- Insmed Incorporated (NJ)
- …-up and/or mid-cap sized company highly desiredFamiliarity/experience with regulatory and pharmaceutical legal promotional review processesSuccessful track record ... Effectiveness to ensure key clinical and research insights inform HCP strategies. Lead development and implementation of tactical planning, sequencing and KPIs,… more
- Cipla (Fall River, MA)
- …on time, ensuring accuracy and completeness. Adhering to all cGMPs, compliance/ regulatory mandates and quality requirements. Complying with company policies and ... and Safety All employees must undergo various training activities at the start of their employment. New trainings and re-trainings will occur periodically.Employees… more
- Insmed Incorporated (NJ)
- …Medical Affairs to ensure scientific and clinical insights inform HCP strategies. Lead development and implementation of tactical plans for health care ... of US HCP activities with field execution.Work closely with Legal, Regulatory , Compliance, Medical Affairs, Market Access, and Commercial Operations team members… more
- Cipla (Fall River, MA)
- …and Safety All employees must undergo various training activities at the start of their employment. New trainings and re-trainings will occur periodically. Operators ... instructions and document results. Knowledge of fundamental cGMP and regulatory requirements in a pharmaceutical manufacturing environment highly preferred. Basic… more
- Cipla (Fall River, MA)
- …and Safety: All employees must undergo various training activities at the start of their employment. New training and re-training will occur periodically.Operators ... instructions and document results. Knowledge of fundamental cGMP and regulatory requirements in a pharmaceutical manufacturing environment highly preferred. Basic… more
- Cipla (Fall River, MA)
- …and Safety: All employees must undergo various training activities at the start of their employment. New training and re-training will occur periodically.Warehouse ... instructions and document results. Knowledge of fundamental cGMP and regulatory requirements in a pharmaceutical manufacturing environment highly preferred. Basic… more
- Cipla (Central Islip, NY)
- …and Safety: All employees must undergo various training activities at the start of their employment. New training and re-training will occur periodically.Employees ... work instructions and document results. Knowledge of fundamental cGMP and regulatory requirements in a pharmaceutical manufacturing environment is highly preferred.… more
- Cipla (Hauppauge, NY)
- …and Safety: All employees must undergo various training activities at the start of their employment. New training and re-trainings will occur periodically.Employees ... work instructions and document results. Knowledge of fundamental cGMP and regulatory requirements in a pharmaceutical manufacturing environment is highly preferred.… more
- Pfizer (Groton, CT)
- POSITION SUMMARY You will lead and coordinate the development of multiple studies of novel biological and small molecules for first in human (FIH), proof of ... in Oncology. You will work in close collaboration with the Global Development Lead (GDL)and members of the development team to establish, lead , coordinate,… more
- AdaptHealth LLC (Philadelphia, PA)
- …while developing expertise in control evaluation, risk assessment, and regulatory compliance frameworks. Essential Functions and Job Responsibilities Audit Planning ... Assist in developing audit plans and programs for SOX and operational audits. Lead or support execution of financial, operational, compliance, and IT audits from … more
