About this role
Provide quality oversight to the manufacturing team to ensure GMP compliance and adherence to quality systems. Responsibilities include reviewing batch records, managing investigations, and supporting regulatory inspections.
Requires a degree in pharmaceutical, life sciences, or a related engineering discipline. Preference is given to candidates with 0-2 years of experience in QA, GMP compliance, or biotech manufacturing.
What they're looking for
Quality SystemsGMP ComplianceRegulatory RequirementsProduct ReleaseProblem SolvingCommunicationDocumentation PracticesInvestigation Management
Frequently asked questions
What does a Quality Operations Specialist I/II at Takeda do?
Provide quality oversight to the manufacturing team to ensure GMP compliance and adherence to quality systems. Responsibilities include reviewing batch records, managing investigations, and supporting regulatory inspections. Requires a degree in pharmaceutical, life sciences, or a related engineerin…
What skills does this Quality Operations Specialist I/II role need?
Key skills for this role include Quality Systems, GMP Compliance, Regulatory Requirements, Product Release, Problem Solving, Communication.
How much does a Quality Operations Specialist I/II at Takeda pay?
The employer did not list a salary for this role. Most similar Singapore roles publish their band on the job page.
Is this Quality Operations Specialist I/II role remote, hybrid, or on-site?
This role is on-site, based in Singapore.
How do I apply for this Quality Operations Specialist I/II role?
You can apply directly on Takeda's careers page. ApplyLah can tailor your résumé and cover letter to this exact role in seconds first.