5,452 Quality Control Specialists jobs in the United States

**Quality Control Specialist**
Kelly® Science & Clinical is seeking a Quality Control Specialist for **a 6-month contract** position at **a premier biotech** company in **Redwood City, CA** . If you're passionate about bringing the latest scientific discoveries to life and are ready to take the next step in your career, trust The Experts at Hiring Experts.
**Pay Rate:**
$65-75/hour
**Overview** :
In this role, you will support the implementation and configuration of Veeva LIMS in the QC laboratory, create and revise SOPs, and assist with day-to-day lab operations and data integrity.
**Schedule:**
Monday-Friday, standard working hours
**Responsibilities:**
+ Support the implementation and configuration of Veeva LIMS and Blue Mountain systems in the QC laboratory.
+ Create and revise standard operating procedures (SOPs) related to stability, validation, and test methods.
+ Perform routine lab activities, including data review, laboratory maintenance, sample receipt and disposal, and chart recorder upkeep.
+ Assist with laboratory investigations, OOT/OOS deviations, change controls, and CAPAs.
+ Collaborate closely with the QC team to ensure smooth system integration and effective documentation.
+ Other duties as assigned.
**Qualifications:**
+ BS in Analytical Chemistry, Biochemistry or Biological Sciences or equivalent
+ 8+ years of industrial Quality Control experience
+ Strong knowledge in QC lab related processes, GDP, and data integrity
+ Strong working knowledge and hands-on experience with Veeva LIMS
**What happens next:**
Once you apply, you'll proceed to next steps if your skills and experience look like a good fit. But don't worry - even if this position doesn't work out, you're still in our network. That means our team of expert Science & Clinical recruiters will have access to your profile, making your opportunities limitless.
As part of our promise to talent, Kelly supports those who work with us through a variety of benefits, perks, and work-related resources. Kelly offers eligible employees voluntary benefit plans including medical, dental, vision, telemedicine, term life, whole life, accident insurance, critical illness, a legal plan, and short-term disability. As a Kelly employee, you will have access to a retirement savings plan, service bonus and holiday pay plans (earn up to eight paid holidays per benefit year), and a transit spending account. In addition, employees are entitled to earn paid sick leave under the applicable state or local plan. Click here ( for more information on benefits and perks that may be available to you as a member of the Kelly Talent Community.
Why Kelly ® Science & Clinical?
Kelly Science & Clinical is your connection to premier scientific and clinical companies looking to hire industry experts just like you. Our team creates expert talent solutions to solve the world's most critical challenges. Every day, we match science professionals with dream jobs that fit their skills, interests, and career goals-it's the way we think job searching should be. Nearly 100 percent of our science recruiters have a professional background and education in science, so we know a thing or two about the science market and how to get your expertise noticed.
About Kelly
Work changes everything. And at Kelly, we're obsessed with where it can take you. To us, it's about more than simply accepting your next job opportunity. It's the fuel that powers every next step of your life. It's the ripple effect that changes and improves everything for your family, your community, and the world. Which is why, here at Kelly, we are dedicated to providing you with limitless opportunities to enrich your life-just ask the 300,000 people we employ each year.
Kelly is committed to providing equal employment opportunities to all qualified employees and applicants regardless of race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, age, marital status, pregnancy, genetic information, or any other legally protected status, and we take affirmative action to recruit, employ, and advance qualified individuals with disabilities and protected veterans in the workforce. Requests for accommodation related to our application process can be directed to the Kelly Human Resource Knowledge Center. Kelly complies with the requirements of California's state and local Fair Chance laws. A conviction does not automatically bar individuals from employment. Kelly participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S.
Kelly Services is proud to be an Equal Employment Opportunity and Affirmative Action employer. We welcome, value, and embrace diversity at all levels and are committed to building a team that is inclusive of a variety of backgrounds, communities, perspectives, and abilities. At Kelly, we believe that the more inclusive we are, the better services we can provide. Requests for accommodation related to our application process can be directed to Kelly's Human Resource Knowledge Center. Kelly complies with the requirements of California's state and local Fair Chance laws. A conviction does not automatically bar individuals from employment.

With Staff Management | SMX, you'll get a weekly paycheck, learn new skills, meet new people, and work with a great management team in a clean and safe environment.
