This position is no longer open for applications

The Opportunity

· Adecco is partnering with a well-established Pharmaceutical company

· The role works together with management and cross functional department

· Work within dynamic environment



The Talent

· Degree in Chemical Engineering or any Science related discipline

· Minimally to have 2 years of Quality Assurance experience in Pharmaceutical industry

· Familiar with Batch Release, deviation, change control and Product review

· Familiar with SAP, LIMS or Trackwise system

· Good knowledge of GMP compliance

· Understanding of ISO 9001, FSSC and HACCP proceed is good to have

· Confident in taking up this role, working independently




The Job

· Responsible to review and approve master batch records and subsequent batch records, packaging and labeling of intermediates and active pharmaceutical ingredients (API),

· Ensure batches produced are compliance with company’s quality standards and regulatory registered specifications.

· Disposition the intermediates and API

· Ensure timely delivery of quality products by working with Supply Chain and Drug product sites

· Ensure impact assessment is adequate and thorough by involving in change control process with cross functional subject matter expert

· Review and approve cleaning records and procedures

· Improve quality assurance systems

· Review and approve deviations according to the site procedures, participating with cross functional team in analysis, performing the impact assessment with the subject matter experts for quality, validation and/ or regulatory impact, ensuring the adequacy of the associated corrective actions and/or preventive actions

· Reviewing and approving the investigation reports

· Handle and investigate product complaints thoroughly with CAPAs effective to prevent recurrence.

· Maintain quality tracking systems and the quality metrics to identify trends and atypical observations.

· Prepare Annual Product Record Reviews, discuss trends & atypical observations and recommend improvement actions.

· Conduct internal audits, ensuring the internal controls are effective.

· Conduct external audits to ensure adequate oversight to suppliers/ service providers and collaborate with supplier to reduce starting material quality issues.

· Participate in GMP walk downs, ensuring site operation and facility is always inspection ready state.

· Participate/ lead continuous improvement project to improve work processes and quality system.

· Other duties and activities as required




Next Steps

Prepare your updated resume (please include your current salary package with full breakdown such as base, incentives, annual wage supplement, expected package and reason for leaving.)

To apply online, please click on the link and contact us to follow-up. Alternatively, please send your resume to technicalstaffing@adecco.com.

For confidential discussion, please contact Patricia Teo (Reg.No: R1873997) at Tel: 6697 7912




All shortlisted candidates will be contacted. All the best!