9 дней назад
PLS Project Manager II (Pharmaceutical Analytical Outsourcing)
Мэтч & Сопровод
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Описание вакансии
Текст:
TL;DR
PLS Project Manager II (Pharmaceutical Analytical Outsourcing): Managing complex pharmaceutical analytical testing projects across laboratory, QA, sales, and client teams with an accent on project planning, scientific data interpretation, regulatory compliance, and customer communication. Focus on coordinating milestones and resources, resolving quality investigations and CAPAs, maintaining LIMS and project documentation, and communicating risks and recommendations.
Location: Morrisville, NC, United States; hybrid schedule, Monday–Friday, 8:30 a.m.–5:00 p.m.
Company
Pace Life Sciences provides analytical testing and laboratory services supporting pharmaceutical and life sciences organizations.
What you will do
- Develop and manage project plans, timelines, budgets, milestones, and deliverables for complex analytical testing projects.
- Act as the primary client liaison, leading meetings, providing updates, managing scope changes, and communicating risks with recommendations.
- Coordinate laboratory, QA, sales, and operational resources across analytical outsourcing laboratories in Minnesota, New Jersey, North Carolina, and Puerto Rico.
- Manage sample coordination, LIMS updates, project documentation, cost details, client information, and testing initiation.
- Provide scientific data analysis and interpretation while supporting investigations, CAPAs, forecasting, and account health tracking.
- Guide project team members and identify opportunities to improve processes and implement best practices.
Requirements
- Bachelor’s degree in Chemistry, Biology, Biochemistry, or a related scientific field; an advanced degree is preferred.
- At least four years of experience in project management or technical operations, preferably in analytical testing or a laboratory environment.
- Extensive knowledge of analytical testing methodologies, instrumentation, and laboratory operations.
- Ability to interpret and communicate complex scientific data and manage multiple complex projects.
- Proficiency in Microsoft Office Suite and strong organizational, communication, client service, and collaboration skills.
- Ability to work in a fast-paced environment while maintaining professionalism, discretion, quality, regulatory, and Environmental Health and Safety requirements.
Nice to have
- PMP certification.
- Familiarity with pharmaceutical industry standards and analytical testing requirements.
- Experience with regulatory compliance and quality systems such as ISO and GLP.
Culture & Benefits
- Full-time employment with medical, dental, vision, life, disability, and voluntary benefits.
- 401(k) retirement savings plan with immediate vesting in the employer match.
- Paid holidays, sick leave, vacation days, parental leave, and an Employee Assistance Program.
- HSA, flexible spending accounts, wellness program, tuition reimbursement, optional legal coverage, and identity theft protection.
- Work aligned with a mission to advance science and improve community health and safety.
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