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Open nowPosted today

Validation & Compliance Specialist

MyCareersFuture94,660 open roles

Pay
SGD 4,000 – SGD 6,500 a month
Where
Singapore
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Your applicationOpen nowValidation & Compliance SpecialistMyCareersFuture · Singapore
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The clock on this job

Early applications get read.

8.0% of postings close within 7 days. Measured by our own scanner across the market. MyCareersFuture postings stay open a median of 3 days.

Share of postings closed within
  1. 1.6%1 day
  2. 3.5%3 days
  3. 8.0%7 days
  4. 14.9%14 days
  5. 34.0%30 days
This job: posted today

MyCareersFuture median: 3 days open

The posting

Responsibilities:

  • Hands-on experience and understanding of automated systems supporting manufacturing, IT infrastructure, Engineering and operations.
  • Strong understanding and applicable regulations (FDA/EU/ICH), with emphasis in 21 CFR Part 11, 210, 211, and 820 and local regulatory expectations.
  • Promoting GMP awareness and a culture of continuous improvement and facilitating manufacturing process improvements, laboratory operational excellence and validation activities, including latest trends in validation and best practices.
  • Assist in review and preparation of process/production equipment validation and computer systems validation
  • Review and approval of all Data Integrity – related activities and training including periodic reviews and status report to management
  • Improve and add to existic Data Integrity knowledge base, identify training requirements and serve as SME for the same
  • Serve as Validation Point of Contact and thus review all validation/qualification documents related to facilities, utilities and equipment.
  • Train all site personnel in validation area, provide training and prepare for both internal and external audit and investigations that follow
  • Hands on Computerized Systems Validation GAMP5/21CFR

Requirements:

  • Minimum 5 years in Quality Management Systems and Proficient in leading Validation, Computerized Systems/SDLC, Change Management, Manufacturing Quality, Deviation Investigation, Data integrity, Audits and Compliance, Documentation Control, Training Management and CAPA management
  • Minimum bachelor’s or master’s degree
  • GMP & GDP Certificate is plus
  • Well versed with Regulatory Guidelines – USFDA, EU GMP, PDA, PICS, 21CFR, BPE, ISPE, USP <1050>,GAMP5, ISO, WHO etc
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