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Evening Fda Investigator Jobs (NOW HIRING)

Nihon Kohden USA

Quality Systems Manager

Irvine, CA · On-site

$100K - $145K/yr

... including investigation and root cause analysis, risk assessment, action plan creation and ... Solid knowledge of FDA regulations and interpretation of FDA regulations, guidelines and policy ...

Nihon Kohden

Quality Systems Manager

Irvine, CA · On-site

$100 - $145/hr

... including investigation and root cause analysis, risk assessment, action plan creation and ... Solid knowledge of FDA regulations and interpretation of FDA regulations, guidelines and policy ...

Nihon Kohden

Quality Systems Manager

Irvine, CA · On-site

$100K - $145K/yr

... including investigation and root cause analysis, risk assessment, action plan creation and ... Solid knowledge of FDA regulations and interpretation of FDA regulations, guidelines and policy ...

Nihon Kohden America

Quality Systems Manager

Irvine, CA · On-site

$100K - $145K/yr

... including investigation and root cause analysis, risk assessment, action plan creation and ... Solid knowledge of FDA regulations and interpretation of FDA regulations, guidelines and policy ...

CEDENT

Process Engineer

Largo, FL · On-site

Conduct technical investigations, write reports, and aid in the close-out of deviations. * Support ... Keep current on regulatory and quality requirements for manufacturing, including FDA-regulated ...

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How much do evening fda investigator jobs pay per year?

As of Aug 27, 2026, the average yearly pay for evening fda investigator in the United States is $70,123.00, according to ZipRecruiter salary data. Most workers in this role earn between $50,000.00 and $85,000.00 per year, depending on experience, location, and employer.

What are the most commonly searched types of Fda Investigator jobs?

The most popular types of Fda Investigator jobs are:

Evening Fda Investigator jobs near you
Infographic showing various Evening Fda Investigator job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 57% Full Time, 39% Part Time, 2% Contract, and 1% Nights. Highlights an 93% Physical, 1% Hybrid, and 6% Remote job distribution, with an average salary of $70,123 per year, or $33.7 per hour.

Quality Assurance Associate - Manufacturing Floor (Evening & Night Shift)

Elwood, KS • On-site

Elanco Animal Health Incorporated
Pharmaceutical and Medicine Manufacturing • 5 - 10K employees

7.8

Company rating: 7.8 out of 10

Based on 25 frontline employees who took The Breakroom Quiz

49th of 86 rated pharmaceutical

People enjoy working here

Good employer

Recommended by parents

Learn more about Elanco Animal Health Incorporatedexternal

Full-time

Retirement

Re-posted 3 hours ago

Job description

At Elanco (NYSE: ELAN) - it all starts with animals!
As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets. At Elanco, we are driven by our vision of Food and Companionship Enriching Life and our purpose - all to Go Beyond for Animals, Customers, Society and Our People.
At Elanco, we pride ourselves on fostering a diverse and inclusive work environment. We believe that diversity is the driving force behind innovation, creativity, and overall business success. Here, you'll be part of a company that values and champions new ways of thinking, work with dynamic individuals, and acquire new skills and experiences that will propel your career to new heights.
Making animals' lives better makes life better - join our team today!
Job Description
Your Role: Quality Assurance Associate - Manufacturing Floor
This position coordinates and conducts activities of the Quality Assurance Department regarding manufacturing floor support and has specific responsibilities for other quality and compliance related activities as directed by the Quality Assurance Manager. This position plays a key role in day-to-day operations and works very closely with the Manufacturing and Process Teams.
Your Responsibilities:
  • Actively interact with Manufacturing and champion compliance through leadership and example in daily processes. Provide quality floor support, including observing daily active processes for: statuses, issues, concerns, and issuance of cell banks. Act as first responder for manufacturing activities and represent QA on cross-functional process teams.
  • Identify, investigate, and resolve complex technical issues using problem-solving skills. Participate in investigation teams, determine next steps and assist in the proper close out and follow up actions. Make decisions independently and notify management of actions taken.
  • Perform QA review/approval of controlled documents including, but not limited to, solution records, batch records, logbooks, autoclave cycles with a high attention to detail, using extensive working knowledge of quality concepts and internal procedures and controls.
  • Review change management documentation, deviations, investigations and CAPA records for completion. Write new documents and revise existing QA documents as needed.
  • Participate and manage QA projects as needed with minimal supervision. Receive overall project direction from management but complete most work independently. Assist other Quality Assurance Associate(s) and Quality Assurance Manager(s) as needed.

What You Need to Succeed (Minimum Qualifications):
  • BA/BS (or Master's) in any Life Science discipline preferred, and/or 3 years' experience in regulated industry (USDA, FDA, ISO etc).
  • Must have direct experience with Quality Assurance within regulated industry (USDA, FDA, ISO, etc.)
  • Understands and applies comprehensive knowledge of quality and GMP principles and maintains current understanding of global GMP drug manufacturing regulations.
  • Must be able to work in controlled / clean room environments requiring gowning qualifications.

What Will Give You the Competitive Edge (Preferred Qualifications):
  • Familiarity with basic statistics, review/approval of documentation; risk tools, technical writing, and writing/reviewing/approving investigations.
  • Ability to handle multiple tasks and competing priorities concurrently and in a timely fashion.
  • Good interpersonal skills and ability to work effectively and efficiently in a team environment to accomplish goals.
  • Demonstrated experience making sound independent decisions.

Additional Information
  • Location: Elwood, KS Manufacturing Site
  • Must be able to work in controlled / clean room environments requiring gowning qualifications.
  • Evening Shift: 4:00pm - 12:30am & Night Shift: 12am - 8:30am, Monday - Friday
  • Rotating weekend schedule required (every 3rd weekend) 24/7 hr. site

Don't meet every single requirement? Studies have shown underrepresented groups are less likely to apply to jobs unless they meet every single qualification. At Elanco we are dedicated to building a diverse and inclusive work environment. If you think you might be a good fit for a role but don't necessarily meet every requirement, we encourage you to apply. You may be the right candidate for this role or other roles!
Elanco Benefits and Perks:
We offer a comprehensive benefits package focusing on financial, physical, and mental well-being while encouraging our employees to pursue our purpose! Some highlights include:
  • Multiple relocation packages
  • 8-week parental leave
  • 9 Employee Resource Groups
  • Annual bonus offering
  • Up to 6% 401K matching

#LI-HL
#LI-Onsite
Elanco is an EEO/Affirmative Action Employer and does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status
Elanco may use automated tools, including AI, to support parts of our recruitment process, such as reviewing applications against job-related criteria and/or transferrable skills. These tools help ensure a consistent, structured evaluation, but they do not make hiring decisions. All decisions involve a human reviewer. For more information on how we handle personal data, please see our Elanco Workforce Privacy Notice.

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