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Resume alert |
Resumes 61 - 70 of 103 |
Greensboro, NC
... Responsible for Market Product Stability Field Alerts, participated in FDA audits. • Approved/released stability results, NDA stability reports, authored Annual Product Review. • System Champion for Product Complaints. • Issued Field Alerts and ...
- 2013 Aug 07
Greensboro, NC, 27518
... Knowledge of ICH-GCP, FDA and EMA guidelines . Knowledge of scientific terms and medical terminology . Knowledge of working on databases Clintrace, ARISg, Oracle AERS . Knowledge of MedDRA and E2B submissions . Able to work in an environment of ...
- 2013 May 01
Elon, NC
... Achieved three years of positive market share growth and code additions even in a period of extraordinary circumstances including multiple recalls, product withdrawal, plant closures, a consent decree and increased FDA investigation. . Managed ...
- 2013 Apr 18
Greensboro, NC, 27455
... on soft gelatin capsules for filings to FDA System installation and validation of Multichrom (chromatographic data system) for R&D and QC Project management (installation and validation) of Atlas chromatographic data system on the entire site. ...
- 2013 Apr 15
Oak Ridge, NC, 27310
... Oversaw the design and building of FDA approved Lab equipment . Oversaw the validation of FDA approved equipment. . Chose and oversaw the work performed by outside contractors. Manufacturing Engineer/Industrial Engineer, R. J. Reynolds Packaging, ...
- 2013 Apr 14
Greensboro, NC, 27282
... Demonstrated ability to effectively train, manage, and measure associates to meet rigorous manufacturing, quality, cGMP, and FDA objectives, building a productive and safe work environment. Degreed professional and certified Six Sigma Green Belt ...
- 2013 Apr 08
High Point, NC
... Regulatory Inspections: FDA, EMEA, Internal Corporate Audits, etc . Quality Systems: Investigations, CAPAs, change controls, materials management, electronic batch records, etc. . Performance Management: Hiring, Coaching, Goal Setting, Development ...
- 2013 Apr 03
Greensboro, NC
... Monitored laboratory procedures and practices to assure compliance with current GMP, FDA, and environmental regulatory requirements. Cross trained in a number microbiology lab techniques. Performed a variety of record keeping and computer data entry ...
- 2013 Feb 20
Jamestown, NC
... Understanding of cGMP, GLP, FDA, ICH and ISO17025 Guidelines. Highly motivated and result oriented professional with strong analytical and team building skills. Ability to manage multiple projects at the same time. Ability to convert technical ...
- 2013 Feb 19
Burlington, NC, 27215
... Participated in internal audits for clinical trails before final review by the FDA. . Conducted final review for departmental clinical studies, final patient reports and quality control. . Conducted test validation studies for molecular based and ...
- 2013 Feb 17