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Aseptic Process Engineer Jobs in Ohio (NOW HIRING)

... and processes required to support an aseptic manufacturing and packing operation. This role ... Work with engineering team to review specifications and provide input * Accept turnover packages ...

... Aseptic Filling, Automated Inspection, Device Assembly, Packaging, Building Automated System, AMHS ... Consult cross-functionally and assist system owners in process development as the automation ...

... Aseptic Filling, Automated Inspection, Device Assembly, Packaging, Building Automated System, AMHS ... Consult cross-functionally and assist system owners in process development as the automation ...

... Aseptic Filling, Automated Inspection, Device Assembly, Packaging, Building Automated System, AMHS ... Consult cross-functionally and assist system owners in process development as the automation ...

Automation Engineer II

West Chester, OH · On-site

$70 - $107.50/hr

... Aseptic Filling, Automated Inspection, Device Assembly, Packaging, Building Automated System, AMHS ... Consult cross‑functionally and assist system owners in process development as the automation ...

Experience in pharmaceutical, biotech, or aseptic manufacturing environments * Ability to manage ... If you need assistance completing the application process, please call 1 (440) 392.7047. This ...

Our team of experts range from product developers to engineers, working across our portfolio of ... Experience working on similar equipment used for thermal and aseptic processing preferred

Showing results 41-60

Aseptic Process Engineer information

See Ohio salary details

$32.3K

$83K

$124K

How much do aseptic process engineer jobs pay per year?

As of Sep 5, 2026, the average yearly pay for aseptic process engineer in Ohio is $82,978.00, according to ZipRecruiter salary data. Most workers in this role earn between $68,300.00 and $93,600.00 per year, depending on experience, location, and employer.

What is an aseptic process engineer?

Aseptic process engineers are professionals who design, develop, and maintain sterile manufacturing systems, primarily in the pharmaceutical, biotechnology, and food industries. Their main responsibility is to ensure that products are produced in a contamination-free environment, using processes that prevent the introduction of microorganisms. This involves overseeing the design of cleanrooms, validating equipment, developing standard operating procedures, and ensuring regulatory compliance. Aseptic process engineers work closely with quality assurance teams to maintain high standards of product safety and efficacy. Their expertise is crucial for industries where product sterility is critical to consumer safety.

What are the key skills and qualifications needed to thrive as an aseptic process engineer, and why are they important?

Aseptic Process Engineers need a strong background in chemical, mechanical, or biomedical engineering, along with experience in aseptic manufacturing environments and a solid understanding of GMP regulations. Familiarity with process automation systems, sterilization equipment, and industry certifications such as Six Sigma or Lean Manufacturing are often required. Attention to detail, strong problem-solving abilities, and effective communication are vital soft skills for ensuring product quality and process efficiency. These skills are crucial for maintaining sterile conditions, regulatory compliance, and the safe production of pharmaceuticals or biotechnology products.

What are some common challenges faced by aseptic process engineers, and how can they be addressed?

Aseptic Process Engineers often encounter challenges such as maintaining strict sterility standards, troubleshooting equipment issues, and ensuring compliance with changing regulatory requirements. Addressing these challenges requires strong attention to detail, proactive communication with cross-functional teams, and staying current with industry best practices and regulations. Collaborating closely with quality assurance, production, and maintenance teams helps to identify and resolve issues quickly, ensuring that processes remain efficient and compliant.

What is the difference between Aseptic Process Engineer vs Pharmaceutical Manufacturing Technician?

AspectAseptic Process EngineerPharmaceutical Manufacturing Technician
CredentialsBachelor's degree in engineering, life sciences, or related field; GMP trainingHigh school diploma or associate degree; GMP training often required
Work EnvironmentCleanroom, sterile environments, manufacturing facilitiesManufacturing floors, production areas, sometimes cleanrooms
Industry UsageDesign, optimize, and validate aseptic processes in pharmaOperate equipment, assemble products, support manufacturing

The Aseptic Process Engineer focuses on designing and validating sterile manufacturing processes, requiring specialized engineering knowledge. In contrast, the Pharmaceutical Manufacturing Technician handles day-to-day production tasks, often with less formal education but essential for maintaining manufacturing flow. Both roles are vital in pharmaceutical production but differ in responsibilities and qualifications.

What job categories do people searching Aseptic Process Engineer jobs in Ohio look for?

The top searched job categories for Aseptic Process Engineer jobs in Ohio are:

What cities in Ohio are hiring for Aseptic Process Engineer jobs?

Cities in Ohio with the most Aseptic Process Engineer job openings:

Infographic showing various Aseptic Process Engineer job openings in Ohio as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 15% Part Time, 1% Temporary, 4% Contract, and 1% Nights. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $82,978 per year, or $39.9 per hour.

Manufacturing Process Technician

530d PETNET Solutions, Inc.

Akron, OH • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

This job post has expired today. Applications are no longer accepted.


Job description

Join us in pioneering breakthroughs in healthcare. For everyone. Everywhere. Sustainably. Our inspiring and caring environment forms a global community that celebrates diversity and individuality. We encourage you to step beyond your comfort zone, offering resources and flexibility to foster your professional and personal growth, all while valuing your unique contributions. Join the global leader shaping the future of PET imaging. At Siemens Healthineers, we operate the world's largest PET radiopharmaceutical network — delivering over 1 million doses annually with a >99% fulfillment rate and supporting more than 2,800 imaging centers worldwide.

