systems, including more complex systems and mechanical assemblies. Follow test process instructions and determine test specifications, methods, and procedures from statements of work.
Responsibilities
<ul>
<li>Perform set-up, calibration, testing, and troubleshooting of circuits, components, instruments, and mechanical assemblies.</li>
<li>Test and troubleshoot assemblies and final systems.</li>
<li>Engage in the set-up and testing of complex systems and mechanical assemblies.</li>
<li>Follow test process instructions and determine test specifications from statements of work.</li>
<li>Complete rework on assemblies and systems.</li>
<li>Prepare technical reports summarizing findings and recommending solutions to technical problems.</li>
<li>Perform additional tasks such as unpacking, packaging, placing labels, and crating.</li>
<li>Execute any other tasks assigned.</li>
</ul>
Essential Skills
<ul>
<li>Proficiency in troubleshooting, reworking, and using test equipment.</li>
<li>Experience in hardware and software testing and installation.</li>
<li>Strong computer skills, including downloading software and troubleshooting software and hardware.</li>
<li>Knowledge in electronics, schematics, blueprints, and familiarity with Linux and C++.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Strong attention to detail.</li>
<li>Good written and verbal communication skills.</li>
<li>Knowledge of basic office applications, such as word processors, spreadsheets, and databases.</li>
<li>Familiarity with troubleshooting or networking computer components.</li>
<li>Ability to regularly lift, push, and move up to 50 pounds.</li>
<li>Ability to stand for prolonged periods.</li>
<li>Capability to work on ladders or stools.</li>
</ul>
Why Work Here?
Enjoy long-term employment with weekly attendance bonuses, high security, and a clean work environment. Experience career advancement in a supportive, innovative setting.
Work Environment
Work in multiple buildings within a large company with room for advancement and promotions. Be a part of a team that values collaboration, innovation, and thought leadership in a fast-changing, high-growth technology environment. The work environment requires standing for long periods, ESD precautions, and loud ear protection.
Job Type &amp; Location
This is a Contract position based out of Fremont, California.
Pay and Benefits
The pay range for this position is $23.50 - $25.00/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
 • Medical, dental &amp; vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in Fremont,CA.
Application Deadline
This position is anticipated to close on Aug 9, 2025.
About Aerotek:
We know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meets their goals, skills and interests. Since 1983, we have provided a variety of career opportunities across North American industry – from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role solving for companies’ construction, manufacturing and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are everything spirit to the test as your career continues to grow.
Aerotek offers weekly pay, employee benefits including medical, dental &amp; vision, life insurance, health advocacy and employee assistance programs, a 401(k) plan, and employee discounts.
The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
Company DescriptionWe know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meet their goals, skills, and interests. Since 1983, we have provided a variety of career opportunities across North American industry – from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role in solving companies’ construction, manufacturing, and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are-everything spirit to the test as your career continues to grow. 
<h3>Company Description</h3>
We know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meet their goals, skills, and interests. Since 1983, we have provided a variety of career opportunities across North American industry – from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role in solving companies’ construction, manufacturing, and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are-everything spirit to the test as your career continues to grow.

Test Technician

<h3>Job Description</h3>
Job Description
🔍 Now Hiring: Quality Inspector – Loves Park &amp; South Beloit, IL
Pay:$19–$24/hr (Based on experience)
Schedule: Full-time | Multiple shifts available
Location :Clients in Loves Park and South Beloit, IL
Are you an experienced Quality Inspector looking for your next opportunity? We’re hiring for several clients in the Loves Park and South Beloit areas who are seeking detail-oriented professionals to join their teams.
✅ Responsibilities:
<ul>
<li>Perform visual and mechanical inspections of parts and products</li>
<li>Use measurement tools such as calipers, micrometers, and gauges</li>
<li>Document inspection results and maintain quality records</li>
<li>Identify and report non-conformities</li>
<li>Work closely with production and engineering teams to ensure quality standards</li>
</ul>
🔧 Requirements:
<ul>
<li>Previous experience as a Quality Inspector is required</li>
<li>Familiarity with inspection tools and quality documentation</li>
<li>Strong attention to detail and problem-solving skills</li>
<li>Ability to read and interpret technical drawings and specifications</li>
</ul>
💼 Why Apply?
<ul>
<li>Competitive pay based on experience</li>
<li>Opportunities for long-term placement</li>
<li>Supportive team environment</li>
<li>Positions available immediately</li>
</ul>
 
