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Supervisory Chemist at US FDA
Excellent fit as they currently hold the exact title at the right agency. Supervisory Chemist at US FDA → Supervisory Chemist at US FDA. Excellent.
This sample report shows what our sourcing engine surfaces for this search. Preview the top 30 matches below.
Supervisory Chemist at US FDA
Excellent fit as they currently hold the exact title at the right agency. Supervisory Chemist at US FDA → Supervisory Chemist at US FDA. Excellent.
Pharmaceutical Scientist at FDA
A direct match: this scientist currently works at the FDA developing and validating analytical methods using exactly the techniques listed, and performs QC analysis. Pharmaceutical Scientist at FDA (21+ years). Excellent.
Supervisory Chemist at FDA
This candidate is a perfect fit, holding the exact title and working directly for the FDA. Supervisory Chemist at FDA. Excellent.
Retired FDA Chemist; Chief Scientist at Autopoiesis Sciences
Excellent fit due to 16 years as a retired FDA Chemist, along with a PhD in Chemistry, despite being retired. FDA Chemist (16 yrs) → USP → current Chief Scientist. Excellent.
Chemist at FDA
This candidate is an excellent match, boasting direct FDA experience and a strong background in analytical chemistry as a chemist. FDA Chemist (4yr) → Mallinckrodt Staff Analytical Chemist (10yr); PhD Analytical Chemistry. Excellent.
Chemist at FDA, Center for Drug Evaluation and Research, Division of Pharmaceutical Analysis
Perfect match as this candidate currently works as a Chemist at the FDA in their analytical division and holds a PhD in Analytical Chemistry. Current Chemist at FDA (CDER) → ORISE Fellow at FDA → Research/Teaching Assistant; PhD Analytical Chemistry. Excellent.
Laboratory Director at FDA
This candidate offers extensive, long-term leadership experience directly within the FDA in chemistry and laboratory director roles. Laboratory Director at FDA (19.5 years) → Supervisory Chemist at FDA → Research Chemist. Excellent.
Analytical Chemist with FDA laboratory and industrial auditing experience.
This candidate is an excellent match, having a long career as a bench chemist directly within the FDA's own laboratory before moving into auditing roles. FDA Drug Lab Chemist (18 years) → bench chemist specializing in HPLC/GC/Spectroscopy/wet chemistry, internal/external auditing for FDA inspections. Excellent.
Lead Chemist at US Food and Drug Administration
This candidate is a direct match, currently serving as a Lead Chemist at the FDA, with 16 years of experience performing regulatory chemistry, method validation, and coordinating QA/instrument maintenance. Lead Chemist at US FDA (16.5 years) → current role. Excellent.
Experienced Chemistry Professional Specializing in Quality Control, Public Safety and Laboratory Excellence.
This individual explicitly worked as a Chemist at the FDA and has direct experience in quality control chemistry roles. Chemist at FDA (1+ year), prior QC Chemist II role, background in analyzing food/drug/cosmetic samples under regulation. Excellent.
Senior Manager | Analytical Chemistry | Method Validation (ICH, USP, FDA) | Regulatory Strategy | Lab Automation | Quality Systems | GMP/GLP Compliance| Audit-Ready Leadership
Excellent fit - current work explicitly involves writing/reviewing protocols for FDA submission, method validation (USP), and working within GMP/GLP frameworks. Principal/CEO Consultant → Validation Specialist (FDA review). 26 years exp. Excellent.
Supervisory Chemist at USFDA
This candidate currently holds the exact title in the target agency, implying direct fulfillment of all criteria. Supervisory Chemist at USFDA. Excellent.
Research Chemist at FDA
This candidate is an active Research Chemist directly employed at the FDA with a strong background in analytical chemistry method development and validation within GLP regulated environments. Research Chemist at FDA → CRO (PPD) doing bioanalytical method dev/validation in GLP/FDA environment, PhD Analytical Chemistry. Excellent.
chemist at FDA
This candidate is an excellent match as they have spent over 41 years working as a chemist directly for the FDA with a Master's in Analytical Chemistry, ticking every box perfectly. Career: Chemist at FDA for 41+ years, MS Analytical Chemistry. Excellent.
Advanced Chemist at U.S. Food and Drug Administration (FDA)
This candidate is an excellent fit, currently working as an Advanced Chemist at the FDA with a heavy background in analytical chemistry. Ex-CDC → ADM Deerland → FDA. Excellent.
Group Leader at Pace Analytical Life Sciences
Excellent background mixing hands-on analytical chemistry, FDA regulated lab experience, and supervisory skills in a CRO environment. Pace Analytical → 3M → Pace Analytical. Excellent.
