If you searched Superstar Sourcing for Quality Assurance Specialist (with 1 additional requirement) on January 3, 2026 you'd find 468 great candidates

This sample report shows what our sourcing engine surfaces for this search. Preview the top 30 matches below.

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V**** N****

Associate Director, Quality Management Systems

Philadelphia, United States 12 years 7 months

Excellent fit, explicitly described as an experienced QA Specialist working in the pharmaceutical manufacturing sector with explicit GMP oversight. Teva Pharmaceuticals (Associate Director, QMS) focusing on GMP commercial/clinical manufacturing oversight. Excellent.

Work Experience

Eastern Mennonite University
Graduate Teaching Assistant · 1 year 10 months
Virginia Tech
Research Assistant · 3 months
Teva Pharmaceuticals
Director, Commercial Quality US
Merck
Environmental Monitoring Technician · 2 years
+ 4 more positions

Qualification Criteria 4 met

GMP knowledge
QA experience
Pharmaceutical industry
Quality Assurance Specialist

Skills & Expertise

root cause analysis quality assurance trend analysis quality management employee training gel electrophoresis quality systems performance metrics supply chain regulatory affairs continuous improvement performance reviews +8 more
100%

J*** P****

Quality Associate III McNeil Consumer Healthcare

Pottstown, Pennsylvania, United States 34 years 1 month

An excellent match with extensive experience in Pharma/Biotech, including dedicated Quality Assurance roles and GMP committee involvement. Quality Associate III at McNeil Consumer Health (current, role implies QA Specialist level) with 15+ years in industry roles. Excellent.

Work Experience

Centocor / Johnson&Johnson
Associate Process Scientist · 3 years 4 months
Neose Technologies, Inc.
Validation Specialist · 3 months
Centocor
Manufacturing Associate III · 5 years 5 months
Janssen, Pharmaceutical Companies of Johnson and Johnson
Process Scientist · 2 years 8 months
+ 3 more positions

Qualification Criteria 4 met

GMP knowledge
QA experience
Pharmaceutical industry
Quality Assurance Specialist

Skills & Expertise

manufacturing assurance performing investigations analysis training management 5s processing metrics auditing compliance +8 more
100%

G**** T****

Quality Assurance Finished Production Specialist II

Wilson, North Carolina, United States 26 years 6 months

This candidate is an exceptional match, holding a specialist role in QA for the pharmaceutical sector for over 26 years with explicit GMP knowledge mentioned. QA Finished Production Specialist II at Novo Nordisk for 26+ years, strong focus on regulatory compliance and GMP. Excellent.

Work Experience

Novo Nordisk
QA Finished Production Specialist II · 26 years 7 months

Qualification Criteria 4 met

GMP knowledge
QA experience
Pharmaceutical industry
Quality Assurance Specialist

Skills & Expertise

regulatory compliance process improvement best practices quality management quality assurance biotechnology industry regulatory requirements problem solving communication skills production compliance regulations +8 more
100%

V**** D****

Quality Assurance

United States 2 years

This candidate is a perfect match, currently working as a QA Specialist in pharma, mentioning direct cGMP adherence experience. QA Specialist at Piramal Pharma Solutions → Co-Founder at RegINTL (regulatory consulting). Excellent.

Work Experience

Piramal Pharma Solutions
Quality Assurance Specialist · 1 year 1 month
RegINTL
Co-Founder · 2 years 1 month

Qualification Criteria 4 met

GMP knowledge
QA experience
Pharmaceutical industry
Quality Assurance Specialist

Skills & Expertise

assurance compliance cgmp pharmaceuticals clinical documentation remediation investigation reports quality assurance regulatory compliance corrective actions +1 more
100%

J*** L*

QA Specialist II at Lonza

San Jose, California, United States 19 years 9 months

This candidate seems like an excellent fit, matching the title, industry, experience, and explicit GMP knowledge. QA Specialist II at Lonza, 19+ years experience, reviewing GMP documents in FDA regulated facility. Excellent.

