What are the responsibilities and job description for the Aseptic Process Project Manager position at Piper Companies?
Piper Companies is seeking an Aseptic Process Project Manager to join a leading organization within the pharmaceutical manufacturing industry for an on-site contract position located in Clayton, NC. The Aseptic Process Project Manager will support large-scale capital projects and RFP-driven initiatives across aseptic production operations, including material flow, inspection, cleaning/sterilization, formulation, and fill/finish systems.
Responsibilities:
Salary Range: $130,000-$145,000/year (USD)
Comprehensive Benefits: Medical, Dental, Vision, sick leave if required by law, and 401K
This job opens for applications on 6/10/26. Applications for this job will be accepted for at least 30 days from the posting date.
Keywords: aseptic processing, sterile manufacturing, fill finish, formulation, GMP, pharmaceutical engineering, capital projects, RFP, validation, material handling, inspection systems, wash and sterilization, cleanroom operations, regulatory compliance, FDA, project management, vendor management, biotech manufacturing, CQV, contamination control
Responsibilities:
- Lead coordination and execution of aseptic processing workstreams tied to capital expansion and vendor RFP activities
- Oversee cross-functional integration of material handling, inspection, wash/sterilization, formulation, and filling systems
- Manage vendor relationships, review proposals, and support technical bid evaluations for multiple project packages
- Ensure alignment with cGMP standards, regulatory expectations, and internal quality requirements throughout project lifecycle
- Collaborate with engineering, validation, and operations teams to drive timelines, mitigate risk, and maintain project milestones
- 5 years of experience supporting pharmaceutical manufacturing projects, preferably within aseptic or sterile environments
- Strong understanding of aseptic processing workflows, including fill/finish and sterilization systems
- Experience working with capital projects, RFP processes, and vendor management
- Familiarity with cGMP, FDA regulations, and validation practices within life sciences manufacturing
- Bachelor’s degree in Engineering, Life Sciences, or a related technical field
Salary Range: $130,000-$145,000/year (USD)
Comprehensive Benefits: Medical, Dental, Vision, sick leave if required by law, and 401K
This job opens for applications on 6/10/26. Applications for this job will be accepted for at least 30 days from the posting date.
Keywords: aseptic processing, sterile manufacturing, fill finish, formulation, GMP, pharmaceutical engineering, capital projects, RFP, validation, material handling, inspection systems, wash and sterilization, cleanroom operations, regulatory compliance, FDA, project management, vendor management, biotech manufacturing, CQV, contamination control
Salary : $130,000 - $145,000