Enable job alerts via email!

Filling Aseptic Process Manager- Vaccines

Scorpion Therapeutics

United States

Remote

USD 80,000 - 120,000

Full time

2 days ago
Be an early applicant

Boost your interview chances

Create a job specific, tailored resume for higher success rate.

Job summary

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.

Benefits

Healthcare benefits
Wellness programs
Parental leave
Diversity and equal opportunity initiatives

Qualifications

  • 1 year relevant experience or 7+ years in manufacturing/filling biological products.
  • Experience in FDA-regulated industry and cGMPs.

Responsibilities

  • Oversee process and personnel in the Filling Department.
  • Ensure compliance with regulatory standards and drive performance improvements.

Skills

Aseptic Processing
Regulatory Compliance
Quality Assurance
Employee Management
Cost Control

Education

BS in Life Sciences
Engineering Degree

Job description

If you're aiming for a job like this, you need an edge.

JobsAI gives you that edge—by helping you upgrade your resume, analyze hiring managers’ LinkedIn profiles, and prepare with a built-in interview coach.

This is the smarter, faster way to compete in today’s job market.

Check out JobsAI
Job Title: Filling Aseptic Process Manager

Location: Swiftwater, PA

About The Job

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.

Main Responsibilities
Context of job/major challenges:

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.

Safety

Follow safety procedures, participate in safety meetings, report issues, and contribute to safety initiatives using +QDCI boards.

Quality

Ensure compliance with regulatory standards, support inspections, lead investigations, and maintain GMP data accuracy. Collaborate with quality teams to uphold standards.

Delivery

Review data, drive performance improvements, support production needs, and ensure proper training. Follow escalation procedures and maintain attendance policies.

Cost

Lead continuous improvement and cost reduction initiatives, support changeovers, and improve operator efficiencies.

Involvement

Complete training modules, train new team members, lead meetings, and ensure proper work procedures and confidentiality are maintained.

Education/Experience
  • BS in Life Sciences, Engineering, or equivalent plus 1 year relevant experience, or 7+ years in manufacturing/filling biological products.
  • Experience in pharmaceutical manufacturing, FDA-regulated industry, and cGMPs.
Why Choose Us?

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.

Get your free, confidential resume review.
or drag and drop a PDF, DOC, DOCX, ODT, or PAGES file up to 5MB.

Similar jobs

BARDA Senior Vaccine and Biologic Development Subject Matter Expert

BryceTech

Washington

Remote

USD 90,000 - 150,000

30+ days ago

BARDA Senior Pharmaceutical Business Development and Portfolio Management Subject Matter Expert

The International Society for Pharmaceutical Engineering, Inc.

Washington

Remote

USD 90,000 - 150,000

30+ days ago

Quality Associate III - Filling (weekend 2nd shift)

Simtra BioPharma Solutions

Bloomington

On-site

USD 50,000 - 90,000

30+ days ago