The Role
The Senior Engineer supports pharmaceutical and biotech final-product packaging and manufacturing. Responsibilities include evaluating primary and secondary packaging materials, applying GMP and GDP standards, conducting distribution and technical testing, writing protocols, performing technical evaluations, and preparing reports supporting packaging component selection. The role requires project management, problem-solving, communication, teamwork, and adaptability in an evolving environment.
Summary Generated by Built In
• General packaging/engineering experience in final product manufacturing within the Pharma/Biotech Industry.
• Excellent understanding of Good Manufacturing Practices (GMP) and Good Documentation Practices (GDP).
• Strong knowledge of common materials used in pharmaceutical primary and secondary packaging (bottles, labels, trays, lidding material, leaflets, paperboard, sterile barrier packaging, corrugate, etc.).
• Familiar with distribution testing per ASTM D4169 and ASTM, ISO, TAPPI, USP and EP testing standards.
• Strong interpersonal, project management, technical problem solving and communication (written and verbal) skills.
• Ability to work in teams and adapt to a continuously evolving environment.
• Ability and experience writing test protocols, performing technical evaluations and testing to support reports used to uphold the use of selected materials and packaging components.
Requirements
Doctorate OR -Masters + 2 years of Engineering experience OR -Bachelors in Engineering + 4 years of Engineering experience
Skills Required
- Doctorate in Engineering
- Master’s degree in Engineering plus 2 years of engineering experience
- Bachelor’s degree in Engineering plus 4 years of engineering experience
- General packaging or engineering experience in final-product manufacturing within the pharmaceutical or biotech industry
- Excellent understanding of Good Manufacturing Practices and Good Documentation Practices
- Strong knowledge of pharmaceutical primary and secondary packaging materials
- Familiarity with distribution testing and ASTM, ISO, TAPPI, USP, and EP testing standards
- Experience writing test protocols and performing technical evaluations and testing
- Strong interpersonal, project management, technical problem-solving, and written and verbal communication skills
- Ability to work in teams and adapt to a continuously evolving environment
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The Company
What We Do
ISPV Inc. is a Life Science company that leads Productivity & Validation projects for the Pharmaceutical and Food industries.
