Responsibilities:
-Ensure computerized systems validation is in compliance with GMP regulatory requirement
-Review and approve procedures, validation protocols and reports.
-Responsible for developing/maintenance of validation documents (facility validation master plan, project validation plan and strategy, installation and operational protocols for new equipment and protocol addendums)
-Provided computerized systems validation training to team members
-Experience in leading a team
-Skills required: planning skills, supervisory skills, communication skills.Requirements:
Candidate must possess at least a Bachelor's Degree, Post Graduate Diploma or Professional Degree in related field.
At least 5 year(s) of working experience in the related field is required for this position.
Preferably Senior Executives specializing in Biotechnology or equivalent.
Job role in Quality Control/Assurance or Supervisor/Team Lead.
Full-Time positions available.
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