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Study Technician Lab Tech Dose Formulation - $1500 Sign On Bonus Potential Opportunity - Madison

Job Overview Do you enjoying following a recipe to mix solutions? If so, you could be a Study Technician in our Dose Formulations department. The Study Technician (Laboratory Technician) is a true laboratory position where you collect and document study data step by step. You will perform study calculations and specific techniques for test material formulation. In addition you will: * Prepare labo

Contact Us   3 months ago
Director, Pharmaceutics and Process Technology - Oral Solid Dose - Cincinnati

Join us as We Transform How Pharmaceuticals are Made. Patheon is looking for people who are passionate about making a difference in people's lives. Patheon is in need of proven leaders to nurture talent, build effective teams and drive engagement in an environment where people are motivated to do their best for the company, its clients and their patients. To inspire collaboration and innovati

Contact Us   9 months ago
Global Product Quality Steward - Solid Dose - Bowdre

Other Locations:Celgene Summit 86 Morris Avenue Summit 07901DescriptionPosition Global Quality Product Steward: Solid Dose Manager VP, Global Quality Operations Prerequisites Bachelor?s Degree in pharmacy, chemistry or related life sciences field. Advanced degree is preferred. A minimum of 15 years related pharmaceutical experience.Location Neuch?tel, Switzerland/Summit, New Jersey USAPURPOSE AND

Contact Us   1 year ago
Lead Validation Engineer - Solid Dose Ashtabula - Ashtabula

Job Description The Lead Validation Engineer is responsible for writing, executing, and reporting validation protocols and other relevant documentation. Other validation lifecycle documentation responsibilities may include User Requirement Specifications (URS), Design Qualification (DQ), installation qualification (IQ), operational qualification (OQ), performance qualification (PQ), cleaning valid

Contact Us   1 year ago
Lead Validation Engineer - Solid Dose New Philadelphia - New Philadelphia

Job Description The Lead Validation Engineer is responsible for writing, executing, and reporting validation protocols and other relevant documentation. Other validation lifecycle documentation responsibilities may include User Requirement Specifications (URS), Design Qualification (DQ), installation qualification (IQ), operational qualification (OQ), performance qualification (PQ), cleaning valid

Contact Us   1 year ago
Lead Validation Engineer - Solid Dose Avon Lake - Avon Lake

Job Description The Lead Validation Engineer is responsible for writing, executing, and reporting validation protocols and other relevant documentation. Other validation lifecycle documentation responsibilities may include User Requirement Specifications (URS), Design Qualification (DQ), installation qualification (IQ), operational qualification (OQ), performance qualification (PQ), cleaning valid

Contact Us   1 year ago
OSD Oral Solid Dose Manufacturing Operator - Harrisburg

Relocation to the greater St. Louis, MO area OSD (Oral Solid Dose) Manufacturing Operator SUMMARY: The OSD (Oral Solid Dose) Manufacturing operator will efficiently, effectively, and safely clean, set-up, and operate machinery in the oral solid dose area to manufacture tablets meeting FDA and company standards of quality and productivity while adhering to applicable cGMPs and SOPs including follow

Contact Us   1 year ago
OSD Oral Solid Dose Manufacturing Operator - Harrisburg

Relocation to the greater St. Louis, MO area OSD (Oral Solid Dose) Manufacturing Operator SUMMARY: The OSD (Oral Solid Dose) Manufacturing operator will efficiently, effectively, and safely clean, set-up, and operate machinery in the oral solid dose area to manufacture tablets meeting FDA and company standards of quality and productivity while adhering to applicable cGMPs and SOPs including follow

Contact Us   1 year ago
OSD Oral Solid Dose Manufacturing Operator - Harrisburg

Relocation to the greater St. Louis, MO area OSD (Oral Solid Dose) Manufacturing Operator SUMMARY: The OSD (Oral Solid Dose) Manufacturing operator will efficiently, effectively, and safely clean, set-up, and operate machinery in the oral solid dose area to manufacture tablets meeting FDA and company standards of quality and productivity while adhering to applicable cGMPs and SOPs including follow


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Last Updated on: November 25, 2017
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