About this role
Responsible for adhering to Cleaning Validation Master Plans and ensuring risk-based cleaning policies comply with GMP standards. The role involves generating and executing protocols for equipment re-qualification and providing quality oversight for API and Biologics manufacturing facilities.
Requires a degree in Science, Engineering, or Pharmacy with at least 3 years of relevant work experience. Essential knowledge of pharmaceutical regulatory requirements (GMP) is required, with a preference for experience in Risk Based Cleaning Validation lifecycles.
What they're looking for
Cleaning ValidationGMP ComplianceRisk Based ValidationEquipment QualificationProtocol GenerationCAPAChange ManagementDeviation Investigation
Frequently asked questions
What does a Validation Engineer II (Cleaning) at AbbVie do?
Responsible for adhering to Cleaning Validation Master Plans and ensuring risk-based cleaning policies comply with GMP standards. The role involves generating and executing protocols for equipment re-qualification and providing quality oversight for API and Biologics manufacturing facilities. Requir…
What skills does this Validation Engineer II (Cleaning) role need?
Key skills for this role include Cleaning Validation, GMP Compliance, Risk Based Validation, Equipment Qualification, Protocol Generation, CAPA.
How much does a Validation Engineer II (Cleaning) at AbbVie pay?
The employer did not list a salary for this role. Most similar Singapore roles publish their band on the job page.
Is this Validation Engineer II (Cleaning) role remote, hybrid, or on-site?
This role is on-site, based in Singapore.
How do I apply for this Validation Engineer II (Cleaning) role?
You can apply directly on AbbVie's careers page. ApplyLah can tailor your résumé and cover letter to this exact role in seconds first.