Staff. QC Chemistry

Lương không công khai

Đồng Nai (On-site)

Nghỉ trọn T7, CN

Hạn chót 05/12/2026

Đăng 7 ngày trước

Ít hơn 20 ứng viên

Yêu cầu công việc

3. Minimum Qualification Requirements

3.1 Education

Minimum College/University Degree (with basic background in science)

3.2 Experience

Minimum 0-1 years of experience in Laboratory operation and management.

3.3 Skills

  • Computer literate and effective communication skills (verbal, written, and listening).
  • Self-motivated and proactive; committed to improving lab performance, workflow, and quality.
  • Team player.
  • Able to perform the job independently.
  • Good planning, coordinating, managing, and time-management skills.
  • Able to engage with cross-functional teams and external stakeholders.

-Or-

An equivalent competency level acquired through a variation of these qualifications may be considered.

Công việc cụ thể là gì?

1. Job Summary

Responsible for routine/non-routine QC Chemistry Laboratory analysis of finished products, process validation, Investigation, NC/CAPA. The candidate must demonstrate experience working in a cGMP laboratory and possess basic knowledge of industry regulations related to pharmaceutical and medical device manufacturing.

2. Essential Duties

  • Check, receive and register of samples, sorting samples to the test areas.
  • Prepare testing samples, solutions, standards and reagents to support testing.
  • Perform chemical analysis with compliance to the procedures and standards, with timely delivery as per sample priority or due date, without compromising the quality and accuracy.
  • Able to perform other testing upon completion training of test methods and Verification of Effectiveness (VOE) of QC Microbiology and QC Function Team.
  • Have analytical skills in the maintenance, operation and interpretation of the results obtained from analytical instruments such as the FTIR, HPLC, IR, UV, GC-MS, etc.
  • Support for the execution of method validations, qualifications, and transfers.
  • Perform routine maintenance activities in the laboratory and participates in the qualification and periodic calibration of equipment.
  • Able to perform review of all worksheets and logbooks.
  • Perform training for entry level staff and peer-to-peer training.
  • Identify and troubleshoot problems with instrumentation and analytical preparations.
  • Support and Perform Lab OOS/NC/CAPA Investigations in his/ her area.
  • Conduct supporting duties such as sample preparation, wash and dry apparatus and vials, and reject and discard samples.
  • Record any verifications, maintenance and calibration or repair works in the respective equipment logbook.
  • Practice 5S and conduct self-audit as per sectional audit checklist.
  • Maintain filing records as per record management retention schedule by filing the worksheets, shredding expired records to ensure that there are no expired records maintained.
  • Must be detail oriented, able to clearly record laboratory testing data and is a creative problem solver.
  • Follow Good Manufacturing Practices (cGMP) as well as all safety regulations and company procedures.
  • Adhere to all safety regulations and practices conforming to EHS regulations.
  • Support with Internal/External Audit such as FDA, ISO, etc.
• Cấp bậc: Nhân viên (associate) • Loại công việc: Toàn thời gian

Quyền lợi có gì?

Bảo hiểm & sức khoẻ

Premium Healthcare & accident insurance 24/7, 100% full salary in probation period