Work Experience

Agilent Technologies
QA Sr. Representative · 1 year 11 months
Lonza
QA Specialist II
Impax Laboratories
QA Sr. Inspector (Manufacturing) · 11 years
Impax Laboratories
QA Associate (Product Release) · 2 years 5 months

Qualification Criteria 4 met

GMP knowledge
QA experience
Pharmaceutical industry
Quality Assurance Specialist

Skills & Expertise

assurance iso gmp production management database surveillance responsible questionnaires manufacturing metrics disposition +8 more
100%

C**** T****

QC Specialist

Murrayville, Georgia, United States 5 years 7 months

Excellent fit as an experienced QC/QA professional deeply rooted in the pharmaceutical industry, reviewing GxP documentation and interacting with global quality leadership. QC Specialist at Patheon → Quality Technician 4 at J&J. Excellent.

Work Experience

The Janssen Pharmaceutical Companies of Johnson & Johnson
Senior Technician Quality Control · 1 year 6 months
Patheon
QC Specialist
Johnson & Johnson
Quality Technician 4 · 10 months

Qualification Criteria 4 met

GMP knowledge
QA experience
Pharmaceutical industry
Quality Assurance Specialist

Skills & Expertise

quality control quality assurance medical devices best practices regulatory requirements quality system information systems problem analysis assurance pharmaceuticals healthcare leadership +8 more
100%

A**** G***

ASQ-CQA Certified | Quality Assurance Specialist

United States 9 years 9 months

This is an excellent fit, experienced QA Consultant/Specialist focused entirely on pharmaceutical manufacturing compliance and cGMP/21 CFR. Consultant at Avet Pharmaceuticals → The Jackson Laboratory. Excellent.

Work Experience

CEVA SANTE ANIMALE
Summer Intern- Water System Validation · 5 months
St. John's University
Adjunct Professor · 8 months
The Jackson Lab
Consulatnt · 1 year 4 months
Avet Pharmaceuticals Inc.
Pharma Consultant · 1 year 10 months
+ 4 more positions

Qualification Criteria 4 met

GMP knowledge
QA experience
Pharmaceutical industry
Quality Assurance Specialist

Skills & Expertise

compliance driving manufacturing management cgmp iso auditing pharmaceuticals laboratory investigations capa clarity +8 more
100%

A*** J****

Quality Assurance Specialist/ CAR-T Cell Therapy. Quality Consultant at Drug and Device.

United States 13 years 11 months

This candidate is an excellent fit, currently serving as a Senior Quality Assurance Specialist in a pharma environment. Pharmacist → Sr QA Exec/Specialist at BMS/Medicaids Pharma/SAMI, working with SOPs, investigations, APQR. Excellent.

Work Experience

Medicaids Pharma
Senior Quality Assurance Executive
Bristol Myers Squibb
Quality Assurance Specialist/ CAR-T Cell Therapy.
SAMI Pharmaceuticals
Management Trainee Officer QA · 7 months
SAMI Pharmaceuticals (Pvt.) Ltd.
Senior Quality Assurance Officer · 9 months
+ 6 more positions

Qualification Criteria 4 met

GMP knowledge
QA experience
Pharmaceutical industry
Quality Assurance Specialist

Skills & Expertise

assurance regulations trend analysis reports triage investigations reconciliation risk cell responsible manufacturing +8 more
100%

T**** R**

Quality Assurance Specialist

Dayton, New Jersey, United States 7 years 8 months

This candidate is an excellent match who explicitly holds the Specialist title while detailing deep QA/GMP experience in pharma. QA Specialist → QA & Compliance Lead, extensive experience in QMS, batch record review, audits, deviations, and strong GMP/GLP foundation. Excellent.

Work Experience

Circle Pharma, Inc.
Sr. Quality Assurance · 2 years 7 months
Aurolife
QA Specialist · 6 months
Merck
QA Representative · 2 years
Bausch + Lomb
Senior Specialist, QA · 2 years 2 months

Qualification Criteria 4 met

GMP knowledge
QA experience
Pharmaceutical industry
Quality Assurance Specialist

Skills & Expertise

assurance management efficiency optimization documentation compliance inspection validation audit investigations iso driving +8 more
100%

C**** V****

Quality Assurance Analyst

Washington, District of Columbia, United States 5 years 5 months

Excellent fit - this candidate has 6 years of dedicated pharmaceutical QA experience explicitly mentioning GMP. Pii → Emergent BioSolutions → Clene Nanomedicine, MQA Associate → QA Analyst → QA Specialist. Excellent.

