What Jobs are available for Qa Analysts in Madison?

Job Title: Temporary Quality Control Analyst
Job Description
The PCR Analyst will perform routine testing support and project support. This includes qPCR testing with a 7-hour turnaround time. The role requires teamwork to manage sample processing, with new samples arriving every 8 hours. The analyst will conduct in-process testing on raw materials, typically from pig origin, and finished product testing on pancreatin powder. Responsibilities also include contaminant monitoring, environmental monitoring, instrument calibration and maintenance, inventory management, and reagent preparation. Training will be provided on validation tasks, including basic centrifuges, spectrophotometers, and liquid handler robots, as well as software programming, lab space validation, and method drafting.
Responsibilities
+ Perform qPCR testing with a 7-hour turnaround time.
+ Conduct in-process testing on raw materials and finished product testing on pancreatin powder.
+ Perform contaminant monitoring and positive control environmental monitoring.
+ Calibrate and maintain instruments.
+ Manage inventory and prepare reagents.
+ Undergo training for validation tasks including centrifuges, spectrophotometers, and liquid handler robots.
+ Validate lab spaces and draft methods.
+ Run speciation assays to identify and quantify different species within a sample.
Essential Skills
+ Experience with PCR, QC, testing, method development, and quality control.
+ Knowledge of GMP, biology, pharmaceutical processes, and environmental monitoring.
+ Familiarity with FDA regulations, molecular biology, microbiology, and assay procedures.
+ Bachelor's degree or above in Microbiology or related discipline preferred.
+ 2+ years of PCR/Micro Lab experience preferred for Associate QC Analyst.
+ 5+ years of experience with GMP preferred for Sr QC Analyst.
Work Environment
This is a 12 month contract role operating on a 3rd shift schedule from Monday to Thursday, 9 PM to 7 AM, with a shift differential of $3.50/hr. The position is based in a brand new lab set to open in March 2025. The team comprises three members per shift, and the work environment is described as laid-back, driven, and hardworking. Initial training will occur on 1st shift for the first few weeks, followed by a transition to the assigned shift.
Pay and Benefits
The pay range for this position is $2.00 - 36.00/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 Madison,WI.
Application Deadline
This position is anticipated to close on Nov 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 (% ) for other accommodation options.

