1,202 Quality Control Analyst jobs in the United States

Today, Lonza is a global leader in life sciences operating across three continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that’s the kind of work we want to be part of.

Lonza Pharma & Biotech is looking for a Manager, Compliance & Validation to join the Quality Assurance team in Bend, OR. This role provides an outstanding opportunity to lead an exceptional QA team in a company that values innovation and collaboration. Join us and help drive the future of life sciences forward!

Key Responsibilities:

• Provide assistance in internal audits, audits from external parties, and regulatory inspections of designated Quality Management Systems as the QA subject matter expert.
• Maintain current knowledge of applicable regulations, mentorship, and standards, and train personnel on cGMPs and applicable regulations.
• Participate in compliance evaluation of regulated activities within pharmaceutical development and cGMP manufacturing.
• Report to management any departures from regulations and cGMP noted during the assessment of manufacturing operations, internal audits, supplier audits, external audits, and regulatory inspections. Help in identifying necessary CAPA and validate the successful execution and efficacy of assigned measures.
• Develop efficient workflows and processes, and appropriate metrics to track compliance, efficiency, and efficiency.
• Manage and supervise designated aspects of the Quality Assurance and Management System.
• Ensure procedures, systems, and processes are effective and meet regulatory requirements and business needs.
• Supervise QA staff at various levels responsible for lifecycle management of quality system documents.
• Review and approve regulatory documents.
• Perform other duties as assigned.

Key Requirements:

• Bachelor's Degree or equivalent experience required.
• Significant experience in the pharmaceutical/biotech industry.
• Compliance and Regulatory experience required.
• Prior Management experience required.
• GMP (Good Manufacturing Practices) experience preferred.
• Strong leadership, writing, and communication/presentation skills are required.
• Must be independent, self-motivated, organized, able to multi-task, and skilled in communication, facilitation, and collaboration.
• Individual must be a great teammate prepared to work in and embrace a team-based culture that relies on collaboration for effective decision-making.

Every day, Lonza’s products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically.

People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference .

Lonza is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a qualified individual with disability, protected veteran status, or any other characteristic protected by law.

Today, Lonza is a global leader in life sciences operating across three continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that’s the kind of work we want to be part of.

Lonza Pharma & Biotech is looking for a Manager, Compliance & Validation to join the Quality Assurance team in Bend, OR. This role provides an outstanding opportunity to lead an exceptional QA team in a company that values innovation and collaboration. Join us and help drive the future of life sciences forward!

Key Responsibilities:

• Provide assistance in internal audits, audits from external parties, and regulatory inspections of designated Quality Management Systems as the QA subject matter expert.
• Maintain current knowledge of applicable regulations, mentorship, and standards, and train personnel on cGMPs and applicable regulations.
• Participate in compliance evaluation of regulated activities within pharmaceutical development and cGMP manufacturing.
• Report to management any departures from regulations and cGMP noted during the assessment of manufacturing operations, internal audits, supplier audits, external audits, and regulatory inspections. Help in identifying necessary CAPA and validate the successful execution and efficacy of assigned measures.
• Develop efficient workflows and processes, and appropriate metrics to track compliance, efficiency, and efficiency.
• Manage and supervise designated aspects of the Quality Assurance and Management System.
• Ensure procedures, systems, and processes are effective and meet regulatory requirements and business needs.
• Supervise QA staff at various levels responsible for lifecycle management of quality system documents.
• Review and approve regulatory documents.
• Perform other duties as assigned.

Key Requirements:

• Bachelor's Degree or equivalent experience required.
• Significant experience in the pharmaceutical/biotech industry.
• Compliance and Regulatory experience required.
• Prior Management experience required.
• GMP (Good Manufacturing Practices) experience preferred.
• Strong leadership, writing, and communication/presentation skills are required.
• Must be independent, self-motivated, organized, able to multi-task, and skilled in communication, facilitation, and collaboration.
• Individual must be a great teammate prepared to work in and embrace a team-based culture that relies on collaboration for effective decision-making.

Every day, Lonza’s products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically.

People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference .

Lonza is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a qualified individual with disability, protected veteran status, or any other characteristic protected by law.

Today, Lonza is a global leader in life sciences operating across three continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that’s the kind of work we want to be part of.

Lonza Pharma & Biotech is looking for a Manager, Compliance & Validation to join the Quality Assurance team in Bend, OR. This role provides an outstanding opportunity to lead an exceptional QA team in a company that values innovation and collaboration. Join us and help drive the future of life sciences forward!

