Validation Intern

WuXi Biologics Group; New Jersey; On-site; USD 27,552 - 41,328; Part time

Benefits offered by this job

Hands-on experience in state-of-the-art facility

Insights from industry professionals

Exposure to leading global biopharmaceutical clients

Professional growth opportunities

Job summary

WuXi Biologics Group in Cranbury, New Jersey, is seeking an Engineering Document Specialist Intern for the summer term. This role involves supporting the Engineering team with documentation, organizing, and digitizing records, along with assisting in validation processes. Interns will engage in meaningful projects, gaining exposure to the biopharmaceutical industry. Candidates should be pursuing a Bachelor's degree with at least a 3.0 GPA and have unrestricted work authorization in the U.S. Pay is between $20-$30 per hour.

Qualifications

• Minimum GPA of at least 3.0.
• Ability to work 40 hours per week during the internship term.

Responsibilities

• Assist the Engineering team with documentation processes.
• Organize and archive Engineering documents.
• Digitize Engineering documents for off-site storage.
• Assist with in-field validation activities.
• Support protocol execution reviews.

Skills

Familiarity with Microsoft Office Applications

Ability to self-teach from technical manuals

Interest in Validation Engineering process

Education

Progress toward a Bachelor’s degree

Job description

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.
• Digitize Engineering documents to prepare them for off‑site storage.
• Assist Engineering staff with in‑field validation activities, including troubleshooting.
• 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.

Familiarity with Microsoft Office Applications.

• 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 toward 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 40 hours 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–$30 per hour.

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.