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An established industry player is seeking a Filling Aseptic Process Manager to oversee critical operations in the Filling Department. This role is essential for ensuring compliance with regulatory standards and driving continuous improvement initiatives. You will manage personnel, ensure quality assurance, and lead cost control efforts while contributing to the delivery of healthcare solutions that impact patients worldwide. Join a supportive team that values diversity and offers comprehensive benefits, including healthcare and wellness programs, while you grow your career in a dynamic environment.
Location: Swiftwater, PA
We deliver 4.3 billion healthcare solutions annually, thanks to our meticulous Manufacturing & Supply teams. With your talent, we can do even more to protect against infectious diseases and bring hope to patients and their families.
Responsible for overseeing process, personnel, and activities in the assigned PCU and shift, ensuring compliance with all +QDCI standards. Drive continual improvement through leading projects, investigations, and CAPA to prevent reoccurrence.
This role is for an exempt employee working in the Filling Department. Pay is based on experience and education.
We are a global healthcare company delivering over 500 million vaccine doses yearly, exploring new technologies to protect communities worldwide. We pursue scientific progress to make a real impact on patients.
Manage process within the shift to meet goals. Ensure operations comply with regulatory standards, including cGMPs, CBER, WHO, and EP. Plan production schedules, coordinate personnel, and review batch records.
Responsibilities include employee management, training, development, cost control, quality assurance, incident investigations, and managing budgets. Provide managerial coverage during shifts, and coordinate maintenance, validation, and process improvements. Background in Aseptic Processing is favorable.
Follow safety procedures, participate in safety meetings, report issues, and contribute to safety initiatives using +QDCI boards.
Ensure compliance with regulatory standards, support inspections, lead investigations, and maintain GMP data accuracy. Collaborate with quality teams to uphold standards.
Review data, drive performance improvements, support production needs, and ensure proper training. Follow escalation procedures and maintain attendance policies.
Lead continuous improvement and cost reduction initiatives, support changeovers, and improve operator efficiencies.
Complete training modules, train new team members, lead meetings, and ensure proper work procedures and confidentiality are maintained.
Join a supportive team, grow your career, and enjoy comprehensive benefits including healthcare, wellness programs, and parental leave. We are committed to diversity and equal opportunity.