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WuXi AppTec Peptide Platform

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Job: Associate Director, Peptide Analysis

Location: Changzhou City, Jiangsu Province

Hiring: 1

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

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.

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Job: Director/Sr. Director, Peptide Process Development

Location: Changzhou City, Jiangsu Province

Hiring: 1

Overview

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

Responsibilities

Projects:

Be able to lead multiple collaborations.

Be able to plan and prioritize projects to ensure projects timely executed according to client’s need.

Finalize the research plan and the execution program; ensure the team fully understand the whole plan and guideline to solve the issues during execution.

Coordinate all the resource and make adjustment according to the progress and timeline on time.

Immediately communicate with upper management and clients when issues to impact the progress and plan of the projects occur; and provide backup plan to ensure success of the project.

Management

Be able to lead multiple groups simultaneously

Be able to manage multiple projects simultaneously

Be able to manage client’s projects independently

Organize all kinds of the trainings on the whole team to continuously improve the ability of the team

Promote talented team members and evaluate on all the group leaders or team members

Optimize the workflow and involve the daily management of the department

Recruit new staff and provide trainings

Ensure team members to strictly comply with all the policies of company and department. Daily Check lab safety, notebook and IP

Ensure the personal safety of team members and the safety of labs. Investigate and prevent any violations and accidents.

Communication

Communicate with clients efficiently by TC or email (carefully organize the materials and the detailed information)

Ensure clients to be satisfied with our communications

Ensure all the reports (including weekly update, final report , PPT file and campaign report) to be ready on time

Response to clients immediately by TC or email for some special requirements.

Assist to build good relationship with clients and to arrange visit for clients.

Qualifications

Master or PhD in chemistry, chemical engineering or equivalent degree.

Expertise in process development of peptide drugs.

Excellent in presentation and communication in English.

5 years or above experience (PhD) in process development peptide drugs, 3 years or above projects management experience.

9 years or above experience (Master) in process development, 5 years or above projects management experience.

At least 5 years of people management experience.

Strong project management and communication skills.

Be able to build a highly productive and effective team, leads and motivates team to be efficient and innovative.

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Job: Senior Scientist/Group Leader, Peptide Process Research & Development

Location: Changzhou City, Jiangsu Province

Hiring: 1

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

Responsibilities

Effective technical and project leadership in the peptide PRD team to supervise peptide synthesis or purification process development, novel technology development, technical transfer, data analysis, project reporting and team management.

Oversee daily operations in peptide process R&D, monitor quality, timelines, cost, and project progression.

Evaluate/execute company’s current platforms and technologies in upstream or downstream process development.

Generate, manage, interpret, and maintain critical data in a highly organized manner; write and present technical reports to management and clients.

Lead/participate in lab maintenance and management.

Demonstrate effectiveness in collaborative projects in a matrix organization and communication with clients in written or verbal English language.

Provide mentorship to the team members and conduct performance assessment

Qualifications

Advance degree in organic chemistry, peptide chemistry, pharmaceutical chemistry, peptide purification or equivalent.

Proven pharmaceutical industry experience in peptide synthesis, purification or close fields is a plus.

Experience in route scouting, process design, scale-up, technology transfer to pilot plant facility and commercial manufacturing plant and regulatory documentation (Qulification& Validation reports, PDF, P&ID, MBR, deviation reports and change request report etc.).

Fluent in Mandarin and English and excellent technical written and verbal communication skills in both.

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Job: Senior Scientist /Group Leader, Peptide and Oligonucleotide Analysis

Location: Changzhou City, Jiangsu Province

Hiring: 1

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

Responsibilities

Effective technical and project leadership in the peptide PRD team to supervise peptide/ oligonucleotide synthesis or purification process development, novel technology development, technical transfer, data analysis, project reporting and team management.

Oversee daily operations in peptide/ oligonucleotide process R&D, monitor quality, timelines, cost, and project progression.

Evaluate/execute company’s current platforms and technologies in upstream or downstream process development.

Generate, manage, interpret, and maintain critical data in a highly organized manner; write and present technical reports to management and clients.

Lead/participate in lab maintenance and management.

Demonstrate effectiveness in collaborative projects in a matrix organization and communication with clients in written or verbal English language.

Provide mentorship to the team members and conduct performance assessment

Qualifications

Advance degree in organic chemistry, peptide chemistry, pharmaceutical chemistry, peptide/ oligonucleotide purification or equivalent.

Proven pharmaceutical industry experience (Master + 8 years or Ph.D.+5 years) in peptide synthesis, purification or close fields.

Experience in route scouting, process design, scale-up, technology transfer to pilot plant facility and commercial manufacturing plant and regulatory documentation (Qualification& Validation reports, PDF, P&ID, MBR, deviation reports and change request report etc.)

Fluent in Mandarin and English and excellent technical written and verbal communication skills in both

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