Looking for your next opportunity? Join Staff Management | SMX as a Quality Control Specialist in Gardena, CA! We're seeking detailed-oriented individuals to support our client's Airport Cargo operations.
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Perks & Benefits: Paid Training, Weekly paychecks, Direct Deposit or Cash Card pay options, Medical / Dental Insurance, Paid Sick Leave, Paid Time Off, Referral Bonus (Restrictions Apply).
Bonus: Bonus is per eligibility requirements.
Shifts: All Shifts, Rotating Shifts.
Employment Types: Full Time, Seasonal, Temporary or Contract, Long Term.
Pay Rate: $19.50 - $2.00 / hour
Duties:
+ Verify assembly compliance to airline/company specifications.
+ Flight is assembled in the correct equipment type.
+ Crew meal count and special dietary specification are correct.
+ All components, entrees, or supply/beverage item are complete.
+ Initiate the correction of missing or wrong items packed with assembly team members and capture the actions taken in QC tracking system (Smartsheet).
+ Partner with assembly leadership to initiate proactive coaching sessions to mitigate repeat defects.
+ Weekly check-ins with CI and Department Manager(s) to discuss defect trends and additional actions needed by department leadership to correct.
+ Other duties as assigned by CI Manager.
.
Position Requirements:
**QUALIFICATIONS:**
+ Basic math skills (add, subtract, multiply, divide).
+ Problem-solving skills: ability to make independent decisions.
+ Effective written and verbal communications.
+ Ability to use computer and mobile /tablet electronic devices.
+ Must have the ability to work under pressure while maintaining composure.
+ Ability to provide constructive feedback and coaching.
+ Fast-paced assembly experience preferred.
+ Quality control experience preferred.
+ Experience working in cold environment preferred.
Requirements: Background Check, Drug Test, Stand for Shift Duration, Must be at least 18 years old., required education: HS Diploma or GED.
Work Location: SMX @ Air Fayre, 1720 W 135th St, Gardena, CA 90249.
Job Types: Distribution, Food Production, General Production, General Warehouse, Hand Packaging, Manufacturing, Administrative/Clerical.
Industry: Warehouse/Distribution.
The hourly rate for this position is anticipated between 19.50 - 22.00 per hour. This range is a good-faith estimate, based on the shift you work and other considerations permitted by law. An employee''s pay history will not be a contributing factor where prohibited by local law. In addition to monetary compensation, we offer medical, dental, vision, life, and more. More details about benefits can be found at .
SMX, LLC is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, sexual orientation, age, gender identification, protected veteran status, or any other characteristic protected by law. We consider qualified applicants with arrest and conviction records in accordance with applicable law.
Accommodations are available on request for candidates taking part in the selection process. If you require disability-related accommodation during the recruitment process, please contact your Recruiter or Employee Relations at or . TrueBlue, Inc. and its brands will consult with all applicants who request disability-related accommodation during the recruitment process to ensure that the accommodation provided takes into account the applicant's individual accessibility needs.
SM | SMX is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, sexual orientation, age, gender identification, protected veteran status, or any other characteristic protected by law.

The Quality Control Specialist serves as a key member of the Quality Control department for the remedial action team for its Shallow Land Disposal Area site in Parks Township, PA, east-northeast of Pittsburgh. This position supports the Contractor Quality Control System Manager (CQCSM) in implementing the Quality Control program and ensures subcontractor performance is tracked to meet project needs. This position reports directly to the CQCSM.
Position Description
Responsible for assisting the CQCSM in implementing the Contractor Quality Control (CQC) System.
Has authority to recommend stop work when conditions adverse to quality are identified.
Review and approve subcontractor submittals, ensuring compliance with requirements identified in the Performance Work Statement, task order Scope of Services, and the CQC Program.
Responsible for assisting the CQCSM in implementing the U.S. Army Corps of Engineers (USACE) three-phase control process.
Inspect (or oversee inspection of) materials and equipment received on site to assure compliance with contractual requirements.
Perform routine Quality surveillances, assessments and audits of work performance as directed by the CQCSM.
Oversee subcontractor work performance for compliance with work plans, drawings and specifications.
Complete daily QC Reports.
Other duties as assigned by the CQCSM.
**Requirements**
- Minimum of Associates degree or equivalent experience.
