Executes and properly documents cGMP Quality Control testing with supervision. * Operates basic cGMP Quality Control equipment. * Performs self-review of analytical data for accuracy and consistency ...
Executes and properly documents cGMP Quality Control testing with supervision. * Operates basic cGMP Quality Control equipment. * Performs self-review of analytical data for accuracy and consistency ...
Designing data models for risk and controls domains, including key risk indicators, issues and defects, risk acceptance, control testing outcomes, audit evidence, and policy exceptions, and enabling ...
Designing data models for risk and controls domains, including key risk indicators, issues and defects, risk acceptance, control testing outcomes, audit evidence, and policy exceptions, and enabling ...
Jr. Data Engineer
Germantown, WI · On-site
$116K - $139K/yr
Follow best practices for version control, testing, and deployment Qualifications * Bachelor's degree in Computer Science, Data Engineering, Information Systems, or related field (or equivalent ...
Quick apply
Jr. Data Engineer
Germantown, WI · On-site
$116K - $139K/yr
Follow best practices for version control, testing, and deployment Qualifications * Bachelor's degree in Computer Science, Data Engineering, Information Systems, or related field (or equivalent ...
Senior Auditor - Compliance
Milwaukee, WI · On-site
$79K - $98K/yr
Responsibilities include performing or overseeing control testing and documenting results in accordance with internal audit standards. The role partners with Lines of Business and RCA stakeholders to ...
Senior Auditor - Compliance
Milwaukee, WI · On-site
$79K - $98K/yr
Responsibilities include performing or overseeing control testing and documenting results in accordance with internal audit standards. The role partners with Lines of Business and RCA stakeholders to ...
Senior Auditor - Corporate Treasury
Milwaukee, WI · On-site
$79K - $98K/yr
Includes using appropriate sampling and control testing techniques; identifying and assessing the relevancy of possible issues; and documenting work performed to support audit scope/conclusions, to ...
Senior Auditor - Corporate Treasury
Milwaukee, WI · On-site
$79K - $98K/yr
Includes using appropriate sampling and control testing techniques; identifying and assessing the relevancy of possible issues; and documenting work performed to support audit scope/conclusions, to ...
Senior Auditor - Payment Services
$79K - $98K/yr
Includes using appropriate sampling and control testing techniques; identifying and assessing the relevancy of possible issues; and documenting work performed to support audit scope/conclusions, to ...
Senior Auditor - Payment Services
$79K - $98K/yr
Includes using appropriate sampling and control testing techniques; identifying and assessing the relevancy of possible issues; and documenting work performed to support audit scope/conclusions, to ...
Senior Auditor - Compliance
$79K - $98K/yr
Includes using appropriate sampling and control testing techniques; identifying and assessing the relevancy of possible issues; and documenting work performed to support audit scope/conclusions, to ...
Senior Auditor - Compliance
$79K - $98K/yr
Includes using appropriate sampling and control testing techniques; identifying and assessing the relevancy of possible issues; and documenting work performed to support audit scope/conclusions, to ...
Manager, Quality Control
Madison, WI · On-site
Provides Quality Control oversight of all cGMP testing of raw materials, in process, product release, clean utility and environmental monitoring testing. Review and approve all QC related ...
Manager, Quality Control
Madison, WI · On-site
Provides Quality Control oversight of all cGMP testing of raw materials, in process, product release, clean utility and environmental monitoring testing. Review and approve all QC related ...
Provides Quality Control oversight of all cGMP testing of raw materials, in process, product release, clean utility and environmental monitoring testing. Review and approve all QC related ...
Provides Quality Control oversight of all cGMP testing of raw materials, in process, product release, clean utility and environmental monitoring testing. Review and approve all QC related ...