Work Experience

Pii (Pharmaceutics International, Inc.).
MQA Associate II · 6 months
Emergent BioSolutions
Quality Assurance Analyst II (OTF) · 1 year 2 months
Clene Nanomedicine
Senior Production Technician · 2 years 3 months
Pii, A Jabil Company
MQA Associate III · 5 months
+ 1 more positions

Qualification Criteria 4 met

GMP knowledge
QA experience
Pharmaceutical industry
Quality Assurance Specialist

Skills & Expertise

quality assurance manufacturing operations gmp manufacturing operations assurance production training documentation management reports metrics
100%

W**** C****

QA Support Specialist @ FUJIFILM Biosciences | Regulatory Science @ JHU AAP

Irvine, California, United States 3 years 1 month

Strong match for a specialist role with current QA experience in biopharma/medical device CMOs explicitly mentioning 21 CFR compliance. QA Support Specialist at FUJIFILM Biosciences → QA/QC Specialist at MedisourceRx. Excellent.

Work Experience

UCI Campus Recreation
Competitive Sports Supervisor · 10 months
FUJIFILM Biosciences
Quality Assurance Support Specialist · 1 year
Cloudbreak Pharma
Pharmaceutical Intern · 7 months
MedisourceRx
Quality Assurance / Quality Control Specialist · 8 months
+ 1 more positions

Qualification Criteria 4 met

GMP knowledge
QA experience
Pharmaceutical industry
Quality Assurance Specialist

Skills & Expertise

assurance manufacturing iso compliance management documentation inspection readiness operations science salesforce sap +8 more
100%

A**** P**

Quality Assurance specialist II| Pharma | CAPA| cGMP and regulatory compliance |Drugs | Biologics | Medical Device

Hurst, Texas, United States 5 years 4 months

Excellent fit – currently in the Specialist QA role within the pharma industry, explicitly mentioning cGMP and CAPA experience. Sovereign/Piramal/ScieGen → QA Specialist roles, explicitly referencing cGMP, batch record review, and CAPA. Excellent.

Work Experience

Ipca Laboratories Limited
Quality Control Specialist · 1 year 7 months
Piramal Pharma Solutions
Quality Assurance Specialist I · 1 year 3 months
Sovereign Pharmaceuticals
Quality Assurance Specialist II · 10 months
ScieGen Pharmaceuticals Inc
Quality Assurance Specialist · 1 year 11 months

Qualification Criteria 4 met

GMP knowledge
QA experience
Pharmaceutical industry
Quality Assurance Specialist

Skills & Expertise

disposition packaging capa compliance cgmp manufacturing management auditing sop writing reporting kpi +8 more
100%

S**** C****

Quality Assurance Specialist

Lubbock, Texas, United States 5 years 1 month

This candidate's current and recent roles perfectly align with the requirements, detailing specific QA tasks under GMP/GLP/FDA compliance. Quality Assurance Specialist lead at Takeda (2y 2m) worked directly on batch record review, compliance, and CAPA. Excellent.

Work Experience

Abbott
Quality Assurance Specialist · 1 year 1 month
Novartis
Quality Assurance Specialist · 2 years 1 month
Takeda
Quality Assurance Specialist lead · 2 years 2 months

Qualification Criteria 4 met

GMP knowledge
QA experience
Pharmaceutical industry
Quality Assurance Specialist

Skills & Expertise

compliance gmp glp iso risk analysis fmea capa validation documentation testing integrity +8 more
100%

T** L***

Quality Assurance Specialist at Gilead Sciences

United States 24 years 3 months

This individual is currently a Quality Assurance Specialist at Gilead Sciences with detailed experience covering validation, compliance, vendor qualification, and investigations in the pharmaceutical industry. Quality Assurance Specialist at Gilead Sciences → Clinical Project Manager at REMEDIAL CORPORATION. Excellent.