Cardinal Health Sonexus Access and Patient Support helps specialty pharmaceutical manufacturers remove barriers to care so that patients can access, afford and remain on the therapy they need for a better quality of life. Our diverse expertise in pharma, payer and hub services allows us to deliver best-in-class solutions-driving brand and patient markers of success. We're continuously integrating advanced and emerging technologies to streamline patient onboarding, qualification, and adherence. Our non-commercial specialty pharmacy is centralized at our custom-designed facility outside of Dallas, Texas, empowering manufacturers to rethink the reach and impact of their products.
**Together, we can get life-changing therapies to patients who need them-faster.**
**What Performance Monitoring contributes to Cardinal Health:**
Performance Monitoring is responsible for establishing, maintaining, and enhancing customer business through contract administration, customer orders, and problem resolution. Performance Monitoring is responsible for monitoring, analyzing, and reviewing customer contact quality.
**Responsibilities:**
+ Evaluate calls and cases to assess performance based on a standard set of criteria, providing constructive feedback and recognition to employees to ensure high performance and continuous improvement.
+ Accurately score transactions to gauge employee's quality performance based on organizational and departmental policies and requirements.
+ Monitor and evaluate team performance, whether voice or non-voice, of assigned entity and team, ensuring adherence to company quality standards, and compliance with industry regulations.
+ Track and report any trends from the customer experience that can be improved or celebrated.
+ Analyze and provide weekly & monthly trend analysis to leadership.
+ Provide support to leadership by participating in and hosting internal/external client calibration sessions.
+ Engage in and lead projects to promote quality enhancements and/or broaden services for the team.
+ Maintain a comprehensive understanding of quality systems and methodologies as well as knowledge of applicable regulations, standards, and operating procedures.
+ Conduct investigations/root cause analysis and formulate corrective action recommendations.
+ Show an understanding of the program requirements and be capable of conducting gap assessments based on those requirements.
+ Uphold quality standards that adhere to company, regulatory, and HIPAA policies and procedures.
+ Collaborate across various functions, interpret requirements, educate and influence others regarding those requirements.
+ Identify training needs or potential disciplinary actions which will be reported to leadership.
+ Build strong customer relationships and deliver customer-centric solutions.
+ Optimize work processes by identifying effective and efficient methods to complete tasks, with an emphasis on continuous improvement.
+ Develop strategic alliances and cooperate with stakeholders to achieve mutual goals.
+ Demonstrate resourcefulness by adeptly securing and efficiently deploying resources.
+ Analyze complex and high-quality, sometimes contradictory, information to solve problems effectively.
+ Hold oneself and others accountable for meeting commitments and objectives.
+ Exhibit situational adaptability by adjusting approach and demeanor in real time to meet the changing demands of various situations.
+ Create and implement diverse communication strategies that clearly address the specific requirements of various target audiences.
**Qualifications:**
+ HS Diploma, GED or technical certification in related field or equivalent experience, preferred. Diploma or degree in relevant field desirable.
+ 3+ years' call quality audit experience strongly preferred.
+ 3+ years' experience in a patient support program or hub field would be an asset.
+ Adverse Event reporting and reconciliation experience strongly preferred.
+ Data collection and trend reporting experience is essential for this role.
+ Proficiency in MS Office applications required - Outlook, Excel, PowerPoint, and Word.
+ Excellent verbal and written communication skills.
+ High regard for superior quality of service.
+ Ability to prioritize and manage multiple responsibilities.
+ Experience handling tasks where attention to detail is critical to success.
+ Bilingual Spanish would be an asset.
**What is expected of you and others at this level:**
+ Demonstrates strong leadership and collaboration skills with a proven ability to develop and execute effective quality assurance programs.
+ Works independently within established procedures; may receive general guidance on new assignments.
+ May provide general guidance or technical assistance to less experienced team members.
+ Excellent attention to detail and problem-solving skills.
+ Strong communication and interpersonal skills.
+ Ability to analyze data and generate reports.
+ Ability to drive process improvements and implement quality assurance procedures.
**TRAINING AND WORK SCHEDULES:** Your new hire training will take place 8:00am-5:00pm CT, mandatory attendance is required.
This position is full-time (40 hours/week). Employees are required to have flexibility to work any of our shift schedules during our normal business hours of Monday-Friday, 7:00am- 7:00pm CT.
**REMOTE DETAILS:** You will work remotely, full-time. It will require a dedicated, quiet, private, distraction free environment with access to high-speed internet. We will provide you with the computer, technology and equipment needed to successfully perform your job. You will be responsible for providing high-speed internet. Internet requirements include the following:
+ Maintain a secure, high-speed, broadband internet connection (DSL, Cable, or Fiber) at the remote location. Dial-up, satellite, WIFI, Cellular connections are NOT acceptable. Download speed of 15Mbps (megabyte per second)
+ Upload speed of 5Mbps (megabyte per second)
+ Ping Rate Maximum of 30ms (milliseconds)
+ Hardwired to the router
+ Surge protector with Network Line Protection for CAH issued equipment
**TRAINING AND WORK SCHEDULES:** Your new hire training will take place 8:00am-5:00pm CT, mandatory attendance is required.
This position is full-time (40 hours/week). Employees are required to have flexibility to work any of our shift schedules during our normal business hours of Monday-Friday, 7:00am- 7:00pm CT.
**REMOTE DETAILS:** You will work remotely, full-time. It will require a dedicated, quiet, private, distraction free environment with access to high-speed internet. We will provide you with the computer, technology and equipment needed to successfully perform your job. You will be responsible for providing high-speed internet. Internet requirements include the following:
Maintain a secure, high-speed, broadband internet connection (DSL, Cable, or Fiber) at the remote location. **Dial-up, satellite, WIFI, Cellular connections are NOT acceptable** . Download speed of 15Mbps (megabyte per second)
+ Upload speed of 5Mbps (megabyte per second)
+ Ping Rate Maximum of 30ms (milliseconds)
+ Hardwired to the router
+ Surge protector with Network Line Protection for CAH issued equipment
**Anticipated hourly range:**  $21.50 per hour - $30.70 per hour
**Bonus eligible:**  No
**Benefits:**  Cardinal Health offers a wide variety of benefits and programs to support health and well-being.
+ Medical, dental and vision coverage
+ Paid time off plan
+ Health savings account (HSA)
+ 401k savings plan
+ Access to wages before pay day with myFlexPay
+ Flexible spending accounts (FSAs)
+ Short- and long-term disability coverage
+ Work-Life resources
+ Paid parental leave
+ Healthy lifestyle programs
**Application window anticipated to close:**  12/22/2025 *if interested in opportunity, please submit application as soon as possible. The hourly range listed is an estimate. Pay at Cardinal Health is determined by multiple factors including, but not limited to, a candidate's geographical location, relevant education, experience and skills and an evaluation of internal pay equity.
_Candidates who are back-to-work, people with disabilities, without a college degree, and Veterans are encouraged to apply._
_Cardinal Health supports an inclusive workplace that values diversity of thought, experience and background. We celebrate the power of our differences to create better solutions for our customers by ensuring employees can be their authentic selves each day. Cardinal Health is an Equal_ _Opportunity/Affirmative_ _Action employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, ancestry, age, physical or mental disability, sex, sexual orientation, gender identity/expression, pregnancy, veteran status, marital status, creed, status with regard to public assistance, genetic status or any other status protected by federal, state or local law._
_To read and review this privacy notice click_ here (