Sr Compliance / Regulatory Analyst - Information Lifecycle Management
Appleton, WI · On-site
$81K - $110K/yr
Conducting control testing, responding to internal audit requests, and responding to regulatory requests as applicable * Managing the offsite storage and onsite shredding processes and vendors
Sr Compliance / Regulatory Analyst - Information Lifecycle Management
Appleton, WI · On-site
$81K - $110K/yr
Conducting control testing, responding to internal audit requests, and responding to regulatory requests as applicable * Managing the offsite storage and onsite shredding processes and vendors
Quality Control
Monroe, WI · On-site
$21/hr
The Quality Control Technician plays a critical role in ensuring product quality, compliance, and ... Perform testing and measurement of products to ensure compliance with Orchid Monroe, LLC and ...
Quality Control
Monroe, WI · On-site
$21/hr
The Quality Control Technician plays a critical role in ensuring product quality, compliance, and ... Perform testing and measurement of products to ensure compliance with Orchid Monroe, LLC and ...
Quality Control
Monroe, WI · On-site
$21/hr
The Quality Control Technician plays a critical role in ensuring product quality, compliance, and ... Perform testing and measurement of products to ensure compliance with Orchid Monroe, LLC and ...
Quality Control
Monroe, WI · On-site
$21/hr
The Quality Control Technician plays a critical role in ensuring product quality, compliance, and ... Perform testing and measurement of products to ensure compliance with Orchid Monroe, LLC and ...
Control System Engineer
Hartford, WI · On-site
Support functional testing, validation, and verification of control systems * Ensure systems comply with applicable electrical and safety standards * Implement safe machine control practices ...
Quick apply
Control System Engineer
Hartford, WI · On-site
Support functional testing, validation, and verification of control systems * Ensure systems comply with applicable electrical and safety standards * Implement safe machine control practices ...
Quality Control Scientist
Madison, WI · On-site
$26 - $32/hr
Quality Control Scientist The Quality Control Scientist supports an in‑house Quality Control team ... This role focuses on DNA and RNA testing, including sequencing and contamination analysis, and ...
New
Quick apply
Quality Control Scientist
Madison, WI · On-site
$26 - $32/hr
Quality Control Scientist The Quality Control Scientist supports an in‑house Quality Control team ... This role focuses on DNA and RNA testing, including sequencing and contamination analysis, and ...
New
Quality Control Scientist
$26 - $32/hr
Quality Control Scientist The Quality Control Scientist supports an in‑house Quality Control team ... This role focuses on DNA and RNA testing, including sequencing and contamination analysis, and ...
New
Quick apply
Quality Control Scientist
$26 - $32/hr
Quality Control Scientist The Quality Control Scientist supports an in‑house Quality Control team ... This role focuses on DNA and RNA testing, including sequencing and contamination analysis, and ...
New
Control Systems Engineer
Beaver Dam, WI · On-site
$72K - $84K/yr
Support control system engineering tasks including design development, testing, and system integration. * Assist with installation, startup, commissioning, and troubleshooting of automation systems.
Control Systems Engineer
Beaver Dam, WI · On-site
$72K - $84K/yr
Support control system engineering tasks including design development, testing, and system integration. * Assist with installation, startup, commissioning, and troubleshooting of automation systems.
$72K - $84K/yr
Support control system engineering tasks including design development, testing, and system integration. * Assist with installation, startup, commissioning, and troubleshooting of automation systems.
$72K - $84K/yr
Support control system engineering tasks including design development, testing, and system integration. * Assist with installation, startup, commissioning, and troubleshooting of automation systems.
Quality Control & Testing: Schedule and lead the internal Factory Acceptance Testing (FAT) process prior to shipment, and inspect machinery exiting production to ensure quality standards.
Quick apply
Quality Control & Testing: Schedule and lead the internal Factory Acceptance Testing (FAT) process prior to shipment, and inspect machinery exiting production to ensure quality standards.
Quality Control Supervisor
Waukesha, WI · On-site
Quality Control Supervisor About Walbec Group Walbec produces high-quality construction materials ... Audit projects, laboratories, and evaluates team members to ensure the testing and reporting is ...
Quality Control Supervisor
Waukesha, WI · On-site
Quality Control Supervisor About Walbec Group Walbec produces high-quality construction materials ... Audit projects, laboratories, and evaluates team members to ensure the testing and reporting is ...
