jobs in EFOR

EFOR Hiring! Full Time QA Operations - Validation Consultant in - Ricebowl

QA Operations - Validation Consultant

EFOR

Undisclosed

Singapore

Share
Save

Working Location

  • Singapore

Job Description

Responsibilities

Consultant – QA Operations & Validation | Singapore


Are you passionate about quality in pharmaceutical manufacturing ? As a Consultant and ambassador for our company, you will play a key role in supporting our clients’ operational quality assurance and validation processes. Join us in Singapore to help drive excellence and compliance in a fast-paced, regulated environment.


Your Responsibilities:


  • Provide on-the-floor Quality Assurance (QA Ops) support to manufacturing operations, ensuring compliance with GMP and internal quality standards
  • Review and support batch records, production documentation, and release activities
  • Investigate and manage deviations, non-conformities, and implement CAPA (Corrective and Preventive Actions)
  • Support and participate in regulatory and internal inspections, and readiness activities
  • Draft, review, and approve quality and validation documentation
  • Define, write, and execute validation protocols (IQ, OQ, PQ) for equipment, processes, cleaning, or computerized systems
  • Plan, coordinate, and follow up validation activities with all stakeholders (production, engineering, laboratories, etc.)
  • Perform risk assessments and contribute to change control and impact analysis
  • Support continuous improvement initiatives in QA operations and validation practices
  • Organize and lead meetings, communicate findings, and train operational teams on quality and validation topics


Your Profile:


  • Degree in Engineering, Pharmacy, Life Sciences, or equivalent
  • At least 3 years’ experience in QA Operations and/or Validation within the pharmaceutical or biotech industry
  • Strong knowledge of GMP and pharmaceutical regulations
  • Experience in batch release, deviation management, and quality documentation
  • Proficient in validation protocols and qualification activities (IQ/OQ/PQ)
  • Excellent communication and teamwork skills
  • Fluent in English (written and spoken)


Ready to play a key part in supporting pharmaceutical quality and regulatory compliance in Singapore ?


Apply now and join a dynamic international team !

Important Information

Never provide your bank or credit card details when applying for jobs. Do not transfer any money or complete unrelated online surveys. If you see something suspicious, Report this Job ad.

Learn More