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Online Resumes with "GMP environment"
Quality Analyst-5-8 yrs experience in medical and pharmaceutical GMP environment
Biological Technician - 15 Years of Experience - Near 94547
Obtain a challenging position to utilize 15 years of experience in the biotechnology industry. Help company achieve optimum operational excellence while producing successful results in lean manufacturing. Increase process efficiency with a focus on safety. Skilled professional to achieve success and increase productivity in a quality controlled safe cGMP environment
Ideal Companies: BioMarin
Tags for this Online Resume: Biotech, cGMP, FDA, AsepticTechnique , ISO, SAP, Quality Control, manufacturing, Compliance, Monitoring
Chemist - 13 Years of Experience
SUMMARY OF QUALIFICATIONS: * Strong organizational and technical skills, highly efficient a quick learner. * 13+ Years of experience with Analytical Testing within GMP environment. * Understands and complies to ICH guidelines, cGMP, GLP, and FDA regulations. * Very enthusiastic and motivated in learning new instrumentation and methods. * Work effectively under high pressure environment and never compromise with ethics and q...
Tags for this Online Resume: Quality, Quality Assurance, High Performance Liquid Chromatography (HPLC), Documentation, Instrumentation, Software, Test, Troubleshooting, 5S, Documentum
Life Scientist - 8 Years of Experience - Near 27617
Summary Ph.D in Pharmaceutics with extensive experience in analytical method development, method transfer and validation for Small and Large molecular API, in a GMP environment. Specialized in mass spectrometry/LC-MS method development and troubleshooting. Good knowledge of the GMP, GLP, SOP practices, the USP, EP, NF, FDA and ICH guidelines. Proven problem solver, motivated team leader and excellent communicator Qualificat...
Tags for this Online Resume: High Performance Liquid Chromatography (HPLC), ELISA, protein, Protocol, LC-MS, MASS, API, Process Improvement, Application Program Interface, FORMULATION, QC, ANALYTICAL, pharmaceutics
Chemist - 1 Years of Experience - Near 48108
Analytical method development for drug excipients and impurities. * Challenging project management and progress report writing. Environmental sample testing using internal SOP as well as ASTM EPA and USP methods. * Expert in designing and synthesis of heterocyclic compounds peptides photocatalysts and biomarkers. * Optimization of catalytic reactions- biomimetic organic reactions. * Collaborative research experience - acade...
Tags for this Online Resume: HPLC, Automatic Call Distribution, Chemistry, GC, High Performance Liquid Chromatography (HPLC), Management, TGA, Research, Research and Development, Spectrophotometer, LC/MS, DSC
Scientist - 15 Years of Experience - Near 30045
PROFESSIONAL SUMMARY * Result oriented, Creative, Passionate, highly focused, experienced Pharmaceutical R&D Scientific Lead with good ethics, possessing over 15 years of experience in Formulation design, Process Development, Optimization and Scale up of various Pharmaceutical Dosage Forms, Solid Orals (IR and ER Tablets and Capsules), Liquid Orals (Solutions, Syrups and IR / ER Oral suspensions), and Parenteral formulation...
Tags for this Online Resume: Product Development, Filing, Pharmaceuticals (Generics), Formulation Research, Management, Budgetary, Process development, Oral solid dosage forms, Manufacturing, ANDAs
Clinical Pharmacovigilance/Drug Safety - 3 Years of Experience - Near 07726
SUMMARY Aggressive resourceful, Take-Charge Program Manager with comprehensive skills in the administration and day- to- day supervision of technical and support systems. Managing product development group for medical and non- medical devices. Specific areas of experience: Pharmaceutical Development Project Management First to File Project Management * Solid Dosage delivery system experience Soft gel delivery system experie...
Tags for this Online Resume: Research, Research and Development, Sourcing, Filing, Packaging, Program Manager, Protocol, Risk Analysis, Technical Requirements, Test
Mechanical Inspector - 10 Years of Experience - Near 28218
SUMMARY OF PROFESSIONAL QUALIFICATIONS As a professional with qualifications in Manufacturing Operations including Compounding, Compression, and Equipment Reliability, I am able to make an immediate contribution to Manufacturing Operations including, but not limited to, FDA and DEA regulated industry. * Skilled Operator with 10 years manufacturing experience in GMP environment * Knowledge of Good Manufacturing Practices, an...
Tags for this Online Resume: Troubleshooting, Documentation, Manufacturing, Pharmaceutical, Reliability, CNC, Forklift, Forklift Operator, Good Manufacturing Practices, Production Schedule
Chemical Equipment Operator - 14 Years of Experience
Summary Manufacturing Associate with broad experience in GMP environments. Strong technical background skilled in equipment repair. Effective working independently or as part of a team. Ability to build strong relationships with vendors and contractors. Quick learner who cross trains to support other departments and provides training to co-workers. Known for problem-solving and troubleshooting skills.
Tags for this Online Resume: manufacturing, production, Biotech, pharmaceutical, Manufacturing, Complaints, Documentation, Inventory, Training, Fabrication, Good Manufacturing Practices, Protocol
Quality Assurance Specialist - 13 Years of Experience - Near 08540
Professional Summary More than 14 years of experience in Pharmaceutical and Life Sciences Industry with key focus in Business Requirements Analysis Data Analysis and Management Software Application Testing Document Management Change Control and Release Management FDA Compliance Verification and Validation Quality Assurance Processes and Methodologies Developing Testing Strategies and Test Plans Test Scenarios and executing ...
Tags for this Online Resume: Test Scripts, Test, Management, Test Cases, Structured Query Language, Audit, CFR Part 11, Test Plan, Application Server, Documentation, validation of protocols
Supervisr, Reagent process
I am seeking to align myself with a progressive company poised for a strong growth and market expansion. With extensive experience of leading and managing production of Reagent products in cGMP environment ensuring compliance.
Tags for this Online Resume: GMP, Non-conforming, Laboratory experience, CAPA, FDA compliance, Auditing
Quality control team leader,Montreal
Result oriented professional with a master’s degree in biology and over 7 years of Pharmaceutical industry experience in positions of increasing responsibilities in cGMP production under sterile conditions, quality assurance, and quality control and process development. Skilled at leading multiple projects, as well as developing and managing laboratory operations and budgets. Familiar with both the US and Health Canada’s or...
Tags for this Online Resume: GMP, CRA certification, Quality Assurance, SOPs , Bilingual French/English, cGMP, Virology/Oncology, HYGIENE, Inventory, Inventory management, clinical, pharmaceutical, trial