Key Responsibilities:

• Provide assistance in internal audits, audits from external parties, and regulatory inspections of designated Quality Management Systems as the QA subject matter expert.
• Maintain current knowledge of applicable regulations, mentorship, and standards, and train personnel on cGMPs and applicable regulations.
• Participate in compliance evaluation of regulated activities within pharmaceutical development and cGMP manufacturing.
• Report to management any departures from regulations and cGMP noted during the assessment of manufacturing operations, internal audits, supplier audits, external audits, and regulatory inspections. Help in identifying necessary CAPA and validate the successful execution and efficacy of assigned measures.
• Develop efficient workflows and processes, and appropriate metrics to track compliance, efficiency, and efficiency.
• Manage and supervise designated aspects of the Quality Assurance and Management System.
• Ensure procedures, systems, and processes are effective and meet regulatory requirements and business needs.
• Supervise QA staff at various levels responsible for lifecycle management of quality system documents.
• Review and approve regulatory documents.
• Perform other duties as assigned.

Key Requirements:

• Bachelor's Degree or equivalent experience required.
• Significant experience in the pharmaceutical/biotech industry.
• Compliance and Regulatory experience required.
• Prior Management experience required.
• GMP (Good Manufacturing Practices) experience preferred.
• Strong leadership, writing, and communication/presentation skills are required.
• Must be independent, self-motivated, organized, able to multi-task, and skilled in communication, facilitation, and collaboration.
• Individual must be a great teammate prepared to work in and embrace a team-based culture that relies on collaboration for effective decision-making.

Every day, Lonza’s products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically.

People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference .

Lonza is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a qualified individual with disability, protected veteran status, or any other characteristic protected by law.

Today, Lonza is a global leader in life sciences operating across three continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that’s the kind of work we want to be part of.

Lonza Pharma & Biotech is looking for a Manager, Compliance & Validation to join the Quality Assurance team in Bend, OR. This role provides an outstanding opportunity to lead an exceptional QA team in a company that values innovation and collaboration. Join us and help drive the future of life sciences forward!

Key Responsibilities:

• Provide assistance in internal audits, audits from external parties, and regulatory inspections of designated Quality Management Systems as the QA subject matter expert.
• Maintain current knowledge of applicable regulations, mentorship, and standards, and train personnel on cGMPs and applicable regulations.
• Participate in compliance evaluation of regulated activities within pharmaceutical development and cGMP manufacturing.
• Report to management any departures from regulations and cGMP noted during the assessment of manufacturing operations, internal audits, supplier audits, external audits, and regulatory inspections. Help in identifying necessary CAPA and validate the successful execution and efficacy of assigned measures.
• Develop efficient workflows and processes, and appropriate metrics to track compliance, efficiency, and efficiency.
• Manage and supervise designated aspects of the Quality Assurance and Management System.
• Ensure procedures, systems, and processes are effective and meet regulatory requirements and business needs.
• Supervise QA staff at various levels responsible for lifecycle management of quality system documents.
• Review and approve regulatory documents.
• Perform other duties as assigned.

Key Requirements:

• Bachelor's Degree or equivalent experience required.
• Significant experience in the pharmaceutical/biotech industry.
• Compliance and Regulatory experience required.
• Prior Management experience required.
• GMP (Good Manufacturing Practices) experience preferred.
• Strong leadership, writing, and communication/presentation skills are required.
• Must be independent, self-motivated, organized, able to multi-task, and skilled in communication, facilitation, and collaboration.
• Individual must be a great teammate prepared to work in and embrace a team-based culture that relies on collaboration for effective decision-making.

Every day, Lonza’s products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically.

People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference .

Lonza is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a qualified individual with disability, protected veteran status, or any other characteristic protected by law.

Today, Lonza is a global leader in life sciences operating across three continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that’s the kind of work we want to be part of.

Lonza Pharma & Biotech is looking for a Manager, Compliance & Validation to join the Quality Assurance team in Bend, OR. This role provides an outstanding opportunity to lead an exceptional QA team in a company that values innovation and collaboration. Join us and help drive the future of life sciences forward!

Key Responsibilities:

• Provide assistance in internal audits, audits from external parties, and regulatory inspections of designated Quality Management Systems as the QA subject matter expert.
• Maintain current knowledge of applicable regulations, mentorship, and standards, and train personnel on cGMPs and applicable regulations.
• Participate in compliance evaluation of regulated activities within pharmaceutical development and cGMP manufacturing.
• Report to management any departures from regulations and cGMP noted during the assessment of manufacturing operations, internal audits, supplier audits, external audits, and regulatory inspections. Help in identifying necessary CAPA and validate the successful execution and efficacy of assigned measures.
• Develop efficient workflows and processes, and appropriate metrics to track compliance, efficiency, and efficiency.
• Manage and supervise designated aspects of the Quality Assurance and Management System.
• Ensure procedures, systems, and processes are effective and meet regulatory requirements and business needs.
• Supervise QA staff at various levels responsible for lifecycle management of quality system documents.
• Review and approve regulatory documents.
• Perform other duties as assigned.

