5 дней назад
Interface Manager (Pharmaceutical Facilities)
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Interface Manager (Pharmaceutical Facilities): Developing and leading interface management plans for large pharmaceutical capital projects with an accent on cross-functional coordination, governance, and interface risk control. Focus on managing technical, organizational, construction, commissioning, and operational interfaces, integrating critical-path activities, and ensuring GMP and regulatory compliance.
Location: Richmond, Virginia, United States
Company
Sustainable Technology Solutions provides technology, advisory, engineering, energy transition, and asset optimization solutions across the full asset life cycle.
What you will do
- Develop, implement, and maintain the project Interface Management Plan, including processes, tools, governance, and reporting systems.
- Identify and manage technical, organizational, construction, commissioning, validation, quality, and operational interfaces throughout the project lifecycle.
- Coordinate interfaces between engineering, procurement, construction management, commissioning, operations, contractors, licensors, clients, and third-party stakeholders.
- Lead interface meetings and workshops, assign ownership, resolve issues, and track actions through closure.
- Maintain interface registers covering risks, dependencies, constraints, decisions, milestones, and critical-path impacts.
- Prepare KPIs, risk assessments, interface reports, and executive updates while ensuring compliance with GMP, quality systems, regulatory expectations, and company procedures.
Requirements
- Bachelor’s degree in engineering or project management.
- Minimum 15 years of industry experience, including at least 10 years supporting pharmaceutical, biotechnology, vaccine, sterile manufacturing, API, or advanced therapy facilities.
- Experience delivering capital projects exceeding $500 million TIC.
- Experience managing interfaces and communications for large multidisciplinary teams and contractors.
- Strong knowledge of communications, governance, project controls, design management, and project delivery processes.
Nice to have
- Experience with GMP-regulated facilities, major capital projects exceeding $1 billion TIC, PMC or Owner’s Representative work, FDA inspection support, or greenfield pharmaceutical projects.
- PE, PMP, or ISPE certification.
Culture & Benefits
- Full-time employment with a Zero Harm and People First culture.
- Benefits may include a 401(k) plan with company match, medical, dental, vision, life insurance, AD&D, flexible spending, disability coverage, and paid time off.
- Flexible work schedules may be available.
- Professional training and career development opportunities.
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