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Live In Fda Scientist Jobs in Springfield, MO (NOW HIRING)

Fitness Coach

Springfield, MO · On-site

$25 - $55/hr

Understand the science behind our workouts specifically, heart-rate focused training programs in ... Fitness is a way of life -- in fact, our brand purpose is to help people live longer, more vibrant ...

The result is an increase in calorie burn post-workout, backed by the science of excess post ... Fitness is a way of life -- in fact, our brand purpose is to help people live longer, more vibrant ...

... in collaboration with other professionals and implement treatment strategies based on scientific ... At UnitedHealth Group, our mission is to help people live healthier lives and make the health ...

... a city in southwestern Missouri. The Discovery Center of Springfield has interactive science ... with live music. The town's main strip is also home to the Titanic Museum, with a half-scale ...

... in collaboration with other professionals and implement treatment strategies based on scientific ... At UnitedHealth Group, our mission is to help people live healthier lives and make the health ...

... and live fulfilling lives. This leadership opportunity offers the chance to influence program ... Bachelor's Degree or Master's Degree in Social Sciences or a related field preferred. Five years of ...

Showing results 21-40

Live In Fda Scientist information

What is the difference between Live In Fda Scientist vs Fda Reviewer?

AspectLive In Fda ScientistFda Reviewer
Required credentialsBachelor's or Master's in Life Sciences, relevant experienceSimilar credentials, often with advanced degrees
Work environmentOn-site, often in government or research facilitiesOffice-based, reviewing submissions at FDA headquarters or regional offices
Employer and industry usageFederal government, regulatory scienceFederal government, regulatory review
Common search intentJob duties, qualifications, work conditionsComparison of roles, responsibilities, career path

The Live In Fda Scientist and Fda Reviewer roles both require scientific expertise and federal employment credentials. While the Live In Fda Scientist often involves conducting research and scientific analysis on-site, the Fda Reviewer primarily focuses on evaluating regulatory submissions and documentation. Both roles are integral to FDA operations, but they differ in daily tasks and work environment, with the scientist more research-oriented and the reviewer more review-focused.

What are the key skills and qualifications needed to thrive as a live in FDA scientist, and why are they important?

To thrive as an FDA Scientist, you need a strong background in life sciences or chemistry, typically with an advanced degree (MS or PhD) and experience in research or regulatory affairs. Familiarity with laboratory instrumentation, data analysis software, and FDA regulatory systems is essential, and certifications like RAC (Regulatory Affairs Certification) can be advantageous. Attention to detail, critical thinking, and excellent communication skills help you interpret data accurately and collaborate effectively with multidisciplinary teams. These skills ensure scientific integrity, regulatory compliance, and the advancement of public health through safe and effective products.

What is a live in FDA scientist?

A Live In FDA Scientist typically refers to a regulatory scientist who works for the U.S. Food and Drug Administration (FDA) and may be involved in on-site or continuous monitoring of studies, often in clinical or laboratory settings. Their role includes evaluating scientific data, ensuring compliance with federal regulations, and overseeing the safety and efficacy of products such as drugs, biologics, or medical devices. Live-in positions might be required for research facilities needing 24/7 oversight, although such roles are rare and specialized. These scientists play a crucial role in public health by supporting the FDA’s mission to protect consumers.

What are some unique challenges faced by a live in FDA scientist, and how can they be managed?

A Live-In FDA Scientist often works in environments such as research facilities or clinical trial sites where on-site presence is essential. This setup can present challenges like maintaining work-life balance, adapting to extended hours, and managing confidentiality due to the sensitive nature of ongoing research. Successful candidates typically develop strong time management skills, set clear personal boundaries, and foster open communication with team members to ensure both professional responsibilities and personal well-being are balanced. Collaboration with multidisciplinary teams is frequent, and adaptability is key to thriving in this dynamic role.
What cities near Springfield, MO are hiring for Live In Fda Scientist jobs? Cities near Springfield, MO with the most Live In Fda Scientist job openings:
Infographic showing various Live In Fda Scientist job openings in Springfield, MO as of August 2026, with employment types broken down into 79% Full Time, 16% Part Time, and 5% Contract. Highlights an 95% In-person, and 5% Remote job distribution.

Full-time

Re-posted 22 days ago


Job description

My Account
Senior Quality Manager
Summary
Title: Senior Quality Manager ID: 1002 Location: Springfield, MO Department: Operations Travel Necessary: No
More about this job >
Description

POSITION SUMMARY:

The Quality Assurance Manager is a member of the site leadership team responsible for ensuring products manufactured at the site are safe, wholesome, and comply with all applicable company, customer, and regulatory requirements. They will support and coach the site team in developing and maintaining a culture of best-in-class Quality through their influence and coaching. The QM is responsible for supporting and optimizing site quality operations and practices through effective data analysis and decision-making.

