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Aseptic Processing Jobs in Pennsylvania (NOW HIRING)

PSC Biotech

Senior Process Engineer

York, PA · On-site

$102K - $132K/yr

Aseptic Processing Support * Support aseptic processing programs in compliance with: * FDA cGMP regulations * EU GMP Annex 1 * ICH Guidelines * USP requirements * Participate in aseptic process ...

PSC Biotech

Senior Process Engineer

York, PA

$102K - $132K/yr

The successful candidate will possess a strong understanding of aseptic processing, sterile manufacturing, cGMP requirements, process validation, and pharmaceutical engineering principles. Process ...

PSC Biotech

Senior Process Engineer

York, PA · On-site

$95K - $120K/yr

The successful candidate will possess a strong understanding of aseptic processing, sterile manufacturing, cGMP requirements, process validation, and pharmaceutical engineering principles. Process ...

PHARMALOGIC HOLDINGS

Quality Specialist

Pittsburgh, PA · On-site

$50K - $60K/yr

Assure aseptic processing of samples and products, as per SOP. Assure aseptic processing area suitably cleaned, maintained, controlled to prevent mix-ups or contamination; assure personnel qualified ...

Gregory Packaging

Aseptic Equipment Mechanic

Bethlehem, PA · On-site

$25.75 - $33.75/hr

ASEPTIC EQUIPMENT MECHANIC All Shifts Available Aseptic Equipment Mechanic will ensure that our High Speed and Automated Processing, Filling and Packaging Equipment are maintained to ensure ...

PSC Biotech

Manufacturing Associate III

York, PA · On-site

$26 - $32/hr

Familiarity with formulation, filling, primary packaging, and aseptic processing. * Willingness to work extended shifts and a variable schedule when required. * Skilled in MS Office/Excel tools.

PSC Biotech

Manufacturing Associate III

York, PA

Familiarity with formulation, filling, primary packaging, and aseptic processing. Willingness to work extended shifts and a variable schedule when required. Skilled in MS Office/Excel tools.

PSC Biotech

Manufacturing Associate III

York, PA · On-site

Familiarity with formulation, filling, primary packaging, and aseptic processing. * Willingness to work extended shifts and a variable schedule when required. * Skilled in MS Office/Excel tools.

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How much do aseptic processing jobs pay per hour?

As of Sep 6, 2026, the average hourly pay for aseptic processing in Pennsylvania is $24.73, according to ZipRecruiter salary data. Most workers in this role earn between $19.76 and $28.17 per hour, depending on experience, location, and employer.

What is aseptic processing?

An Aseptic Processing job involves maintaining sterile conditions while handling pharmaceutical or food products to prevent contamination. Responsibilities typically include sterilizing equipment, monitoring environmental conditions, and following strict regulatory guidelines. Workers must adhere to Good Manufacturing Practices (GMP) and use specialized techniques to ensure product integrity and safety.

What are the typical daily responsibilities of someone working in aseptic processing?

Aseptic Processing professionals are responsible for preparing, operating, and monitoring equipment within sterile environments, ensuring all procedures are performed according to strict quality and safety guidelines. Tasks may include gowning and entering cleanrooms, performing aseptic transfers, documenting activities for regulatory compliance, and troubleshooting equipment or process deviations. Teamwork is essential, as you will collaborate closely with quality assurance, maintenance, and production teams to maintain consistent standards. The role requires a high level of concentration, adherence to protocols, and readiness to promptly address any contamination risks or procedural issues.

What are the key skills and qualifications needed to thrive in aseptic processing?

To thrive in Aseptic Processing, you need knowledge of sterile manufacturing practices, attention to detail, and often a background in microbiology, biotechnology, or a related field. Familiarity with cleanroom operations, automated filling equipment, and compliance with Good Manufacturing Practices (GMP), as well as certifications like HACCP or aseptic processing training, are valuable. Strong teamwork, communication skills, and a commitment to safety set top performers apart. These skills are crucial to maintaining product purity, preventing contamination, and meeting strict regulatory standards in industries such as pharmaceuticals or food production.

What are the most commonly searched types of Aseptic Processing jobs in Pennsylvania?

The most popular types of Aseptic Processing jobs in Pennsylvania are:

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

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

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

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

What cities in Pennsylvania are hiring for Aseptic Processing jobs?

Cities in Pennsylvania with the most Aseptic Processing job openings:

Aseptic Processing jobs near you
Infographic showing various Aseptic Processing job openings in Pennsylvania as of August 2026, with employment types broken down into 84% Full Time, 5% Part Time, and 11% Contract. Highlights an 100% In-person job distribution, with an average salary of $51,442 per year, or $24.7 per hour.

Process SME - Asceptic Processing - GMP Design

Genesis AEC

Blue Bell, PA • On-site

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 14 days ago

Key responsibilities

  • Support and guide process engineering teams through complex project work, including developing deliverables, supporting quality reviews, and troubleshooting technical challenges.

  • Represent Genesis as a subject matter expert by building client relationships, supporting proposal development, and participating in client meetings and industry events.

  • Contribute to the advancement of the company's market position by creating technical content, participating in industry forums, and supporting internal training and standards development.

