Integrated Services For Productivity & Validation, Inc

Preferably resource should have experience in GMPrelated field (manufacturing operations engineering operations).Resources should be capable of resolving equipmentrelated problems by using technical skills to analyze the condition understand variables that impact the process and propo More...

Experience with change control product disposition process cleaning validations and quality aspects of the manufacturing process.RequirementsDoctorate degree or Masters degree and 3 years of directly related experience or Bachelors degree and 5 years of directly related experience or More...

Foundation in quality assurance roles focused in Quality Management Systems and GMP documentation (must have) Support development of new equipment/technology introduction projects preferably within Packaging Area (must have) Be knowledgeable about compliance and regulatory a More...

Engineering (any field) or scientific background (Biology Microbiology Biotechnology Chemistry etc.Previous experiences in regulated environment (Biotechnology Pharmaceutical Medical Devices etc.. Experience in Validation with preference in Process Validation.RequirementsDoctorate deg More...

Technical Writing (SOP FORMS)Change Control ProcessRequirementsDoctorate degree OR Masters degree and 3 years of Manufacturing Operations experience Alternatively Bachelors degree and 5 years of Manufacturing Operations experience Alternatively Associate s degree and 10 years of Man More...

Quality Professional with Manufacturing Process Audit and Batch Record Review experience. In addition some knowledge or to be familiar with DAI process PASx/MES application MAXIMO SAP and LIMS. Available for nonstandard shift which includes nights and weekends.RequirementsDoctorate de More...