- Minimum of 5 years of experience, including 2 years of experience in USACE projects is desired.
- Current USACE "Construction Quality Management for Contractors" certification, or ability to obtain, is desired.
- Understanding of USACE Hazardous, Toxic, and Radioactive Waste (HTRW) Remediation is desired.
- General understanding of procurement and construction concepts and principles, and their attendant quality requirements.
- Good written, verbal and Microsoft Office skills are required.
- USA Citizenship is required.
- A person already residing withing commuting distance of Vandergrift, PA is highly desired
- Knowledge and application of the USACE Construction Quality Management requirements.
- Technical knowledge of the application of procurement and construction practices sufficient to comprehend Quality requirements, including interpreting drawings and specifications.
- Experience participating in and supporting quality assessments, surveillances, and audits.
- Demonstrated ability to effectively communicate with all levels of personnel across multiple organizations within a construction and remedial action environment.
- Desired Skills
- Possess effective communication skills. Listens carefully and speaks professionally and clearly in all situations. Is able to create, read, and interpret written information.
- Capable of identifying and resolving problems in a timely manner, gathering and reviewing information appropriately.
- Adaptable to changes in the work environment, manages competing demands and is able to deal with frequent interruptions, changes, delays, or unexpected events.
- Strong writing skills. Good communication, computer and interpersonal skills. Good organization skills and ability to balance oversight of multiple work phases at multiple locations on the project.
**Additional Details**
Position will be located in Parks Township, Pennsylvania (near Pittsburgh)
Requires ability to pass beryllium sensitivity testing blood test.
**Essential Functions:** Intermittent sitting, walking, standing, bending, squatting, climbing, kneeling, twisting, and lifting. Lifting requirements limited to 20 lbs. in the form of supplies, drawings, etc. Longest distance carried of 50 feet. Hand manipulation is required for simple grasping, pushing and pulling, and fine manipulation. Right and/or left hands utilized. Occasional need to reach and/or work above the shoulder, for supplies, as well as below the shoulder for same. Must be alert to equipment in the field, there will be occasional travel, will work near construction job site equipment when in the field, occasional need to work near hazardous equipment and machinery, occasional need to walk on uneven ground, exposure to dust, gas or fumes, exposure to noise, extremes in temperature or humidity, and potential work at heights. We help prepare people for new opportunities and challenges. With positions at every level, openings in multiple disciplines, expertise in a range of markets and offices around the globe, we create an environment where you can learn, grow, and thrive. From our competitive benefits program to our Health and Safety initiative of zero workplace injuries, we believe that you'll find a flourishing career here.

**About Oshkosh AeroTech, an Oshkosh company**
**Oshkosh AeroTech is a leading provider of aviation ground support products, gate equipment and airport services to commercial airlines, airports, air-freight carriers, ground handling and military customers. Oshkosh AeroTech offers products that make a difference in people's lives by supporting those in our communities who do some of the toughest work. They own many of the most trusted brands in the air transportation industry, including LEKTRO®, JetAire®, JetPower®, AmpTekÔ, Jetway®, and more.**
Perform and verify visual, dimensional, electrical, and mechanical inspection functions relating to source, first article, receiving, in process, final check and test operations using company supplied drawings, equipment, procedures, and work instructions.
**YOUR IMPACT**
+ Analyze and interpret blueprints, data, manuals, and other materials to determine specifications, inspection and testing procedures, adjustment and certification methods, formulas, and measuring instruments required.
+ Discard or reject products on materials and equipment not meeting specification to ensure consistent quality standards.
+ Inspect, test or measure materials, products, installations, and/or work to verify conformance to specifications.
+ Record inspection or test data, such as weights, temperatures, or grades and quantities inspected or graded to verify conformance to standards.
+ Observe and monitor production operations and equipment to ensure conformance to specifications and shop practices and order necessary process or assembly adjustments.
+ Analyze test data and make computations as necessary to determine test results.
+ Notify supervisors and other personnel of production problems and assist in identifying and correcting these problems to reduce defects.
+ Discuss inspection results with those responsible for products and recommend necessary corrective actions to maintain or improve standards of quality.
+ Mark items with details such as grade and acceptance or rejection status so items can be easily identified and processed.
