Validation Intern

Career Opportunities: Validation Intern (5381)

Requisition ID 5381 - Posted 04/15/2026 - Cranbury, NJ - United States

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Job Title - Validation Intern

Work Location - Cranbury NJ (Onsite)

About Us

Welcome to the epicenter of innovation in healthcare! At Wuxi Biologics MFG18, in Cranbury New Jersey, we''re not just about making medications; we''re on a mission to rewrite the future of medicine. Picture a place where science fiction meets reality, and breakthroughs happen daily. That''s us!

Job Summary

Are you ready to dive into the heart of biopharmaceutical magic? Join us for an electrifying summer as an Engineering Document Specialist Intern! As part of our squad, you''ll be at the forefront of cutting-edge discoveries, tinkering with processes that could change lives. Buckle up for an adrenaline-fueled ride through the world of biotech!

Job Responsibilities

• Assist the Engineering team with documentation processes.
• Organize and archive Engineering documents.
• Digitizing Engineering documents to prepare them for off-site storage.
• Assist Engineering staff with in the field validation activities, including trouble shooting.
• Assist Engineering staff with protocol execution reviews.
• Internships are your chance to shine. Depending on your skills and interests, you might tackle projects usually reserved for seasoned pros, giving you a taste of what it''s like to be a biopharma professional.

Qualificatoins

Familiarity with Microsoft Office Applications.

Strong communication skills.

• Ability to self-teach from technical manuals and documentation.
• Interest in gaining knowledge in the Validation Engineering process.
• Currently possess unrestricted authorization to work in the United States
• Progress towards a Bachelor's degree program in a discipline utilizing technical document, investigative, and instrument skills, with a minimum GPA of at least 3.0.
• Ability to work 40hrs per week during the term (June to August/September)

Perks of a Co-Op/Internship Position:

• Dive into hands-on experiences in our state-of-the-art facility.
• Gain insights from industry titans and level up your skills faster than you can say "biopharmaceutical."
• Gain invaluable exposure to industry giants as we collaborate with leading global biopharmaceutical clients.
• Experience the prestige of working alongside top players in the field, enriching your internship journey with unparalleled opportunities for learning and professional growth.

The pay range for this internship depends on level of education. Pay range - $20-30hr

The job description does not intend to list all the duties and responsibilities assigned to this position. Employees in this position would be required to perform other job-related duties/responsibilities based on their expertise and company business needs.

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Job Title - Validation Intern

Work Location - Cranbury NJ (Onsite)

About Us

Welcome to the epicenter of innovation in healthcare! At Wuxi Biologics MFG18, in Cranbury New Jersey, we''re not just about making medications; we''re on a mission to rewrite the future of medicine. Picture a place where science fiction meets reality, and breakthroughs happen daily. That''s us!

Job Summary

Are you ready to dive into the heart of biopharmaceutical magic? Join us for an electrifying summer as an Engineering Document Specialist Intern! As part of our squad, you''ll be at the forefront of cutting-edge discoveries, tinkering with processes that could change lives. Buckle up for an adrenaline-fueled ride through the world of biotech!

Job Responsibilities

• Assist the Engineering team with documentation processes.
• Organize and archive Engineering documents.
• Digitizing Engineering documents to prepare them for off-site storage.
• Assist Engineering staff with in the field validation activities, including trouble shooting.
• Assist Engineering staff with protocol execution reviews.
• Internships are your chance to shine. Depending on your skills and interests, you might tackle projects usually reserved for seasoned pros, giving you a taste of what it''s like to be a biopharma professional.

Qualificatoins

Familiarity with Microsoft Office Applications.

Strong communication skills.

• Ability to self-teach from technical manuals and documentation.
• Interest in gaining knowledge in the Validation Engineering process.
• Currently possess unrestricted authorization to work in the United States
• Progress towards a Bachelor's degree program in a discipline utilizing technical document, investigative, and instrument skills, with a minimum GPA of at least 3.0.
• Ability to work 40hrs per week during the term (June to August/September)

Perks of a Co-Op/Internship Position:

• Dive into hands-on experiences in our state-of-the-art facility.
• Gain insights from industry titans and level up your skills faster than you can say "biopharmaceutical."
• Gain invaluable exposure to industry giants as we collaborate with leading global biopharmaceutical clients.
• Experience the prestige of working alongside top players in the field, enriching your internship journey with unparalleled opportunities for learning and professional growth.

The pay range for this internship depends on level of education. Pay range - $20-30hr

The job description does not intend to list all the duties and responsibilities assigned to this position. Employees in this position would be required to perform other job-related duties/responsibilities based on their expertise and company business needs.