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Online Resumes with "Validations Qualifications"
Administrative Assistant
Ideal Companies: Pharmaceutical
Tags for this Online Resume: Administrative Assistant
QA Supervisor
Currently I’m looking for a Quality Assurance position in industry, where my previous experience and education will be utilized to achieve rewarding and long-term growing opportunities. I have a significant work experience in Quality Assurance and Quality Control departments. My responsibilities as a Head of QA Department involve wide range of quality assurance tasks, assigned but not limited to overseeing daily t...
Tags for this Online Resume: quality assurance, supervisor, GMP regulated industry, improving quality
Senior Quality Validation Engineer-FDA,GXP,QSR,Validation, Qualification experience
Providing guidance and direction at a director/president level heading the quality organization
Tags for this Online Resume: Valdiation, Quality, FDA, QSR, GAMP, GXP
To work in a professional, goal-driven, team-oriented environment.
Monitored and adjusted control levels in a manufacturing environment to produce the highest purities of industrial gases. Led all process validation, instrument calibration and qualification projects
Ideal Companies: Lab enviroment/ Outside. Production, hazardous material
Recruiter
Tags for this Online Resume: Human Resources, Marketing, Recruiting, interviewer, investigator
Business Analyst
Experienced in the Pharmaceutical, Agriculture, Automotive, and Distribution
Industries. Have demonstrated talent to excel in diverse organizations. Extensive
development/involvement of concept, design and completion of various projects and
compliance areas including Sharepoint, Computer System Validation, Qualification, and
...
Tags for this Online Resume:
Requirements, Business Analyst, Sharepoint, Systems Analyst, Change Control, Documentation
Microbiology Laboratory Analyst - 11 years experience - cGMP, GOP/SOP, SAP experience
I am looking to relocate to the greater Philadelphia region, to a job either in a microbiology laboratory in a QA position.
Tags for this Online Resume:
Quality experienced, cGMP, Aseptic technic, GOP/SOP, Validations/Qualifications, Microbiology
Engineer- Professional with over nine (9) years of experience in Validation and Qualification study under the FDA regulations. Strong knowledge in Electrical Engineering, mainly in Communication and Electronic. Excellent analytical and problem solving c
Validation Qualification Specialist
Featured Profile
Validation Documentation Writer, Validation Coordinator, Quality Assurance - 10 years Experience - Indianapolis
To work in a quality-driven environment, such as the biotechnical field, as a Validation Coordinator, Validation Writer, or Quality Assurance Manager.
Ideal Companies: Convance, Clarian, Roche Diagnostics
Tags for this Online Resume:
GxP guidelines, Planning Documentation, Regulus, CFR21 Part 11, Testing Documentation, TrackWise, Good Documentation Practices, Microsoft Office
Biologist - 13 Years of Experience - Near 07208
Qualifications Summary Highly competent, diligent, and detail-oriented management professional, equipped with extensive experience and expertise focused on various areas of quality improvement, process validation and qualification, manufacturing, risk analysis, as well as implementation of standard procedures and policies within the pharmaceutical industry. Possess solid instrumental analysis skills and expertise in categor...
Tags for this Online Resume:
Management, Complaints, CFR Part 11, High Performance Liquid Chromatography (HPLC), FDA, New Jersey, MSDS, Policies and Procedures, Process Improvement, Protocol, CAPA
Validation Documentation Writer, Validation Coordinator, Quality Assurance - 10 years Experience - Indianapolis
To work in a quality-driven environment, such as the biotechnical field, as a Validation Coordinator, Validation Writer, or Quality Assurance Manager.
Ideal Companies: Convance, Clarian, Roche Diagnostics
Tags for this Online Resume: GxP guidelines, Planning Documentation, Regulus, CFR21 Part 11, Testing Documentation, TrackWise, Good Documentation Practices, Microsoft Office
