USP Associate Scientific Liaison Post Vacancy - Apply Online

USP Associate Scientific Liaison Post Vacancy – Apply Online

The U.S. Pharmacopeial Convention (USP) is a scientific nonprofit organization that sets standards for the identity, strength, quality, and purity of medicines, food ingredients, and dietary supplements manufactured, distributed, and consumed worldwide. Check out all the details

Job Title: Associate Scientific Liaison

Location: Hyderabad, India

Eligibility Criteria:

  • Ph.D. degree in Chemistry, Pharmacy, or a related field and five (5) years, or M.S. degree and eight (8) years of relevant industry experience in quality assurance.
  • An equivalent combination of experience and education may be substituted.

Preferred Qualifications

  • Experience with conducting reviews of scientific and technical documents.
  • Experience with reference standards development is a plus.
  • Working knowledge of general analytical methodologies is required.
  • Ability to write technical reports related to material characterization, references standard evaluations, and method development.
  • Ability to establish and nurture relationships with individuals of varying backgrounds and learning styles.
  • Ability to operate independently where appropriate, yet understands when to escalate issues and how to establish effective working relationships.
  • Strong presentation and communication skills (written and oral).
  • Well-developed organizational, interpersonal communications, negotiation, writing, and strong listening skills.
  • Project Management skills. Must have the ability to prioritize and manage multiple, concurrent projects with often long life cycles.
  • Experience with, and knowledge of the USP-NF is preferred.

Roles and Responsibilities

  • Performs technical and quality reviews of documents to ensure a high level of quality within the department.
  • Manages and tracks efforts for continuous improvements.
  • Develops and reviews SOP’s, Operation Manuals, and training documents.
  • Assists in investigations of quality-related issues resulting from customer complaints to include root cause analysis, corrective action identification, action planning, and implementation monitoring.
  • Develops and implements a database for quality measurement and improvement. Monitors database and performs trend analysis to improve quality in daily operations.
  • Supports the day-to-day operation of the reference standard stability program.
  • Works with internal stakeholders to develop new and innovative standards for analytical analysis of biopharmaceutical products.
  • Communicates and maintains working relationships with other USP departments regarding projects related to validation studies, methods development, reference standards, and other cross-cutting activities.

Apply Online

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