- Tanjong Pagar Central Region (Singapore) Singapore
全职 CQV Engineer 工作, 薪水 up to SGD 6,000, AMARIS ACT PTE. LTD. Central Region (Singapore) 公司招聘中 - Ricebowl
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Job Description
You’ll have the opportunity to work within our Life Sciences team, supporting commissioning, qualification, and validation activities in a pharmaceutical environment. This role is ideal for junior professionals interested in developing their careers in CQV, equipment qualification, and computerized system validation.
ABOUT THE JOB
Support commissioning, qualification, and validation activities for pharmaceutical equipment and systems
Prepare, execute, and review qualification protocols, test scripts, and reports
Support the qualification of QC equipment, production equipment, HVAC systems, and related instrumentation
Contribute to computerized system validation activities associated with equipment and validation software
Perform testing and accurately document results in accordance with approved procedures
Identify, document, and support the resolution of deviations arising during qualification activities
Ensure qualification documentation complies with applicable quality, GMP, and data integrity requirements
Support performance qualification activities, including process, cleaning, or single-use material qualification
Work closely with validation, engineering, quality, manufacturing, and QC teams
Support other CQV-related activities as assigned
ABOUT YOU
Degree in Pharmaceutical Science, Life Sciences, Chemical Engineering, Biomedical Engineering, Instrumentation, Automation, or a related field
1 to 3 years of experience in commissioning, qualification, or validation within a pharmaceutical or similarly regulated environment
You have between 1 and 3 years of experience in commissioning, qualification, or validation within a pharmaceutical or similarly regulated environment
You have experience with QC equipment, production equipment, or HVAC qualification
You have knowledge or practical experience in computerized system validation
Experience in process validation, cleaning qualification, or single-use material qualification is an advantage
You are familiar with qualification documentation, including protocols, test scripts, deviations, and reports
You demonstrate strong attention to detail and a good understanding of quality and compliance requirements
You are able to follow approved procedures and document your work accurately
You work effectively with cross-functional stakeholders
You are fluent in English
Our organisation is a global HR consulting company dedicated to providing the full spectrum of HR-related services to our clients who range from small-medium enterprises (SME's) to multi-nationals and government agencies.
With 23 years of experience, we have grown our client base steadily with more than 300 successful engagements.
You’ll have the opportunity to work within our Life Sciences team, supporting commissioning, qualification, and validation activities in a pharmaceutical environment. This role is ideal for junior professionals interested in developing their careers in CQV, equipment qualification, and computerized system validation.
ABOUT THE JOB
Support commissioning, qualification, and validation activities for pharmaceutical equipment and systems
Prepare, execute, and review qualification protocols, test scripts, and reports
Support the qualification of QC equipment, production equipment, HVAC systems, and related instrumentation
Contribute to computerized system validation activities associated with equipment and validation software
Perform testing and accurately document results in accordance with approved procedures
Identify, document, and support the resolution of deviations arising during qualification activities
Ensure qualification documentation complies with applicable quality, GMP, and data integrity requirements
Support performance qualification activities, including process, cleaning, or single-use material qualification
Work closely with validation, engineering, quality, manufacturing, and QC teams
Support other CQV-related activities as assigned
ABOUT YOU
Degree in Pharmaceutical Science, Life Sciences, Chemical Engineering, Biomedical Engineering, Instrumentation, Automation, or a related field
1 to 3 years of experience in commissioning, qualification, or validation within a pharmaceutical or similarly regulated environment
You have between 1 and 3 years of experience in commissioning, qualification, or validation within a pharmaceutical or similarly regulated environment
You have experience with QC equipment, production equipment, or HVAC qualification
You have knowledge or practical experience in computerized system validation
Experience in process validation, cleaning qualification, or single-use material qualification is an advantage
You are familiar with qualification documentation, including protocols, test scripts, deviations, and reports
You demonstrate strong attention to detail and a good understanding of quality and compliance requirements
You are able to follow approved procedures and document your work accurately
You work effectively with cross-functional stakeholders
You are fluent in English
Our organisation is a global HR consulting company dedicated to providing the full spectrum of HR-related services to our clients who range from small-medium enterprises (SME's) to multi-nationals and government agencies.
With 23 years of experience, we have grown our client base steadily with more than 300 successful engagements.
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