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Online Resumes with "CHANGE CONTROL DEVIATION"
Quality Assurance Manager - 9 years experiance in pharma
To be a part of a pharmaceutical professional organization that would enhance and elevate my credentials towards the growth of the organization and myself.
Tags for this Online Resume: Maintaining Quality Management Systems like: Change control, Deviations, CAPA, OOS and OOT., Performing Annual Product Quality Reviews, Vendor Qualification, Qualification of Equipments (FAT, SAT, DQ, IQ, OQ PQ)., Prepare, maintain, control and issued quality system documents while adequately maintaining the Documents Management System, Performing Batch Release, In-process Control Management,
Laboratory Supervisor
24 years in Pharmaceuticals as a scientist/chemist.
Ideal Companies: Dupont, Invitrogen
Tags for this Online Resume: laboratory supervisor, Chemist, Cleaning Validation, Validation, Protocol, Risk management
Pharmacist
Tags for this Online Resume: Quality Assurance, Pharmaceuticals, SAP,LIMS,TRACKWISE, Quality Management System, INPROCESS CHECKS, CHANGE CONTROL, DEVIATION
Pharmaceutical Quality Assurance Specialist- 10 years Experince- Atlanta
Seeking a challenging assignment in Quality Assurance in the pharmaceutical sector to utilize acquired expertise and deliver best-in-class results. PROFESSIONAL SNAPSHOT: •A Quality Assurance Professional bestowed with 10+ years of experience in Corporate Quality Assurance, Plant Quality Assurance, Manufacturing, Validation and different International Quality audits in Solid Dosage. •Hands on experience with Quality Manage...
Tags for this Online Resume: QMS, Batch Record Review, Preparation of SOP, CAPA, Investigation, Change Control, Deviation, Internal Audit, Document Control, Batch Release, Solid Dosage, Process Validation, APQR, Market Complaint, GMP, OOS, Self Inspection, Third Party Audit
Biologist - 13 Years of Experience - Near 20874
Summary Downstream process professional with ten years of experience spanning development, clinical manufacturing, and commercial manufacturing in biotechnology companies. * Experienced in biologics process development, process scale-up, process optimization, and manufacturing. * Authored, reviewed, implemented, and executed technical reports, science journal articles, process run summaries, investigation reports, CAPA, cha...
Tags for this Online Resume: Manufacturing, Compliance, Science, Support, Biotechnology, Inventory, Logistics, Management, Microsoft Office, Microsoft Visio
Quality Control
SUMMARY OF QUALIFICATIONS Quality Systems - Quality Control /Quality Assurance Management of Analytical Laboratories/Quality Audits/Scientific Technical Services Liaison Highly motivated, key contributor in Quality Management and cGMP compliance with more than twenty five years of demonstrated growth and success in scientific applications with Contract Manufacturing Organizations in Quality, R&D and manufacturing. Recognize...
Tags for this Online Resume: Analytical Chemistry, Chemistry, Manufacturing, Research and Development, Commercial Production, Compliance, Packaging, Pharmaceutical, Documentation, Quality, validation, Audits
Department Manager - 20 Years of Experience - Near 00693
Professional validation expert and scientist with up to thirty years of overall experience in the Pharmaceutical Medical Device and Biotechnology Industry. Proficient in manufacturing industry environment including but not limited to facilities utilities solid dosage equipment HVAC water systems chemical plant equipment chemical biotechnology and microbiology instrumentation handling validation (IQ OQ PQ) validation plans c...
Tags for this Online Resume: Quality, Quality Assurance, Project Leader, Project Management, Support, Manufacturing, Test, High Performance Liquid Chromatography (HPLC), Injection Molding, Instrumentation
Pharmaceutical CMC Development | cGMP Manufacturing | Product Quality
Senior manager and director of pharmaceutical process chemistry, manufacturing and controls (CMC) specializing in cGMP, quality and regulatory compliance of novel small and large molecule therapeutic drugs including peptides, nucleotides, protein biologics and antibody drug conjugates (ADCs). Skilled in technology transfer, analytical method development and validation, quality risk assessment, deviation management, investi...
Ideal Companies: Shire, Biogen, Lonza, Genzyme, Sarepta.
Tags for this Online Resume: Chemical Process Development, API, cGMP Manufacture, Technology Transfer, Management, Quality, Risk Assessment, Pharmaceutical Operations, FDA and ICH Drug Regulations, CRO, CDMO and CMO Oversight, CMC Process Chemistry, TrackWise QMS, Change Controls, Deviation Management, Investigations, Root Cause Analysis, CAPA, Antibody Drug Conjugates, IND, IMPD, NDA, MAA and BLA