Key Requirements:

• Bachelor's Degree or equivalent experience required.
• Significant experience in the pharmaceutical/biotech industry.
• Compliance and Regulatory experience required.
• Prior Management experience required.
• GMP (Good Manufacturing Practices) experience preferred.
• Strong leadership, writing, and communication/presentation skills are required.
• Must be independent, self-motivated, organized, able to multi-task, and skilled in communication, facilitation, and collaboration.
• Individual must be a great teammate prepared to work in and embrace a team-based culture that relies on collaboration for effective decision-making.

Every day, Lonza’s products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically.

People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference .

Lonza is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a qualified individual with disability, protected veteran status, or any other characteristic protected by law.

Job Title: Quality Control Inspector
Job Description
We are seeking a dedicated Quality Control Inspector to support quality control efforts for raw materials in process manufacturing. This role involves adhering to SOP requirements and ensuring the release of approved raw materials for testing. The analyst will perform OOS investigations for all rejected materials and manage GMP document authoring and revisions.
Responsibilities
+ Support all quality control efforts for raw materials in process manufacturing.
+ Follow all SOP requirements for quality control processes.
+ Release approved raw materials for testing purposes.
+ Perform OOS investigations for all rejected materials.
+ Author and revise all GMP documents as required.
Essential Skills
+ Proficiency in quality control processes.
+ Experience with raw materials and OOS investigations.
+ Familiarity with clean room operations.
+ Understanding of Quality Systems and ERP.
+ Knowledge of GMP requirements.
Additional Skills & Qualifications
+ Associate's degree in life sciences.
+ 1-3 years of experience in a QA/QC role within a GMP facility; internships considered.
+ Proficiency in Microsoft Office and quality systems.
Work Environment
This position is 100% onsite in Bedford. ; Monday - Friday 9am - 6pm (occasional overtime required)
Pay and Benefits
The pay range for this position is $25.00 - $30.00/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 Bedford,MA.
Application Deadline
This position is anticipated to close on Nov 4, 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 - Pay Rate**
Our client in **(city, state)** is looking for hardworking, motivated talent to join their team. **(add 1 client specific selling statement)** Don't wait. apply today!
Whats in it for you?
+ **Payrate**
+ **Shift**
+ Paid training
+ Full time hours
+ Clean and safe work environment
+ **(add 1-2 other key selling points Ex: Opportunity for growth, on public transportation, etc.)**
What will you be doing?
+ (Enter text)
+ (Enter text)
What do you bring?
+ Positive, can-do attitude
+ **(add 1-3 desired candidate attributes. Ex: High School Diploma, 6 months related experience, etc.)**
Why should you choose Manpower?
+ Free training to upgrade your skills, including a free college tuition program
+ Medical, dental, vision, 401k
+ Weekly pay with direct deposit
+ 24/7 Manpower customer care support
+ Dedicated Career Partner to help you achieve your career goals
+ Voted #1 best places to work by Glassdoor 2021
Are you Interested?
Stop your job search and apply today! A recruiter will be in touch within 24 hours.
Share this job with friends and family and earn dollars with every successful hire.
ManpowerGroup recognizes the importance of providing an accessible and barrier-free environment. We are committed to creating a welcoming, fair and inclusive environment by offering equal opportunity to access our services. At ManpowerGroup, we are committed to providing accommodations, and will work with you to meet your needs.
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.

