6 manager biotech jobs at 6 companies in Rockford, IL
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Quality Manager, NPI
Rockford or United States
$87k-$98k/yrOnsiteFull Time
PCI Pharma Services: Global contract development and manufacturing organization for biopharma.
10+ YOEBachelor's in engineering/life sciences, 10+ years pharma/biotech/device quality experience, expertise in GAMP5 and FDA 21 CFR (820/210/211/11), product lifecycle and design control, risk management, team leadership, and strong reporting skills.
Hospital Senior Account Manager, Anti-Infectives - Milwaukee, WI / Rockford, IL
Milwaukee or Appleton or Rockford or United States
$165k-$275k/yrFieldFull Time
GSKLondon Stock Exchange (LSE): GSK: Global biopharmaceutical focused on medicines and vaccines.
5+ YOEBA/BS degree, valid driver's license, 5+ years in pharmaceutical, medical, or biotech industries, 3+ years calling on hospitals and health systems, and willingness to travel up to 50%.
Neuroscience Therapeutic Sales Specialist (Chicago N, IL)
Chicago or Rockford or Northbrook
$165k-$195k/yrFieldFull Time
Compass PathwaysNasdaq Global Select Market: CMPS: Public British biotechnology developing investigational COMP360 psilocybin treatment for people with serious mental health conditions.
5+ YOEBachelor's degree and 5–8+ years of pharmaceutical or biotech sales experience required; specialty therapeutics, psychiatry, reimbursement, treatment centers, territory management, and complex scientific communication preferred.
Inizio Engage: Commercialization and patient engagement partner for life sciences.
3+ YOEBachelor's degree, 3+ years pharma/biotech/healthcare sales, experience with hospitals/IDNs/specialty pharmacies preferred, CRM proficiency, strong communication and territory management, ability to travel ~70%.
NorthStar Medical Radioisotopes: U.S. radiopharmaceutical manufacturer and CDMO producing therapeutic and diagnostic radioisotopes for pharmaceutical partners.
10+ YOE5+ MgmtBachelor's in a life science,10+ years quality experience in cGMP pharma/biotech/radiopharma with 5+ years management; hands-on startup experience; knowledge of FDA 21 CFR, data integrity, audits, method validation; ASQ preferred; must be authorized to work in the U.S.