+ Uses measuring instruments such as tape measures, gauges, calipers, micrometers, or other devices to verify conformity to standards of components and assemblies
+ Monitors compliance to the ISO 9001 business system and ensures action is taken to address noncompliance when identified.
+ Follow Safety, Health, Environment, and Hazardous Waste Rules and Responsibilities.
+ Conduct in process audits of products and work with product team members to implement corrective actions to eliminate repetitive non-conformances.
+ Conduct unit inspections per specifications and record non-conformances in a Windows based program.
+ Participate in Customer inspections and document suggestions and findings in Windows based program.
+ Other projects and responsibilities may be added at the company's discretion.
**QUALIFICATIONS**
**Education and Experience**
+ High school diploma or GED. Associates degree or greater preferred
+ Technical / vocational / or military training or related experience is helpful
+ Typically has eight or more years manufacturing experience with at least four (4) years of experience in a similar environment
+ At least six (6) months working with heavy mobile equipment in a manufacturing environment.
+ Ability to work productively and cohesively in a diverse and multicultural environment
Oshkosh is committed to working with and offering reasonable accommodations to job applicants with disabilities. If you need assistance or an accommodation due to a disability for any part of the recruitment process, please contact our talent acquisition team by email .
Oshkosh Corporation is a merit-based Equal Opportunity Employer. Job opportunities are open for application to all qualified individuals and selection decisions are made without regard to race, color, religion, sex, national origin, age, disability, veteran status, or other protected characteristic. To the extent that information is provided or collected regarding categories as provided by law it will in no way affect the decision regarding an employment application.
Oshkosh Corporation will not discharge or in any manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with Oshkosh Corporation's legal duty to furnish information.
Certain positions with Oshkosh Corporation require access to controlled goods and technologies subject to the International Traffic in Arms Regulations or the Export Administration Regulations. Applicants for these positions may need to be "U.S. Persons," as defined in these regulations. Generally, a "U.S. Person" is a U.S. citizen, lawful permanent resident, or an individual who has been admitted as a refugee or granted asylum.

Our client, a leading manufacturing company, is seeking a **Quality Control Specialist** to join their team. As a **Quality Control Specialist** , you will be part of the QA Department supporting the quality assurance and training initiatives. The ideal candidate will have strong interpersonal skills, attention to detail, and a proactive attitude, which will align successfully in the organization.
**Job Title:** **Quality Control Specialist**
**Location: Durham, NC**
**Pay Range: $18.50 - $19.50**
**Shift: 7AM-7PM OR 7PM-7AM (2-2-3 ROTATING SHIFT)**
**What's the Job?**
+ Conduct talent assessments to identify skill gaps among QA staff
+ Facilitate training sessions using various methods including coaching, workshops, shadowing, and mentoring
+ Evaluate the effectiveness of training and facilitation techniques
+ Ensure all QA employees are properly trained and understand their responsibilities
+ Perform periodic audits to assess employee progress and document findings
**What's Needed?**
+ High School diploma or equivalent
+ Minimum of 1 year of relevant experience in quality assurance or training
+ Proficiency in using Microsoft and management information systems (MIS)
+ Ability to manage multiple priorities in a fast-paced environment
+ Must have physical capability to lift 25lbs frequently, 60lbs occasionally
+ Must be able to work for 12 hour shifts
**What's in it for me?**
+ Active referral program available.
+ Weekly pay - every Friday!
+ Long term contract position.
+ Gain valuable experience in quality control processes
+ Be part of a dynamic team committed to excellence
**Upon completion of waiting period associates are eligible for:**
+ Medical and Prescription Drug Plans
+ Dental Plan
+ Supplemental Life Insurance
+ Short Term Disability Insurance
+ 401(k)
If this is a role that interests you and you'd like to learn more, click apply now and a recruiter will be in touch with you to discuss this great opportunity. We look forward to speaking with you!
