- Singapore
全职 Validation Engineer (MNC-pharmaceutical) 工作, 薪水 up to SGD 6,000, RRECRUITER INT PTE. LTD. 公司招聘中 - Ricebowl
分享
保存
工作地点
职位描述
岗位职责
Key Responsibilities
Execute CQV activities for GMP-regulated pharmaceutical and biopharmaceutical facilities.
Prepare and review validation documents, including plans, IQ/OQ/PQ protocols, test scripts, and reports.
Support validation of equipment, utilities, facilities, and computerized systems in compliance with GMP, GAMP 5, and 21 CFR Part 11.
Coordinate with Engineering, QA, clients, and vendors on validation activities.
Conduct risk/impact assessments, deviation investigations, and CAPA.
Support FAT, SAT, commissioning, and qualification of new equipment and systems.
Maintain accurate validation records and data integrity.
Requirements
Bachelor’s Degree in Engineering, Life Sciences, Pharmaceutical Sciences, or related field.
3–5 years of CQV/validation experience in pharmaceutical or biopharmaceutical industries.
Strong documentation, analytical, problem-solving, and communication skills.
Experience with equipment, utilities, cleanrooms, HVAC, water systems, or CSV is preferred.
Knowledge of FDA 21 CFR Part 11, EU GMP, GMP, GAMP 5, and data integrity.
For interested applicant, kindly send your resume in Word/PDF format, include the following informations:
1. Current Salary
2. Expected Salary
3. Availability
4. Reason for leaving
Thank you for your application and we regret that only shortlisted applicants will be notified
By submitting any application or resume to us, you will be deemed to have agreed & consented to us collecting, using, retaining & disclosing your personal information to prospective employers with the services provided by us.
VU TRA MY | R25158108
RRECRUITER INT PTE. LTD. | 22C1414
OUR PASSION
Is to deliver OUTSTANDING customer service
To the companies and candidates that we PARTNER !!
Developing long term and mutually beneficial relationships is the key to our success.
Extensive experience in sourcing and selecting for key positions
Recruitment Experts in Singapore, Thailand, Vietnam, Philippines & Indonesia market
Execute CQV activities for GMP-regulated pharmaceutical and biopharmaceutical facilities.
Prepare and review validation documents, including plans, IQ/OQ/PQ protocols, test scripts, and reports.
Support validation of equipment, utilities, facilities, and computerized systems in compliance with GMP, GAMP 5, and 21 CFR Part 11.
Coordinate with Engineering, QA, clients, and vendors on validation activities.
Conduct risk/impact assessments, deviation investigations, and CAPA.
Support FAT, SAT, commissioning, and qualification of new equipment and systems.
Maintain accurate validation records and data integrity.
Requirements
Bachelor’s Degree in Engineering, Life Sciences, Pharmaceutical Sciences, or related field.
3–5 years of CQV/validation experience in pharmaceutical or biopharmaceutical industries.
Strong documentation, analytical, problem-solving, and communication skills.
Experience with equipment, utilities, cleanrooms, HVAC, water systems, or CSV is preferred.
Knowledge of FDA 21 CFR Part 11, EU GMP, GMP, GAMP 5, and data integrity.
For interested applicant, kindly send your resume in Word/PDF format, include the following informations:
1. Current Salary
2. Expected Salary
3. Availability
4. Reason for leaving
Thank you for your application and we regret that only shortlisted applicants will be notified
By submitting any application or resume to us, you will be deemed to have agreed & consented to us collecting, using, retaining & disclosing your personal information to prospective employers with the services provided by us.
VU TRA MY | R25158108
RRECRUITER INT PTE. LTD. | 22C1414
OUR PASSION
Is to deliver OUTSTANDING customer service
To the companies and candidates that we PARTNER !!
Developing long term and mutually beneficial relationships is the key to our success.
Extensive experience in sourcing and selecting for key positions
Recruitment Experts in Singapore, Thailand, Vietnam, Philippines & Indonesia market
重要安全守则
申请工作时，切勿提供您的银行或信用卡详细资料。不要转账或完成无关的在线调查问卷。如果您发现可疑内容，请举报此招聘广告。
了解更多