Pay and Benefits
The pay range for this position is $18.00 - $18.00/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
 • Medical, dental &amp; vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in South Beloit,IL.
Application Deadline
This position is anticipated to close on Jul 31, 2025.
About Aerotek:
We know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meets their goals, skills and interests. Since 1983, we have provided a variety of career opportunities across North American industry – from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role solving for companies’ construction, manufacturing and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are everything spirit to the test as your career continues to grow.
Aerotek offers weekly pay, employee benefits including medical, dental &amp; vision, life insurance, health advocacy and employee assistance programs, a 401(k) plan, and employee discounts.
The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
Company DescriptionWe know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meet their goals, skills, and interests. Since 1983, we have provided a variety of career opportunities across North American industry – from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role in solving companies’ construction, manufacturing, and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are-everything spirit to the test as your career continues to grow. 
<h3>Company Description</h3>
We know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meet their goals, skills, and interests. Since 1983, we have provided a variety of career opportunities across North American industry – from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role in solving companies’ construction, manufacturing, and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are-everything spirit to the test as your career continues to grow.

<h3>Job Description</h3>
Job DescriptionQuality TechnicianJob Description
We are seeking a dedicated Technician to perform daily evaluations and approvals of finished products, process quality checks, and routine product testing. This role requires responsible operating equipment calibration, troubleshooting, and documentation. The Technician will conduct ingredient inspections, packaging inspections, inventory control, and maintain sample archives. Accurate recording of test results and effective communication with operating departments and management are crucial. The role also involves performing in-process quality checks, collecting test samples, troubleshooting equipment, and performing mechanical maintenance. A commitment to maintaining a clean and safe laboratory environment is essential.
Responsibilities
<ul>
<li>Perform daily evaluation and approval of finished products and process quality checks.</li>
<li>Conduct basic microbiological testing.</li>
<li>Calibrate equipment, troubleshoot issues, and calculate dilutions.</li>
<li>Inspect ingredients and packaging, manage inventory, and maintain sample archives.</li>
<li>Conduct laboratory tests including solvent extraction, sieving, pH etc.</li>
<li>Test raw ingredients and finished packaged products.</li>
<li>Record test results and communicate with operating departments and management.</li>
<li>Perform in-process quality checks and collect test samples.</li>
<li>Troubleshoot equipment and perform mechanical maintenance.</li>
<li>Maintain a clean and safe laboratory work environment.</li>
</ul>
Essential Skills
<ul>
<li>0-2 years of production experience.</li>
<li>Background in food manufacturing.</li>
</ul>
Pay and Benefits
The pay range for this position is $19.00 - $19.00/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
 • Medical, dental &amp; vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in Saint Joseph,MO.
Application Deadline
This position is anticipated to close on Aug 8, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email <a href="mailto:actalentaccommodation@actalentservices.com" target="_blank">actalentaccommodation@actalentservices.com</a> for other accommodation options.

<h3>Job Description</h3>
Job Description Description:
Position Summary:
The Quality Systems Specialist works with management and staff to ensure that the organization's quality systems are effectively implemented and maintained. The Quality Systems Specialist will be responsible for overseeing and managing the company's quality management systems in compliance with ISO 17020, ISO 17025, and ISO 17065 standards.
 