Bring more to life.
Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?
At Aldevron, one of Danaher's ( 15+ operating companies, our work saves lives-and we're all united by a shared commitment to innovate for tangible impact.
You'll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher's system of continuous improvement, you help turn ideas into impact - innovating at the speed of life.
At Aldevron, we deliver world-class CDMO services that accelerate the development of groundbreaking therapies. Our mission is to be the engine of innovation for genomic medicine pioneers. As a member of our team, you'll help bring life-changing innovations to life-impacting millions around the world. We bring together deep scientific expertise, an unwavering commitment to quality, and a collaborative spirit to drive progress. Whether you're launching your career or bringing years of experience, we value the unique perspective you bring. Join us and become part of a mission-driven team advancing science and unlocking human potential-one discovery at a time.
Learn about the Danaher Business System ( which makes everything possible.
The Scientist II, Quality Control is responsible for performing a broad range of QC assays to support manufacturing, stability, and method validation. The Scientist II is a Subject Matter Expert in one or more analytical technical areas.
This position reports to the Quality Control Supervisor and is part of the Quality Control Group located in Madison, Wisconsin and will be an on-site role.
In this role, you will have the opportunity to:
+ Independently perform complex QC assays for biological macromolecules (Concentration, Purity, Activity, Residual, Compendial) according to established standard operating procedures under minimal direction from the QC Supervisor
+ Represent Aldevron in internal and external client meetings as a Subject Matter Expert in one or more analytical technical areas
+ Lead investigations for Out of Specification / Out of Trend results using hypothesis tests and root cause analysis techniques; applies sustainable corrective actions
+ Train and mentor Quality Control Scientists and Analysts
+ Write and revise Standard Operating Procedures, Forms, Protocols, and Reports
The essential requirements of the job include:
+ Bachelor's degree in Scientific field + 5 years of experience working in a related laboratory environment OR Master's +2 years OR Ph.D. + 1 year
+ Knowledge of Quality Management Systems (ISO 13485 or cGMP) and Good Documentation Practices
+ Experience in writing complex technical SOPs for clarity and ease of use
It would be a plus if you also possess previous experience in:
+ Analytical Method Optimization and Transfer
+ Electronic Laboratory Information Management Systems (LIMS)
Aldevron, a Danaher operating company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether it's a health care program or paid time off, our programs contribute to life beyond the job. Check out our benefits at Danaher Benefits Info ( .
#LI-GC1
Join our winning team today. Together, we'll accelerate the real-life impact of tomorrow's science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.
For more information, visit .
Danaher Corporation and all Danaher Companies are committed to equal opportunity regardless of race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law.
The U.S. EEO posters are available here ( .
We comply with federal and state disability laws and make reasonable accommodations for applicants and employees with disabilities. If reasonable accommodation is needed to participate in the job application or interview process, to perform essential job functions, and/or to receive other benefits and privileges of employment, please contact: or .

