Quality Inspector
$20 - $23/hr
APEX Placement and Consulting has partnered with an exciting company in Fort Wayne, IN looking to ... ISO, FDA, and internal quality requirements · Collect, analyze, and document quality data to ...
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$20 - $23/hr
APEX Placement and Consulting has partnered with an exciting company in Fort Wayne, IN looking to ... ISO, FDA, and internal quality requirements · Collect, analyze, and document quality data to ...
Quick apply
$20 - $23/hr
APEX Placement and Consulting has partnered with an exciting company in Fort Wayne, IN looking to ... ISO, FDA, and internal quality requirements · Collect, analyze, and document quality data to ...
Indianapolis, IN · On-site
$80K - $95K/yr
ELIQUENT Life Sciences is the leading global consulting firm providing solutions to life science ... Working knowledge of FDA and cGMP regulations and documentation practice * Ability to read and ...
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Indianapolis, IN · On-site
$80K - $95K/yr
ELIQUENT Life Sciences is the leading global consulting firm providing solutions to life science ... Working knowledge of FDA and cGMP regulations and documentation practice * Ability to read and ...
Indianapolis, IN · On-site
$70K/yr
At Performance Validation, you'll work directly in FDA-regulated facilities such as pharmaceutical ... What We Do Performance Validation is a 100% employee-owned consulting firm with over 30 years of ...
New
Indianapolis, IN · On-site
$70K/yr
At Performance Validation, you'll work directly in FDA-regulated facilities such as pharmaceutical ... What We Do Performance Validation is a 100% employee-owned consulting firm with over 30 years of ...
New
Carmel, IN · On-site
... R consultation, ensuring operational continuity during off-shift hours. This is an off-shift ... HR Compliance & Regulatory Risk Management Ensure adherence to applicable labor laws, FDA ...
Carmel, IN · On-site
... R consultation, ensuring operational continuity during off-shift hours. This is an off-shift ... HR Compliance & Regulatory Risk Management Ensure adherence to applicable labor laws, FDA ...
Indianapolis, IN · On-site
$55 - $64/hr
Provide technical support for audits of software suppliers and consultants, including cybersecurity ... Provide expertise in applicable industry standards and regulations (e.g., IEC 62304, FDA guidance ...
Indianapolis, IN · On-site
$55 - $64/hr
Provide technical support for audits of software suppliers and consultants, including cybersecurity ... Provide expertise in applicable industry standards and regulations (e.g., IEC 62304, FDA guidance ...
Indianapolis, IN · On-site
$151K - $251K/yr
... FDA regulations (specifically 21 CFR Part 820), ISO 13485 , and IEC 62304 (the standard for medical device software lifecycle). * Sales/BD Track Record : Proven track record in the consultative life ...
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Indianapolis, IN · On-site
$151K - $251K/yr
... FDA regulations (specifically 21 CFR Part 820), ISO 13485 , and IEC 62304 (the standard for medical device software lifecycle). * Sales/BD Track Record : Proven track record in the consultative life ...
Indianapolis, IN · On-site
$151K - $251K/yr
... FDA regulations (specifically 21 CFR Part 820), ISO 13485 , and IEC 62304 (the standard for medical device software lifecycle). * Sales/BD Track Record : Proven track record in the consultative life ...
Quick apply
Indianapolis, IN · On-site
$151K - $251K/yr
... FDA regulations (specifically 21 CFR Part 820), ISO 13485 , and IEC 62304 (the standard for medical device software lifecycle). * Sales/BD Track Record : Proven track record in the consultative life ...
Indianapolis, IN · On-site
Barry-Wehmiller is a diversified global supplier of engineering consulting and manufacturing ... Experience with project management, good documentation practices, cGMP, & FDA validation methods ...
Indianapolis, IN · On-site
Barry-Wehmiller is a diversified global supplier of engineering consulting and manufacturing ... Experience with project management, good documentation practices, cGMP, & FDA validation methods ...
Barry-Wehmiller is a diversified global supplier of engineering consulting and manufacturing ... Experience with project management, good documentation practices, cGMP, & FDA validation methods ...
Barry-Wehmiller is a diversified global supplier of engineering consulting and manufacturing ... Experience with project management, good documentation practices, cGMP, & FDA validation methods ...
Indianapolis, IN · On-site
Barry-Wehmiller is a diversified global supplier of engineering consulting and manufacturing ... Experience with project management, good documentation practices, cGMP, & FDA validation methods ...
Indianapolis, IN · On-site
Barry-Wehmiller is a diversified global supplier of engineering consulting and manufacturing ... Experience with project management, good documentation practices, cGMP, & FDA validation methods ...
Indianapolis, IN · On-site
Barry-Wehmiller is a diversified global supplier of engineering consulting and manufacturing ... Responsible for developing and executing a variety of validation and FDA compliance related ...
Indianapolis, IN · On-site
Barry-Wehmiller is a diversified global supplier of engineering consulting and manufacturing ... Responsible for developing and executing a variety of validation and FDA compliance related ...
Indianapolis, IN · On-site
Barry-Wehmiller is a diversified global supplier of engineering consulting and manufacturing ... Responsible for developing and executing a variety of validation and FDA compliance related ...