Important:

This is a primarily overnight role. Candidates must be willing to work overnight and have the flexibility to rotate into alternative shifts as business needs evolve. Why You'll Love Working Here Industry‐leading 5‐week paid training program (in‐person + virtual). Competitive Benefits Competitive benefits: medical/dental/vision, 5% bonus, 100% 401(k) match. 20 days PTO + 5 floating holidays. Meaningful work that supports patient care and advanced medical imaging.

Responsibilities

You are responsible for the synthesis, quality control, packaging, logistics, and strict regulatory compliance of radiopharmaceuticals used in the diagnostic imaging and treatment of disease. You support manufacturing through regular preventive maintenance, calibration, and troubleshooting of analytical equipment used in operations. You also communicate regularly with couriers and customers to ensure the accurate and timely delivery of biomarkers.

In addition, you assist with facility housekeeping, maintenance of laboratory inventory levels, creation of quality control documentation as needed, and adherence to strict safety protocols and regulations related to the production and transport of radioactive materials. Operate chemistry instruments (HPLC, GC, TLC, and chemistry modules) and advanced systems (cyclotron) for the routine manufacturing and quality control of radiopharmaceuticals.

Author and maintain precise documentation for manufacturing, quality control, preventive maintenance, customer support, laboratory investigations, deviations, and out-of-specification events. Perform preventive maintenance, inspections, and troubleshooting of critical equipment. Prepare products for shipment, coordinate courier logistics, and provide customer support. Maintain aseptic environments (cleanroom) to create sterile consumables and prevent contamination during the production of injectable materials.

Conduct environmental monitoring on a regular and defined basis. Maintain compliance with strict safety, sterile environment, and regulatory standards.

Physical Demands:

Applicants should be comfortable working in a fast‐paced laboratory environment and able to lift up to 100 lbs.

Minimum Qualifications

High school diploma or equivalent required. Specialized skill training or certification may be required.

Preferred Qualifications

Associates degree in Chemistry, Biochemistry, Biology, Medical Technology, or a related Life Science field. Licensed Pharmacy Technician. Understanding of current Good Manufacturing Practices and Good Documentation Practices. Previous work experience in a laboratory environment or related role. Previous experience with analytical laboratory equipment and laboratory software systems. Familiarity with radiation safety or ALARA principles.

Knowledge, Skills, and Abilities

Excellent communication and interpersonal skills. Strong command of Good Documentation Practices (GDP) to ensure data integrity and audit readiness. Excellent problem-solving and analytical skills, as well as critical thinking ability. Excellent organizational skills and attention to detail. Ability to treat confidential information with sensitivity. Ability to meet deadlines and work in a fast‐paced, multi‐priority environment. Ability to plan and organize job responsibilities and priorities. Ability to apply standard operating procedures (SOPs) in a production environment. Demonstrated ability to maintain a sterile environment. Ability to understand, prioritize, and implement laboratory safety protocols.

Who we are

We are a team of more than 72,000 highly dedicated Healthineers in more than 70 countries. As a leader in medical technology, we constantly push the boundaries to create better outcomes and experiences for patients, no matter where they live or what health issues they are facing. Our portfolio is crucial for clinical decision‐making and treatment pathways.

How we work When you join Siemens Healthineers, you become one in a global team of scientists, clinicians, developers, researchers, professionals, and skilled specialists, who believe in each individual's potential to contribute with diverse ideas. We are from different backgrounds, cultures, religions, political and/or sexual orientations, and work together, to fight the world's most threatening diseases and enable access to care, united by one purpose: to pioneer breakthroughs in healthcare. For everyone. Everywhere. Sustainably.

Our culture We are part of an incredible community of scientists, clinicians, developers, researchers, professionals, and skilled specialists pushing the boundaries versus to improve people's lives around the world. The base pay range for this position is: $46,040 - $63,305. Factors which may affect starting pay within this range may include geography/market, skills, education, experience, and other qualifications of the successful candidate.

If this is a commission eligible position the commission eligibility will be in accordance with the terms of the Company's plan. Commissions are based on individual performance and/or company performance. Benefits medical/dental/vision 5% bonus 100% 401(k) match 20 days PTO 5 floating holidays medical insurance dental insurance vision insurance 401(k) retirement plan life insurance long-term disability insurance short-term disability insurance paid parking/public transportation paid time off paid sick and safe time Equal Employment Opportunity Statement Siemens Healthineers is an Equal Opportunity and affirmative Action Employer encouraging diversity in the workplace.

All qualified applicants will receive consideration for employment without regard to their race, color, creed, religion, national origin, citizenship status, ancestry, sex, age, physical or mental disability unrelated to ability, marital status, family responsibilities, pregnancy, genetic information, sexual orientation, gender expression, gender identity, transgender, sex stereotyping, order of protection status, protected veteran or military status, or an unfavorable discharge from military service, and other categories protected by federal, state or local law. EEO is the Law: Applicants and employees are protected under federal law from discrimination.

To learn more, click here. Export Control A successful candidate must be able to work with controlled technology in accordance with US export control law.

It is Siemens Healthineers' policy to comply fully and completely with all United States export control laws and regulations, including those implemented by the Department of Commerce through the Export Administration Regulations (EAR), by the Department of State through the International Traffic in Arms Regulations (ITAR), and by the Treasury Department through the Office of Foreign Assets Control (OFAC) sanctions regulations.

Data Privacy We care about your data privacy and take compliance with GDPR as well as other data protection legislation seriously. California Privacy Notice California residents have the right to receive additional notices about their personal information. To learn more, click here. We are a team of 72,000 highly dedicated employees across more than 70 countries passionately pushing the boundaries of what's possible in healthcare to help improve people's lives around the world.