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We are committed to improving our world by making it healthier and safe for everyone and everywhere. Sannova strives to engage colleagues through a high-performance culture where employees are energized, excited and committed to shared goals.
Sannova is seeking scientific talent who are capable of anticipating and responding quickly to the dynamic environment and industry that we work in. At Sannova, you will have the chance to work with talented people, put your creativity and enthusiasm in high gear, flourish as a professional and enrich the lives of others in a rewarding career.
We value Innovation, Collaboration and Leader Behaviors and recognize and reward team members for their creative performance and contributions to the company.
Sannova is an equal opportunity employer. Full-time employees are eligible to participate in a variety of benefit programs offered by the Company.
Job Opening:
Analytical Chemist - Develop and validate sensitive Bioanalytical methods using LCMS/MS; Prepare technical protocols and documentation in compliance to USFDA guidelines; Analyze biological samples following GLP specifications for bioequivalence and bioavailability studies; Compile test information to write reports on analytical methods; Perform assay studies of active drug ingredients and metabolites; Maintain and calibrate analytical instruments, pH meters, UV-VIS, HPLC and LCMS/MS; Organize and maintain drug information in laboratory notebook for FDA documents.
Requirements:
Require a Master’s Degree or equivalent in Chemistry or Pharmacy and skills and working knowledge in HPLC, UV-VIS, pH meters, LCMS/MS and Analysis of Biological Sample
Location of job:
Somerset, NJ
Submit résumé referencing job code MIJ001 to HR,
Sannova Analytical, Inc.,
155 Pierce Street,
Suite A, Somerset,
NJ 08873.
Submit your updated resume to hr@sannova.net |
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Robust Methods for several ther- |
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-apeutic areas. |
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Controlled substance methods |
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(CII-CV). |
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Preclinical and clinical sample an- |
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-alysis. |
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BA/BE studies & PK/TK data ana- |
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-lysis. |
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State of the art equipment. |
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Reports in eCTD format. |
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Access to clinics in USA, Canada& |
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India. |
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Complete project management. |
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Electronic submission services. |
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Strict adherence to GLP. |
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Strict security and confidentiality. |
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Method Development |
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Method Validation |
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Pre clinical & clinical sample ana- |
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-lysis. |
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Report preparation for bioanalyt- |
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-ical studies reporting. |
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Pharmacokinetic & Toxicokinetic |
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Statistics |
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