A Pharmaceutical Validation Engineer is an integral part of the pharmaceutical production team, ensuring the validity and reliability of manufacturing processes. This role focuses on validating processes, systems, and equipment used in drug development and production.

Responsibilities and Duties:

• Develop and execute validation plans for processes, systems, and equipment.

• Analyze and interpret validation test data and prepare detailed reports.

• Work closely with production and QA teams to address any issue identified during the validation process.

• Familiarize with US FDA and EU EMA regulatory requirements.

• Ensure all operations, processes, and methods comply with GMP, ISO and other relevant regulatory standards.

Qualifications and Skills:

• A Bachelor's degree in Pharmacy, Chemistry, Chemical Engineering, or a related field.

• At least two years of experience in process validation, pharmaceutical engineering, or related roles.

• Working knowledge of GMP and regulatory standards.

• Strong data analysis and report writing skills.

• Excellent problem-solving and teamwork skills.

Additional Requirements:

Candidates are expected to be highly detail-oriented, organized, and proactive. Regular travel may be required.

Benefits and Perks:

We offer a competitive salary package, health benefits, pension scheme, life insurance, and continuous professional development opportunities. Our work culture promotes work-life balance, inclusion, and collaboration.

Application Process:

To apply, submit a cover letter and resume to our email. Please use “Pharmaceutical Validation Engineer Application - "[Your Name]” as the subject of your email. Only candidates selected for interviews will be contacted.

Our company is an equal opportunity employer. We encourage applicants of different backgrounds, experiences, abilities, and perspectives to apply.

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