Work Experience

REMEDIAL CORPORATION
Clinical Project Manager · 1 year 10 months
Wilco Imports
Project Manager · 4 years 2 months
eGuanxi
Project Manager · 1 year 4 months
Gilead Sciences
Quality Assurance Specialist

Qualification Criteria 4 met

GMP knowledge
QA experience
Pharmaceutical industry
Quality Assurance Specialist

Skills & Expertise

clinical commercialization liaison projects validation management compliance commercial vendor readiness assurance disposition +8 more
100%

C**** W****

Quality Assurance Consultant at PharmaLex

Simi Valley, California, United States 25 years 6 months

This individual represents an excellent match, offering decades of deep QA consulting and leadership experience specifically in pharma/biopharma supporting CMOs. Quality Assurance Consultant at PharmaLex (5y 5m) → Associate Director, Disposition & QA Operations Lead at Takeda (3y 10m) → Sr. Quality Manager at Shire (4y 1m) → Sr. Manager, External Quality at Baxter International Inc. (1y 1m). Excellent.

Work Experience

Baxter International Inc.
QAI · 1 year
Baxter International Inc.
Sr. Manager, External Quality at Baxter BioScience · 1 year 1 month
Takeda
Associate Director, Disposition & QA Operations Lead (US), Plasma OpU · 3 years 10 months
Baxter Healthcare
Quality Associate III · 2 years 11 months
+ 6 more positions

Qualification Criteria 4 met

GMP knowledge
QA experience
Pharmaceutical industry
Quality Assurance Specialist

Skills & Expertise

management compliance inspection preparedness assurance director disposition operations training api manufacturing less +4 more
100%

M**** P****

Senior Quality Specialist at Merck

Lancaster, Pennsylvania, United States 14 years

This candidate is an excellent fit, currently working as a Senior Quality Specialist in pharmaceuticals with extensive QA and GMP experience. Sr Quality Specialist at Merck → Quality Specialist at GSK, MSc Pharmacology. Excellent.

Work Experience

Johnson & Johnson
Compliance Specialist II · 1 year 11 months
Cadista Pharmaceuticals
Quality Assurance Specialist · 2 years 7 months
Merck
Senior Quality Specialist
GSK
Quality Specialist · 4 years 11 months

Qualification Criteria 4 met

GMP knowledge
QA experience
Pharmaceutical industry
Quality Assurance Specialist

Skills & Expertise

change management aseptic processing quality assurance preventive maintenance process management process improvement production management regulatory requirements environmental monitoring problem solving pharmacology biotechnology +8 more
100%

C**** D****

Pharmaceuticals/Medical Devices/Clinical Trials/Gene Therapy

Raleigh, North Carolina, United States 13 years 5 months

This candidate is an excellent fit, detailing extensive QA experience within the pharmaceutical sector ensuring GMP compliance. Sr. Quality Associate (QA Operations Consultant) at Sage Therapeutics (1y 5m) → Sr. Specialist II at Taysha Gene Therapies (9m) → Sr. Compliance Specialist at PPD (1y 6m) → Specialist, Quality Systems & Compliance at Merck (1y 11m). Excellent.

Work Experience

Catalent Pharma Solutions
Laboratory Associate · 2 months
Taysha Gene Therapies
Sr. Specialist II, External Quality Operations · 9 months
PPD
Sr. Compliance Specialist (Clinical Supplies QA - EQA) · 1 year 6 months
Beckman Coulter Diagnostics
Sample Management Coordinator · 2 months
+ 6 more positions

Qualification Criteria 4 met

GMP knowledge
QA experience
Pharmaceutical industry
Quality Assurance Specialist

Skills & Expertise

self motivated quality assurance regulatory affairs communication skills manufacturing operations laboratory equipment quality management medical devices regulatory compliance product quality complaint investigations change control +8 more
100%

S**** T****

Quality Assurance | Quality Batch Disposition SME Raleigh - Durham - Chapel Hill Area

United States 20 years 7 months

Excellent fit - senior QA professional with extensive experience across pharma/biologics focusing on batch disposition and GMP manufacturing. Merck → Eli Lilly, 20+ years experience. Excellent.

