| Resume alert | Resumes 81 - 90 of 96 |
Manager Plant
Hamden, CT, 06514
... Ensure proper cleaning and sanitation of the plant through preventive maintenance programs that meet USDA, OSHA and FDA regulations. Manage a 23-person administrative and operations staff in all personnel matters. Key Achievements: - Improved bottom ... - 2013 Jul 18
... Ensure proper cleaning and sanitation of the plant through preventive maintenance programs that meet USDA, OSHA and FDA regulations. Manage a 23-person administrative and operations staff in all personnel matters. Key Achievements: - Improved bottom ... - 2013 Jul 18
Quality Assurance Engineer
Stratford, CT, 06614
... location in USA following their quality controls Organization Project Details Role Duration Covidien Inc., Mansfield, MA USA DHF Remediation of Dialysis Catheters The DHF of hemodialysis catheters were remediated as per FDA / TUV guidelines. ... - 2013 Jun 05
... location in USA following their quality controls Organization Project Details Role Duration Covidien Inc., Mansfield, MA USA DHF Remediation of Dialysis Catheters The DHF of hemodialysis catheters were remediated as per FDA / TUV guidelines. ... - 2013 Jun 05
Manager Manufacturing
Oxford, CT, 06478
... Coordinate plant preparations for successful FDA pre and post approval site inspections . Conduct cGMP monitoring and training, operational training, as well as develop and administer SOPs. . Assist in coordinating fiscal year budget for department ... - 2013 Feb 22
... Coordinate plant preparations for successful FDA pre and post approval site inspections . Conduct cGMP monitoring and training, operational training, as well as develop and administer SOPs. . Assist in coordinating fiscal year budget for department ... - 2013 Feb 22
Medical Device Quality Assurance
Plantsville, CT
|Sharon Coffey |Summary of Qualifications | |** Rutherford St |Extensive experience in QA/RA within the medical device | |New Britain, CT |industry adhering to FDA (21 CFR 820), ISO13485 and MDD | |06051 |requirements with regards to documentation, ... - 2012 Nov 19
|Sharon Coffey |Summary of Qualifications | |** Rutherford St |Extensive experience in QA/RA within the medical device | |New Britain, CT |industry adhering to FDA (21 CFR 820), ISO13485 and MDD | |06051 |requirements with regards to documentation, ... - 2012 Nov 19
Assistant Medical
Wallingford, CT
... Hartford, Ct – worked part time to full time while earning degree-1992 ABSTRACTS, REPORTS & PUBLICATIONS (Some abstracts and reports are proprietary.) Internal Reports • Co-author to multiple documents to the FDA and internal proprietary reports. ... - 2012 Oct 19
... Hartford, Ct – worked part time to full time while earning degree-1992 ABSTRACTS, REPORTS & PUBLICATIONS (Some abstracts and reports are proprietary.) Internal Reports • Co-author to multiple documents to the FDA and internal proprietary reports. ... - 2012 Oct 19
Clinical Management
Madison, CT
... More importantly, we contributed many novel markers and validated assays used in phase 2 and phase 3 clinical programs and data subsequently used in FDA filings and internal decision-making. I left this position over 6 years later due to a ... - 2012 Oct 18
... More importantly, we contributed many novel markers and validated assays used in phase 2 and phase 3 clinical programs and data subsequently used in FDA filings and internal decision-making. I left this position over 6 years later due to a ... - 2012 Oct 18
Project Manager Customer Service
Fairfield, CT
... Accomplished 80% of the objectives outlined by the company-wide Business Success Scorecard (BSS) by effectively managing the MRO Work Plan and integrating the BSS, FDA Submissions and Intellectual Property Expirations. Increased MROaiis ability to ... - 2012 Oct 12
... Accomplished 80% of the objectives outlined by the company-wide Business Success Scorecard (BSS) by effectively managing the MRO Work Plan and integrating the BSS, FDA Submissions and Intellectual Property Expirations. Increased MROaiis ability to ... - 2012 Oct 12
Research Associate
Stratford, CT
... NIH, FDA); assisted in grant applications; Performed literature research on specified topics; evaluated related methods and trends and applied them in the data analysis as appropriate; Developed method for documenting, and archiving statistical ... - 2012 Jun 28
... NIH, FDA); assisted in grant applications; Performed literature research on specified topics; evaluated related methods and trends and applied them in the data analysis as appropriate; Developed method for documenting, and archiving statistical ... - 2012 Jun 28
Quality Assurance Testing
Seymour, CT, 06483
... Responsible for chemical and physical testing mandated by the FDA per USP, Ph. Eur., and in-house methodologies. Position required familiarity with cGMP's and GLP. Utilized spreadsheets and other programs to calculate and check results of various ... - 2012 May 14
... Responsible for chemical and physical testing mandated by the FDA per USP, Ph. Eur., and in-house methodologies. Position required familiarity with cGMP's and GLP. Utilized spreadsheets and other programs to calculate and check results of various ... - 2012 May 14
Mechanical Engineer Project
Newington, CT, 06111
... • Teamed with multiple engineering disciplines and R&D product development to facilitate and identify modifications required for ease of assembly, part minimization and maximum performance in a fast-paced FDA-regulated environment. • Compiled ... - 2012 Apr 15
... • Teamed with multiple engineering disciplines and R&D product development to facilitate and identify modifications required for ease of assembly, part minimization and maximum performance in a fast-paced FDA-regulated environment. • Compiled ... - 2012 Apr 15