Biologics Manufacturing Ops & Tech Intern

MSD

Wilmington (DE)

On-site

USD 40,000 - 111,000

Full time

14 days+
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Job summary

MSD offers a Future Talent Program internship lasting up to 12 weeks at the Wilmington, Delaware site, focused on Biologics Manufacturing Operations and Technical Operations Support. Interns may work on drug substance or drug product lines and collaborate with cross‑functional teams to optimize processes.

The program includes exposure to project management, cGMP practices, and opportunities to contribute to safety and compliance initiatives within our Global Biologics Organization.

Qualifications

  • Candidates should have pharmaceutical or biologics manufacturing‑related experience.
  • Candidates should have strong collaboration skills, strong communication skills, lean six sigma experience/ knowledge, and strong project management skills.
  • Candidates should have knowledge of current Good Manufacturing Practices (cGMPs), some data analytics experience, and strong problem‑solving skills.

Responsibilities

  • Work as part of the team starting up the manufacturing plant.
  • Work could be in either a drug substance or a drug product manufacturing line.
  • Collaborate with cross‑functional teams to improve and/or optimize manufacturing processes.
  • Support/lead projects directly tied to improving the safety and/or compliance performance of the manufacturing areas.

Skills

Collaboration skills
Communication skills
Lean six sigma experience
Project management skills

Education

Pursuing associate/bachelor/master degree in Engineering or related science

Job description

MSD offers a Future Talent Program internship lasting up to 12 weeks at the Wilmington, Delaware site, focused on Biologics Manufacturing Operations and Technical Operations Support. Interns may work on drug substance or drug product lines and collaborate with cross‑functional teams to optimize processes.

The program includes exposure to project management, cGMP practices, and opportunities to contribute to safety and compliance initiatives within our Global Biologics Organization.

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