Position Responsibilities: 
<ul>
<li>Responsibility for the integrity and efficacy of ICC Conformity Assessment Group's quality systems, including ICC-ES' test labs and surveillance quality systems.</li>
<li>Ensure company's quality management systems remain compliant with ISO 17020, ISO 17025, and ISO 17065 standards.</li>
<li>Develop and maintain quality-system manuals, standard operating procedures, and other essential documents.</li>
<li>Conduct internal audits to ensure compliance of operations with the documented quality systems. </li>
<li>Provide reports to the ICC-NTA President and management on the performance of the quality systems.</li>
<li>Establish records on internal deficiencies and their resolution.</li>
<li>Resolve complaints from outside sources.</li>
<li>Collect and analyze information on client satisfaction, utilizing the results to promote, throughout the organization, a sensitivity to client requirements.</li>
<li>Maintain ICC Conformity Assessment Group, including ICC-ES' test labs and surveillance accreditations, and coordinate activities as necessary with accreditation bodies.</li>
<li>Travel as necessary for accreditation activities and to ensure smooth operation of the quality systems throughout the organization.</li>
<li>Perform other tasks as may be directed by the Conformity Assessment Group Presidents or Sr. VP, Quality System</li>
</ul>
 
Requirements:
Essential Skills and Education / Experience:
<ul>
<li>Bachelor's degree in Engineering, Quality Management, or a related field (Master's degree preferred). </li>
<li>Completion of ISO 9001 training/internal auditing course given by a nationally recognized training organization (or equivalent knowledge/experience).</li>
<li>Demonstrated knowledge of quality systems, including the creation and maintenance of quality documentation. </li>
<li>In-depth knowledge of ISO/IEC 17065, ISO/IEC 17025 and ISO/IEC 17020 (latest versions) and accreditation requirements for various ICC Conformity Assessment Group programs.</li>
<li>Certifications are preferred.</li>
<li>Ability to prepare and present clear and concise written and oral reports.</li>
<li>Ability to facilitate efficient and effective assessments of quality systems.</li>
<li>Ability to train and lead staff in activities related to the quality systems, and in the preparation and presentation of written materials. </li>
<li>Familiarity with the International Family of Codes and relevant test standards and ICC-ES Acceptance Criteria is desired.</li>
</ul>
ICC Family of Solutions offers a competitive starting salary and comprehensive benefits package that includes paid vacation and sick time, health/dental/vision insurance, 401k with generous company match, company paid basic life insurance, short-term and long-term disability coverage. Additional voluntary benefit offerings are available. 
 
Compensation details: 85000-105000 Yearly Salary
 
PI26dde8e97ac3-25405-38128735

Quality Systems Specialist

<h3>Job Description</h3>
Job DescriptionJob Title: QA Specialist Job Description
This position requires reviewing label content to ensure accuracy, consistency, and compliance. The role involves using labeling software to prepare and submit SPL, collaborating with customers for private labeling, and communicating labeling requirements and timelines to internal stakeholders.
Responsibilities
<ul>
<li>Coordinate label approvals and manage version controls and updated labeling.</li>
<li>Support change control processes related to labeling updates.</li>
<li>Coordinate labeling projects to ensure regulatory compliance.</li>
<li>Facilitate project completion through effective and detailed project management.</li>
<li>Provide guidance to team members on labeling regulations and process requirements.</li>
<li>Initiate, review, and implement label creation/updates with extreme attention to detail.</li>
<li>Identify and recommend process improvements to enhance business practices.</li>
<li>Provide regular updates regarding labeling projects to cross-functional departments.</li>
<li>Foster collaborative, efficient, and effective working relationships with internal teams.</li>
<li>Prepare and submit Annual Reports.</li>
<li>Mentor team members and act as a recognized resource to local team.</li>
<li>Perform other duties as assigned based on business requirements.</li>
</ul>
Essential Skills
<ul>
<li>Quality assurance expertise.</li>
<li>Knowledge of FDA regulations.</li>
<li>Understanding of SOPs.</li>
<li>Ability to partner with members across departments like Regulatory and Quality to ensure compliance.</li>
<li>Proficient knowledge of GMP and Quality Management Systems.</li>
<li>Computer literacy in Windows applications and MS Office (Word, Excel, Outlook).</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>A minimum of a BS in a scientific discipline.</li>
<li>1-3 years of experience in pharmaceutical manufacturing.</li>
<li>1-2 years of quality experience with pharmaceutical FDA submissions.</li>
</ul>
Work Environment
This role operates within a GMP environment on the QA team, offering room for growth. The position requires collaboration with teams based both in the US and India.
Pay and Benefits
The pay range for this position is $80000.00 - $87000.00/yr.
401k is really great! We offer 3% contribution regardless of contribution and offer an additional match up to 1.5%. So if they contribute 1.5% they get 6% toward 401k.
Workplace Type
This is a fully onsite position in Basking Ridge,NJ.
Application Deadline
This position is anticipated to close on Jul 31, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email <a href="mailto:actalentaccommodation@actalentservices.com" target="_blank">actalentaccommodation@actalentservices.com</a> for other accommodation options.