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Chemical Laboratory Technician/SS
Wauwatosa, WI · On-site
$22 - $24/hr
Prepare samples for internal testing and customer evaluations. * Support quality control and product validation activities. * Maintain laboratory cleanliness, organization, and safety standards ...
New
Quick apply
Be Seen First
Chemical Laboratory Technician/SS
Wauwatosa, WI · On-site
$22 - $24/hr
Prepare samples for internal testing and customer evaluations. * Support quality control and product validation activities. * Maintain laboratory cleanliness, organization, and safety standards ...
New
Control Testing information
What is Control Testing?
Control testing is the process of evaluating whether an organization's internal controls are properly designed and operating effectively to manage risks and achieve business objectives. It involves assessing procedures, policies, and activities to ensure compliance with laws, regulations, and internal standards. Control testing is commonly used in auditing, risk management, and compliance to identify weaknesses or gaps in controls, helping organizations improve their processes and reduce the likelihood of errors or fraud.
What are some common challenges faced by professionals in Control Testing, and how can they be addressed?
Professionals in Control Testing often encounter challenges such as keeping up with constantly evolving regulatory requirements and ensuring comprehensive coverage of all control activities. Another common challenge is coordinating with various departments to gather accurate documentation and evidence, which can be time-consuming. To address these issues, it's helpful to stay current with industry standards, build strong communication channels across teams, and use automation tools to streamline testing processes. Developing a systematic approach to documentation and regularly reviewing control frameworks also contribute to more effective testing outcomes.
What are the key skills and qualifications needed to thrive in Control Testing, and why are they important?
To thrive in Control Testing, you need a strong understanding of risk management, internal controls, and auditing principles, often supported by a degree in accounting, finance, or a related field. Familiarity with audit software, data analytics tools (such as ACL or IDEA), and certifications like CIA or CISA are typically required. Attention to detail, analytical thinking, and effective communication are essential soft skills for evaluating processes and reporting findings clearly. These skills and qualifications are crucial for accurately identifying control weaknesses and ensuring regulatory compliance within organizations.
What is the difference between Control Testing vs Control Documentation?
| Aspect | Control Testing | Control Documentation |
|---|---|---|
| Primary Focus | Evaluating the effectiveness of controls through testing procedures | Documenting controls, policies, and procedures for compliance and reference |
| Required Credentials | Typically CPA, CIA, or similar certifications; auditing experience | Often similar credentials; focus on documentation standards and compliance |
| Work Environment | Audit engagements, testing environments, internal or external audits | Policy writing, process mapping, compliance documentation |
| Industry Usage | Used in internal controls, SOX compliance, audit processes | Used in control frameworks, policy development, regulatory filings |
Control Testing and Control Documentation are related but distinct roles. Control Testing involves evaluating the effectiveness of controls through testing procedures, while Control Documentation focuses on creating and maintaining detailed records of controls and policies. Both roles often require similar credentials and are essential in compliance and audit processes, but they serve different functions within an organization’s control environment.
What are popular job titles related to Control Testing jobs in Wisconsin? For Control Testing jobs in Wisconsin, the most frequently searched job titles are:
What job categories do people searching Control Testing jobs in Wisconsin look for? The top searched job categories for Control Testing jobs in Wisconsin are:
Full-time
Life, PTO
Posted 19 hours ago
Catalent rating
7.4
Based on 52 frontline employees who took The Breakroom Quiz
53rd of 73 rated pharmaceutical
Job description
Associate Scientist I - Quality Control, AQC
Position Summary:
Catalent Biologics is a fast-growing business within Catalent Pharma Solutions focused on providing innovative technologies and solutions to help more and better biologic treatments get to patients. The business includes our proprietary GPEx cell line engineering platform, our new state-of-the-art biomanufacturing facility in Madison, WI, and our leading biologics analytical services in Kansas City, MO and Research Triangle Park, NC, as well as SMARTag Antibody Drug Conjugate technology in Emeryville, CA. Leveraging our growing differentiated technology portfolio, world class manufacturing capability, and other integrated services across the Catalent network, Catalent Biologics is positioned to drive significant growth for Catalent.
