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Principal Research Scientist/Research Advisor-Analytical Development

Direct Staffing
Location
Indianapolis, IN, United States
Workplace
Employment
Full Time
Salary
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Posted 10y ago

Principal Research Scientist/Research Advisor-Analytical Development

Responsibilities

The Principal Research Scientist/Research Advisor is responsible for analytical control strategies and for leading a team in the development, qualification/validation, and use of analytical, bioanalytical and characterization methods in support of biotherapeutic product development.

  • Ensure work and team activities are aligned with all relevant development quality, regulatory, HSE, GLP, and GMP requirements.
  • Serve as key analytical technical lead co-formulated drug products.
  • Responsible for development of analytical strategies for co-formulated drug products
  • Develop all or portions of analytical control strategies.
  • Development and verification/qualification/validation of analytical methods to support in-process, release, characterization analysis, and stability testing of active pharmaceutical ingredient and drug product.
  • Provide support for discovery, toxicology, cell culture, purification, formulation, and manufacturing.
  • Oversight for method transfers to development, QCL, or third party personnel.
  • Coaching, training, and administration of performance management to personnel (primarily, but not limited to, direct reports).

Basic Qualifications

  • Ph.D. in analytical, biophysical, biochemistry, molecular/cell biology, or related field
  • Minimm of 8+ years experience in analytical development in industrial, pharmaceutical or biotech setting

Additional Skills/Preferences

  • Experience with the supervision, mentoring and development of direct reports.
  • Demonstration of scientific leadership skills.
  • Effective oral and written communication skills.
  • Must be able to work productively in an interdisciplinary team environment.
  • Experience with the drug development process, including knowledge of regulatory compliance issues.
  • Fundamental knowledge of cGMP/GLP compliance requirements.

CANDIDATE DETAILS

7+ to 10 years experience

Minimum Education - Doctorate Degree

.

ADDITIONAL DETAILS

Location

Indianapolis

Industry

Job Category

Research & Development

Hours Per Week

Visa Candidate Considered

No

Basic Qualifications

  • Ph.D. in analytical, biophysical, biochemistry, molecular/cell biology, or related field
  • Minimm of 8+ years experience in analytical development in industrial, pharmaceutical or biotech setting

All your information will be kept confidential according to EEO guidelines.

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