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Recruit Express Pte Ltd

QA Specialist (Pharma) - 6months / NORTH #HHL

Early Applicant
  • 8 days ago
  • Be among the first 50 applicants

Job Description

Contract Duration: 6 months
Working Hours: Monday to Friday, office hour
Location: Kranji
Start Date: ASAP

Salary: 6000-8000

Responsibilities :

  • Support site projects on Qualification/Validation.
  • Review and approve Quality Control related protocols, reports, procedures, and other documents.
  • Evaluate and approve discrepancies related to qualification/validation protocols.
  • Collaborate and participate in projects as a Quality Representative for Quality Systems and Validation.
  • Provide validation expertise and support for Analytical Instrument Qualification, Analytical and Microbiology Method Validation, and Critical Reagent Qualification.
  • Ensure information in approved qualification/validation documents is understandable and defendable during inspections.
  • Provide quality oversight on Quality Control validation maintenance activities and the Master Validation Plan.
  • Support multisite initiatives to harmonize Quality Systems and qualification/validation activities between plants.
  • Build strong partnerships with other departments to ensure open communication and acceptance.
  • Adhere to applicable EHS requirements.
  • Commit to fair and respectful relationships and behavior in accordance with the company's Code of Conduct.
  • Perform other duties as assigned by the Manager/Supervisor.

Education and Experience Requirements:

  • Min. Degree in pharmaceutical sciences, life sciences, biology, biotechnology, chemistry, chemical engineering, engineering, or a related discipline.
  • Additional certifications and training such as Certified Quality Engineer or specific Validation topics are advantageous.
  • Minimum of 2-3 years of experience in the pharmaceutical or biotechnology industry in quality assurance, manufacturing operations, or validation, ideally in a multinational company.
  • Hands-on experience in performing equipment, process, cleaning, computer systems, and shipping validation is advantageous.
  • Knowledge of FDA/EU cGMP validation requirements/expectations (e.g., CFR 21 part 11, PAT) and ICH guidelines.

Interested candidates, do submit your resume to [Confidential Information] or telegram @alexgohhl

-

Alex Goh Hock Leong

(CEI.No: R1763413 l Recruit Express Pte Ltd (Healthcare & Life Science) | 99C4599)

[HIDDEN TEXT]

Date Posted: 16/11/2024

Job ID: 100516261

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