Key Responsibilities

* Support the Operations team throughout the commissioning and Process Performance Qualification (PPQ) phases.

* Provide operational expertise for recipe creation, as well as batch record design and review.

* Oversee operations related to Media / Buffer preparation OR Extraction / Purification (including Grinder, Centrifuge, UF, Chrom, and Sterile filtration).

* Execute qualification protocols for loose equipment (e.g., spectrophotometers, incubators, fridges, and freezers)."

Key Deliverables

"• Designed and reviewed batch records and recipes.

* Completed loose equipment qualification protocols and reports.

* Operations readiness and support documentation for commissioning to PPQ phases."

Required Skills & Qualifications

* 5 to 8 years of experience in the pharmaceutical manufacturing industry.

* Familiarity with DeltaV and Manufacturing Execution Systems (MES).

* Strong background in manufacturing operations.

* Note: This is a 1.5 to 2-year contract role (starting with a 1-year contract with the possibility of extension).