Indianapolis, IN · On-site
Barry-Wehmiller is a diversified global supplier of engineering consulting and manufacturing ... Responsible for developing and executing a variety of validation and FDA compliance related ...
Barry-Wehmiller is a diversified global supplier of engineering consulting and manufacturing ... Responsible for developing and executing a variety of validation and FDA compliance related ...
Barry-Wehmiller is a diversified global supplier of engineering consulting and manufacturing ... Responsible for developing and executing a variety of validation and FDA compliance related ...
$23 - $25/hr
Follow quality procedures (ISO 13485, FDA, OSHA standards) * Lift up to 35+ lbs occasionally and stand for 6+ hours per shift * Work overtime as needed to meet delivery goals What We're Looking For:
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$23 - $25/hr
Follow quality procedures (ISO 13485, FDA, OSHA standards) * Lift up to 35+ lbs occasionally and stand for 6+ hours per shift * Work overtime as needed to meet delivery goals What We're Looking For:
$75K - $106K/yr
We provide commissioning, qualification, validation, startup, project management, and other consulting services associated with operational readiness to FDA-regulated and other mission-critical ...
$75K - $106K/yr
We provide commissioning, qualification, validation, startup, project management, and other consulting services associated with operational readiness to FDA-regulated and other mission-critical ...
... consultation to Elanco M&Q. This role serves as a strategic advisor to global sites, defining and ... Working knowledge of USDA and FDA regulatory requirements pertaining to animal health manufacturing.
... consultation to Elanco M&Q. This role serves as a strategic advisor to global sites, defining and ... Working knowledge of USDA and FDA regulatory requirements pertaining to animal health manufacturing.
Indianapolis, IN · On-site
$75K - $106K/yr
We provide commissioning, qualification, validation, startup, project management, and other consulting services associated with operational readiness to FDA-regulated and other mission-critical ...
Indianapolis, IN · On-site
$75K - $106K/yr
We provide commissioning, qualification, validation, startup, project management, and other consulting services associated with operational readiness to FDA-regulated and other mission-critical ...
... labeling, providing guidance and consultation for domestic and international regulations ... Advanced knowledge of FDA and EU regulations (including labeling regulations) and regulations ...
... labeling, providing guidance and consultation for domestic and international regulations ... Advanced knowledge of FDA and EU regulations (including labeling regulations) and regulations ...
$75K - $106K/yr
We provide commissioning, qualification, validation, startup, project management, and other consulting services associated with operational readiness to FDA-regulated and other mission-critical ...
Quick apply
$75K - $106K/yr
We provide commissioning, qualification, validation, startup, project management, and other consulting services associated with operational readiness to FDA-regulated and other mission-critical ...
... consultation to Elanco M&Q. This role serves as a strategic advisor to global sites, defining and ... Working knowledge of USDA and FDA regulatory requirements pertaining to animal health manufacturing.
... consultation to Elanco M&Q. This role serves as a strategic advisor to global sites, defining and ... Working knowledge of USDA and FDA regulatory requirements pertaining to animal health manufacturing.
$22.66 is the 25th percentile. Wages below this are outliers.
$18.07 - $23.37
29% of jobs
$23.37 - $28.68
0% of jobs
$28.68 - $33.98
0% of jobs
$33.98 - $39.28
0% of jobs
$39.28 - $44.58
0% of jobs
$44.58 - $49.89
19% of jobs
The median wage is $51.21 / hr.
$49.89 - $55.19
10% of jobs
$55.19 - $60.49
3% of jobs
$64.78 is the 75th percentile. Wages above this are outliers.
$60.49 - $65.79
18% of jobs
$65.79 - $71.10
9% of jobs
$71.10 - $76.40
12% of jobs
$18
$49
$76
An FDA Consulting job involves providing expert guidance to businesses seeking regulatory approval for their products from the U.S. Food and Drug Administration (FDA). Consultants help companies navigate complex FDA regulations, ensure compliance, and prepare necessary documentation for submissions. They may work with pharmaceuticals, medical devices, food, and biotech industries. Their role includes strategy development, risk assessment, and communication with the FDA to facilitate approvals and avoid compliance issues.
To thrive in FDA Consulting, you need expertise in regulatory affairs, a deep understanding of FDA guidelines, and often a degree in life sciences or a related field. Familiarity with regulatory submission systems such as eCTD, knowledge of GxP standards, and certifications like RAC (Regulatory Affairs Certification) are valuable. Strong communication, analytical thinking, and project management skills set outstanding consultants apart. These competencies are essential to effectively guide clients through complex regulatory landscapes and ensure successful product approvals.
As an FDA Consultant, your day might involve reviewing regulatory documentation, preparing submissions for FDA approval, and advising clients on compliance strategies. You’ll often attend meetings with cross-functional teams including R&D, quality assurance, and legal experts to ensure alignment on regulatory requirements. Consultants also stay updated on changes in FDA guidelines, draft correspondence to regulatory agencies, and address client questions or concerns. This dynamic role requires adaptability and strong collaboration skills to manage multiple projects and effectively support clients through all stages of the regulatory process.

$20 - $23/hr
Full-time
Medical, Dental, Vision, Retirement, PTO
Re-posted 3 days ago