**About ManpowerGroup, Parent Company of: Manpower, Experis, Talent Solutions, and Jefferson Wells**
_ManpowerGroup® (NYSE: MAN), the leading global workforce solutions company, helps organizations transform in a fast-changing world of work by sourcing, assessing, developing, and managing the talent that enables them to win. We develop innovative solutions for hundreds of thousands of organizations every year, providing them with skilled talent while finding meaningful, sustainable employment for millions of people across a wide range of industries and skills. Our expert family of brands -_ **_Manpower, Experis, Talent Solutions, and Jefferson Wells_** _-_ creates substantial value for candidates and clients across more than 75 countries and territories and has done so for over 70 years. We are recognized consistently for our diversity - as a best place to work for Women, Inclusion, Equality and Disability and in 2023 ManpowerGroup was named one of the World's Most Ethical Companies for the 14th year - all confirming our position as the brand of choice for in-demand talent.
ManpowerGroup is committed to providing equal employment opportunities in a professional, high quality work environment. It is the policy of ManpowerGroup and all of its subsidiaries to recruit, train, promote, transfer, pay and take all employment actions without regard to an employee's race, color, national origin, ancestry, sex, sexual orientation, gender identity, genetic information, religion, age, disability, protected veteran status, or any other basis protected by applicable law.

Job Title: Quality Control Specialist
Job Description
We are seeking a dedicated Quality Control Specialist to join our dynamic team in the cell and gene therapy sector. This role offers the opportunity to work at a brand new site, supporting our cutting-edge CDMO operations. The successful candidate will be trained in a variety of analytical methods and will be responsible for maintaining high-quality standards in a fast-paced environment.
Responsibilities
+ Perform and be trained in ELISA-based assays, Endotoxin testing, Flow Cytometry, and PCR analytical methods.
+ Support operations at both the Newark and Princeton locations.
+ Conduct quality inspections and manage materials, reagents, and live cells.
+ Interact effectively with clients and health authorities, ensuring clear communication and maintaining professional relationships.
Essential Skills
+ Master's Degree with 1+ years of experience in the pharmaceutical industry or GMP environment, focusing on analytical methods or Quality Control, OR a Bachelor's Degree with 2+ years of relevant experience.
+ In-depth knowledge and hands-on experience with analytical assays, including Flow Cytometry, PCR, and ELISAs.
+ Extensive Quality Control experience with a comprehensive understanding of compendial methods and regulatory guidance.
+ Ability and willingness to learn and perform microbiological assays as part of the evolving needs of the team.
+ Capability to thrive in a dynamic environment, manage multiple priorities, and adapt to evolving demands.
+ Willingness to travel between facilities and work flexible hours, including evenings, weekends, and shift-based schedules as operational needs dictate.
Additional Skills & Qualifications
+ Experience with LIMS, Endotoxin, Sterility, mycoplasma, and method qualification/validation, including supporting method transfer activities.
+ Familiarity with FDA, EMEA, ICH, USP, GMP guidelines, and cGMP regulations related to QC labs and cell-based product manufacturing.
+ Proven ability to support lab investigations, deviations, CAPAs, and change controls.
+ Knowledge of Gene/Cell therapy products, particularly in clinical production.
Work Environment
This role is based in a growing CDMO specializing in Cell/Gene Therapy at a brand new site. The work environment is dynamic, offering opportunities to work with the latest technologies in a supportive team-oriented setting. Flexible hours, including evenings and weekends, may be required to meet operational demands.
Job Type & Location
This is a Contract to Hire position based out of Princeton, NJ
Pay and Benefits
The pay range for this position is $25.00 - $35.00/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 & vision - Critical Illness, Accident, and Hospital - 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available - Life Insurance (Voluntary Life & AD&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 Princeton,NJ.
Application Deadline
This position is anticipated to close on Oct 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 (% ) for other accommodation options.

Job Title: Quality Control Specialist
Job Description
We are seeking a dedicated Quality Control Specialist to join our dynamic team in the cell and gene therapy sector. This role offers the opportunity to work at a brand new site, supporting our cutting-edge CDMO operations. The successful candidate will be trained in a variety of analytical methods and will be responsible for maintaining high-quality standards in a fast-paced environment.
Responsibilities
+ Perform and be trained in ELISA-based assays, Endotoxin testing, Flow Cytometry, and PCR analytical methods.
+ Support operations at both the Newark and Princeton locations.
+ Conduct quality inspections and manage materials, reagents, and live cells.
+ Interact effectively with clients and health authorities, ensuring clear communication and maintaining professional relationships.
Essential Skills
+ Master's Degree with 1+ years of experience in the pharmaceutical industry or GMP environment, focusing on analytical methods or Quality Control, OR a Bachelor's Degree with 2+ years of relevant experience.
