CV, Curriculum Vitae and Online Resumes Search

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Online Resumes with "GMP environment"

Quality Control Microbiolgist

Position in the Quality Unit of pharmaceutical/Biotech sector. Expertise in conformance/compliance regulations in cGMP environment.

Validation Engineer, Clayton

Demonstrated scholar and proven achiever in the pharmaceuticals, who utilizes leadership, teamwork and creativity to support the demands of a project. Highly motivated, inquisitive chemist desiring to acquire further knowledge in a cGMP environment. Particular interests include design qualification, system impact assessment and component criticality assessment.

Senior Manufacturing Scientist with fifteen years of expertise in early stage and phases II&III of downstream purification, process development and cGMP environments. Experience in both technical and management capacities.

Obtain a career as a downstream specialist of protein or antibody purification utilizing extensive professional expertise.

Tags for this Online Resume: Protein Purification , Downstream Process Development, technical reviews for GMP , GMP operations , Downstream GMP specialist, Coordinator of raw material storage, Protein or antibody Purification

Bio Production Technician - 4 years Experience - Durham, NC - Fortune 500 Experience - GMP

I am a a four year experienced Merck biopharmaceutical technician and exceptional assistant floor lead who has 4 years experience in the pharmaceutical field and GMP environment. Knowledgable in Operations Reviews, cGMP production, Auditing Batch Records, MMD Sigma Yellow Belt Certified,

Tags for this Online Resume: Durham, NC, SAP, GMP, Operations Reviews, Auditing Batch Records, Experienced

Chemist - 16 Years of Experience - Near 08016

Result oriented professional with many years of experience in pharmaceutical and consumer health care related industry within a cGMP environment. Worked on various solid, semi-solids, liquid, dosage forms. Performed Method development, Method Validation, Method Verification and Method Transfer. Hands on experience on UPLC (Acvity H-Class), HPLC, GC, Auto-Dissolution USP apparatus I,II and IV(Sotax)Flow through Cell, AA,...

Chemist - 20 Years of Experience - Near L5W0C1

I have been involved in research in the bioanalytical field as well as worked in preclinical/clinical studies in the drug discovery process which include anticancer, antihistamines, specific target pain relievers and others. I have more than 20 years experience in bioanalytical chemistry which includes preclinical/clinical assays, research in a GLP/GMP environment. I have managerial experience in setting up and running of...

Clinical Quality Assurance - 3 Years of Experience - Near 94404

Organized and detail oriented professional with almost 3 years of clinical Quality Assurance/ Quality Control experience in a regulated GMP environment. Good communication and problem solving skills, adept at managing multiple projects. Authored multiple Standard Operating Procedures (SOP), Qualification Protocols and Methods. Acted as the de-facto supervisor of the QA team for the last 5 months. Supervisory responsibilitie...

Tags for this Online Resume: Auditing, Batch Production Record, CMC, SOP , Qualification Protocol, Data trending, Clinical, Quality

Biological Technician - 6 Years of Experience - Near 27513

My qualifications include my Bachelor's in Biology. Also of note is my most recent position as an Associate Bio-Processioning Technician for Merck and Company. In this role, I am responsible for performing various operational tasks as part of an empowered team. I currently work in a cGMP environment, while operating and monitoring equipment. I attend safety training and compliance events on a regular basis, and I routinely...

Tags for this Online Resume: Technician , Chemist, HPLC, FDA, CAPA, Anaytical

Validation Consultant-18 years experience in cGMP regulated environment-Dallas, Georgia

Technically accomplished, results oriented professional with 17 years CFR Part 11and GAMP 5, Part 58, Parts 210 & 211, Part 600, 601,610, Part 1270, 1271and Part 820 cGMP regulated environment with 10 years working experience writing, developing and executing validation protocols, managing calibration programs, maintaining and upgrading automated systems in a cGMP environment. Creative Metrologist/Chemist/Biologist and (IQ,...

Clinical Quality Assurance -13 Years of Experience - Near 92121

Experienced Document Control Associate for the pharmaceutical, device and technology industry working in a GLP, GCP, and cGMP environment. Demonstrated project manager for several document management types, with ability to self-prioritize to meet management and customer demands. Responsible for the successful execution of change control activities for all document types. Effective communicator with strong grammatical, wr...

Tags for this Online Resume: San Diego, CA, GLP, GCP, cGMP, Document Control, Quality Assurance