Our client is seeking a meticulous and experienced Senior Quality Control Engineer to join their advanced manufacturing facility in **Madison, Wisconsin, US**. This role is essential in ensuring the highest standards of product quality and process integrity throughout the manufacturing lifecycle. The ideal candidate will possess a strong background in quality management systems, statistical process control, and root cause analysis, coupled with a proactive approach to identifying and mitigating potential defects.
Responsibilities:

• Develop, implement, and maintain comprehensive quality control plans and procedures.
• Oversee and manage all quality assurance activities on the production floor.
• Conduct regular inspections and audits of raw materials, in-process components, and finished goods.
• Utilize statistical process control (SPC) techniques to monitor and improve manufacturing processes.
• Lead root cause analysis investigations for non-conformances and implement corrective and preventive actions (CAPA).
• Collaborate with engineering, production, and supply chain teams to address quality issues promptly.
• Develop and manage quality metrics and reporting systems, providing insights to management.
• Ensure compliance with industry standards, regulatory requirements, and customer specifications.
• Train and mentor quality technicians and other production personnel on quality procedures and best practices.
• Manage calibration and maintenance programs for quality testing equipment.
• Participate in the qualification and validation of new equipment and processes.
• Drive continuous improvement initiatives to enhance product quality and reduce waste.
• Review and approve production documentation, including work instructions and inspection records.

Qualifications:

• Bachelor's degree in Engineering (Mechanical, Electrical, Industrial) or a related technical field.
• Minimum of 7 years of experience in quality control or quality assurance within a manufacturing environment.
• In-depth knowledge of quality management systems (e.g., ISO 9001, AS9100, IATF 16949).
• Proficiency in statistical analysis tools and software (e.g., Minitab, JMP).
• Experience with Six Sigma methodologies and Green/Black Belt certification is highly desirable.
• Strong understanding of various manufacturing processes and quality inspection techniques.
• Excellent analytical, problem-solving, and decision-making abilities.
• Superior communication, interpersonal, and leadership skills.
• Ability to read and interpret blueprints, technical drawings, and specifications.
• Experience with metrology and calibration principles.
• Familiarity with Lean Manufacturing principles.

This role offers a competitive salary, excellent benefits, and the opportunity to make a significant impact on product excellence.

Our client is seeking a highly skilled and meticulous Advanced Quality Control Technician to join their dynamic manufacturing facility in Madison, Wisconsin, US . This is a critical role responsible for ensuring the highest standards of product quality throughout the production process. The ideal candidate will possess a strong understanding of manufacturing processes, quality control methodologies, and statistical analysis. You will be instrumental in identifying, analyzing, and resolving quality issues, contributing directly to the efficiency and reputation of our production lines.

Key Responsibilities:

• Conduct thorough inspections and tests on raw materials, in-process components, and finished goods to verify compliance with specifications and quality standards.
• Operate and maintain a variety of precision measurement and testing equipment.
• Analyze test results, identify trends, and report deviations to engineering and production teams.
• Develop and implement corrective actions to address quality issues and prevent recurrence.
• Participate in root cause analysis investigations for non-conforming products.
• Contribute to the continuous improvement of quality control procedures and documentation.
• Maintain accurate and comprehensive records of all quality control activities.
• Collaborate with production staff to ensure adherence to quality protocols and standards.
• Stay updated on industry best practices and emerging quality control technologies.
• Assist in the training of new quality control personnel.
• Ensure a safe and organized work environment, adhering to all safety regulations.

Qualifications:

• Associate's or Bachelor's degree in a related field (e.g., Manufacturing Technology, Engineering) or equivalent practical experience.
• Proven experience (3+ years) in a quality control role within a manufacturing environment.
• Proficiency in using various quality control instruments and testing equipment.
• Solid understanding of ISO 9001 or similar quality management systems.
• Familiarity with statistical process control (SPC) techniques.
• Strong analytical and problem-solving skills with a keen eye for detail.
• Excellent communication and interpersonal skills, with the ability to work effectively in a team.
• Proficiency in Microsoft Office Suite, particularly Excel for data analysis.
• Ability to read and interpret technical drawings and specifications.
• Must be able to work effectively in a hybrid model, balancing on-site responsibilities with potential remote collaboration.
• Physical ability to stand for extended periods, lift moderate weights, and perform manual tasks as required.

This role offers a competitive salary and benefits package. Join us and make a significant impact on the quality of our products.

Our client is seeking an experienced and meticulous Quality Control Manager to lead their quality assurance initiatives within their manufacturing operations in **Madison, Wisconsin, US**. This crucial role will be responsible for establishing and maintaining robust quality control systems to ensure products consistently meet high standards and regulatory requirements. You will oversee inspection processes, implement quality improvement programs, manage a team of quality technicians, and collaborate with production and engineering teams to identify and resolve quality issues. The ideal candidate will possess a strong understanding of manufacturing quality principles, excellent analytical skills, and proven leadership capabilities.