Work Experience

Charles River Laboratories
Quality Assurance Auditor · 2 years
Merck
Senior Specialist, Product Release · 1 year 2 months
Next Century Incorporated
Associate Scientist · 1 year
AppTec
Quality Assurance · 1 year
+ 4 more positions

Qualification Criteria 4 met

GMP knowledge
QA experience
Pharmaceutical industry
Quality Assurance Specialist

Skills & Expertise

biologics gmp manufacturing director compliance disposition assembly packaging health integrity assurance testing +3 more
100%

M**** M****

Raleigh, North Carolina, United States 28 years 11 months

This individual is an excellent match, currently working as a Senior Quality Assurance Specialist in a biopharma setting with extensive GMP knowledge. KBI Biopharma (QA Specialist II, Sr. QA Specialist) → bioMerieux (QC/Analyst/Group Leader) → KBI Biopharma. Excellent.

Work Experience

KBI Biopharma
Quality Assurance Specialist II · 3 years 1 month
KBI Biopharma
Senior Quality Assurance Specialist · 1 year 5 months
bioMerieux
Senior Application Specialist · 14 years
bioMerieux
QC Analyst/Senior QC Analyst/Group Leader · 11 years

Qualification Criteria 4 met

GMP knowledge
QA experience
Pharmaceutical industry
Quality Assurance Specialist

Skills & Expertise

assurance compliance preparation assembly gmp disposition projects capa manufacturing laboratory responsible quality assurance
100%

A**** A****

Quality Assurance Specialist at Miltenyi Biotec

Gaithersburg, Maryland, United States 17 years 5 months

Perfect match occupying the exact specialist QA role within the pharmaceutical sector, boasting explicit GMP and 21 CFR knowledge over 10 years in quality. Miltenyi Biotec/Jubilant/Hikma → QA roles, citing GMP/GLP and 21 CFR familiarity. Excellent.

Work Experience

Jubilant Pharma
Quality Assurance Associate II · 1 year
Hikma Pharmaceuticals
Quality Control Analyst · 2 years
Miltenyi Biotec
Quality Assurance Specialist
Hikma Pharmaceuticals
Quality Assurance Specialist · 6 years
+ 2 more positions

Qualification Criteria 4 met

GMP knowledge
QA experience
Pharmaceutical industry
Quality Assurance Specialist

Skills & Expertise

assurance collaboration iso gmp glp sap manufacturing hplc sop operation production quality assurance +3 more
100%

D**** S**

Pharmaceutical Quality Manager

Chicago, Illinois, United States 28 years 6 months

This candidate is highly experienced Quality Manager with deep roots in Pharmaceutical R&D Quality and compliance, strongly implying all required competencies. Manager PharmSci QO at Pfizer → GMP Officer at Pfizer → Compliance Specialist at Hospira. Excellent.

Work Experience

Hospira
Senior Validation Analyst, Chemical Method Validations Group (CMV) · 6 years 2 months
Pfizer
GMP Officer · 7 years 6 months
Abbott Laboratories
Senior Microbiologist, Method Development Laboratory · 6 years 5 months
Hospira
Compliance Specialist, Global Pharma R&D · 2 years 2 months
+ 2 more positions

Qualification Criteria 4 met

GMP knowledge
QA experience
Pharmaceutical industry
Quality Assurance Specialist

Skills & Expertise

quality management operational excellence risk management method development raw materials root cause analysis compliance r management laboratory investigations capa +8 more
100%

K**** G****

Sr Quality Assurance Associate and System Manager at Solaris Pharma Corporation

Hackettstown, New Jersey, United States 15 years 8 months

This candidate is an excellent fit, explicitly holding the title Sr Quality Assurance Associate and referencing a deep history in the pharmaceutical industry with strong regulatory expertise. Solaris Pharma Corp → Systems Manager/QA Associate, 15+ years in pharma, references GLP/FDA/global regulators. Excellent.

Work Experience

Lupin
QC Officer · 1 year 1 month
Gufic Biosciences Ltd.
Quality Assurance Officer · 2 years
Span Diagnostics Ltd.
Production Officer · 7 months
Lupin
Quality Assurance Executive · 3 years 8 months
+ 5 more positions

Qualification Criteria 4 met

GMP knowledge
QA experience
Pharmaceutical industry
Quality Assurance Specialist

Skills & Expertise

assurance pharmaceuticals laboratory glp biotechnology validation calibration food administration science tga iso +8 more
100%

A*** R****

Quality Assurance Supervisor at ADMA Biologics, Inc.