+ In-depth knowledge and hands-on experience with analytical assays, including Flow Cytometry, PCR, and ELISAs.
+ Extensive Quality Control experience with a comprehensive understanding of compendial methods and regulatory guidance.
+ Ability and willingness to learn and perform microbiological assays as part of the evolving needs of the team.
+ Capability to thrive in a dynamic environment, manage multiple priorities, and adapt to evolving demands.
+ Willingness to travel between facilities and work flexible hours, including evenings, weekends, and shift-based schedules as operational needs dictate.
Additional Skills & Qualifications
+ Experience with LIMS, Endotoxin, Sterility, mycoplasma, and method qualification/validation, including supporting method transfer activities.
+ Familiarity with FDA, EMEA, ICH, USP, GMP guidelines, and cGMP regulations related to QC labs and cell-based product manufacturing.
+ Proven ability to support lab investigations, deviations, CAPAs, and change controls.
+ Knowledge of Gene/Cell therapy products, particularly in clinical production.
Work Environment
This role is based in a growing CDMO specializing in Cell/Gene Therapy at a brand new site. The work environment is dynamic, offering opportunities to work with the latest technologies in a supportive team-oriented setting. Flexible hours, including evenings and weekends, may be required to meet operational demands.
Job Type & Location
This is a Contract to Hire position based out of Princeton, NJ
Pay and Benefits
The pay range for this position is $25.00 - $35.00/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 & vision - Critical Illness, Accident, and Hospital - 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available - Life Insurance (Voluntary Life & AD&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 Princeton,NJ.
Application Deadline
This position is anticipated to close on Oct 27, 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 (% ) for other accommodation options.

Job Title: Quality Control Specialist
Job Description
We are seeking a dedicated Quality Control Specialist to join our dynamic team in the cell and gene therapy sector. This role offers the opportunity to work at a brand new site, supporting our cutting-edge CDMO operations. The successful candidate will be trained in a variety of analytical methods and will be responsible for maintaining high-quality standards in a fast-paced environment.
Responsibilities
+ Perform and be trained in ELISA-based assays, Endotoxin testing, Flow Cytometry, and PCR analytical methods.
+ Support operations at both the Newark and Princeton locations.
+ Conduct quality inspections and manage materials, reagents, and live cells.
+ Interact effectively with clients and health authorities, ensuring clear communication and maintaining professional relationships.
Essential Skills
+ Master's Degree with 1+ years of experience in the pharmaceutical industry or GMP environment, focusing on analytical methods or Quality Control, OR a Bachelor's Degree with 2+ years of relevant experience.
+ In-depth knowledge and hands-on experience with analytical assays, including Flow Cytometry, PCR, and ELISAs.
+ Extensive Quality Control experience with a comprehensive understanding of compendial methods and regulatory guidance.
+ Ability and willingness to learn and perform microbiological assays as part of the evolving needs of the team.
+ Capability to thrive in a dynamic environment, manage multiple priorities, and adapt to evolving demands.
+ Willingness to travel between facilities and work flexible hours, including evenings, weekends, and shift-based schedules as operational needs dictate.
Additional Skills & Qualifications
+ Experience with LIMS, Endotoxin, Sterility, mycoplasma, and method qualification/validation, including supporting method transfer activities.
+ Familiarity with FDA, EMEA, ICH, USP, GMP guidelines, and cGMP regulations related to QC labs and cell-based product manufacturing.
+ Proven ability to support lab investigations, deviations, CAPAs, and change controls.
+ Knowledge of Gene/Cell therapy products, particularly in clinical production.
Work Environment
This role is based in a growing CDMO specializing in Cell/Gene Therapy at a brand new site. The work environment is dynamic, offering opportunities to work with the latest technologies in a supportive team-oriented setting. Flexible hours, including evenings and weekends, may be required to meet operational demands.
Job Type & Location
This is a Contract to Hire position based out of Princeton, NJ
Pay and Benefits
The pay range for this position is $25.00 - $35.00/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 & vision - Critical Illness, Accident, and Hospital - 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available - Life Insurance (Voluntary Life & AD&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 Princeton,NJ.
Application Deadline
This position is anticipated to close on Oct 21, 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 (% ) for other accommodation options.

