Senior Scientist - Supply Analytical Sciences (SAS)

MSDUpper Gwynedd Township, PA
$117,000 - $184,200Hybrid

About The Position

Our company is currently seeking an exceptional individual for a Senior Scientist position within the Supply Analytical Sciences (SAS) - Analytical Chemistry in Development and Supply (ACDS) organization. This is a laboratory-based scientific role in a fast-paced, multidisciplinary team environment. The successful candidate will join a group of innovative analytical scientists with broad deliverables to support commercial pharmaceutical products, ensuring an undisrupted supply of our company products to patients globally. This role offers the opportunity to interact closely with internal sites and external partners within our company network, identifying issues, implementing solutions, and providing strong analytical support.

Requirements

  • Bachelor’s Degree (BS) in Chemistry or related discipline with at least seven (7) years of relevant pharmaceutical development experience, OR Master’s Degree (MS) in Chemistry or related discipline with at least five (5) years of relevant pharmaceutical development experience, OR PhD in Analytical Chemistry or related discipline
  • Strong chemistry knowledge
  • Demonstrated problem-solving ability, including the ability to perform investigations with strong technical troubleshooting skills
  • Experience with common analytical techniques such as chromatography, spectroscopy, dissolution, and Karl Fischer
  • Strong communication (verbal and written) and interpersonal skills
  • Demonstrated ability to work in an interdisciplinary team environment
  • Ability to quickly adapt to changes and develop appropriate plans for managing risks

Nice To Haves

  • Working knowledge of pharmaceutical API and/or drug product development and commercialization
  • Working knowledge of CMC filing requirements and regulatory guidances (e.g., ICH) for API and/or drug product
  • Working knowledge of GMP and data integrity and recent industry trends in commercial production space
  • Experience supporting regulatory inspections and internal audits as an analytical subject matter expert
  • Experience working with CMOs and CROs
  • Experience assisting in developing/implementing CAPAs
  • Strong interpersonal skills, including the ability and sensitivity to deal with different cultures

Responsibilities

  • Support commercial pharmaceutical products to ensure undisrupted supply.
  • Interact closely with internal sites and external partners to identify issues and implement solutions.
  • Provide strong analytical support, including troubleshooting laboratory test methods and workflows.
  • Ensure compliant, robust, and responsive supply of materials.
  • Understand the global regulatory and business environment related to pharmaceutical API and Drug Product development.
  • Ensure GMP compliance in commercial manufacturing and data integrity.

Benefits

  • medical, dental, vision healthcare and other insurance benefits (for employee and family)
  • retirement benefits, including 401(k)
  • paid holidays
  • vacation
  • compassionate and sick days
  • annual bonus
  • long-term incentive
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