Key Responsibilities:

• Develop, implement, and manage the company's quality control system in accordance with industry standards and customer requirements.
• Oversee all quality inspection and testing activities, ensuring product conformity at various stages of the manufacturing process.
• Manage and train a team of quality control inspectors and technicians, providing guidance and support.
• Establish and monitor key quality metrics, analyzing trends and implementing corrective and preventive actions (CAPA).
• Collaborate closely with production and engineering teams to address quality concerns and implement process improvements.
• Conduct regular internal audits of manufacturing processes and quality systems.
• Ensure compliance with relevant quality standards (e.g., ISO 9001) and regulatory requirements.
• Manage the disposition of non-conforming materials and products.
• Develop and maintain quality documentation, including inspection procedures and quality reports.
• Lead continuous improvement initiatives aimed at enhancing product quality and reducing defects.
• Act as the primary point of contact for quality-related customer inquiries and audits.
• Stay abreast of evolving quality control technologies and best practices.

Qualifications:

• Bachelor's degree in Engineering, Quality Management, or a related field.
• Minimum of 5 years of experience in quality control or quality assurance within a manufacturing environment.
• Proven experience in developing and implementing quality management systems.
• Strong understanding of manufacturing processes and quality control methodologies (e.g., Six Sigma, Lean, SPC).
• Experience with quality inspection tools and techniques.
• Excellent leadership, communication, and problem-solving skills.
• Proficiency in quality management software and data analysis tools.
• Ability to interpret technical drawings and specifications.
• Experience with regulatory compliance and audits is a plus.
• Strong attention to detail and a commitment to upholding quality standards.

Our client, a leading pharmaceutical company, is looking for a meticulous and experienced Senior Pharmaceutical Quality Control Analyst to join their team in Madison, Wisconsin, US . This role is critical in ensuring the quality and safety of our pharmaceutical products through rigorous testing and analysis. You will be responsible for performing a variety of analytical tests on raw materials, in-process samples, and finished products using advanced laboratory equipment and techniques. This includes developing and validating analytical methods, troubleshooting instrumentation, and maintaining detailed laboratory records in compliance with regulatory standards (e.g., FDA, GMP). The ideal candidate will have a strong background in analytical chemistry, pharmaceutical sciences, or a related field, with extensive experience in QC laboratory operations. You must be proficient in various analytical techniques such as HPLC, GC, spectroscopy (UV-Vis, FTIR), and dissolution testing. Excellent understanding of current Good Manufacturing Practices (cGMP) and regulatory requirements is essential. This position requires strong problem-solving skills, the ability to interpret complex data, and meticulous attention to detail. You will also be involved in investigations of out-of-specification (OOS) results and contribute to continuous improvement initiatives within the QC department. Collaboration with R&D, manufacturing, and regulatory affairs teams is expected. This is a challenging and rewarding opportunity for a dedicated scientist seeking to make a significant impact in the pharmaceutical industry. You will work within a state-of-the-art facility in Madison, Wisconsin, US and contribute to the development and production of life-changing medicines. The role demands accuracy, efficiency, and a commitment to upholding the highest quality standards. A Bachelor's or Master's degree in a relevant scientific discipline is required, along with significant hands-on experience in pharmaceutical QC.

