Manager - Drug & Device Product Labeling - Medical Device
Sterling Life Sciences - Newark, NJ

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1) Review, revise and approve content and context required of labeling materials for drug and medical device products2) Ensure that labeling and training material meet regulatory and company requirements3) Manage work and resolve conflicts4) Ensure all labeling materials are in compliance with relevant laws and regulations5) Coordinate with Regulatory Affairs, Marketing and Operations on the timely implementation of requested labeling changes 6) Work in a team environmentTAGS: Biotechnology Jobs, Pharmaceutical Jobs, Medical Device Jobs, Small Molecule, Biologic, Oncology, Hematology, Dermatology, Neurology, Cardiology, Urology, Nephrology, Vaccine, Disease, Drug Development, Surgery, Physician, EMR, Pfizer, Merck, Amgen, Genentech, Healthcare, Life Sciences, Scientist, R&D, Ferring, Stryker, Boston Scientific, Medtronic, Abraxis, Gilead, Glaxosmithkline, Clinical Research, Clinical Trial, Regulatory Affairs, FDA, Johnson & Johnson, Schering, Nutraceutical, Surgeon, MD, Hospital, Immunology, Medimmune, Abbott, Roche, Therapeutic, Hospira, Covidien, Quintiles, PPD, Parexel, Quality, QC, Validation, Engineer, QA, Manufacturing, Engineering, Aseptic, Sterility
1) University degree is required (preference will be given to those with degree in relevant field, though all candidates are welcome and encouraged to apply)2) Appropriate full-time work experience is mandatory (no students or fresh graduates please)3) Recent experience in the pharmaceuticals industry is strongly preferred4) Preference will be given to people who have recent experience in regulatory and labeling management