QA Specialist

<h3>Job Description</h3>
Job Description Wagstaff Description:
Wagstaff Applied Technologies manufactures equipment for the nuclear industry. 
 
Pay: $29.55- $39.98 per hour, depending on experience
 
As an employee of Wagstaff, you'll enjoy:
Paid non-working holidays
Monthly, site-wide BBQs
Up to 8% retirement contribution
Annual bonus program
1200 Sqft onsite gym, accessible 24/hrs a day
Family-friendly, company-wide events
 
To view our full benefits summary, please visit <a href="https://www.wagstaff.com/Wagstaff/Careers.htm" target="_blank">https://www.wagstaff.com/Wagstaff/Careers.htm</a>
Want to learn more about Wagstaff AT? Visit <a href="https://www.WagstaffAT.com" target="_blank">https://www.WagstaffAT.com</a>
 
Job Summary
Perform inspections of electrical control panels and equipment utilizing knowledge of UL 508A and the National Electric Code (NFPA 70). 
Primary Job Responsibilities
<ul>
<li>Read, understand, and interpret electrical drawings.</li>
<li>Conduct documented inspections of control panels and equipment to ensure compliance with drawings, specifications and codes </li>
<li>Complete quality documentation as applicable to the inspection</li>
<li>Electrically and mechanically test, calibrate and perform various quality control and process control functions on finished product</li>
<li>Review customer provided electrical designs and specifications and turn them into packages necessary for equipment production.</li>
<li>Create bills of material in the ERP system</li>
<li>Review customer designs for compliance with UL 508 A and the National Electric Code, bringing any nonconformance's to the attention of the project manager.</li>
<li>Identify potential design, reliability and functionality issues and provide possible solutions that minimize impact on productivity, production schedules and or the customer.</li>
<li>Accurately estimate hours to complete production tasks.</li>
<li>Represent Wagstaff AT when interacting with auditors, customers, suppliers and visitors</li>
<li>Abide by company policies</li>
<li>In order to achieve business objectives, work weeks in excess of 40 hours may be required </li>
<li>Other duties as assigned</li>
</ul>
Requirements:
<ul>
<li>Minimum of 4 years' experience as an industrial electrician. </li>
<li> Current journeyman electrician license preferred </li>
<li> Demonstrated working knowledge of UL 508A and the National Electric Code</li>
<li> Prior experience in electrical inspection preferred.</li>
<li> Detail oriented, accurate, and thorough</li>
</ul>
Working Environment
While performing the duties of this job, work is performed primarily in an adequately lit, well ventilated, climate controlled general office environment. Close computer work is regularly required. The work usually involves minimal physical exertion. The noise level in the general office environment is usually moderate. 
This job may require occasional or more frequent interaction with employees on the manufacturing shop floor. While on the shop floor, the employee may be exposed to fumes, airborne particles, toxic or caustic chemicals, risks of moving equipment and parts, and other risks associated with a manufacturing environment. Because of this environment and associated risks, coordination with shop floor managers/employees may be necessary before entering the shop floor, and use of job appropriate personal protective equipment and clothing is required on the shop floor. The noise level on the shop floor is often loud.
 
