Posting ID: #8471SMH
Generic Pharma: ANDA Submissions and Project Management
Location: Minneapolis, MN
Salary: $85,000-$103,000 + Bonus
A dynamic, growing Midwestern-based generic pharmaceutical company seeks an experienced and Regulatory Affairs Project Manager to help our team manage our growing volume of regulatory submissions and project management work.
Our history as a successful generic drug company is long and very well-established. Year after year, we’ve demonstrated consistent growth. We fully expect this growth to continue, and we need your help today!
WHAT WILL YOU DO?
· Manage regulatory aspects of products/projects.
· Write ANDA submissions.
· Directly liaise with regulatory authorities to facilitate review and approval of submissions.
WHAT MAKES YOU A TOP-NOTCH CANDIDATE?
· BS with 7 years pharma industry experience. Less experience required for advanced degrees.
· ECTD experience required.
· Hands-on ANDA experience required.
We fully intend to increase the velocity of our ANDA submissions, so we need strong performers to help us achieve our ambitious goals. We continue to invest in our company and our people so when people come to work here, they stay for a long time. Come join our team!
Jump to the head of the line by sending your resume to Scott Hobar today.
Talented employees: those that fit in, add to the culture and exceed expectations are nearly as rare as they are valuable. They have equal parts of drive, personality, boldness and tact. I look to find the right candidate for the right position. If you are an "Impact Player" in the pharmaceutical and biotech industry then we need to talk! Submit your information to Scott Hobar for consideration.
Click here, ONLINE APPLICATION to apply for this job.
www.mrindianapolis.com For the latest Regulatory Affairs / Quality Assurance jobs, news, industry links, and career guidance.
Desk Identifiers: mri indy-north smh.mr.industry
Position ID: 8471SMH
