Associate Director, CMC Regulatory Affairs Working with Us Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here,...
Responsibilities Well versed in performing CMC compliance activities including Gap Analysis, CMC comparison and validation for the quality reports Experienced in authoring of assessment reports and Part2/ Expert reports for Dossiers ...
Responsibilities: Observe and record production operationsReview operational schedules and coordinate manufacturing activities to ensure minimum costs and prevent operational...
The candidate will be leading the regulatory strategies for biologic products and combination products for the product portfolio assigned. In this role, a typical day might include the following: Responsible for...
Title: CMC Manager Location: Short Hills,NJ(Remote) Duration: 12 Months Job Description: Well versed in performing CMC compliance activities including Gap Analysis, CMC comparison and validation...
Job Title: CMC Regulatory Documentation Coordinator Location: New Brunswick, NJ- Remote Hours/Schedule: Mon - Fri, Business Hours Type: Contract Responsibilities + Manage document preparation of CMC...
Join a Legacy of Innovation 110 Years and Counting! Daiichi Sankyo Group is dedicated to the creation and supply of innovative pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of...
Equipment OperatorPay: $20.75 hrlyDay Shifts Available1st Shifts: Sun - Wed 6am - 4:30pmSun-Tues 6am-6pmWed - Sat 6am - 4:30pmMon, Tues, Thurs & Fri; 5:45am-4:15pmMid shift: Mon-Fri; 10am-6:30pmWe are Wayfair; we continue to deliver a best-in-class...
Company Information Legend Biotech is a global biotechnology company dedicated to treating, and one day curing, life-threatening diseases. Headquartered in Somerset, New Jersey, we are developing advanced cell therapies...
As the Associate Director of Regulatory CMC, reporting to the Director of Regulatory CMC, you will be pivotal in managing the development and submission of regulatory filings for gene therapy projects both domestically and internationally. You...