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!
...Assistant Director, Inpatient Services (Hospice) High Point, NC A respected nonprofit hospice organization in High Point is seeking... ...Responsibilities: Provide daily leadership and supervision for inpatient nursing and support staff Support referrals, admissions, and...
...One year of supervisory experience or experience in health service administration required. Home health or related experience preferred. Essential Functions... ...: 1. Reports to .Sr Dir of Homecare services. 2. Travel may be required for this position. Pay range min $5...
...of being in a cleanroom this position is a non-smoking position. Job Description Insight Global is seeking 2 Cleanroom Assembly Technicians for our client, a key partner in the pharmaceutical sector, based in Easthampton, MA. These Assembly Technicians will...
...Regional Operations Manager Job Purpose The Regional Operations Manager serves as the primary point of contact for operational leadership and execution across the organization. This role is responsible for carrying out ownership directives and leadership standards...
...Job Description The Construction Project Superintendent is responsible for the first-line supervision of a work crew (usually four crews with 1... ...company will provide vehicle transportation and fuel for travel to and from projects. Work hours start and end at the location...