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Lancaster, PA
... We are the first company to have a non-systemic and non-invasive depression treatment cleared by the FDA for patients who have not benefited from prior antidepressant medication. Neuronetics markets the medical device Neurostar Advanced Therapy ...
- 2020 Oct 19
York, PA
... Demonstrated skills in several ISO Standards and FDA Guidelines to mitigate risks, reduce liabilities, increase speed-to-market, and accelerate compliance with internal policies and legal requirements related to medical devices. Creator of company ...
- 2020 Aug 26
Mount Joy, PA
... Early in my career at GE, I was responsible for all HHS reporting for new Radiology Installations and CT Tube replacements via the processing of FDA 2579 Documentation 7. Also during my time at GE worked for a Surgical Laser Technology start-up ...
- 2020 Apr 03
Stewartstown, PA
... The group also provided documentation in response to deficiency inquiries from the FDA and other Regulatory agencies. PFIZER, INC. (FORMERLY WYETH, INC.), Princeton, NJ A $210 B Global Pharmaceutical Company Sr. Scientist III (2008-2010), Analytical ...
- 2019 Jul 22
Marietta, PA, 17547
... Regulated environment compliance experience with FDA Medical Device, EPA Small Engine, and ITAR Programs Management Skills: Operations and Facility Development, Program Management, Risk Management, Requirements Management, Stage Gate PDP, Resource ...
- 2018 Apr 20
York, PA, 17406
... KS 913-***-**** ac46hl@r.postjobfree.com Client Dan Shiflet Quality Manager Keystone Certifications, Inc 717-***-**** ac46hl@r.postjobfree.com Colleague Joshua Simms Branch Chief CDRH FDA 301-***-**** ac46hl@r.postjobfree.com Personal Reference
- 2018 Apr 18
Stewartstown, PA, 17363
... Demonstrated professional expertise and leadership in the Quality function as it relates to CGMP and PAI FDA inspections and internal / external audits. Quality Assurance Skills CGMP Inspections PAI FDA Inspections Internal/External Audits ...
- 2018 Jan 02
Lancaster, PA
... How to Manage Conflict, Criticism, and Anger Introduction to FDA Regulations and Device Submission Dale Carnegie Customer Relation & Employee Development Baxter Bio-Tech products Training LOTUS CHEMICAL TECHNOLOGY TRAINING PROGRAMS KRAUSS MAFFEI ...
- 2017 Sep 11
Hershey, PA
... Experienced in cGMP and GLP processes, FDA guidelines and other government regulations SCIENTIFIC SKILLS (PRECLINICAL & CLINICAL RESEARCH): Leverages experience in vitro and in vivo model selection and evaluation, design of PK/PD and efficacy ...
- 2017 Jul 18
Mechanicsburg, PA
... Prepared reports complying with FDA, ISO, cGMP and internal regulations; and coordinated material, instrument and process validations. Maintained lab set up by ordering common supplies and chemicals. Titanium dioxide nanoparticles with blank ...
- 2017 Jun 20