MSD-posted 4 months ago
$39,600 - $105,500/Yr
Intern
5,001-10,000 employees

The Future Talent Program features internships that last up to 12 weeks and will include one or more projects. These opportunities in our Research and Development Division can provide you with great development and a chance to see if we are the right company for your long-term goals. Our company's Global Pharmacovigilance Quality (PV QA) team is focused on advancing patient care and promoting safe and effective use of our companies' medicinal products and vaccines. The team ensures that the pharmacovigilance (PV) activities performed by Research and Development and Human Health (HH) comply with the relevant procedures and regulations across the globe. Quality assurance, including auditing, is a critical function in the pharmaceutical industry. In pharmacovigilance effective audits focus on compliance with regulatory requirements, data integrity and patient safety. Audits may identify and resolve compliance issues in a timely manner preventing negative outcomes of regulatory inspections. Global Pharmacovigilance Quality also engages in providing support to the business through partnership with key business stakeholders, process improvement and more. The position is anticipated to be located at our company Rahway, NJ site. The Global Pharmacovigilance Quality intern will have the opportunity to interact with the Quality Assurance Leadership Team, exposing the intern to a broad perspective on quality throughout the drug development continuum. They will also: Gain an understanding of the phases of drug development. Gain an understanding of the importance of quality in ensuring the rights and well-being of patients and the welfare of animals; helping to meet the intent of global regulatory requirements through robust processes and procedures; and ensuring subject, company, and regulator confidence and public trust in our company. Interact with our company employees who have broad experience across the pharmaceutical industry.

  • Gain an understanding of the phases of drug development.
  • Gain an understanding of the importance of quality in ensuring the rights and well-being of patients and the welfare of animals.
  • Help meet the intent of global regulatory requirements through robust processes and procedures.
  • Ensure subject, company, and regulator confidence and public trust in the company.
  • Interact with company employees who have broad experience across the pharmaceutical industry.
  • Candidates must have completed at least two (2) years of study toward a Bachelor’s degree by June 2026.
  • Candidates must be a current student (sophomore, junior or senior) enrolled in a B.S. or graduate student enrolled in an M.S. in Scientific/Public Health/Nursing/Epidemiology or related field.
  • Candidates must have an interest in Biology/Chemistry, Health Care, Health Science or Pharmacy.
  • Candidates must have strong organizational skills.
  • Candidates must have demonstrated ability to take initiative and own deliverables.
  • Candidates must have demonstrated interpersonal skills including flexibility, collaboration and inclusion skills, and ability to work in a team environment.
  • Candidates must have demonstrated the capability to develop innovative solutions to challenges.
  • Candidates must have strong written and verbal communication skills.
  • Experience with or exposure to the development of dashboards, analytics or other systems.
  • Proficiency with Microsoft Office tools (Outlook, Word, Excel, PowerPoint, Teams).
  • Advanced Excel, Word, PowerApps, Photoshop, Illustrator, or InDesign skills.
  • Project Management skills.
  • Experience with document management systems (e.g. FirstDoc, Veeva, Documentum, SharePoint).
  • Salary range: $39,600.00-$105,500.00 USD
  • Hybrid work model with three days on-site per week.
  • Equal Employment Opportunity Employer.
© 2024 Teal Labs, Inc
Privacy PolicyTerms of Service