Director, Quality Auditing & Compliance
Sterling Life Sciences - New York, NY

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1) Manage the effective operation of the document control system and maintenance of the relevant records2) Ensure effective external and internal audit programs and determine compliance with regulations3) Manage document for all company documentation (policies, procedures and controlled forms), including document change requests, notifications of new documents mastered4) Participate in cross-functional teams to identify effective corrective and preventive actions to improve process quality5) Establish all quality assurance and quality management activities in the company6) Prepare and submit submissions and ensure compliance with all regulatory requirements pertaining to product approval7) Ensure company and products are compliant with applicable regulations and lawsTAGS: 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 healthcare industry is strongly preferred4) Preference will be given to people who have recent experience in quality & compliance management