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Online Resumes with "GLP GCP"



Senior Manager Capital Project Engineering

Interested in a management position within the scientific or mechanical segments of the biotech/pharma industry, utilizing my technical and development strengths, expanding my areas of expertise and increasing the scope of my responsibility within a world-class organization.

Tags for this Online Resume: Project Leadership, GMP, GLP, GCP, Budget Planning & Cost Control, Client Relations, Proposal Development, Contract Administration

Clinical supply coordinator

Senior scientist/clinical supply coordinator with broad experience managing and coordinating pharmaceutical clinical supply systems for API’s, Excipients, Packaging components, Finished drug products including Controlled substances, Reserve samples, and Chemical archives. Labeling and distribution of GMP Clinical supplies for worldwide GLP and GCP studies. Reconciliation and disposition of returned clinical supplies. Pro...

Tags for this Online Resume: Organization, Document control, Inventory management, Leadership, Proactive

Director of Quality Assurance

Direct quality assurance for biopharma company, quality systems lot release investigations, audits, GLP GCP interface with GMP. Department of 20 -50, with increasing responsibility world-wide.

Tags for this Online Resume: quality assurance, biopharma, quality systems, lot release, investigations, GLP GCP interface with GMP

Analyst

Tags for this Online Resume: Certified Medical Technologist, Laboratory Expertise, GLP, GCP, FDA Compliance, Data Management, Quality Assurance, Biology

Compliance Manager/Auditor

To obtain a position working as a Microbiology Business Analyst and Project Manager in a pharmaceutical/biotech validation environment, oriented toward management advancement. Over 20 years of experience in the Pharmaceutical Industry, 16+ years of those years are with GxP (GMP, GLP, GCP) systems compliance/QA and 21 CFR Part 11. Experience includes GxP system implementation projects, documentation/SOP writing/review.

Regulatory Affairs Associate, New Jersey

Regulatory Affairs professional with a strong regulatory and compliance foundation, well-versed in the laws, regulations and requirements of the FDA; over six years of experience as an International Coordinator for a pharmaceutical organization, currently completing a graduate degree in Regulatory Affairs in Drug Development, Biologics and Medical Devices, studying all facets of regulatory requirements including processes a...

Regulatory Affairs, Clinical Research, Quality Assurance

A degreed professional with over 4 years of experience in the pharmaceutical/Biotech industry with multi-functional Regulatory, Clinical and Quality background. Demonstrated ability to expand beyond the scope of assigned responsibilities to gain proficiency in new areas. Responsibilities have ranged from managing the preparation, submission of INDs, BLAs, ANDAs/NDA, to reviewing QMS, essential regulatory documents to ensure...

Tags for this Online Resume: Regulatory Affairs, Clinical Research, FDA, GCP, GCP, ICH, GLP, Pharmaceuticals, Quality Assurance

Senior Quality Control Auditor- 13 years experience in GLP, GCP, GMP

I'd like to use my people and organization skills to communicate compliance requirements to cross-functional departments emphasizing the legal obligation biotech/pharma has to regulatory agencies and patients in an organization who supports the Quality Systems.

Tags for this Online Resume: Quality Control, Quality Assurance, Quality Auditor, Promotional, GCP GMP, Compliance Auditor

Medical Device Project Manager, Indiana

Seeking a position with a start up or established company where I can apply my diverse management and quality compliance experiences and skills to further my professional and personal growth.

Tags for this Online Resume: Medical Devices , Project Management, Veterinary Technology , Communication , Biomedical Leadership & Training , Preclinical & Clinical Trials , Safety Protocols , Regulatory Compliance Process Improvement , Facility Management , Research, Quality Assurance , Regenerative Medicine, Product Development , Supply Chain Management , Vendor Relations, Strategic & Tactical Planning , ISO 13485, GMP/GLP/GCP, Administrative

Clinical Research Associate, Chicago, IL

I have been working in the Biotechnology industry for the last 9 years in the Pharmacokinetics & Drug Metabolism group at Amgen. I worked to characterize the pharmacokinetics (PK), pharmacokinetics/pharmacodynamics (PK/PD), and metabolic fate of novel drug candidates using state-of-the-art procedures and technologies. I supported discovery from research into the clinical. I developed and validated analytical methods whic...

Agricultural Technician

I am Compliance Auditor, with over 8 years of GLP and GCP experience from Amgen.

Chemist - 2 years of experience in pharmaceutical industry- San Francisco, CA

Looking for a position as a Chemist in the pharmaceutical or biotechnology company.

Tags for this Online Resume: HPLC, GC, AAS, GLP, GCP, Method development, validation, Separation techniques