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Resumes 61 - 70 of 90 |
North Providence, RI
... Responsible for general laboratory organization and maintaining the readiness for non-GMP production activities. LONZA BIOLOGICS, Hopkinton, MA 2008-2013 Manufacturing Science and Technology Assistant (Sep.2012-Sep.2013) . Organized, edited and ...
- 2014 Apr 20
Holliston, MA
... Functional Expertise in Global Business Operations: ( Global Supply Chain ( Lean & Quality Improvement ( Strategic Planning ( Negotiation skills ( Manufacturing & Distribution ( GMP, GDP, C-TPAT EDUCATION & CERTIFICATIONS . Bachelor of Arts, New ...
- 2014 Apr 01
Hudson, MA
... Excellent knowledge of production,quality assurance, documentation in Pharmaceutical Manufacturing In-depth knowledge of GMP, ICH, SOPs, ISO,USFDA quality management system and internal and external audits Team leader and team player, dedicated ...
- 2014 Mar 12
Marlborough, MA
... Gained experience as a QA person in the GMP facility involved in the production and evaluation of Tablets, Capsules, syrups and semisolid preparations. . Performed various quality control tests such as friability test, hardness test, disintegration ...
- 2013 Dec 13
North Brookfield, MA
... skills (Microsoft Office) KNOWLEDGE OF: Western, Northern, Southern Blotting, ELISAs, BSL3 Safety regulations, GLP and GMP EDUCATION: Saint Michael’s College, Colchester, VT 2009-2013 Bachelor’s of Science Major: Biology Minor: Chemistry GPA: 3 ...
- 2013 Oct 22
Natick, MA
... Documentation Consultant 2007 - 2009 Genzyme Corporation – W rote Standard Operating Procedures (SOPs) for the implementation of an engineering content management (ECM) application that supports FDA compliant Good Manufacturing Practices (GMP) for ...
- 2013 Aug 20
Shrewsbury, MA
... using rodent /rabbit/canine models design analyze modify experimental protocols according to clients needs • Experienced in all aspects of wet molecular biology research worked under GLP and GMP environments in compliance with FDA/NIH/USDA/ICH
- 2013 Aug 05
Shrewsbury, MA, 01545
... Buy Analysis Manufacturing Transfers Strategic Sourcing 6-Sigma Black Belt GMP /QSR Audits FDA CFR Part 820, ISO 13485 PROFESSIONAL EXPERIENCE INDEPENDENT CONSULTANT, GREATER BOSTON AREA 2013 - Present Lead manufacturing and supply chain initiatives ...
- 2013 Jul 11
Shrewsbury, MA
... Perform executed Batch Production Control Record (BPCR) review to ensure compliance with approved procedures and GMP expectations. Review release test and stability data ensuring data accuracy, conformance to test procedures, specifications and ...
- 2013 May 11
Natick, MA
... various test equipment Question suspect parts or processes and verify product passes all functional test in an ISO-9001 and GMP environment 11/94-1/97 TEST/REPAIR TECHNICIAN Bell Atlantic, Northboro MA Troubleshoot and repair Sun monitors including ...
- 2013 Jan 22