Associate Scientific Liaison Job Opening @ USP – Apply Online
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Job Title: Associate Scientific Liaison (Excipients)
No.of posts: 01
Eligibility:
- Assistant Scientific Liaison: PhD in Chemistry or Biochemistry and 2 years or MS in Chemistry or Biochemistry and 5 years, respectively, or relevant experience. An equivalent combination of experience and education may be substituted.
- Associate Scientific Liaison: PhD in Chemistry or Biochemistry and 5 years or MS in Chemistry or Biochemistry and 7 years, respectively, of relevant experience. An equivalent combination of experience and education may be substituted.
- Scientific Liaison: PhD in Chemistry or Biochemistry and 8 years or MS in Chemistry or Biochemistry and 10 years, respectively, of relevant experience. An equivalent combination of experience and education may be substituted.
Experience:
- Experience and knowledge of the pharmaceutical industry and the associated regulatory framework is essential.
- Ability to review, analyze, interpret and report effectively on data from various analytical tests.
- Proficient in related analytical analysis and instrumentation (e.g., GC, HPLC, NMR, ICP, AA, KF, UV, LC/MS, GC/MS).
- Should possess strong technical knowledge in the areas of complex molecules/compounds such as polymers, fats, oils, waxes and plants.
- Must be able to share technical information with non-technical or non-scientific staff, and to communicate effectively with representatives from pharmaceutical companies,
- government, and academic institutions. Ability to rapidly assess technical complications to identify, define, and solve technical issues
- Well-developed organizational, interpersonal communications, negotiation, writing, and strong listening and presentation skills.
- Proficient with pharmaceutical testing requirements and test protocols involving USP-NF compendial methods development for Excipient monographs.
- The ability to influence without direct authority.
- Results driven with demonstrated successful outcomes.
- Project Management skills and ability to prioritize tasks and manage multiple projects simultaneously.
- Able to operate independently where appropriate, yet understands when to escalate issues and how to establish effective working relationships.
- Ability and desire to work well with diverse employees and customers in a cooperative and friendly manner.
- Ability to handle multiple priorities in a fast-paced environment.
- Able to work flexible hours when needed.
- Prior experience in a scientific based industry.
- Excellent written and verbal communications skills
Roles and Responsibilities
- Works with USP staff, relevant USP Excipient Expert Committee(s) (EC), subcommittees (SC), and Expert panels (EP), external stakeholders as related to Excipient monograph and RS development;
- Supports in the preparation of data packages and briefing materials to present to the Excipients EC/SC/EP; manages projects appropriately, and ensures impeccable work-product delivery.
- Participates in USP EC/SC/EP meetings, scientific conferences/meetings, outreach visits and other events sponsored by USP and/or pharmaceutical industry , trade associations, and regulatory agencies and provides supporting scientific expertise at EC/SC/EP meetings, internal and external meetings, scientific symposia, industry forums.
Standard setting responsibilities include: - Prepares data summary packages, briefing materials and other technical documents for correspondence with EC/CS/EP.
- Manages action items from monthly EC /SC/EP telecom meetings.
- Tracks and reports frequently on the status of assignments to management;
- Facilitates the accomplishment of key departmental metrics.
- Assists in writing manuscripts for publication by USP (e.g., PF proposals, stimuli articles) or in peer-reviewed journals;
- Applies knowledge of current trends in public health to prepare information for Expert Committee to facilitate decision-making.
- Performs other related duties in support of the Excipients –Science Program Unit as assigned.
Apply Online
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