19 часов назад
Entry Level Associate Project Manager (Biopharmaceutical Product Testing)
Мэтч & Сопровод
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Описание вакансии
Текст:
TL;DR
Entry Level Associate Project Manager (Biopharmaceutical Product Testing) (GMP/CMC): Planning and coordinating GMP-compliant biopharmaceutical testing projects in a regulated laboratory environment with an accent on client delivery, regulatory compliance, and cross-functional coordination. Focus on tracking schedules and financial performance, mitigating project risks, managing investigations, and reporting KPIs to stakeholders.
Location: Lancaster, Pennsylvania, USA; candidates must live within a commutable distance. Full-time, Monday–Friday, 8:00 a.m.–4:00 p.m., with additional hours as needed.
Company
Scientific provides analytical testing, laboratory, clinical diagnostics, and contract research services across pharmaceutical, food, environmental, cosmetics, and life sciences industries.
What you will do
- Plan, coordinate, and manage multiple GMP testing projects from initiation through closure.
- Build and maintain schedules, action trackers, dashboards, turnaround-time metrics, and schedule variance reports.
- Monitor project progress, identify risks, implement mitigation plans, and ensure timely delivery of compliant results.
- Act as the primary client contact and facilitate project kickoffs, status calls, technical visits, closure meetings, and business reviews.
- Track FTE utilization, planned versus actual hours, budget variance, and cash flow.
- Coordinate with Operations, QA, Sample Registration, Pricing, Business Development, partner sites, and subcontractors.
Requirements
- Bachelor’s degree in Chemistry, Biology, Pharmaceutical Sciences, or a related field.
- Background in pharmaceutical sciences, analytical chemistry, or biologics, with experience in GMP laboratory operations, especially CMC testing.
- Ability to manage complex projects and cross-functional teams, with strong organizational, time-management, communication, and stakeholder-management skills.
- Knowledge of GMP regulations, including 21 CFR Part 210/211 and EU GMP, as well as GLP, regulatory requirements, and quality standards.
- Proficiency with project management tools such as MS Project and Smartsheet.
- Must be authorized to work in the United States indefinitely without restriction or sponsorship.
Culture & Benefits
- Work in a regulated laboratory environment supporting pharmaceutical and biopharmaceutical testing.
- Medical coverage, dental and vision options, and life and disability insurance.
- 401(k) plan with company match.
- Paid holidays and vacation.
- Collaboration with international sites and cross-functional laboratory teams.
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