Validation Specialist - QA
Summary:
Prepare and implement all validation activities including: process, cleaning and computer system validation, quality risk management activities, qualification activities, and change management activities before being presented to validation lead for final revision and approval.
Job requirements:
Prepare validation activities plans and issue
protocol that comply with regulatory requirements and company policy.
Witness and follow up validation runs execution,
collect all necessary data and register and assess any anomalies.
Issue validation report, communicate validation
outcome with management and concerned stakeholders and archive reports.
Register, communicate and assess any changes will be conducted in
site prior change execution and track execution of change actions.
Raise deviation and NCR risk assessment and review CAPAs relevant to
validation activities.
Register and evaluate identified current or potential quality
risks, suggest with key stakeholders proper mitigation actions and re-evaluate
risk after their implementation.
Provide periodical reports to superior with appropriate analysis
regarding all validation updates to ensure effective and accurate updated
records.
Fulfill other related tasks as asked by management and as arising
from the business.
Qualifications:
B.Sc.
Degree in Pharmaceutical Science, Science or Engineering.
Years of Experience:
1
Posting Date:
18 January 2022
Application End Date:
2 February 2022
Available Vacancies:
1
Job Level:
Specialist
Function:
QA - Validation
apply
Go Back