Bachelor's degree required; graduate degree in Food or Pharma Sciences preferred.
Professional certification in relevant fields (e.g., GFSI, CQA, RAC) is mandatory.
Minimum four years of experience in manufacturing, retail operations, or quality assurance.
Willingness to travel extensively (70-80% annually) is essential.
Strong written and verbal communication skills in English; proficiency in a second language is a plus.
Excellent analytical and mathematical skills for problem-solving.
Experience leading audit teams and proficient in Microsoft Office.
Responsibilities
Conduct high-level assessments of quality systems across various manufacturing sites.
Report findings according to UL and industry standards for GMP and Food Safety.
Mentor and train junior auditors and trainees in the field.
Lead complex audits requiring advanced methodologies and detailed reporting.
Complete audit agendas and reports within strict timelines (14 and 4 days respectively).
Submit audit expenses promptly and maintain a minimum of 10 audit days per month.
Benefits
Comprehensive health benefits including medical, dental, and vision.
Wellness programs focusing on mental and financial health.
401K retirement savings plan available.
Generous paid time off including 15 vacation days and 12 holidays.
Additional sick leave of 72 hours.
Full Job Description
Job Description
Lead Auditor - GMP Quality Audits will perform high level assessments of quality systems in a variety of manufacturing sites, farms, processing plants and/or other work related sites throughout a region or country.
Assess and report in accordance with UL, industry scheme, and client audit protocols on facilities working and/or operational conditions as it relates to established industry standard(s) for GMP, Quality Systems, Food Safety initiatives and/or client programs.
Maintain a high level of technical knowledge and play an active mentoring role with trainees, auditors and lead auditors in the field.
Participate and lead higher level audits; and as such this will involve complex methodologies, advanced analysis, and comprehensive / intricate reporting. Reports will be written in English in an objective, accurate, detailed and timely manner.
Specific Regulatory Standard(s) Competency are a focus including:
OTC Drug/Pharmaceuticals: 21CFR211/210
Nutritional Supplements: 21CFR111
Medical/Homecare Devices: 21CFR820
Cosmetics: ISO22716
Complete audit agendas within 14 calendar days of the audit
Complete reports within 4 calendar days of the audit
Submit audit expenses in a timely manner
Complete at least 10 days of audits per month minimum capacity.
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Qualifications
University Degree (Equivalent to Bachelor's degree) required. Prefer Graduate Science Degree in Food or Pharma Sciences, Engineering, Technology, or similar.
Must hold one or more scope specific professional credential(s), such as: GFSI recognized auditor credential; CQA, RABQSA, IRCA, RAC, Pharmaceutical GMP Professional Certification (CPGP)
Four years related work experience in manufacturing or retail sectors in technical, supply chain, retail operations, quality assurance or food safety and/or equivalent experience in environmental health, public health or relevant experience.
Willingness and ability to travel to other countries, states, regions, provinces and or throughout any assigned or designated country (up to 70 to 80% annually).
Excellent written and verbal communication skills in English and if required fully proficient/literate in a 2nd language.
Excellent oral communication skills; capable of addressing high executive audiences and conduct opening and closing conferences in front of multiple people.
Excellent mathematical skills and analytical skills. Creative and innovative thinking to problem solve and streamline processes.
Ability to lead a team of auditors during the execution of a project and/or specialized audits. Proficient in internet navigation, e-mail and PC software such as Microsoft Word, Excel.
PCQI Certification a plus.
Ability to travel locally and regionally and work remotely. This position does not generally report to a specific UL office.
Candidate needs to be located close to airport due to high travel requirements.
What we offer:
Total Rewards: We understand compensation is an important factor as you consider the next step in your career. The estimated salary range for this position is $85,000 to $110,000 and is based on multiple factors, including job-related knowledge/skills, experience, geographical location, as well as other factors. This position is eligible for annual bonus compensation with a target payout of 10% of the base salary. This position also provides health benefits such as medical, dental and vision; wellness benefits such as mental and financial health; and retirement savings (401K) commensurate with the standard rewards offered in each individual location or country. We also provide full-time employees with paid time off including vacation (15 days), holiday including floating holidays (12 days) and sick time off (72 hours).
Learn More:
Curious? To learn more about us and the work we do, visit UL.com
This application deadline for this position is April 16, 2027.
About UL
UL is a global safety certification company headquartered in Northbrook, Illinois. It was founded in 1894 and has been providing safety testing, inspection, and certification services for over 125 years. UL operates in over 100 countries and has more than 14,000 employees worldwide. The company's mission is to promote safe living and working environments by advancing safety science. UL's services cover a wide range of industries, including consumer products, industrial equipment, building materials, and more.
