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Develop strong working relationships with Rheumatology experts and all additional Rheumatology specialists in assigned geography as well as nurses, office staff and other important health care personnel and key patient advocacy support groups as directed. Coordinate and communicate with other field-based and home office personnel teams to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives within their assigned geography.

Sanofi Pasteur is a world leader in human vaccines.Producing a portfolio of high quality vaccines that match our areas of expertise and ensure a sustainable future.

Providing more than 1 billion doses of vaccines each year making it possible to immunize more than 500 million people worldwide per year.

Sanofi

Rheumatology Key Account Specialist - Puerto Rico

The role provides technical leadership for contamination control, environmental monitoring, microbiological laboratory testing, cleanroom qualification, and sterility assurance activities to support product quality, Quality and Regulatory compliance across manufacturing and laboratory operations. Collaborate with Quality, Operations, Engineering, and other cross-functional teams to conduct GEMBA walks, execute Quality Risk Management activities (including FMEA), support audits and inspections, and advance continuous improvement initiatives.

Danaher is a global science & technology innovator committed to helping our customers solve complex challenges and improve quality of life worldwide. Our world class brands are leaders in some of the most demanding and attractive industries, including life sciences, medical diagnostics, dental, environmental and applied solutions. Our globally diverse team of 71,000 associates is united by a common culture and operating system, the Danaher Business System, which serves as our competitive advantage. We generated $19.9B in revenue last year. We are ranked #162 on the Fortune 500 and our stock has outperformed the S&P 500 by more than 5,200% over 25 years.
At Danaher, you can build a career in a way no other company can duplicate. Our brands allow us to offer dynamic careers across multiple industries. We're innovative, fast-paced, results-oriented, and we win. We need talented people to keep winning. Here you'll learn how DBS is used to shape strategy, focus execution, align our people, and create value for customers and shareholders. Come join our winning team.
Danaher is committed to competitive compensation that typically has key components including base salary, variable annual incentive compensation based on personal and company performance, and long-term incentive.

Danaher Corp

Contamination Control and Sterility Assurance Sr. Specialist

In addition to the base salary, Amgen offers a Total Rewards Plan comprising health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities including:A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental & vision coverage, and life & disability insurance A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan Stock-based long-term incentives Award-winning time-off plans and an annual site shutdown Flexible work models where possible. In this vital role you will will serve as a Quality leader accountable for the investigation and resolution of major deviations, safeguarding product quality and patient safety through sound judgment, strong ownership, cross‑functional collaboration, and effective risk management in a dynamic drug product manufacturing environment.

At Amgen, we believe in a “biology first” approach. We use cutting-edge science and technology to study the subtlest biological mechanisms in search of therapies that will improve the lives of those who suffer from serious diseases. Amgen believes the cure for disease can be found inside each and every one of us.

Amgen Inc

Specialist Quality Assurance - Major Deviations

In addition to the base salary, Amgen offers a Total Rewards Plan comprising health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities including: A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental & vision coverage, and life & disability insurance. In this vital role you will lead and support Quality Risk Management (QRM) and Change Control Quality System activities that enable proactive, science-based decision making to protect patient safety, product quality, regulatory compliance, and business continuity across GxP-regulated operations.

Specialist QA

Compensation Information: The compensation offered to a candidate may be influenced by a variety of factors, including the candidate's relevant experience; education, including relevant degrees or certifications; work location; market data/ranges; internal equity; internal salary ranges; etc. Current Employees: If you are a current employee at Ryder, please click here ( https://wd5.myworkday.com/ryder/d/task/2998$46522.htmld ) to log in to Workday to apply using the internal application process.

Ryder System Inc

Routing Specialist (remote)

If you have a disability and either need assistance applying online or need to request an accommodation during any part of the application process, please call 1-800-EY-HELP3, select Option 2 for candidate related inquiries, then select Option 1 for candidate queries and finally select Option 2 for candidates with an inquiry which will route you to EY's Talent Shared Services Team (TSS) or email the TSS at ssc.customersupport@ey.com. Fueled by sector insights, a globally connected, multi-disciplinary network and diverse ecosystem partners, EY teams can provide services in more than 150 countries and territories.

