-NEW- 12 Month Quality Check Chemist (Pharmaceutical Industry)

AMBITION GROUP SINGAPORE PTE. LTD.; Town of Islip (NY); On-site; USD 50,000 - 70,000; Full time

Job summary

A well-established company in the pharmaceutical sector is looking for a Quality Control professional. The role involves conducting method transfers, performing analytical tests, and ensuring compliance with regulatory standards. Candidates should have at least a diploma and 2 years of relevant experience, with immediate availability preferred.

Qualifications

• Minimum 2 years of relevant quality check experience.
• Experience within the Pharmaceutical industry preferred.
• Able to start immediately or within short notice.

Responsibilities

• Conduct analytical method transfer and validation studies.
• Perform analytical testing in accordance with GMP and GLP requirements.
• Write and review SOPs and perform laboratory incident investigations.

Skills

Analytical Testing

Method Validation

Data Integrity

Regulatory Compliance

Training

Education

Minimum Diploma in a related discipline

Job description

Job Responsibilities:

· Conduct analytical method transfer, validation, verification, and equivalency studies in compliance with SOPs, ALCOA principles, and data integrity standards.

· Perform analytical testing in accordance with GMP and GLP requirements, ensuring accuracy and efficiency.

· Lead or participate in 5S and housekeeping initiatives, maintaining adherence to safety procedures.

· Assess product impact due to changes or updates in compendial monographs.

· Support regulatory submissions and respond to queries related to post-transfer activities.

· Write and review SOPs, OJT materials, protocols, reports, test procedures, and position papers.

· Investigate laboratory incidents, identify root causes, and implement appropriate CAPAs.

· Provide hands-on training to colleagues on instruments and analytical methods.

· Review and approve laboratory test results.

· Manage QTS actions and handle GMP-impacting change controls.

· Coordinate with donating sites to facilitate smooth method transfers.

· Conduct training on new laboratory methods for QC team members.

· Contribute to continuous improvement initiatives within QC or cross-functional teams.

· Actively participate in Tier meetings by updating performance metrics, highlighting issues, and supporting solution development.

· Perform cleaning method development and validation.

· Ensure documentation complies with GDP practices and is accurately maintained.

· Execute method verification per site or pharmacopeial standards on schedule.

· Keep training records current and properly filed to reflect testing qualifications.

· Adhoc tasks and projects as assigned

Job Requirements

· Minimum Diploma in a related discipline

· Minimum 2 years of relevant quality check experience

· Experience within the Pharmaceutical industry would be an added advantage

· Able to start immediately or within short notice

Interested candidates, kindly email your detailed resumes in MS word format to [e-mail]

Attention to Joseph Koh Wei Jie (R1873431)

Shortlisted candidates will be notified

www.ambition.com.sg

EA Registration Number: R1873431

Data provided is for recruitment purposes only

Business Registration Number: 200611680D. License Number: 10C5117