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Browse Online Resumes by Occupation
Science & Biotech Online Resumes
Technical Director
Performs validation amangement and management of technical staff soving business problems
Ideal Companies: Genentech, Amgen, Gilead
Quality Professional
Efficient, organized professional with excellent communication skills, great attention to detail.
Ideal Companies: Pharmaceutical, Biotech, Medical Device
Tags for this Online Resume: Quality Assurance, Quality Control, Marketing, Customer Service
Clinical Quality Assurance
Ideal Companies: apples
Clinical Quality Assurance
Ideal Companies: GVK, SHANTHO, REDDYS, GENOVO ETC
Tags for this Online Resume: quality assurance
Quality Engineering Associate I
? Highly motivated and results orientated individual with over 9 years experience in the biotech and medical industries. ? Effectively manage different responsibilities simultaneously ? Highly Organized individual with a strong attention to detail ? Experience with documentation systems in a GMP Regulated environment. ? Ability to work independently or cooperatively as a team
Ideal Companies: Genzyme, Genetech, Wyeth, novaritis
Tags for this Online Resume: quality
Clinical Quality Assurance
Quality Assurance Professional
Military History History in general Biographies
Ideal Companies: Watson Pharmaceutical, Genentech
Tags for this Online Resume: Commercial Specifications, Annual Product Review, Audit, CAPA, Document Control, Regulatory Compliance
Six Sigma Manager
Detail oriented and a good team player.
Opportunity to utilize my knowledge and skills for the upliftment of the company.
Ideal Companies: Pharmaceutical and Biotech companies
Tags for this Online Resume: Quality Assurance Specialist
Accomplished manager of quality and manufacturing departments in the biotech and pharmaceutical industry
An fast-paced environment where I can use my skill sets to make major contributions to the department and the company as a whole
Ideal Companies: Established or startup companies
Tags for this Online Resume: quality assurance, manufacturing, manager
Clinical Quality Assurance - 20 Years of Experience - Near 94403
QA/QC experience working with FDA ICH and Japanese regulations 21 CFR reviewing Writing editing submission documentation SOPs Protocols Reports. Product/Project analytical requirements evaluation budget in-house vs. out-source estimation. Upgrading of R&D laboratories to GLP/GMP level.
Ideal Companies: small start-up company
Tags for this Online Resume: methods transfer validation, phase I, II, III protocols and reports, GMP GLP, Laboratory management, hiring training budgeting, FDA ICH regulations, validation monitoring transfer, medical devices, Consulting, Document Review, Documentation, DSC, High Performance Liquid Chromatography (HPLC)
Validation Specialist
I am looking a professional growth.
Ideal Companies: I would like to work with Pharmaceuticals, Biotechnology, Medical Device or Chemical Industry.