VeristaHighlight
Summary
About the Role
About You
- Bachelor's degree in Engineering, Scientific field, Business, or relevant experience.
- 10+ years of relevant industry experience.
- Experience in Project Management, managing multiple small projects or large projects in excess of $500K.
- Strong written and verbal communication skills.
- Experience working in a fast-paced, results-driven organization.
- Broad knowledge of Commissioning, Qualification and Validation, process engineering, and Regulatory/Quality within Pharmaceutical manufacturing environments.
- A network of contacts within the pharmaceutical industry.
Benefits
- High growth potential and fast-paced organization with a people-focused culture.
- Competitive pay plus performance-based incentive programs.
- Company-paid Life, Short-Term, and Long-Term Disability Insurance.
- Medical, Dental & Vision insurances.
- 401(k) Retirement Plan (Employer Matching benefit).
- Paid Time Off (Rollover Option) and Holidays.
- Tuition Reimbursement.
- Team Social Activities.
- Paid Parental Leave and Bereavement.
Verista is a leading business and technology consultancy firm that provides systems, compliance, validation and quality solutions to life science companies - enabling them to improve health and improve lives. We help clients solve their most critical and complex challenges across the GxP lifecycle, from preclinical and clinical to commercialization, manufacturing and distribution – bringing together decades of knowledge, the most advanced engagement platforms and transformative technologies. This allows clients to benefit from the ease, efficiency and trust that results from working with one partner who excels across specialties. Verista’s clients trust the company’s 650+ experts to deliver consistent, safe, and high-quality results across the product development lifecycle. Verista is based in Fishers, Indiana, Wayne, Pennsylvania, Westford, Massachusetts, and San Mateo, California. For more information, visit www.verista.com