An agile career and dynamic working culture in a global life sciences leader.
An inclusive and ethical workplace that values diversity and integrity.
Competitive compensation programs that recognize high performance.
Professional growth opportunities through cross-functional projects and global exposure.
Comprehensive medical insurance, with the option to enroll family members at partially subsidized premiums.
Company transport provided from designated MRT locations to and from the Tuas site.
Access to Lonza's full suite of employee benefits:
What you'll do
Provides QA oversight to QC/DS laboratory services
Review and approval of protocols and reports.
Provide QA oversight in deviation investigation, discrepancy reports and CAPA implementation.
Participate actively, utilizing Root Cause Analysis tools to enable effective and timely closure of records.
Provides Quality Change Request oversight for Lab service changes.
Liaise with cross functions, communicating information and updates in timely manner
Develops good working relationships with internal & external customers.
Participate in cross-functional walk down and provide feedback
Develop skills to be Qualified Trainer in area of expertise
Develop skills to front auditors as SME/ supporting QA oversight
What we're looking for
Bachelor's degree with significant years experience in Quality Assurance in the Biopharmaceutical industry.
Familiarity with Regulatory requirements and local Codes & Standards (eg. FDA, EMA and ICH Quality Guidelines)
Fair knowledge and experience of the practical and theoretical requirement of quality management system in a GMP facility.
Able to operate independently with minimum supervision for routine work within established policies and procedures and receives detailed instructions on new projects and assignments.
Meticulous and Systematic.
Team player, with strong focus on safety, quality and timelines.
