1,000+ matching jobs for “Associate Product Operations”How results work Exact titles rank first, then title variations and keywords in descriptions. These labels aren't qualification scores. Without keywords, recently added jobs appear first.
… planning, and/or cross-functional collaboration Preferred Skills/Education 1 year of leadership experience Product data governance experience Experience in Microsoft products (Outlook, PowerPoint, etc.) and relational …
Added Oct 27, 2026
… of the Amgen team. Join us and transform the lives of patients while transforming your career. Sr. Digital Product Manager, Product Operations - Tech Enablers & PDLC What you will do The Senior Product Manager, Product …
Added Oct 15, 2026
2 postings
Pay posted by employer $41,600–$66,560
… initiatives. Qualifications & Experience • Bachelor’s degree or equivalent work experience. • 2–4 years of operations experience within asset management, custody, fund accounting, or ETF servicing is a plus • Working …
Added Oct 27, 2026
2 postings
Pay posted by employer $41,600–$66,560
The Associate II, Basket Operations supports the daily production, validation, and release of ETF creation and redemption …
Added Oct 27, 2026
2 postings
Pay posted by employer $41,600–$66,560
… initiatives. Qualifications & Experience • Bachelor’s degree or equivalent work experience. • 2–4 years of operations experience within asset management, custody, fund accounting, or ETF servicing is a plus • Working …
Added Oct 27, 2026
Pay posted by employer $41,600–$66,560
The Associate II, Basket Operations supports the daily production, validation, and release of ETF creation and redemption …
Added Oct 27, 2026
Pay posted by employer $90,000–$110,000 per year
… Where Your Career is a Force for Good! WHAT YOU NEED TO KNOW (Job Overview): The Humanitarian Services Product Management team aspires to create human-centered digital experiences for our clients and workforce and to …
Added Oct 13, 2026
Pay posted by employer $71,900–$113,200
… improved manufacturing process development, and seamless technology transfer to commercial sites. The SSO Operations Specialist will provide hands on assistance for daily production activities while ensuring compliance with …
Added Oct 18, 2026
Pay posted by employer $71,900–$113,200
… improved manufacturing process development, and seamless technology transfer to commercial sites. The SSO Operations Specialist will provide hands on assistance for daily production activities while ensuring compliance with …
Added Oct 18, 2026
Pay posted by employer $41,600–$66,560
From technology and product innovation to corporate responsibility and community development, we’re making our mark on the financial …
Added Oct 28, 2026
Pay posted by employer $41,600–$66,560
of Derivative Operations Specialist you will be responsible for: Job Duties and Responsibilities: Use the OTC HUB application to …
Added Oct 28, 2026
Pay posted by employer $195,670–$253,220
The Associate Director, Digital Asset Management (DAM) leads the strategy, product vision, governance, operations, and …
Added Oct 15, 2026
Pay posted by employer $41,600–$66,560
Who we are looking for As an Associate 2 in cash settlement team located in Sacramento, you will be responsible for the oversight/review of daily …
Added Oct 27, 2026
Pay posted by employer $41,600–$66,560
Job Description Who we are looking for As an Associate 2 in cash settlement team located in Sacramento, you will be responsible for the oversight/review of daily …
Added Oct 27, 2026
Pay posted by employer $50,700–$101,300
The Associate Product Support Scientist role will support and assist in a variety of technical support activities within …
Added Oct 15, 2026
Pay posted by employer $134,400–$153,300 per year
Here are a few of the ways our Product Managers are helping people create meaningful interactions with Capital One: Give customers the confidence …
Added Oct 27, 2026
In person Full time Regular … customer focus, and a demonstrated ability to deliver measurable improvements to the customer and associate experience. Key Responsibilities: Analyze the fundamental components of problems and communicate the …
Added Oct 16, 2026
+1 location
Pay posted by employer $95,000–$105,000
… and establishment of Digital Asset solutions. This individual will work across the Digital Asets product team to support strategy, product development, risk governance, business planning and commercialization …
Added Oct 27, 2026
… throughout the packaging process for accuracy and compliance. Conducts final audit prior to submitting to Product Release. Performs serialization activities, including but not limited to sending print, releasing, …
Added Oct 27, 2026
. Manage complaints for commercial Drug Product and Medical Device and Combination Product, ensuring that investigation reports are appropriate and …
Added Oct 16, 2026
Pay posted by employer $50,700–$101,300
Minimum Qualifications · employer excerpt Bachelor’s degree in life sciences or field related to the essential duties of the job. 2+ years of experience in the life sciences industry. Master’s or Doctoral degrees may be considered in lieu of 2 years of experience. Proficient in MS Office Suite (Word, Excel, Outlook, PowerPoint). Demonstrated ability to perform the essential duties of the position with or without accommodation. Authorization to work in the United States without sponsorship.
About this opportunity Original employer description Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 122,000 colleagues serve people in more than 160 countries.
JOB DESCRIPTION: The Associate Product Support Scientist role will support and assist in a variety of technical support activities within Operations. This position will investigate issues through root cause analysis and implement correction actions through use of the Quality Management System supporting Production and Quality Control groups through continuous improvement.