**Quality Control (QC) Analyst / Senior Analyst**
**Kelly® Science & Clinical** is looking for a motivated **Quality Control (QC) Analyst / Senior Analyst** to join the QC analytical team. This individual will directly support the culture and operation of an early phase QC group. This position will collaborate across functions and will have an opportunity to learn in a dynamic start up environment.
**Type: Contract (6-month)**
**Shift: M-F, 1** **st**
**Pay Range: Analyst - $28-$3/hr**
** Sr Analyst: 33- 40/hr**
**CORE ACCOUNTABILITIES**
**Specific responsibilities include:**
+ With management supervision, perform QC Analytical laboratory testing and review for product release, stability, and in-process testing.
+ Execute sample management tasks such as sample receipt, aliquoting, and sample chain of custody in support of manufacturing and QC testing
+ Collaborate with the Analytical Development team to perform testing in support of method qualification and transfer, provide QC perspective and input for method troubleshooting activities
+ Willingness to learn and participate in Operational Excellence/Continuous Improvement activities including application of OE/CI philosophies in a regulated laboratory environment
+ Independently own daily laboratory tasks such as inventory management, critical reagent qualification, cell passaging, etc.
+ Other responsibilities/duties as required to support QC Operations (i.e., QC Microbiology tasks, stability timepoint pulls, etc.)
**The successful candidate will have:**
+ **Analyst Level:** Bachelor's Degree in Biochemistry, Molecular and Cellular Biology, Immunology, Biology, or other life science with a minimum of 1 year in a cGMP regulated QC environment. Equivalent combinations of advanced education and experience will be considered.
+ **Senior Analyst Level:** Bachelor's Degree in Biochemistry, Molecular and Cellular Biology, Immunology, Biology, or other life science with a minimum of 2+ years in a cGMP regulated QC environment. Equivalent combinations of advanced education and experience will be considered.
+ Quality Control experience in cGMP regulated laboratory
+ Molecular biology background, including dPCR, ELISA, Flow Cytometry and Cell-based assays
+ Ability to execute against approved documents (SOPs, Methods, Protocols, etc.) with basic knowledge of relevant pharmaceutical regulations and regulatory guidance
+ A passion for teamwork and unwavering commitment to purpose, team success, and the championing of an outstanding workplace culture
+ Ability to excel through teamwork, collaboration and effective knowledge sharing
**Preferred Qualifications:**
+ Experience with laboratory startup, quality systems, and analytical methods
+ Laboratory experience and understanding of molecular assays including digital PCR, Flow Cytometry, ELISA and/or cell-based test methods
+ Experience in cGMP cell and gene therapy manufacturing and/or testing facility
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.

**Quality Control Analyst**
Kelly® Science & Clinical is seeking a **Quality Control (QC) Analyst / Senior Analyst** for a 6 month **contract** position at a cutting-edge client in **Louisville, CO** . 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:**
+ Analyst: $56,100 - $9,300
+ Senior Analyst: 68,000 - 84,000
**Schedule:**
Day Shift Full-time, on-site
**Overview**
This client is an industry-leading company that's transforming the treatment of cancer with a novel integrated immunotherapy platform. Their vision is to develop off-the-shelf therapies capable of treating any tumor, any time. The team operates from brand-new facility in Louisville, CO. and is driven by groundbreaking science, technology, and a commitment to Diversity, Equity, and Inclusion.
In this role, you will join the Quality Control Analytical team to support early-phase QC operations. You'll collaborate across functions, perform analytical testing, and contribute to method development and operational excellence in a dynamic biotech start-up environment.
**Responsibilities:**
+ Demonstrate the Client's values as part of a high-performing, inclusive, and collaborative organization.
+ Perform QC analytical laboratory testing for product release, stability, and in-process testing under supervision.
+ Execute sample management tasks including receipt, aliquoting, and chain of custody.
+ Collaborate with Analytical Development for method qualification, transfer, and troubleshooting.
+ Participate in Operational Excellence/Continuous Improvement initiatives.
+ Independently manage daily lab tasks such as inventory, reagent qualification, and cell passaging.
+ Support QC operations including microbiology tasks and stability timepoint pulls.
**Qualifications:**
**Analyst Level:**
+ Bachelor's degree in Biochemistry, Molecular and Cellular Biology, Immunology, Biology, or related life science.
+ Minimum 1 year in a cGMP-regulated QC environment (or equivalent education/experience).
**Senior Analyst Level:**
+ Bachelor's degree in Biochemistry, Molecular and Cellular Biology, Immunology, Biology, or related life science.
+ Minimum 2+ years in a cGMP-regulated QC environment (or equivalent education/experience).
**Required Skills:**
+ Experience in cGMP QC laboratory.
+ Molecular biology background including dPCR, ELISA, Flow Cytometry, and cell-based assays.
+ Ability to follow SOPs, methods, and protocols with basic regulatory knowledge.
+ Strong teamwork and commitment to purpose and culture.
**Preferred Qualifications:**
+ Experience with lab startup, quality systems, and analytical methods.
+ Familiarity with molecular assays and cell-based test methods.
+ Experience in cell and gene therapy manufacturing/testing.
+ QC Microbiology and aseptic technique experience.
**Physical Requirements:**
+ Ability to gown aseptically and work in a Clean Room.
+ Wear PPE including gloves, protective clothing, and safety glasses.
+ Work while gowned for extended periods.
+ Lift up to 20 lbs regularly.
**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.
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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.