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Manager Aseptic Processing Jobs in Pennsylvania (NOW HIRING)

Batching Manager

Hazleton, PA ยท On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Manages and directs activities of the aseptic batching department, ensuring product adheres to ... Collaborates with System Engineers, R&D and commercialization on Aseptic process improvements.

Batching Manager

Hazle Township, PA ยท On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Manages and directs activities of the aseptic batching department, ensuring product adheres to ... Collaborates with System Engineers, R&D and commercialization on Aseptic process improvements.

Batching Manager

Hazleton, PA ยท On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Manages and directs activities of the aseptic batching department, ensuring product adheres to ... Collaborates with System Engineers, R&D and commercialization on Aseptic process improvements.

Manufacturing Associate III

York, PA

$26 - $32/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Ability to manage floor activities in the absence of the Supervisor. * Experience in reviewing and ... Familiarity with formulation, filling, primary packaging, and aseptic processing. * Willingness to ...

New

Manufacturing Associate III

York, PA ยท On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Ability to manage floor activities in the absence of the Supervisor. * Experience in reviewing and ... Familiarity with formulation, filling, primary packaging, and aseptic processing. * Willingness to ...

New

Manufacturing Associate III

York, PA ยท On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Ability to manage floor activities in the absence of the Supervisor. Experience in reviewing and ... Familiarity with formulation, filling, primary packaging, and aseptic processing. Willingness to ...

New

Knowledge of clean utilities, HVAC systems, aseptic processing, and GMP facility operations * Familiarity with deviation management, CAPA, and change control systems * Ability to read and interpret P ...

Manage accurate reporting of all in-bound product, materials, supplies and inventories in storage ... Experience with thermal processing, pasteurization, and / or experience with aseptic processing ...

Manage accurate reporting of all in-bound product, materials, supplies and inventories in storage ... Experience with thermal processing, pasteurization, and / or experience with aseptic processing ...

Senior Process Engineer

Blue Bell, PA ยท On-site

$99K - $128K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

... aseptic processing - each with its own diverse subsets of process types. Based on experience, a ... Lead process-driven projects independently or manage a small team of process engineers on more ...

Senior Process Engineer

Blue Bell, PA ยท On-site

$99K - $128K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

... aseptic processing - each with its own diverse subsets of process types. Based on experience, a ... Lead process-driven projects independently or manage a small team of process engineers on more ...

Showing results 21-40

Manager Aseptic Processing information

What is a manager aseptic processing?

A Manager of Aseptic Processing oversees the sterile production environments in pharmaceutical or biotechnology manufacturing. They are responsible for ensuring that products are processed and packaged without contamination, following strict regulatory and safety standards. Their role includes supervising staff, maintaining compliance with Good Manufacturing Practices (GMP), conducting risk assessments, and implementing process improvements. They also play a key part in training employees and managing documentation to ensure product quality and patient safety.

What are the key skills and qualifications needed to thrive as a manager aseptic processing?

To thrive as a Manager Aseptic Processing, you need a strong background in microbiology, pharmaceutical manufacturing, quality assurance, and regulatory compliance, often supported by a relevant degree and experience in sterile production environments. Familiarity with Good Manufacturing Practices (GMP), cleanroom management systems, and environmental monitoring tools is essential. Leadership, attention to detail, and effective communication are crucial soft skills for managing teams and ensuring strict adherence to protocols. These skills and qualities are vital to maintain product sterility, meet regulatory standards, and ensure patient safety in pharmaceutical operations.

What are some common challenges faced by a manager aseptic processing, and how can they be addressed?

Managers in Aseptic Processing often face challenges related to ensuring strict compliance with regulatory standards, maintaining a contamination-free environment, and leading cross-functional teams in high-pressure situations. Addressing these challenges requires staying updated on evolving industry guidelines, fostering a culture of continuous training, and implementing robust monitoring systems. Effective communication and collaboration with Quality Assurance, Maintenance, and Production teams are also crucial for swiftly resolving issues and upholding product safety.

What is the difference between Manager Aseptic Processing vs Aseptic Processing Technician?

AspectManager Aseptic ProcessingAseptic Processing Technician
CredentialsBachelor's degree in life sciences or related field, GMP training, leadership experienceHigh school diploma or associate degree, GMP training
Work EnvironmentSupervisory role overseeing aseptic processes in pharmaceutical manufacturingHands-on role operating aseptic equipment in cleanroom settings
ResponsibilitiesManaging teams, ensuring compliance, process optimizationPerforming aseptic procedures, equipment setup, documentation

The Manager Aseptic Processing oversees the aseptic manufacturing process, focusing on team management and compliance, while the Aseptic Processing Technician handles the direct operation of aseptic equipment. Both roles require GMP training and work in sterile environments, but the manager has additional leadership and oversight responsibilities.

