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Resume alert |
Resumes 41 - 50 of 574 |
Levittown, PA
... Responsible for providing website/email launch documentation required by the FDA. Managed website/email campaign implementations as well as post-production data capture. Oversaw the code review process upon receiving initial assets to ensure the ...
- 2023 Nov 04
New Brunswick, NJ, 08989
... Monitor, organize and execute all functions associated with packaging of pharmaceutical commercial products and ensuring compliance with cGMP, SOP, FDA, DEA and OSHA rules and regulations. Accountability of manpower utilization, departmental ...
- 2023 Oct 30
New Jersey
... research records of study activity, including case report forms, drug dispensation records or other regulatory forms as per FDA guidelines • Directed the collection, labeling, storage and transport of all specimens • Made sure that all equipment and ...
- 2023 Oct 27
Robbinsville Center, NJ
... as per ICH guidelines Evaluation Tests - Disintegration Time, Friability, Dissolution, Particle size Analysis, DSC, Colorimeter Supported in FDA Audit by providing necessary documentation, protocols, procedures Dissolution Apparatus. UV ...
- 2023 Oct 24
Franklin Park, NJ
... Experience in dealing with FDA and DEA while ensuring the safe and efficient execution of job duties. Troubleshoot and make appropriate adjustments to maintain production specifications. Adhere to quality standards during the manufacturing process. ...
- 2023 Oct 23
Somerset, NJ
... • Educated colleagues and healthcare providers regarding new medications recently approved by the FDA. Walgreens Specialty Pharmacy Pharmacy Extern March 2023 – April 2023 • Counseled patients on their discharge medications and conducted ...
- 2023 Oct 22
Marlton, NJ
... Instrumental in facilitating internal and external audits, mentoring high-performing teams, and verifying compliance with cGMP and FDA standards. Skilled researcher with a solid understanding of synthesis patterns and properties determination. ...
- 2023 Oct 20
Mount Laurel, NJ
... Work with FDA on REMS assignments to ensure that the benefits of a Merck drug outweigh the risks associated with the drug. Bristol Meyers Squibb 10/17- 03/18 Global Procurement Buyer Princeton, New Jersey Strategic Sourcing Excellence Confer with ...
- 2023 Oct 13
Moorestown, NJ
... ●Enforcing safety policies are followed as defined by OSHA, FDA, and cGMP guidelines ●Creating and overseeing employee training to increase production, using the LMS Bridge software enhance safe operations and ensure profitability and semi-automated ...
- 2023 Oct 08
Cranbury, NJ
... Supported more than 35 products for submission batches, filed to US FDA 23 New products ANDA applications and secured 9 products approvals in 3 years time. Working closely with BD folks for bringing in CMO & CDMO business. Working with several ...
- 2023 Oct 05