**Catalyst + Talent**
A Catalent internship offers you countless opportunities to have direct impact on the health and well-being of millions of people globally! Your passion for learning coupled with Catalent's superior technologies will help drive the advancement of medicine in collaboration with leading pharmaceutical, biotech and health care innovators.
The Catalent Internship Experience includes
+ **Opportunity** to make an impact in the lives of patients all over the world!
+ **Experience** through hands-on projects that support more superior drug development and delivery technologies than anyone else.
+ **Exposure** to top-tier scientists and industry leaders.
+ **Commitment** from dedicated managers and mentors who are advocates for your success and career development.
+ **Access** to collaborative and highly engaged colleagues across the globe excited to share their knowledge and provide you support.
**The Role**
The Quality Control team is responsible for ensuring that all manufactured products meet specified standards for quality and safety. This is accomplished by inspecting, testing and/or measuring materials of the products being produced. The Quality Control Interns will support the department by performing the day-to-day activities needed to ensure that this process continues seamlessly.
**Additional responsibilities could include:**
+ Defining, measuring, analyzing, and improving identified processes within the quality organization
+ Performing data analysis for established metrics and identifying potential new metrics
+ Supporting continuous improvement projects assigned potentially within regulatory compliance, internal/supplier auditing, or customer focus activities
+ Performing the necessary daily responsibilities in accordance with current Standard Operating Procedures (SOPs) and GMP regulations
+ Maintaining open and effective communication with all other Quality Control team members
+ Database entry
+ Other duties as assigned
**The Candidate**
In order to be eligible for a Quality Control, Analytics internship at Catalent, you must meet the following requirements:
+ Currently enrolled in an accredited college or university
+ Must be an undergraduate/graduate student in the sciences, engineering, public health, pharmacy, or related field of study
+ Eligible to legally work in the United States
+ Ability to work full-time (40 hours/week) for a 10-12-week period over the summer
+ Individual may be required to sit, stand, walk regularly and occasionally lift 0-15 pounds
**Catalent offers rewarding opportunities to further your career!** Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference.
personal initiative. dynamic pace. meaningful work.
Visit Catalent Careers ( to explore career opportunities.
Catalent is an Equal Opportunity Employer, including disability and veterans.
If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to . This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process.
Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.
Important Security Notice to U.S. Job Seekers:
Catalent NEVER asks candidates to provide any type of payment, bank details, photocopies of identification, social security number or other highly sensitive personal information during the offer process, and we NEVER do so via email or social media. If you receive any such request, DO NOT respond- it is a fraudulent request. Please forward such requests to for us to investigate with local authorities.
California Job Seekers can find our California Job Applicant Notice HERE ( .

**Intern - Quality Control, Microbiology**
**Catalyst + Talent**
A Catalent internship offers you countless opportunities to have direct impact on the health and well-being of millions of people globally! Your passion for learning coupled with Catalent's superior technologies will help drive the advancement of medicine in collaboration with leading pharmaceutical, biotech and health care innovators.
The Catalent Internship Experience includes
+ **Opportunity** to make an impact in the lives of patients all over the world!
+ **Experience** through hands-on projects that support more superior drug development and delivery technologies than anyone else.
+ **Exposure** to top-tier scientists and industry leaders.
+ **Commitment** from dedicated managers and mentors who are advocates for your success and career development.
+ **Access** to collaborative and highly engaged colleagues across the globe excited to share their knowledge and provide you support.
**The Role**
The Quality Control team is responsible for ensuring that all manufactured products meet specified standards for quality and safety. This is accomplished by inspecting, testing and/or measuring materials of the products being produced. The Quality Control Interns will support the department by performing the day-to-day activities needed to ensure that this process continues seamlessly.
**Additional responsibilities could include:**
+ Defining, measuring, analyzing, and improving identified processes within the quality organization
+ Performing data analysis for established metrics and identifying potential new metrics
+ Supporting continuous improvement projects assigned potentially within regulatory compliance, internal/supplier auditing, or customer focus activities
+ Performing the necessary daily responsibilities in accordance with current Standard Operating Procedures (SOPs) and GMP regulations
+ Maintaining open and effective communication with all other Quality Control team members
+ Database entry
+ Enhance documentation and compliance skills in a regulated environment.
+ Participate in laboratory housekeeping and equipment maintenance.
+ Other duties as assigned
**The Candidate**
In order to be eligible for a Quality Control - Microbiology internship at Catalent, you must meet the following requirements:
+ Currently enrolled in an accredited college or university
+ Must be an undergraduate/graduate student majoring in life sciences to include Biology, Cell Biology, Microbiology, Molecular Biology, Biochemistry, Engineering or related field of study
+ Eligible to legally work in the United States
+ Ability to work full-time (40 hours/week) for a 10-12-week period over the summer
+ Individual may be required to sit, stand, walk regularly and occasionally lift 0-15 pounds
**Catalent offers rewarding opportunities to further your career!** Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference.
personal initiative. dynamic pace. meaningful work.
Visit Catalent Careers ( to explore career opportunities.
Catalent is an Equal Opportunity Employer, including disability and veterans.
If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to . This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process.
Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.
Important Security Notice to U.S. Job Seekers:
Catalent NEVER asks candidates to provide any type of payment, bank details, photocopies of identification, social security number or other highly sensitive personal information during the offer process, and we NEVER do so via email or social media. If you receive any such request, DO NOT respond- it is a fraudulent request. Please forward such requests to for us to investigate with local authorities.
California Job Seekers can find our California Job Applicant Notice HERE ( .