本文发表在 rolia.net 枫下论坛Regulatory Compliance Coordinator
Job Title: Regulatory Compliance Coordinator,morning shift 8:00Am-4:30Pm
Reporting to QA Manager - a junior sub-coordinate works under the direction of Regulatory Compliance Specialist in maintaining the quality systems.
Duties and Responsibilities:
Maintain SOP index, database, controlled, master copies and QA documents.
Maintain SOP training records and training matrix.
Collect and trend KPI monthly data and other test data as required e.g. stability program.
Coordinate and maintain the calibration maintenance program with contractors for the facility.
Perform in-house calibration duties.
Assist to prepare apostille documents e.g. INCL, MSDS, TDS, CoA, CFS, GMP and export certificates.
Assist to revise SOPs, when appropriate, write change control, deviations and protocols.
Assist to execute corrective actions for closing out audit observations as directed.
Assist to prepare coordinate and execute quality improvement or validation projects.
Maintain other quality systems as directed e.g. batch record review and filing.
Perform other duties as assigned.
Qualifications:
Bachelor of Science preferable in Chemistry or equivalent.
1-2 years related work experience.
Good technical writing skills.
Detail oriented and good organization skills.
Effective communication skills with employees across different levels.
Knowledge of cosmetic, OTC, NHP product regulations and GMP.
Exposure to one of the areas in manufacturing, QC or laboratory will be an asset.
Ability to work in a team environment and independently with limited supervision.
If you are interested in the position,Please send your resume to : jefftop@hotmail.com
Please note:
We thank all applicants.
However, only those selected for an interview will be contacted更多精彩文章及讨论，请光临枫下论坛 rolia.net
Job Title: Regulatory Compliance Coordinator,morning shift 8:00Am-4:30Pm
Reporting to QA Manager - a junior sub-coordinate works under the direction of Regulatory Compliance Specialist in maintaining the quality systems.
Duties and Responsibilities:
Maintain SOP index, database, controlled, master copies and QA documents.
Maintain SOP training records and training matrix.
Collect and trend KPI monthly data and other test data as required e.g. stability program.
Coordinate and maintain the calibration maintenance program with contractors for the facility.
Perform in-house calibration duties.
Assist to prepare apostille documents e.g. INCL, MSDS, TDS, CoA, CFS, GMP and export certificates.
Assist to revise SOPs, when appropriate, write change control, deviations and protocols.
Assist to execute corrective actions for closing out audit observations as directed.
Assist to prepare coordinate and execute quality improvement or validation projects.
Maintain other quality systems as directed e.g. batch record review and filing.
Perform other duties as assigned.
Qualifications:
Bachelor of Science preferable in Chemistry or equivalent.
1-2 years related work experience.
Good technical writing skills.
Detail oriented and good organization skills.
Effective communication skills with employees across different levels.
Knowledge of cosmetic, OTC, NHP product regulations and GMP.
Exposure to one of the areas in manufacturing, QC or laboratory will be an asset.
Ability to work in a team environment and independently with limited supervision.
If you are interested in the position,Please send your resume to : jefftop@hotmail.com
Please note:
We thank all applicants.
However, only those selected for an interview will be contacted更多精彩文章及讨论，请光临枫下论坛 rolia.net