United States 17 years 4 months

This candidate is an experienced QA Specialist working in the pharmaceutical industry with demonstrated GMP knowledge. Determined and detailed Quality Assurance Specialist with a dedication to quality and accuracy. Over 15 years of experience in Pharmaceutical Industry. QA Supervisor at ADMA Biologics, Inc. → QA Specialist II at ADMA Biologics, Inc. → QA Material Disposition Auditor at Actavis, FL. Excellent.

Work Experience

Azopharma
Technical Writer · 2 years 5 months
ADMA Biologics, Inc.
Quality Assurance Specialist II · 2 years 7 months
Actavis, FL
QA Material Disposition Auditor · 8 years 10 months
Watson Laboratories, Florida
R&D · 1 year 9 months
+ 1 more positions

Qualification Criteria 4 met

GMP knowledge
QA experience
Pharmaceutical industry
Quality Assurance Specialist

Skills & Expertise

quality assurance creative thinking problem solving time management multitasking skills pharmaceutical industry writing skills quality control jd edwards team leadership laboratory techniques continuous improvement +8 more
100%

H**** A****

Quality Assurance Specialist | Medical Device Industry | Regulatory Compliance | CAPA Management

United States 6 years 11 months

Perfect profile match, explicitly stating experience as a Quality Assurance Specialist in the pharmaceutical industry with strong CAPA/SOP/Audit skills. Ex-Medline → Abbott → Fresenius Kabi (6+ yrs). Excellent.

Work Experience

University of Illinois College of Medicine
Undergraduate Research Assistant · 1 year 7 months
University of Illinois Chicago
Math and Science Learning Center Peer Leader · 6 months
Abbott
Quality Assurance Product Support Specialist · 2 years 2 months
Ferrero
Quality Assurance Laboratory Technician · 3 months
+ 3 more positions

Qualification Criteria 4 met

GMP knowledge
QA experience
Pharmaceutical industry
Quality Assurance Specialist

Skills & Expertise

assurance compliance management investigations capa sop collaboration r research eeg recording science +8 more
100%

A** S****

Quality Systems Specialist at Boehringer Ingelheim Chemicals

Petersburg, Virginia, United States 12 years 2 months

Perfect fit; currently a Quality Systems Specialist possessing deep knowledge of cGMPs/FDA requirements within chemical/pharma manufacturing. Quality Systems Specialist at Boehringer Ingelheim Chemicals → QA Product Release Chemist, explicit mention of cGMP focus. Excellent.

Work Experience

Boehringer Ingelheim Chemicals
Quality Control Chemist · 4 years 7 months
Boehringer Ingelheim Chemicals
Quality Assurance Product Release Chemist · 4 years 5 months
Boehringer Ingelheim Chemicals
Quality Systems Specialist · 3 years 5 months

Qualification Criteria 4 met

GMP knowledge
QA experience
Pharmaceutical industry
Quality Assurance Specialist

Skills & Expertise

quality systems quality assurance quality control regulatory requirements interpersonal communication communication skills laboratory equipment contractor management regulatory submissions leading meetings process improvement process mapping +8 more
100%

D*** E****

Quality Assurance Associate at Societal

Lawrenceville, Georgia, United States 28 years 1 month

Excellent match with extensive experience as a Quality Assurance Associate explicitly within the pharmaceuticals industry and mentioning GMP skills. QA Associate/Specialist roles across multiple pharma/CDMO companies (Societal, Bend, Recro, Novoste) for over 28 years. Excellent.

