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Veranova · 2 weeks ago

Senior Scientist, Analytical Research & Development

West Deptford, NJ

Full-time

Onsite

Senior Level, Lead/Staff

$115K/yr - $125K/yr

8+ years exp

Veranova is a global leader in the development and manufacturing of complex active pharmaceutical ingredients (APIs) for pharma and biotech customers. The Sr. Scientist is responsible for the implementation, development, and validation of analytical test methods in support of process research and cGMP production, focusing on various analytical techniques for small molecules and other compounds.

BiotechnologyHealth CareManufacturingPharmaceutical

No H1B

Responsibilities

Develop and validate new analytical procedures. Independently, detects and solves complex problems of high technical difficulty

Perform sample analysis using various analytical techniques (e.g., LC, GC, LC-MS, GC-MS, ICP-MS, ELISA, SEC-MALS, CE-SDS, cIEF, etc.), interpret results, and prepare high-quality documentation such as protocols, analytical reports, and summary reports

Document all analyses per SOPs

Prepare SOPs, test methods, and other GMP documentation

Independently, detect and solve complex problems of high technical difficulty

Apply knowledge and expertise from multiple disciplines (including QA, QC, Analytical and production) to achieve project goals

Conduct investigations independently

Troubleshoot analyses and instruments

Support qualification of reference materials

Develop new analytical procedures

Validate analytical methods

Prepare and review scientific reports

Interface with internal and external clients

Qualification

Analytical ChemistryMethod DevelopmentMethod ValidationGMP ExperienceLCGCGC-MSProject ManagementMicrosoft OfficeComplex Problem SolvingMentoring

Required

PhD in Analytical Chemistry or equivalent

Minimum of 8 years' experience in a GMP environment

Minimum of 5 years' experience in method development and validation for small molecules Active Pharmaceutical Ingredients (APIs). Experience with Process Development of APIs

Experience with LC, GC, GC-MS, LC-MS, IC, spectroscopy, and wet chemistry

Experience mentoring staff members in an analytical department

Formal project management training

Experience with writing method validation protocols and reports desirable

Experience with Microsoft Office and other complex computer software (UPLC, Empower 3) desirable