Are you a Regulatory Affairs professional looking to work independently and take ownership of the writing of CMC sections of DMF, BLA, and NDA submissions? Have you supported full product development activities from pre-clinical/clinical to FDA submissions? Are you interested in helping a company expand their client base in new countries? Do you have experience independently writing CMC sections of global regulatory submissions? This position could be for you!
If you're interested in a Lead Regulatory Affairs Specialist position with a well established pharmaceutical company in Madison, Wisconsin, apply here for more details!
...Job Description Job Description For the Fort Payne, AL location : We are seeking Light Industrial to become a part of our team! If you haven't already came by our Fort Payne office to apply in person; click this link to apply with us today: Must have proof...
...Description Physician Affiliate Group of New Yor k (PAGNY) is adding an Anesthesiologist to the Anesthesiology group at NYC Health + Hospitals/Kings County .The department of Anesthesia at Kings County Hospital handles over 5500 cases annually and averages about...
...posture throughout the enterprise. This role will enable the continued success in meeting all financial services and payments industry security standards such as PCI and SOC-1 compliance requirements through the implementation of sound policies, procedures, and tools needed...
...Schedule :Full time schedule. Days andhours may vary. Night and overnight shifts available. More details upon interview. Requirement :No... ...light cleaning duties to maintain establishments, including hotels, restaurants and hospitals, in a clean and orderly manner....
Domestic Violence Case Manager FJC LACABACSALARY$40,000 to $43,400 a year, part time on site (30 hrs. a week) $25.64 to $27.56 HourlyBENEFITSGenerous Vacation and Holiday Allowances, Employee Wellness Program, Employee ParkingLOCATIONLos Angeles (POV Metro...