- Insight Global (Holly Springs, NC)
- Job Description A large pharmaceutical client is seeking a team of Cleaning Equipment Validation Engineers to support their site build out in Raleigh-Durham. The ... on validation experience, documentation experience and experience working within regulated pharmaceutical environment. The first 3-4 months will be heavily focused… more
- Lilly (Indianapolis, IN)
- …organizations + Manage TS/MS technical projects (experimental, modeling and/or production data analysis) to improve process control, yield, and/or productivity. + ... summary reports, processing records, procedures, PFDs, VMPs, etc. + Review /approve relevant technical documents, such as: Change Controls, Regulatory Submissions,… more
- University of Colorado (Aurora, CO)
- …of Colorado Anschutz Medical Campus** **Skaggs School of Pharmacy and Pharmaceutical Science | Dean's Office** **Job Title:** **Position: #** **- Requisition: ... timely triage and resolution of HR inquiries. + Maintain accurate HR data and records to support reporting, compliance, and decision-making. + Support equitable… more
- United Therapeutics (Silver Spring, MD)
- …are as follows:** Who we are We are the first publicly-traded biotech or pharmaceutical company to take the form of a public benefit corporation. Our public benefit ... a brighter future for patients through the development of novel pharmaceutical therapies; and technologies that expand the availability of transplantable organs.… more
- Insight Global (San Diego, CA)
- …keep, and process your private information, please review Insight Global's Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/. Skills ... * 8+ years of Technical Project management experience (working in a pharmaceutical company with exposure to FDA regulations preferred) * Experience managing… more
- Lilly (Indianapolis, IN)
- …automation development (ie, integrated control systems) between PAT tools and process data systems (ie, synTQ or other systems). + Mentor and develop scientific ... Plan and manage short-term and long-term development activities. Develop and/or review technical agendas and timelines for project work. Recommend resource… more
- J&J Family of Companies (Raritan, NJ)
- …Leader will be responsible for the following: + Lead the development, revision, review , agreement, and maintenance of primary labeling (Company Core Data Sheet ... + A minimum of 4 years of relevant experience in the pharmaceutical industry (eg, Regulatory Affairs, Clinical, Medical Information, Pharmacovigilance, etc.) is… more
- BeOne Medicines (San Mateo, CA)
- …and documents. + Designs and conducts quality issue trending, analysis and review activities to proactively identify broader issues and/or patterns within GCO ... and to relevant leadership. + Ensures provision of actionable data and insights regarding the state of quality and...Degree with minimum of 10 years of experience in pharmaceutical or biotechnology drug development, preferably in a relevant… more
- Vighter Medical Group (Phoenix, AZ)
- …patients regarding appropriate use of medications. + Deliver comprehensive pharmaceutical services within the personnel, supply, and equipment capabilities of ... medication for which the patient should seek additional + medical care as appropriate. Review patient profiles at the time of dispensing in order to closely monitor… more
- Merck (Rahway, NJ)
- …the assigned projects. + Prepare materials for program presentations for management review and regulatory submissions, ensuring clarity and thoroughness. + Lead the ... experience and skills:** + Minimum of 6 years of experience in pharmaceutical development, device development, device systems operations, quality management, or a… more