CV, Curriculum Vitae and Online Resumes Search

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Online Resumes with "cGMP GLP"

I am a strong contributor performing routine tasks and other duties assigned under cGMP and GLP methods. I am a versatile individual with keen attention to details and provide input to increase productivity and quality. I participate in IQ, OQ and PQ in

As a technician, I would bring focus on quality and ease of use to your system development. Furthermore, I am eager and determined to work as team in order to achieve success.

Ideal Companies: Bio-tech, Pharmaceuticals, engineering

Analytical Chemist, Lab Manager, Lab Supervisor, Quality Control Officer

Methods Development • Procedure/SOP Writing • Method Validation Quality Control (NELAP, cGMP, GLP, ISO, FDA) • Organics Lab Start-up and Initialization • Process Improvement • Effective Communications Relationship Building • Strategic Planning • Resource Management • Problem Solving • Budgeting • Lab Safety • Laboratory Certification

People, projects and laboratory equipment management

Highly accomplished PRODUCTION and PROJECT MANAGER with multi-Project Management experience in the Pharmaceutical/Biotech Industry (Generic Drug Production, Drug Discovery, Assay Development and High-Throughput Laboratory Automation and equipment). Proven track record in the arena of Robotic Engineering including on-time delivery of custom Automated Robotic Screening Platforms for High-Throughput Screening (HTS), as well as...

Ideal Companies: People, projects and laboratory equipment management (including but not limited too market analysis, ordering, installation, operation, maintenance and removal from operation).

Tags for this Online Resume: project management, HTS, screening, robotic , laboratory equipment, biology, chemistry , pharma, Environmental Health and Safety, pharmaceutical , academic, Drug Discovery, automation

Regulatory Pharmaceutical Document Specialist and Technical Writer

Brenda is a Technical Writer and Quality Assurance Regulatory Document Specialist with over ten years of experience in the pharmaceutical industry. She has extensive experience with all types of document project work, including writing, editing, formatting. She has experience as a team member for non-conformance investigations (NCs) and Corrective Action and Preventative Actions (CAPAs). Her analytical and research skil...

I have extensive Chemical and Biological experience with a working knowledge of USP and cGMP and GLP. I have 12 years of Laboratory experience in Chemistry, Biology, Microbiology and Textile industry. I have repaired and operated Caliper (Sotax) Tablet P

To advance career as a scientist where my education, experience and motivation will have a valuable application for company and personal growth.

Tags for this Online Resume: HLPC, Dissolution/EMC, Wet Chemistry, Vitek , Autoclave/Kaye Validation, Qualified Trainer/Reviewer/Documenation

Chemist

I have 14 years of experience in pharmaceutical industries. Results oriented individual with a track record of instituting and maintaining high levels of Quality Assurance and leadership. I’m seeking additional opportunities for professional development in consulting, validation, compliance or technical areas. Strong analytical and planning skills. Six Sigma Black Belt trained. Knowledge in FDA, cGMP, GLP, 21 CFR - Part 820...

Ideal Companies: Pharmaceuticals or food industries

Tags for this Online Resume: qa, validation, lims, qc

Scientist - >15 years experiece in biotechnolgy process and analytical development

Scientist with 25 years of extensive experience in the Biotechnology industry. Expertise in protein purification, process development and assay development under cGMP and GLP environments. Highly motivated, productive, inquisitive, logical and known as a good team player.

Tags for this Online Resume: Massachusetts, Biotechnology, HPLC, Process , Analytical , Development

Quality Assurance - 11 yrs experience - Phila., PA 19145

• Works to build a rapport giving guidance and support to operational staff to develop an environment of teamwork and effective communication with a result of achieving organizational goals. Responsible for goals pertaining to cGMP, GLP, CFR's, Association of Blood Bank (AABB) regulations and assure compliance with 22 organization Quality Systems.

Tags for this Online Resume: Auditing, Inspections, guidance, support, CAPA, writing polcies and proceudres

QA ASSOCIATE - 3 Years of Experience - 08873

Manufacturing & Production Resumes - Quality Engineer Resumes - Somerset, NJ

• Ensure implementation of cGMP, GLP and GDP • Monitoring processing and laboratory activities in the facility on a daily basis • Hosting regulatory audits • Member of internal audit team • Preparation and implementation of Standard Operating Procedures, Stability Protocols, Master Batch Production Records, etc. • Evaluation and Qualification of vendors for raw materials, packaging materials and contract services • Samplin...

Tags for this Online Resume: QUALITY ASSURANCE, QA TECNICIAN, VALIDATION, DOCUMENTATION, QA AUDITOR, BMR, Test, Audit, Documentation, Internal audit, Manufacturing, Microsoft, Microsoft Office, Packaging

QC Chemist-15 years experiance

Science & Biotech Resumes - Agricultural Technician Resumes - Edison, NJ

• Hands of experience in Chemist for Dissolution and wet chemistry in pharmaceutical • Extensive knowledge of cGMP, GLP, USP, and OSHA requirements • Successfully validated Dissolution method and cleaning validation.

Tags for this Online Resume: QC Chemist

Featured Profile

Global Regulatory Affairs - 14 Years of Experience- New Delhi India 110021

Science & Biotech Resumes - Clinical Regulatory Affairs Resumes - Floral Park, NY

Seeking assignments as a Global Regulatory Affairs Professional - NCEs, GENERICS- Pharma, Biotech products, Botanicals & Medical Devices in Global Regions and/or Quality & Compliance professional across the Pharma & Medical Devices Industry. Overall Profile * With overall 15+ years industrial experience, with 14+ years in the field of Global Regulatory Affairs, Compilation & Submissions of Technical Packages for IND/CTA, ND...

Ideal Companies: BBraun Medical Pvt Ltd, New Delhi, India, Glenmark Pharmaceuticals Ltd., Mumbai, India, Panacea Biotec Ltd., New Delhi, India

Tags for this Online Resume: Regulatory Affairs, Management, Medical Devices, Pharmaceutical Industry, IND/CTA, Formulations & APIs, Regulatory Audits & Compliances, NCEs/NMEs/Generics, CT, Regulatory Consultancy, Regulatory Due Diligence & Gap Assessment

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