What are popular job titles related to Manager Aseptic Processing jobs in Pennsylvania?

For Manager Aseptic Processing jobs in Pennsylvania, the most frequently searched job titles are:

What job categories do people searching Manager Aseptic Processing jobs in Pennsylvania look for?

The top searched job categories for Manager Aseptic Processing jobs in Pennsylvania are:

What cities in Pennsylvania are hiring for Manager Aseptic Processing jobs?

Cities in Pennsylvania with the most Manager Aseptic Processing job openings:

Process & Validation Project Manager

LAPORTE L.C.C.

Philadelphia, PA โ€ข On-site

Full-time

PTO

Re-posted 16 days ago


Job description

Process & Validation Project Manager (a minimum of 5 years of experience required)
Location: Philadelphia, PA
Employment Type: Full-time, mostly onsite
About Us
Are you ready to take the next step in your career? LAPORTE, a consulting engineering firm with 25 years of experience and a strong presence in North America and Europe, is seeking an Process & Validation Project Manager to join our growing team. With 25 offices and over 480 employees worldwide, we specialize in delivering innovative solutions for the pharmaceutical and food & beverage industries.
As we continue to expand our presence in the Greater Philadelphia life sciences market, we are seeking an experienced Process & Validation Project Manager to lead capital projects, facility improvements, commissioning and qualification initiatives, and GMP manufacturing enhancements for our pharmaceutical and biotechnology clients.
This role offers the opportunity to work directly with industry-leading organizations while contributing to technically challenging projects that improve manufacturing performance, quality, and compliance.
At LAPORTE, we offer:
  • Competitive Salary
  • Comprehensive Benefits
  • Compensatory Paid Time Off (PTO)
  • Paid Parental Leave
  • A Flexible Work Environment that values work-life balance
  • Opportunities for Professional Growth

Responsibilities and Duties:
  • Plan, coordinate, and execute facility improvement projects, including scope definition, scheduling, contractor coordination, and closeout documentation.
  • Serve as the primary on-site liaison for all project-related activities, ensuring minimal disruption to GMP operations and maintaining a safe working environment throughout project execution.
  • Initiate, author, and shepherd change control records through the site quality management system (QMS) in accordance with GMP change control procedures.
  • Coordinate and support the vendor approval and qualification process for new contractors and service providers, partnering with Procurement and QA as required.
  • Develop and maintain project schedules, status trackers, and progress reports for review by site leadership.
  • Identify and escalate project risks, scope changes, and schedule impacts in a timely manner, proposing mitigation strategies as appropriate.
  • Ensure all project activities comply with applicable GMP regulations, site SOPs, EHS requirements, and local building codes.

Qualifications:
  • Bachelor's degree in Engineering, Life Sciences, Construction Management, Project Management, or a related technical field.
  • Minimum of 5 years of project management experience supporting pharmaceutical, biotechnology, medical device, or other regulated manufacturing environments.
  • Demonstrated success managing engineering, facility, equipment installation, capital improvement, or operational excellence projects from initiation through closeout.
  • Experience developing and maintaining project schedules, coordinating resources, tracking milestones, and driving projects to successful completion.
  • Strong experience managing contractors, vendors, and cross-functional teams in a GMP-regulated environment.
  • Proven ability to lead project meetings, communicate project status, and effectively manage stakeholder expectations at all organizational levels.
  • Working knowledge of cGMP regulations and quality systems, including change management processes.
  • Exceptional organizational, communication, problem-solving, and relationship management skills.
  • Ability to manage multiple priorities and adapt to changing project requirements in a fast-paced environment.
  • Willingness to travel to client sites as required.

Preferred Qualifications
  • Experience overseeing facility renovations, equipment installations, utility upgrades, or manufacturing process improvement projects.
  • Familiarity with project budgeting, forecasting, cost tracking, and resource planning.
  • Experience coordinating activities across Engineering, Manufacturing, Quality Assurance, Validation, Maintenance, and Procurement teams.
  • PMP certification or similar project management credential.
  • Knowledge of commissioning, qualification, and validation processes within life sciences manufacturing environments.
  • Experience working in aseptic processing, biotechnology, cell and gene therapy, or sterile manufacturing facilities.
  • Familiarity with risk management methodologies and structured problem-solving tools.

Send us your application today. We look forward to meeting you!
The LAPORTE team