Knowledge of regulatory requirements for Food, Feed, Infant Formula as well as chemical manufacturing is desired. This individual will develop, analyze, and drive associated programs to ensure maximum production quality, compliance to the Quality Management System, and compliance with cGMP requirements while supporting the company's mission

The Quality Manager is directly responsible for the implementation of quality systems and initiatives within the facilities. This position is responsible for the daily operations as they relate to the production, packaging, receipt, storage, and release of food products manufactured within the facility. The individual in this position must establish relationships with not only her/his direct reports but within all departments in the organization to effectively cultivate a culture in which safety, quality, and productivity goals are met.
 

ESSENTIAL FUNCTIONS:

  • Responsible for performing all job requirements in a safe manner using the proper PPE and being a proactive safety role model with co-workers
  • Responsible for correcting/reporting unsafe behaviors or equipment to ensure a safe working environment
  • Responsible for cleanliness within the work department
  • Perform/execute job duties keeping the company's commitment to quality in mind, developing strategy and executing tactical plans to support the department's mission, and by being a role model for GMP on the floor
  • Monitor, maintain, and continuously improve all food safety activities. Enforce product safety plan while producing the product.
  • Develop, implement, and maintain policies and processes that ensure the product manufactured meets or exceeds quality expectations defined within the QMS, the specific product specifications, and applicable quality agreements
  • Manage the internal audit process to confirm compliance to the QMS, with the expectation of creating and maintaining a state of audit readiness for both the system and overall facility within all company locations
  • Create and manage relationships with 3rd Party laboratories, consultants, and services that can support company initiatives
  • Manage customer expectations and relations in the manufacturing of products
  • Establish and implement metrics for monitoring quality standards and departmental effectiveness
  • Primary contact for all regulatory audits (FDA) within all facilities; management of internal and external negotiation of all corrective actions associated with customer and 3rd party audits
  • Prepare reports, analyze data, and make recommendations for improving operations
  • Provide mentoring and solutions to challenges for direct reports
  • Lead the effort in harmonizing the quality activities in all facilities
  • Initiate and support continuous improvement and elimination of waste and variation in processes using established improvement processes
  • Must develop cooperative relationships with other departments

QUALIFICATIONS:

  • Bachelor's Degree in a science-related field and 7 - 10 years of quality experience, including successful experience as a mid-level manager or equivalent level of experience
  • Proficiency in procedural and policy auditing, development, and implementation
  • Mastery of Root Cause, CAPA investigation, documentation and follow up to verify effectiveness
  • Experience with applicable 21 CFR regulations for Dietary Supplements, Infant Formula, Food, Feed preferred
  • Experience leading a Manufacturing Analytical Chemistry and Microbiology laboratory
  • Successful track record of effectively managing and developing staff within an entrepreneurial environment
  • Demonstrated management skills including delegation, time management, leadership, and mentoring
  • Proven ability to work collaboratively with the operations team
  • Communicates clearly, written, and orally, with all levels within an organization, both internally and externally
  • Demonstrated ability to work with and develop others in a team environment
  • A clear sense of urgency and ability to manage priorities to meet both immediate and long-term goals
  • Self-motivated with the ability to work independently
  • Advanced computer skills, specifically with Microsoft Office products
  • Sensitive to other cultures/backgrounds, able to work in a multi-cultural workplace
  • Ability and willingness to learn, understand and follow documented work procedures
  • Demonstrated ability to function in a fast-paced environment while moving multiple simultaneous projects forward

WORKING CONDITIONS:

  • While performing the functions of this job, the employee is regularly required to sit, stand, walk, talk, and hear
  • The employee is occasionally required to kneel, crouch, crawl, bend, ascend and descend stairs and/or ladders
  • The employee is frequently required to use hands and fingers to feel, handle, or operate objects, tools, or controls; and reach with hands and arms
  • The employee may occasionally lift and/or move up to 50 pounds
  • Vision requirements include close vision, depth perception, color vision, and the ability to adjust focus
  • The employee will be required to have professional employee and customer interaction frequently
  • This job is performed in a production environment in a manufacturing location
  • The noise level in the plant is moderate to loud
  • There will be exposure to machine noise and food dust when in the plant
  • While performing the duties of this job, the employee regularly works near moving mechanical parts and with or around various chemicals
  • The employee is occasionally exposed to vibration and risk of electric shock
  • The production environment includes varying temperatures (heat, cold, and moisture)
  • While performing certain job duties, employees may be exposed to allergens of the industry such as eggs, wheat, peanuts, dairy products, tree nuts, and soy products, as well as latex and powders
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