2026 Future Talent Program - Assoc. Spclst, Quality Assurance - Rotational Program

Merck Sharp & Dohme Corp

West Point, Pennsylvania, United States
Base: $70,500.00 - $110,900.00; bonus/equity: annu...
Hybrid (3 days on-site, 1 day remote)
Bachelor's degree in engineering or sciences
Willing to work alternate shifts and weekends
Visual inspection of vials and syringes
Merck Sharp & Dohme Corp is seeking candidates for its 2026 Future Talent Program as an Associate Specialist in Quality Assurance within a rotational program. This entry-level position offers hands-on experience in pharmaceutical quality assurance, focusing on vaccine manufacturing, with opportunities for mentorship and career development

Job Summary

  • This entry-level 2-year rotational program provides hands-on experience in pharmaceutical quality assurance at Merck's largest vaccine manufacturing plant.
  • The role involves direct shop floor support including visual inspections, line clearance verification, and GMP documentation review for 24/7 operations.
  • Successful candidates will be eligible for an annual bonus, long-term incentives, and a comprehensive benefits package including medical, dental, vision, and 401(k).

Matching Summary

Match Score: 85

Merck Sharp & Dohme Corp is seeking candidates for its 2026 Future Talent Program as an Associate Specialist in Quality Assurance within a rotational program. This entry-level position offers hands-on experience in pharmaceutical quality assurance, focusing on vaccine manufacturing, with opportunities for mentorship and career development.

Salary

Base: $70,500.00 - $110,900.00; Bonus/Equity: Annual bonus and long-term incentive eligible; Benefits: Medical, dental, vision, 401(k), paid holidays, vacation

Skills & Requirements

Must-have

  • Bachelor's Degree in Engineering or Sciences
  • Willing to work alternate shifts and weekends
  • Visual inspection of vials and syringes
  • GMP document and batch record review
  • Line clearance verification between batches

Nice-to-have

  • Experience using Lean/Six Sigma tools
  • 0-2 years cGMP pharmaceutical environment experience
  • Strong analytical and organizational skills
  • Ability to enact conflict resolution
  • High personal integrity and credibility

Key Requirements

  • Bachelor's Degree in Engineering or Sciences
  • 0-2 years pharmaceutical industry experience preferred
  • US and Puerto Rico Residents Only
  • No VISA Sponsorship available

Work Rights

US and Puerto Rico Residents Only

Tailored Resume

Cover Letter