- Merck (Providence, RI)
- …Areas of Interest consultation, dissemination, data highlights, training, and scientific review as requested by the GMSA ED. **Required Qualifications, Skills & ... of 3 years of working in therapeutic area (clinical, research, or pharmaceutical environment) or within a highly relevant TA with demonstrated scientific acumen… more
- UPMC (Pittsburgh, PA)
- …therapeutic interchange protocols, and promoting rational drug therapy selection. + Review , maintain, and screen patient medication records and profiles for ... aides, student interns and other ancillary personnel involved in providing pharmaceutical care. + Adhere to all regulatory requirements, professional standards of… more
- Chiesi (Cary, NC)
- …care and consumer-facing self-care). We are proud to be the largest global pharmaceutical group to be awarded B Corp Certification, a recognition of high social ... many other enriching diversities. Chiesi USA Chiesi USA is a specialty pharmaceutical company focused on developing and promoting products for the hospital, adjacent… more
- Bayer (Silver Spring, MD)
- …& reshaping sales strategy based upon what is working and not working; + Review sales data, assesses trends, and adjusts sales strategy based upon insights; + ... QUALIFICATIONS:** + Minimum of a Bachelor's Degree; + Relevant specialty pharmaceutical sales, biotech sales, or medical sales experience; + Some specialty… more
- Gilead Sciences, Inc. (Foster City, CA)
- …thorough understanding of internal customers' business needs. + Lead quarterly functional review with VP, Brand Leadership, and business unit stakeholders. + Manage ... MA plus 8 years of experience in a biotechnology or pharmaceutical company is desirable; relevant experience in biopharmaceutical-focused marketing consulting would… more
- Boehringer Ingelheim (Athens, GA)
- …Regulatory Affairs (RA) Chemistry, Manufacturing and Controls (CMC) function for pharmaceutical products in line with Company policies, business strategies and ... technical topics. **Duties & Responsibilities** + Spearheads the preparation, critical review , and timely submission of regulatory dossiers to global Health… more
- Curia (Albuquerque, NM)
- …organization (CDMO) with over 30 years of experience partnering with pharmaceutical and biotech companies to provide life-saving treatments to patients. At ... ensuring secure, reliable, and compliant operations that support regulated pharmaceutical manufacturing activities. The position plays a critical role in… more
- Bayer (Manchester, PA)
- …and air movements in and out of the North America region for the Pharmaceutical (PH) and Consumer Health (CH) divisions to ensure seamless execution to foster the ... the North America region for end to end oversight. Review and assess 4PL performance on a regional level....the logistics industry or as a shipper in the pharmaceutical , consumer health, or FMCG (Fast Moving Consumer Goods)… more
- Bristol Myers Squibb (Devens, MA)
- …are inspection-ready, including pre-inspection audits, mock interviews, training, storyboard review , logistics, and escalation of critical issues. * Disseminate ... & Experience** * A minimum of five (5) years' experience in the Biopharm/ Pharmaceutical industry with knowledge of audits and inspections. * Bachelor's degree in… more
- Takeda Pharmaceuticals (Lexington, MA)
- …knowledge. **Job Description** **Associate Director, Lifecyle Management, Entyvio** **Takeda Pharmaceutical ** **Lexington, MA** **About the role:** Join Takeda as ... teams to thrive in a dynamic market landscape. + Participate in PRT Review process; partnering with Agency teams to support resource generation, approval, and… more