Catalent Pharma Solutions in Madison, WI is hiring an Associate Scientist I - Quality Control, Raw Materials. This position requires a variety of skills necessary for biotech company operations. The position is an entry level laboratory role with the expectation that the candidate can be trained in technical procedures and once trained, execute them consistently and reliably. Additionally, this position may support preventative maintenance and basic laboratory maintenance activities while maintaining a GMP quality system.
The Role:
The Candidate:
Why you should join Catalent:
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 DisabilityAccommodations@catalent.com. 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 spam@catalent.com for us to investigate with local authorities.
California Job Seekers can find our California Job Applicant Notice HERE.
Position Summary:
- Work Schedule: M-F 11am-7pm (2nd shift)
- 100% on-site
Catalent Biologics is a fast-growing business within Catalent Pharma Solutions focused on providing innovative technologies and solutions to help more and better biologic treatments get to patients. The business includes our proprietary GPEx cell line engineering platform, our new state-of-the-art biomanufacturing facility in Madison, WI, and our leading biologics analytical services in Kansas City, MO and Research Triangle Park, NC, as well as SMARTag Antibody Drug Conjugate technology in Emeryville, CA. Leveraging our growing differentiated technology portfolio, world class manufacturing capability, and other integrated services across the Catalent network, Catalent Biologics is positioned to drive significant growth for Catalent.
Catalent Pharma Solutions in Madison, WI is hiring an Associate Scientist I - Quality Control, Raw Materials. This position requires a variety of skills necessary for biotech company operations. The position is an entry level laboratory role with the expectation that the candidate can be trained in technical procedures and once trained, execute them consistently and reliably. Additionally, this position may support preventative maintenance and basic laboratory maintenance activities while maintaining a GMP quality system.
The Role:
- Executes and properly documents cGMP Quality Control testing with supervision.
- Operates basic cGMP Quality Control equipment.
- Performs self-review of analytical data for accuracy and consistency with SOP.
- Enters data into Laboratory Information Management System (LIMS) or laboratory reports.
- Frequently lift and/or move up to 10 pounds and occasional lifting and/or moving up to 50 pounds.
- Handles products using material handling equipment.
- Conducts inspections on inbound single use manufacturing materials in a warehouse environment.
- Performs general lab housekeeping in adherence to 5S standards.
- Accurately completes routine and preventive maintenance on basic equipment.
- Actively participates in team meetings and/or training sessions.
- Other duties as assigned.
The Candidate:
- Bachelor's Degree in Biology, Biotechnology, Chemistry, or related life sciences field.
- Associate Degree in Biology, Biotechnology, Chemistry, or related life sciences field with a minimum of 1 year of industry experience.
- High School Diploma or equivalent with a minimum of 4 years of industry experience.
- Preferred:
- Basic understanding of analytical chemistry and simple lab equipment.
- Familiarity with clean room procedure, aseptic technique, and general lab equipment experience.
- cGMP, Good Documentation Practices (GDP), or Good Laboratory Practices (GLP) knowledge.
- Experience following standard operating procedures (SOP).
- General laboratory equipment experience, including micropipettes.
Why you should join Catalent:
- Defined career path and annual performance review and feedback process
- Diverse, inclusive culture
- Positive working environment focusing on continually improving processes to remain innovative
- Potential for career growth on an expanding team within an organization dedicated to preserving and bettering lives
- 152 hours of PTO + 8 paid holidays
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 DisabilityAccommodations@catalent.com. 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 spam@catalent.com for us to investigate with local authorities.
California Job Seekers can find our California Job Applicant Notice HERE.
About Catalent
Sourced by ZipRecruiter
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.Catalent is committed to the health and safety of its employees, visitors and the customers and patients we serve.
Industry
Pharmaceutical product wholesalers
Company size
10,000+ Employees
Headquarters location
Somerset, NJ, US
Year founded
2007