Chemist at FDA
This candidate holds the exact job title mentioned in the search criteria and has relevant industry experience prior to that role. Chemist at FDA (current) → Analyst at Catalent, 5 years+ total experience. Excellent.
Supervisory Pharmaceutical Scientist at FDA, Center for Drug Evaluation and Research (CDER), Office of Pharmaceutical Quality (OPQ), Office of Product Quality Assessment I (OPQA I)
This candidate has direct, extensive experience as a Chemist and Supervisory Scientist at the FDA performing drug quality assessment roles. FDA Chemist/Supervisory Scientist (8y 4m) → Merck (12y Principal/Senior Scientist). Excellent.
Analytical Chemist
This candidate has decades of relevant experience as an analytical chemist heavily focused on pharmaceutical product testing and quality control operations. Analytical Chemist → Stability Coordinator, Bayer → Quality Control Lead, TriRx, BS Chemistry. Excellent.
Senior Manager, Quality Control, CMC
This candidate is a highly experienced analytical chemist specializing in QC within cGMP pharma, directly aligning with the role requirements. Senior Manager QC at Pharma Co → Analytical Chemist at CRO/CMO. Strong.
Analytical Chemist at Naval Air (NAVAIR) Warfare Center Aircraft Division (NAWCAD)
This specialist has deep analytical instrumentation expertise and explicit knowledge of FDA guidelines, aligning well with an FDA Laboratory Chemist role. NAVAIR → Analytical Chemist, extensive instrumentation, explicitly mentions FDA (21 CFR) and cGLP/cGMP knowledge. Excellent.
Scientist II at Pacific BioLabs, Inc.
This candidate is a highly experienced scientist whose background centers entirely on analytical chemistry techniques essential for a Laboratory Chemist role, including cGMP work and method validation. Scientist II → extensive experience in HPLC/GC/MS/Spectroscopy, trace analysis, method validation, cGMP testing, QC review, 41 years total experience. Strong.
Quality Assurance Supervisor
This candidate has significant recent experience as a Chemist performing QC, method development, and stability testing within pharmaceutical settings. QOL Medical → Formulated Solutions → Lonza → Baxter Chemist (13+ years). Excellent.
Skills: Regulatory Compliance - Quality Assurance - Software Validation / Administration - Laboratory Instrument Qualification - Audit - 21CFR 210, 820
This individual is a strong candidate with direct experience supporting FDA audits and extensive work in method validation, fitting the QC/analytical mold perfectly across pharma/devices. Principal Scientist (Teva) → Adjunct Professor, 33 years experience, specialized in method dev/validation, data integrity, and point person for FDA audits. Excellent.
Supervisor, Quality Control, Method and Cleaning Validation at Sigma Aldrich
This candidate has extensive quality and analytical chemistry experience, including direct FDA audit exposure. Sigma Aldrich → various management roles, 28+ years experience, deep pharmacopeia knowledge matched with HPLC/GC/FTIR QA/QC oversight. Excellent.
Discovery Chemistry Lab/Project Manager
This candidate has deep analytical chemistry experience supporting GMP environments, including specific FDA data integrity remediation, which strongly suggests FDA regulatory experience. Discovery Chemistry Sr Lab/Project Manager → SMACQC Lab Manager → Research Associate II; Supported GMP Empower environments with various analytical equipment; Data Integrity SME for analytical equipment, complete remediation project to meet current FDA requirements. Excellent fit, highly relevant analytical and regulatory background.
Manager Analytical Development at Pfizer
This individual has extensive senior experience developing and running analytical methods in pharmaceutical settings with direct FDA interaction. Pfizer → KV Pharma → Sandoz, 37 years exp, focused on method validation/submission. Excellent.
Quality Control & Analytical Chemist | HPLC/GC Testing | Pharmaceutical & Biotech Industries
This profile strongly indicates a current analytical chemist focused on quality control within pharmaceutical/biotech settings, possessing the core technical skills requested. Analytical Chemist/Specialist → HPLC/GC specialization, GMP compliance, SOP drafting, supporting regulatory audits, current/recent role in Bio-manufacturing Process Specialist (contamination control/environmental monitoring). Strong.
Pharmaceutical, Analytical Development & Quality
Exceptional background managing analytical sciences and laboratory compliance within a pharmaceutical context, explicitly showing deep knowledge of FDA regulations and handling PAI/CRL responses. Manager of Analytical Sciences, comprehensive FDA/cGMP knowledge, 16.9 years. Excellent.
Director of analytical and Quality Control Services
Excellent fit—director level experience spanning commercial pharmaceutical analytical chemistry, deep regulatory knowledge including FDA, and strong leadership in QC services. Director → 23.9 years in pharma/analytical/QC services, explicitly mentions FDA guidelines. Excellent.
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