Job Description

Job Description

PLEASE NOTE WE DO NOT WORK ON C2C BASIS

Open to Candidates with citizenship from the US and Canada

Role Summary

We’re seeking an experienced and hands-on engineering professional to support the design, implementation, and documentation of equipment and processes for automated syringe assembly and packaging. This position will contribute to cross-functional technical transfer initiatives, process optimization, and documentation development in a regulated environment.

Documentation & SOP Development

• Author and revise SOPs for flexible operating parameters and process requirements
• Draft SOPs and six Work Instructions (WIs) for recipe development
• Update Engineering Equipment Assessment SOPs to ensure alignment with process requirements
• Perform technical writing tasks including regulatory document reviews, specifications, and training content creation

Operational & Material Coordination

• Support onboarding of materials and vendors into relevant systems
• Coordinate material movement and inventory management activities with Procurement, Warehouse, and Operations
• Prepare and process move order requests and onboarding documentation

🎓 Qualifications & Skills

• Bachelor’s degree in Engineering or a related technical field (preferred)
• Min 3 years experience in regulated manufacturing environments (e.g., pharmaceutical, biotech, medical devices)
• Proficiency in SOP development and technical writing
• Strong data analysis and cross-functional collaboration skills
• Familiarity with equipment qualification, process validation, and packaging automation

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