Ernst & Young Global Ltd

Document Specialist - San Juan

We are seeking an experienced Project Manager (PM) to lead the implementation and delivery of Manufacturing Execution Systems (MES) within a highly regulated medical devices/life sciences environment. NTT DATA recruiters will never ask for payment or banking information and will only use @nttdata.com and @talent.nttdataservices.com email addresses.

NTT DATA Services, LLC

Project Manager - MES (Medical Devices / Life Sciences)

OTHER

The ideal candidate will have approximately 2–3 years of hands-on validation experience and demonstrated experience working with Kneat , an electronic validation lifecycle management platform used to develop, execute, review, approve, and maintain validation documentation. This position requires working within a regulated pharmaceutical manufacturing environment and collaborating closely with site Engineering, Quality, Manufacturing, Automation, and Validation teams.

HR Works

Validation / CSV Specialist

BreezyHR

We are seeking an AutoCAD Specialist to turn field measurements, sketches, photographs, and inspection findings into accurate technical drawings for our NDT and Mechanical Integrity projects. We partner with leading pharmaceutical, biotechnology, medical device, healthcare, and laboratory organizations to deliver specialized services for critical environments.

Scientific Safety Alliance

AutoCAD Specialist

YEAR

Our company is flexible, family-oriented and focused on our resources' well-being, while providing our Pharmaceutical, Medical Device and Manufacturing industry clients with top-notch quality talent. Picture as well an environment of healthy competition, teamwork, being ethical and of using the scientific method in all ways possible.

Flexible & Integrated Technical Services, LLC

Quality Specialist- 02

partner JazzHR

Assess supplier change notifications and quality records to determine their impact on raw materials, processes, and product quality, coordinating with Supplier Quality, Materials Management, Quality Control, and Manufacturing. In this role, you’ll ensure every change to a raw material or component is assessed, documented, and implemented correctly, and you’ll manage supplier-related non-conformances and CAPAs through closure.

Supplier Quality Specialist

Our company is flexible, family-oriented and focused on our resources' well-being, while providing our Pharmaceutical, Medical Device and Manufacturing industry clients with top-notch quality talent. Picture yourself in a lab… with all the equipment you need to put your multitasking, scientific, creative (to come up with all those experiments!) skills to work.

Change Control Specialist

Packaging/inspection operations, strong knowledge of GDP and electronic quality systems, and the ability to collaborate effectively with Manufacturing, Engineering, and Process Development. Our company is flexible, family-oriented and focused on our resources' well-being, while providing our Pharmaceutical, Medical Device and Manufacturing industry clients with top-notch quality talent.

HOUR

Support major/trend deviation investigations throughout the whole lifecycle including Root Cause Analysis investigation, determination of Corrective/Preventive Actions, authoring process investigation reports, and presenting within regulatory inspections. Design, coordinate, and support execution of functional tests, water tests, and other runs to challenge process and operations during major changes, or campaign readiness.

Quality Consulting Group

JT922 - SPECIALIST MANUFACTURING

Bachelor’s Degree in Science, or Engineering field with at least 2 years of proven experience in commissioning and qualification processes, protocol generation and execution. Support and influence effectively to ensure all necessary Commissioning, Qualification, and Validation (CQV) activities are completed on time and according to the validation program.

C&Q Specialist

Attends client's GMP Buildings Quality system forums and or Management Review meetings to present environmental and critical utilities data and recommend actions based on the data evaluation. QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and manufacturing industry, is looking for a talented, highly motivated and enthusiastic to join our team.

SPECIALIST QA

Support major/trend deviation investigations throughout the whole lifecycle including Root Cause Analysis investigation, determination of Corrective/Preventive Actions, authoring process investigation reports, and presenting within regulatory inspections. QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and manufacturing industry, is looking for a talented, highly motivated and enthusiastic to join our team.

JT787 - SPECIALIST MANUFACTURING

Perform all store opening/closing duties, including performing day end procedures, verifying/securing money/deposits according to company policy, preparing bank deposits as needed, ensuring all night security lights are on, locking doors and securing building, arming/disarming security alarms, and checking/securing/locking delivery vehicle(s) parked in secure designated area. Ensure retail customer returns and exchanges are processed in an efficient and friendly manner, refunds are issued accurately using the correct payment methods, and returned merchandise is processed or staged in the returns area correctly.