Work Experience

Bend Bioscience
Senior Quality Assurance Associate · 1 year 2 months
Clyde Bergemann Power Group
QA Tester · 7 months
Novoste Corporation
QA Specialist · 2 years 10 months
Societal™ CDMO (formerly Recro)
Quality Assurance Associate · 20 years 1 month
+ 2 more positions

Qualification Criteria 4 met

GMP knowledge
QA experience
Pharmaceutical industry
Quality Assurance Specialist

Skills & Expertise

assurance pharmaceuticals pharmaceutics validation investigations reporting lims gmp commercial clinical science biochemistry +4 more
100%

R**** G****

Sr. Specialist QA

Spring Valley, New York, United States 15 years 2 months

This person consistently holds QA Specialist/Senior Specialist roles within pharmaceutical companies and explicitly mentions cGMP adherence. Senior Quality Assurance Specialist at Moderna → QA Specialist at Leadiant Biosciences, explicit cGMP maintenance, deviation participation, raw material/finished product release. Excellent.

Work Experience

RIJ Pharmaceuticals
Quality Assurance Analyst · 1 year 5 months
Par Pharmaceutical
Quality Specialist, Systems · 3 months
MasterPharm
Quality Analyst I; QA/QC · 2 years 1 month
Moderna
Senior Quality Assurance Specialist · 2 years 7 months
+ 5 more positions

Qualification Criteria 4 met

GMP knowledge
QA experience
Pharmaceutical industry
Quality Assurance Specialist

Skills & Expertise

assurance laboratory cgmp testing reports investigations sop pharmacists compliance prescription audit production +8 more
100%

C**** G****

Quality Assurance Specialist at FDA/ Certified Quality Management System Auditor

Silver Spring, Maryland, United States 10 years 2 months

This person is currently working in the exact stated role, complete with FDA and pharmaceutical industry experience demonstrating GMP knowledge. QA Specialist at FDA → QA Manager/Supervisor at Amneal Pharma, 10 years experience, focused on QMS, cGMP compliance, deviations, batch release. Excellent.

Work Experience

Amneal Pharmaceuticals
QA Supervisor · 3 years 9 months
Amneal Pharmaceuticals
QA Associate · 2 years 7 months
FDA
Quality Assurance Specialist · 3 years 2 months
Ipca Laboratories Limited
Intern · 2 months
+ 1 more positions

Qualification Criteria 4 met

GMP knowledge
QA experience
Pharmaceutical industry
Quality Assurance Specialist

Skills & Expertise

education training cgmp assurance management compliance preparation sop specifications reports commercial manufacturing +8 more
100%

N**** V****

Quality Assurance Specialist, Neurogene Inc.

Houston, Texas, United States 10 years 10 months

This candidate holds the exact current title and has deep relevant experience in Gene Therapy/Pharma QA roles, including GMP compliance, CAPA, and investigations. QA Specialist at Neurogene Inc. → Deviation Investigator at Lonza → J&J Janssen roles. Excellent.

Work Experience

Lonza
Cell & Gene Therapy Deviation Investigator III · 1 year 1 month
ORVISV Corporation
CAPA Expert, Investigation Specialist at Johnson & Johnson Janssen Pharmaceutical · 2 years 2 months
ORVISV Corporation
Documentation Specialist, Compliance at Johnson & Johnson Janssen Pharmaceutical · 1 year 1 month
Kelly Services
Quality Assurance Technician at Johnson & Johnson Mcneil Pharmaceutical · 11 months
+ 4 more positions

Qualification Criteria 4 met

GMP knowledge
QA experience
Pharmaceutical industry
Quality Assurance Specialist

Skills & Expertise

assurance cell capa investigation risk assessment trackwise compliance completion investigations manufacturing packaging +8 more
100%

R**** G****

Director, Quality Assurance | Results-oriented.

Vega Alta, United States 20 years 10 months

This senior professional has extensive QA leadership experience within the pharmaceutical context, heavily involving GMP processes. Director QA → Associate Director Quality at Lantheus (managing QMS for GMP processes, aseptic processing, sterile preparations). Excellent.

Work Experience

Bristol-Myers Squibb
Quality Assurance Manager · 6 years 10 months
Lantheus
Associate Director Quality

Qualification Criteria 3 met

GMP knowledge
QA experience
Pharmaceutical industry
Quality Assurance Specialist

Skills & Expertise

quality assurance aseptic processing communication skills analytical skills product planning quality management field operations team management corrective actions patient safety risk analysis assurance +8 more
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