8 дней назад
Visual Inspection Manager 2nd Shift (Biopharma)
90 000 - 130 000$
Вакансия из Hirify Global, списка международных tech-компанийДля мэтча и отклика нужен Plus
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Visual Inspection Manager 2nd Shift (Biopharma): Leading visual inspection operations for a regulated vaccine manufacturing environment with an accent on safety, quality, delivery, cost, and people performance. Focus on managing manual and automated inspection processes, driving root cause investigations and corrective actions, and developing inspectors and frontline leaders on the second shift.
Location: Swiftwater, Pennsylvania, United States; onsite second-shift leadership role
Salary: $90,000–$130,000 per year
Company
is an R&D-driven biopharmaceutical company developing medicines and vaccines through science, digital capabilities, and AI-driven innovation.
What you will do
- Lead visual inspection operations during the second shift in a regulated vaccine manufacturing environment.
- Ensure safe, compliant, and right-first-time execution across inspection activities.
- Review batch records and inspection documentation and support deviation investigations, root cause analysis, audits, and regulatory inspections.
- Oversee production planning, staffing, scheduling, throughput, waste reduction, and process optimization.
- Lead or support automation initiatives for visual inspection systems and collaborate with Manufacturing, Quality, Engineering, and Supply Chain.
- Recruit, onboard, train, coach, and manage the performance of inspectors and frontline leaders.
Requirements
- Bachelor’s degree in any field or five years of equivalent pharmaceutical operations experience.
- At least five years of relevant pharmaceutical or biologics manufacturing experience.
- At least two years of experience leading teams with direct reports.
- Strong knowledge of cGMP requirements, quality systems, FDA requirements, and EU Annex 1.
- Experience driving accountability and performance improvement and leading root cause investigations with corrective actions.
- Applicants must be US or Puerto Rico residents.
Nice to have
- Direct visual inspection experience in a GMP-regulated environment.
- Experience with manual and automated inspection processes.
- Experience in high-volume manufacturing operations.
Culture & Benefits
- Supportive, future-focused environment with opportunities for promotion and lateral career growth.
- Health, wellbeing, prevention, and wellness benefits.
- At least 14 weeks of gender-neutral parental leave.
- Rewards package and opportunities to work with digital, data, and AI-driven manufacturing technologies.
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