Employment at Wagstaff is dependent on successfully passing a company-paid drug screening and background check upon hire. Benefits eligibility is subject to the terms and conditions of the applicable policies, plans and programs of Wagstaff.
 
Wagstaff is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, pregnancy, genetic information, disability, status as a protected veteran, or any other protected category under applicable federal, state, and local laws.
 
PM22
 
Compensation details: 29.55-39.98 Hourly Wage
 
PI1e1b0ec00299-25405-37967206

Quality Assurance Electrical Inspector - AT

<h3>Job Description</h3>
Job DescriptionJob Title: QA Inspector Job Description
The QA Inspector ensures that all products released for distribution comply with applicable specifications. This role involves managing materials in the warehouse to ensure they are appropriately identified as to status and stored correctly. The QA Inspector is responsible for verifying that only released materials are used in production and that all materials are appropriately sampled, tested, and meet specifications before their use in production.
Responsibilities
<ul>
<li>Assure compliance with applicable SOPs.</li>
<li>Ensure manufacturing complies with Batch Record Instructions and requirements.</li>
<li>Receive and sample all raw materials and components for appropriate testing.</li>
<li>Quarantine and release finished products for shipping.</li>
<li>Ensure all items in the plant, including raw materials, components, packaging, labels, finished products, reject materials, and rework materials, are appropriately labeled and stored according to SOPs.</li>
<li>Administer the label program.</li>
<li>Inspect production lines.</li>
<li>Conduct appropriate sampling, storage, and status labeling of pallets of incoming materials until tested for compliance with specifications and released for use.</li>
<li>Conduct appropriate sampling and storage of finished products until tested and released for production.</li>
<li>Review batch records to ensure only released ingredients, components, and labeling are used in production.</li>
<li>Assist the Quality Manager in product investigations where deviations have occurred in manufacturing, or complaints or product failures have been reported.</li>
<li>Maintain label inventory, issue labels to production, return labels to inventory, and facilitate reconciliation of label inventory.</li>
<li>Inspect production lines, checking for PPE, labels, codes, weights, and compliance with product specifications.</li>
</ul>
Essential Skills
<ul>
<li>1+ years of quality inspection experience in a GMP environment required, 3+ years preferred.</li>
<li>HS Diploma required.</li>
<li>Proficient computer skills to work within the QMS/Database, including basic skills or experience in a similar system like SAP or equivalent ERP.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Experience in quality assurance, quality inspection, and quality check processes.</li>
</ul>
Work Environment
The QA Inspector will work primarily Monday through Friday from 8:00 AM to 4:30 PM, with moderate overtime of 4-6 hours weekly. There is a possibility of Saturday work, typically one Saturday a month. The team consists of three inspectors and a supervisor, interfacing with production and warehouse personnel. Sampling duties are typically performed one day a week, constituting 80% of the workday compared to 20% in the office. Other days will involve 70% office release work and 30% inspections and auditing in production/warehouse environments. The work environment can be dusty due to the powdered products or animal feed-based products. The role offers 6 paid holidays and 40 hours of PTO, with a plan for conversion at the end of the assignment as there is an open headcount already approved.
Pay and Benefits
The pay range for this position is $22.00 - $26.00/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
 • Medical, dental &amp; vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in Saint Louis,MO.
Application Deadline
This position is anticipated to close on Aug 5, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email <a href="mailto:actalentaccommodation@actalentservices.com" target="_blank">actalentaccommodation@actalentservices.com</a> for other accommodation options.

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