Must-Have Qualifications:

• Bachelor’s Degree in Engineering or related technical field
• 1–5+ years of experience in CQV, validation, or pharmaceutical/biotech manufacturing
• At least 1 year of hands-on experience in large-scale biotech manufacturing environments
• Experience working with:
• Pumps, bioreactors, or large stainless-steel equipment
• Strong experience with:
• IQ/OQ/PQ execution
• GMP documentation practices
• Ability to troubleshoot equipment and support real-time issues in the field
• Strong communication and cross-functional collaboration skills

Nice-to-Have Skills:

• Experience with Kneat validation software (or willingness to learn)
• Exposure to: Chromatography systems, UF/DF operations
• Background in: Chemical Engineering, Mechanical Engineering, Process Engineering
• Prior experien...