Location : Onsite - Position is based in Madison, WI
Hours: 1st shift, 8am-4:30pm
Essential Duties
Include, but are not limited to, the following:
Provide technical and product support to Operations working cross-functionally with the Production, QC, Supply Chain, R&D, and Quality teams. Perform investigative testing for Out of Specification events (OOS), non-conformances (NCMRs), and corrective action preventive action (CAPA) plans through root cause investigation, experiment design, study execution, data analysis, and reporting. Provide support for PCR-based and/or NGS-based reagents and products. Provide support to Operations teams for qualifying new raw materials and alternative supply channels for products. Demonstrated proficiency in a variety of basic laboratory skills and techniques. Basic knowledge base in Molecular Biology, Biochemistry, Biotechnology, Chemistry, or a related field. Good understanding of in-vitro diagnostic product manufacturing processes and relevant assays (e.g. biochemical, RT-PCR, and NGS). Program, operate, and troubleshoot complex instrumentation such as microplate readers, real-time and digital polymerase chain reaction (PCR) instruments, next-generation sequencers, and liquid handling automation. Assist development and characterization of simple manufacturing processes incorporating industry standard techniques. Assist characterization of basic assay variability for simple measurement systems. Apply basic statistical techniques: assessing data normality, control charting and data trending, hypothesis testing, assessing variation, linear regression and model fitting. Analyze data to identify trends, assists troubleshooting and root cause investigation efforts with ability to utilize recognized root cause analysis tools. Assist investigations into analytical and functional assays, associated equipment, materials, and/or processes. Clearly and accurately generate experimental protocols, draft work instruction procedures, test methods, and summarize development activities through technical summary reports. Support Process and Test Method Validation readiness and execution. Provide support and review in generating Validation documentation. Write new and edit existing Quality System documents (e.g. work instructions, standard operating procedures). Responsible for generating/driving corrective actions/action plans for changes. Collaborate with other departments (Quality Engineering, R&D, Regulatory Affairs, Supply Chain, Production, Validation, Quality Control) to achieve business results. Able to meet objectives without negatively impacting other functions. Actively participates in project execution. Consistently hit deliverables as outlined by manager. Function independently with limited guidance from supervisor as well as part of a team. Adaptable to rapid changes in priorities, strong sense of urgency, and able to identify ways to work together to achieve results needed for all requests. Strong verbal and written communication skills. Uphold company mission and values through accountability, innovation, integrity, quality, and teamwork. Support and comply with the company’s Quality Management System policies and procedures. Maintain regular and reliable attendance. Ability to act with an inclusion mindset and model these behaviors for the organization. Ability to work designated schedule. Ability to work nights and/or weekends, as needed. Ability to work on a mobile device, tablet, or in front of a computer screen and/or perform typing for approximately 80% of a typical working day. Ability to work on a computer and phone simultaneously. Ability to use a telephone through a headset. Ability to work seated for approximately 80% of a typical working day. Ability to work standing for approximately 20% of a typical working day. Ability to lift up to 40 pounds on an occasional basis. Ability to grasp with both hands; pinch with thumb and forefinger; turn with hand/arm; reach above shoulder height. Ability to comply with any applicable personal protective equipment requirements. Ability to use various types of laboratory equipment; including microscopes, microtomes, blades, strainers, and pipettes for extended periods of time. May perform repetitious actions using lab tools. Ability to use near vision to view samples at close range. May be exposed to hazardous materials, tissue specimens, and instruments with moving parts, lasers, heating and freezing elements, and high-speed centrifugation. Ability to work with blood, tissue, stool, or other human specimen samples. Ability and means to frequently travel between local Exact Sciences locations. Ability to travel 5% of working time away from work location, may include overnight/weekend travel. Minimum Qualifications
Bachelor’s degree in life sciences or field related to the essential duties of the job. 2+ years of experience in the life sciences industry. Master’s or Doctoral degrees may be considered in lieu of 2 years of experience. Proficient in MS Office Suite (Word, Excel, Outlook, PowerPoint). Demonstrated ability to perform the essential duties of the position with or without accommodation. Authorization to work in the United States without sponsorship. Preferred Qualifications
Proficiency with statistical analysis software and/or programming (e.g. JMP, R). Experience working within an FDA 21 CFR 820, ISO 13485, and/or cGMP structured environment. Experience with in-vitro diagnostic product development, design transfer, manufacturing, or product support. Experience in a biotech or molecular diagnostics laboratory with nucleic-acid–based workflows (e.g. PCR/qPCR). Familiarity with CAP/CLIA regulatory requirements as they pertain to in vitro diagnostics. We are an equal employment opportunity employer. All qualified applicants will receive consideration for employment without regard to age, color, creed, disability, gender identity, national origin, protected veteran status, race, religion, sex, sexual orientation, and any other status protected by applicable local, state, or federal law. Applicable portions of the Company’s affirmative action program are available to any applicant or employee for inspection upon request.
The base pay for this position is
$50,700.00 – $101,300.00
In specific locations, the pay range may vary from the range posted.
JOB FAMILY: Manufacturing
DIVISION: ONCO Cancer Diagnostics
LOCATION: United States > Madison : 650 Forward Dr
ADDITIONAL LOCATIONS:
WORK SHIFT: Standard
TRAVEL: Not specified
MEDICAL SURVEILLANCE: No
SIGNIFICANT WORK ACTIVITIES: Not Applicable
Abbott is an Equal Opportunity Employer of Minorities/Women/Individuals with Disabilities/Protected Veterans.
EEO is the Law link - English: http://webstorage.abbott.com/common/External/EEO_English.pdf
EEO is the Law link - Espanol: http://webstorage.abbott.com/common/External/EEO_Spanish.pdf
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