WuXi AppTec

Associate Director, Peptide Analysis

Job Locations CN-Changzhou
Job ID
2019-5669

Overview

STA Pharmaceutical Co., Ltd., a WuXi AppTec company (WuXi STA), is a global leading small molecule pharmaceutical development and manufacturing capability and technology platform company serving the life science industry, with operations in China and the United States. As a premier Contract Development and Manufacturing Organization (CDMO), STA offers our worldwide partners efficient, flexible and high-quality solutions for small molecule Active Pharmaceutical Ingredients (APIs) and finished dosage forms.

  • A Leading Company of Contract Development and Manufacturing Organization(CDMO)
  • The World’s Largest Process Chemistry Team
  • To learn the most cutting edge technologies in the pharmaceutical development field
  • To work with 200+ global new drug development companies
  • Systemic and Multiple Training Programs(Technical/Soft skills/Management)
  • Diversified Career Development and Promotion Trails

 

Job Location: Changzhou City, Jiangsu Province

Responsibilities

  • Effective technical and project leadership in the analytical team with both R&D and Quality Control functionalities in support of the company’s peptide R&D and manufacture projects.
  • As a key member for the peptide business unit, oversee daily operations in the analytical method development in R&D, as well as method validation and execution activities in GMP QC.
  • Monitor quality, timelines, cost, and project progression.
  • Ensure effective communication internally with process development team and manufacture team, and externally with clients regarding scientific findings in written or verbal English language, and host teleconference for corresponding discussion.
  • Implementation of the company’s policies, quality systems and training programs. Follow the company’s code of conduct and compliance rules;
  • Lead a group of analysts and quality control chemists
  • Provide mentorship to the team members and conduct performance assessment

Qualifications

  • Advance degree in analytical chemistry, bioanalytical chemistry, pharmaceutical analysis or equivalent.
  • Proven pharmaceutical industry experience (Master + 8 years or Ph.D.+5 years) in peptide analysis or close fields.
  • Experience in analytical method development, validation, transfer and GMP compliance system.
  • Hands-on experience in various analytical instrumentation (e.g. LC, GC, LC-MS, GC-MS, NMR)
  • Experience of peptide analytical method development and quality control is highly desirable.
  • Strong communication skills in both English and Chinese, and outstanding interpersonal skills are essential job requirements.

 

Equal Opportunity Employer Minorities/Women/Veterans/Disabled

 

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