**Position Description**
If you seek a rewarding, high profile and challenging position supporting projects for the US Navy, then Serco has a wonderful opportunity for you!
As our Surface Radar Technician, you will be on a team in Pascagoula, MS, where you will be evaluating and managing the delivery of new amphibious ships and landing craft to the fleet. You will also work closely with Government and industry professionals, shipbuilders, and other support personnel.
Serco is part of a team led by a Program Manager and Deputy Program Manager having decades of experience working in the DoD and Shipbuilding Industry. We have only one objective: to ensure our clients' mission objectives are achieved with the highest level of capability and assurance, and at the lowest possible cost.
Our Naval Acquisition and Sustainment Operation, which is part of Serco's Maritime Engineering, Technology and Sustainment (METS) business, provides critical services to nearly all U.S. Navy amphibious ships and craft. Bring your expertise and collaborative skills to make an impact towards our military defense and safety of our sailors and marines.
In this role you will:
+ Provide installation, troubleshooting, repair and operational test and evaluation support for Radar Systems on LPD 17 Class vessels
+ Review, update, and develop test procedures for shipboard testing events related to Combat Systems
+ Support development and update of Suitability Plans, and develop test objectives, test scenarios, test plans, test reports and briefings.
+ Establish and maintain productive liaison with Government Project teams, Production Teams and Shipbuilder.
+ Monitor Installation of Combat Systems in New Construction shipyard environment.
+ Identify performance issues with the Radar System; isolate issues to either hardware or software or particular interfaces during testing.
+ Draft and submit software trouble reports that describe the performance issue compared to performance requirements.
+ Participate as a test team member for all troubleshooting, training and scenarios.
**Qualifications**
To be successful in this role you will have:
+ An a DoD Secret clearance.
+ U.S. citizenship.
+ Ability to communicate effectively with Navy and shipyard teams both orally and in written reports and briefings using Microsoft Office Products.
+ Combat system and weapon system experience with one or more of the following is required:
+ AN/SPQ-9B Radar System
+ AN/SPS-73 Radar System
+ Bachelor's degree preferred but may be substituted with at least 5 years experience in Combat Systems installation and testing.
+ Specialized education or training in the field of combat systems - particularly within shipboard naval settings is required.
+ Up tp 10% travel
If you are interested in supporting and working with our military and sailors and a passionate Serco team - then submit your application now for immediate consideration. It only takes a few minutes and could change your career!
**Company Overview**
Serco Inc. (Serco) is the Americas division of Serco Group, plc. In North America, Serco's 9,000+ employees strive to make an impact every day across 100+ sites in the areas of Defense, Citizen Services, and Transportation. We help our clients deliver vital services more efficiently while increasing the satisfaction of their end customers. Serco serves every branch of the U.S. military, numerous U.S. Federal civilian agencies, the Intelligence Community, the Canadian government, state, provincial and local governments, and commercial clients. While your place may look a little different depending on your role, we know you will find yours here. Wherever you work and whatever you do, we invite you to discover your place in our world. Serco is a place you can count on and where you can make an impact because every contribution matters.
To review Serco benefits please visit: .If you require an accommodation with the application process please email: or call the HR Service Desk at , option 1. Please note, due to EEOC/OFCCP compliance, Serco is unable to accept resumes by email.
Candidates may be asked to present proof of identify during the selection process. If requested, this will require presentation of a government-issued I.D. (with photo) with name and address that match the information entered on the application. Serco will not take possession of or retain/store the information provided as proof of identity. For more information on how Serco uses your information, please see ourApplicant Privacy Policy and Notice ( .
Serco does not accept unsolicited resumes through or from search firms or staffing agencies without being a contracted approved vendor. All unsolicited resumes will be considered the property of Serco and will not be obligated to pay a placement or contract fee. If you are interested in becoming an approved vendor at Serco, please email .
Serco is an equal opportunity employer. We evaluate qualified applicants without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, and other legally protected characteristics.
Click here to apply now ( to Serco?**
Join our Talent Community! ( _71610_
**Recruiting Location : Location** _US-MS-Pascagoula_
**Category** _Engineering/Ship Construction_
**Position Type** _Full-Time_
**Security Clearance** _Secret_
**Telework** _No - Teleworking not available for this position_