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WuXi AppTec

Global contract research, development, manufacturing organization

Scientist 3

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeCranbury, NJ, USANo salary listedIn-person

About the Job

Requirements

  • A PhD, Master’s, or Bachelor’s degree in Chemistry, Biology, or a related science field, or an equivalent combination of education and work experience.
  • A PhD requires 0–3 years of related experience; a Master’s degree requires 8 or more years; a Bachelor’s degree requires 11 or more years.
  • Knowledge and experience with methods, concepts, and techniques relevant to small- or large-molecule bioanalytical work, including LC-MS, ELISA/MSD, PCR, flow cytometry, and western blotting.
  • Understanding of bioanalytical guidance and acceptance criteria in discovery and development stages.
  • Ability to perform independent scientific thought and technical creativity, and to stay current with relevant science and literature.
  • Oral, written, and interpersonal communication skills.
  • Time-management skills to handle multiple projects within timelines and ability to work in a team environment.
  • Ability to follow non-GLP guidelines and standard operating procedures.
  • Ability to work in an office and/or laboratory environment with variable noise conditions and exposure to biohazards or chemicals, and to wear appropriate personal protective equipment.
  • Ability to stand, sit, or walk for long periods; routinely lift, push, or pull 15 pounds; crouch, bend, twist, and reach; distinguish colors; perform repetitive motions; and work in variable temperatures from high to freezing.

Responsibilities

  • Independently perform bioanalytical method development using an LC-MS/MS platform or immunochemistry platforms such as ELISA/MSD, PCR, flow cytometry, and western blotting.
  • Apply bioanalytical acceptance criteria appropriate to different stages of application.
  • Conduct bioanalytical sample analysis in various biological matrices, including small- and large-molecule samples, and write bioanalytical reports.
  • Serve as study director, principal investigator, or project coordinator, including acting as the primary project contact.
  • Write or present clear, concise reports on studies, processes, and accomplishments.
  • Maintain organized research notebooks and record all necessary documentation.
  • Supervise or train others on bioanalytical studies and demonstrate leadership through example, motivation, and performance recognition.
  • Review other scientists’ calculations and records.
  • Develop and share technical knowledge of DMPK, including ADME, PK, metabolism, and bioanalysis.
  • Participate in writing and reviewing standard operating procedures and bioanalytical acceptance guidelines, suggest practical changes, and comply with procedures, guidelines, and housekeeping policies.
  • Follow company safety policies and procedures; work with the EHS team to identify safety hazards and corrective actions.
  • Perform other job-related duties as assigned.

About the Company

WuXi AppTec

Global contract research, development, manufacturing organization

WuXi AppTec provides an open-access, global platform that offers contract research, development, and manufacturing services (CRDMO) for the pharmaceutical, biotechnology, and medical device industries. Its services cover the full product lifecycle—from discovery and preclinical work to clinical and commercial manufacturing—delivered through a wide range of lab, testing, process development, and manufacturing capabilities that clients can access as needed. The company distinguishes itself by combining broad geographic reach with a comprehensive, end-to-end service portfolio and strategic acquisitions to support projects worldwide. Its goal is to help innovators bring new medicines and healthcare products to market faster and with high quality.

Company size
1,001-5,000
Company stage
IPO
Headquarters
Huangpu, China
Founded
2000

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