10 life sciences jobs at 7 companies in Lafayette, IN
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Quality & Compliance Manager onsite in Lebanon, IN- Life Sciences/ Pharmaceutical
Lebanon, Indiana, United States
OnsiteFull Time
3+ YOESupervisory experience with 3+ years relevant experience, knowledge of audits/CAPAs in life sciences/pharmaceutical/GMP, strong leadership, organizational and communication skills, and Microsoft Office proficiency.
Microsoft Word, Microsoft Excel, Microsoft Outlook
2mo
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Quality Supervisor, Life Science Division 2nd shift
Whitestown, Indiana, United States
OnsiteFull Time
3+ YOELead quality team in raw material sampling; ensure GMP/FDA compliance; manage quality systems and audits; drive continuous improvement.
LIMS, Raman, Calipers, Go/No Go gauges, Microsoft Office
3mo
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VP, Client Solutions
US Remote - AL or US Remote - MA or US Remote - NJ or US Remote - FL or US Remote - IN or US Remote - AL or US Remote - CA or US Remote - DC or US Remote - PA or US Remote - CO or US Remote - MD or US Remote - IL or US Remote - OH or US Remote - TX
$200k-$250k/yr RemoteFull Time
20+ YOESenior leader with 20+ years in life sciences or biotech; strong client leadership, strategic growth, and delivery of services; willing to travel 50-75%; US remote locations.
CRM/PSA, Salesforce, Kantata, Data Visualization, Collaboration Platforms
3w
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Principal Scientist GMP Environmental Monitoring Lilly Medicine Foundry
Lebanon or Carmel or Indianapolis
$65k-$169k/yr OnsiteFull Time
5+ YOEBS/MS in life sciences,5+ years GMP pharmaceutical microbiology/EM experience,authorized to work in the US,cGMP/ALCOA+ knowledge,regulatory inspection experience,EM sampling and investigation skills.
MODA, LabVantage, Metasys, TrackWise, Veeva Vault, Met One, Climent, Air Ideal, MAS 100, Lighthouse, PMS, MALDI-TOF, Vitek
3w
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Clinical Scientist
West Lafayette, Indiana, United States
OnsiteFull Time
3+ YOEBachelor's in life sciences or engineering required; 3+ years clinical research experience; knowledge of GCP/ISO 14155 and regulatory requirements; experience designing studies, analyzing clinical and imaging data; must be authorized to work in the US.
1mo
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Quality Control Microbiology Specialist
Madison or Rensselaer
OnsiteFull Time
eGenesis: Developing genetically engineered animal organs for human transplantation.
0+ YOEB.S./M.S. in life sciences; 0–3 years GMP QC lab experience; proficiency in microbiology methods and aseptic technique; knowledge of US/EU cGMP; strong communication; environmental monitoring and data trending experience.
2mo
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Bioprocess Scientist (Downstream) - Advanced Therapies Manufacturing
Lebanon, Indiana, United States
$66k-$172k/yr OnsiteFull Time
3+ YOEB.S. in a quantitative life-science or engineering field, 3+ years cGMP manufacturing experience, hands-on downstream operations (chromatography, TFF, viral/sterile filtration), process validation/tech transfer, data analysis, and cross-functional collaboration.
1mo
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Quality Assurance Specialist
Westfield, Indiana, United States
OnsiteFull Time
5+ YOEBachelor's in life sciences or technical field required; 5+ years QA/QC experience supporting GMP manufacturing; experience with radiopharmaceutical or PET drug manufacturing and cGMPs preferred; strong organization, record-keeping, communication, and ability to work shifts.
2w
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Warehouse Operations Manager
Brownsburg, Indiana, United States
OnsiteFull Time
5+ YOE3+ Mgmt5+ years in regulated warehouse operations with 3+ years managerial experience preferred; bachelor’s in supply chain/operations/life sciences preferred; strong GDP/GxP knowledge; Blue Yonder/WMS and Microsoft Excel/Outlook/Teams experience; Lean/Six Sigma a plus.
Microsoft Excel, Microsoft Outlook, Microsoft Teams, Blue Yonder, Warehouse Management Systems (WMS), Artificial Intelligence (AI)
1mo
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Lead Clinical Research Associate (CRA)/ Clinical Monitoring Lead
West Lafayette, Indiana, United States
OnsiteFull Time
3+ YOEBachelor's in life sciences/nursing/pharmacy or equivalent experience; extensive CRA experience including 3+ years as senior/lead CRA; medical device monitoring experience; knowledge of FDA/GCP/ISO-14155; Veeva Vault experience desirable; periodic travel; US work authorization required.
Veeva Vault