It started with a father and son - Charles Francis "C.F." and Charles H. "Chub" O’Reilly. Together they had the courage and confidence to venture out on their own. Along with 11 others who shared the same desire to offer great customer service and auto parts availability, the doors of O’Reilly Automotive, Inc. opened on December 2, 1957.

Now, more than 61 years later, the 77,000-plus team members at O’Reilly Auto Parts are proud of the company’s achievements over the years.

During our early years, we focused on sales and slow and steady growth. At the end of our first year, sales totaled $700,000, and by 1961 volume reached $1.3 million. For the first seven years of operation, there was one store in Springfield, MO, until the second opened in July 1964. In March 1975, annual sales volume rose to $7 million and a 52,000 square-foot facility was built in Springfield for the O’Reilly/Ozark warehouse operation. By that time, the company had nine stores, all located in southwest Missouri.

The long range plans and stability of the company were solidified by a public offering of company stock in April 1993. Since that time, the Company has grown through new store and distribution center openings, as well as numerous mergers and acquisitions. O’Reilly currently operates stores in 47 states, including Alaska and Hawaii, and distribution centers in 27 locations.

Dramatic changes in technology, inventory control, facilities, and sheer size mark the O’Reilly growth and success story. But, it is our spirit of teamwork - how important it was then and how important it remains - that drives our performance. The company’s values and culture that started with the original 13 employee/owners remain evident and strong as we expand and develop Team O’Reilly.

We serve two distinct customer bases - the professional (installer) customers who provide auto repair services to their customers (DIFM - do it for me), and retail "walk-in" customers (DIY - do it yourself). Our dual-market strategy continues to differentiate us from the competition and is a major factor in our ongoing success. Depending on a store’s professional versus retail customer mix, more than 95 percent of our locations have team members dedicated to our professional customers, offering them separate counters, phone lines, and a delivery fleet that totals 18,455 vehicles. We also have a professional sales team, consisting of territory sales managers and in-store sales specialists, responsible for calling on our professional customers and building sound business partnerships to ensure O’Reilly is the First Call for their auto parts needs.

O'Reilly Automotive Inc

Retail Service Specialist

JT599 - SPECIALIST MANUFACTURING

Physical Requirements: May require the ability to stand or walk for moderate periods, manual dexterity to handle devices and perform otoscopy, capacity to lift and transport moderate equipment (e.g., hearing devices, toolkits), fine coordination of hands/fingers for precise tasks like earmold impressions and auditory checks. The Department of Veterans Affairs performs pre-employment reference checks as an assessment method used in the hiring process to verify information provided by a candidate (e.g., on resume or during interview or hiring process); gain additional knowledge regarding a candidates abilities; and assist a hiring manager with making a final selection for a position.

Accounting Associate Jobs in Clayton, MO

Rheumatology Key Account Specialist - Puerto Rico Sanofi

Contamination Control and Sterility Assurance Sr. Specialist Danaher Corp

Specialist Quality Assurance - Major Deviations Amgen Inc

Specialist QA Amgen Inc

Routing Specialist (remote) Ryder System Inc

Document Specialist - San Juan Ernst & Young Global Ltd

Project Manager - MES (Medical Devices / Life Sciences) NTT DATA Services, LLC

Validation / CSV Specialist HR Works

AutoCAD Specialist Scientific Safety Alliance

Quality Specialist- 02 Flexible & Integrated Technical Services, LLC

Supplier Quality Specialist Flexible & Integrated Technical Services, LLC

Change Control Specialist Flexible & Integrated Technical Services, LLC

Specialist QA Flexible & Integrated Technical Services, LLC

JT922 - SPECIALIST MANUFACTURING Quality Consulting Group

C&Q Specialist Flexible & Integrated Technical Services, LLC

SPECIALIST QA Quality Consulting Group

JT787 - SPECIALIST MANUFACTURING Quality Consulting Group

Retail Service Specialist O'Reilly Automotive Inc

JT599 - SPECIALIST MANUFACTURING Quality Consulting Group

Health Technician (Hearing Instrument Technician) U.S. Department of Veterans Affairs

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