Job description

Process SME - Aseptic Processing / GMP Design
Are you ready to shape the future of life sciences facilities? Do you thrive at the intersection of aseptic processing, GMP design, and technical leadership? If you're energized by guiding complex projects, mentoring teams, and helping clients bring safe, compliant manufacturing environments to life, we'd love to hear from you.
WHO WE ARE
We're Genesis AEC - an award-winning architecture, engineering, construction management, and CQV firm and a leader in the life sciences industry. Ranked #5 in Pharmaceutical Design by ENR magazine, we design and construct facilities that advance worldwide health. We're proud to contribute to our clients' success, earning honors that include a 2021 ISPE Facility of the Year (FOYA) award and an ENR Mid-Atlantic's Best Manufacturing Project award for our work at the National Institutes of Health.
Description:
The selected candidate will serve as the Aseptic Processing and GMP Design Subject Matter Expert (SME), advising AE teams and clients across project stages while maintaining current knowledge of regulatory environments, industry trends, and emerging equipment technologies.
In this role, you will support aseptic processing and broader GMP projects across all stages of design, from front-end capital planning and feasibility through concept and detailed design, while contributing to key process engineering deliverables such as facility interface requirements, flow diagrams, equipment selections, technical reports, and quality reviews.
ROLE & RESPONSIBILITIES
Role Expectations (No Direct Reports)
  • You will serve as a key technical project resource, supporting deliverable development, quality reviews, process engineering standards, mentoring, proposal support, and thought leadership activities.
  • This hybrid role is primarily project-focused, with opportunities to contribute to internal training, technical guidance, conferences, presentations, and industry publications.
  • The position is hybrid, with an expected office presence of two to three days per week and limited travel as needed.

Operations
  • You will lead and guide process engineering teams through complex project work, helping develop deliverables, support quality reviews, troubleshoot technical challenges, and shape design strategies during front-end studies and early project development.
  • You will support regulatory reviews, risk assessments, facility definition efforts, peer reviews, and project guidance for process engineers and process architects across assignments.
  • You will also help strengthen the Process Engineering group by mentoring staff, facilitating internal training, and contributing to the development and maintenance of design standards, tools, details, specifications, and best practices.

Client-Facing
  • You will represent Genesis as a trusted subject matter expert, building strong client relationships through excellent engineering, responsive service, and confident technical leadership.
  • You will support proposal development, participate in client presentations and project meetings, and help guide clients toward innovative, practical solutions.
  • You will also contribute to early project and proposal discussions as an SME and represent Genesis Process Engineering at relevant conferences, symposiums, and industry events.

Strategic
  • You will help advance Genesis' market leadership by creating technical content for publications and presentations, participating in industry forums, and strengthening the firm's visibility in the life sciences community.
  • You will identify opportunities to engage in local and national industry events, including organizations such as ISPE, ASME BPE, and PDA, while helping recognize potential talent and strategic personnel who can support future growth.

MINIMUM QUALIFICATIONS
  • Bachelor's degree in Chemical Engineering, Mechanical Engineering, Biomedical Engineering, or a related engineering discipline. A Master's degree in Chemical Engineering is a plus.
  • 15+ years of relevant experience in process engineering, aseptic processing, GMP facility design, or biopharmaceutical manufacturing environments.
  • Demonstrated expertise in aseptic processing design, GMP facility planning, process equipment selection, and facility/process interface requirements.
  • Strong understanding of applicable regulatory expectations and industry guidance related to sterile manufacturing, including FDA, EU GMP, and relevant industry standards.
  • Experience supporting life sciences projects across multiple design phases, including feasibility, concept design, basis of design, detailed design, and quality review.
  • Ability to serve as a technical subject matter expert for internal teams and clients, including advising on design strategy, risk assessment, regulatory considerations, and technical problem-solving.
  • Strong communication, facilitation, presentation, and client-facing skills.
  • Ability to mentor engineers, contribute to internal standards and tools, and support technical knowledge sharing across project teams.
  • Ability to manage multiple priorities, work independently, and support project commitments in a hybrid work environment.

Preferred Qualifications
  • Master's degree in Chemical Engineering, Mechanical Engineering, Biomedical Engineering, or a related discipline.
  • Professional Engineer license (P.E.) or other relevant professional certification.
  • Experience with both design-side and owner-side project environments.
  • Prior experience contributing to proposals, client presentations, technical publications, conference presentations, or industry thought leadership.
  • Active involvement in industry organizations such as ISPE, PDA, ASME BPE, or similar life sciences/biopharma groups.
  • Experience developing or maintaining process engineering standards, design tools, specifications, details, or best practices.
  • Experience mentoring or technically guiding process engineers, process architects, or multidisciplinary project teams.
  • Familiarity with emerging aseptic processing technologies, sterile manufacturing equipment, contamination control strategies, and current industry trends.
  • Strong proficiency with Microsoft Office applications and relevant engineering/design tools.

WHY YOU'LL LOVE IT HERE
  • Our collaborative and positive culture sets us apart
  • We offer schedule flexibility. *For field-based personnel, flexible scheduling may be subject to client/project site requirements.
  • Comprehensive medical, dental, vision, and RX insurance plans, with two-thirds of your premiums and deductible paid!
  • Competitive 401(k) match program
  • Generous paid time off (PTO)
  • Paid Parental Leave time
  • Thought leadership opportunities, including a $1,000 award for presenting or publishing your technical expertise!
  • Competitive company-paid training opportunities
  • A 5% salary increase for earning your professional license!
  • Endless opportunities to grow your career

Apply