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Aseptic Process Engineer Jobs in New York (NOW HIRING)

Process & Improvements: • Participate in cross functional aseptic governance and provide insight ... Salary Range $88,000.00 - $132,000.00 Skills Desired Change Control, Chemical Engineering ...

Senior Process Engineer

Manhattan, NY · On-site

$105.50 - $166.10/hr

We are seeking a highly skilled and experienced Process Engineer who will be part of the process ... Experience in hygienic process design, cultured dairy products, and aseptic processing is a plus.

Process Technician

Edison, NJ · On-site

$23.50/hr

Process human tissue products using aseptic techniques in an ISO-certified cleanroom. * Follow ... Collaborate with Quality, Engineering, Supply Chain, Facilities, R&D, and other cross-functional ...

Monitor process systems and equipment for proper operation. * Perform daily and weekly preventative ... About Actalent Actalent is a global leader in engineering and sciences services and talent ...

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Field Service Engineer

Springfield, NJ · Remote

$80K - $100K/yr

The Field Service Engineer will work closely with customers to ensure equipment operates ... Experience with sterile injectable or aseptic processing equipment. * Experience supporting ...

Be Seen First

Field Service Engineer

Springfield, NJ · Remote

$80K - $100K/yr

The Field Service Engineer will work closely with customers to ensure equipment operates ... Experience with sterile injectable or aseptic processing equipment. * Experience supporting ...

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Aseptic Process Engineer information

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 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 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 job categories do people searching Aseptic Process Engineer jobs in New York look for? The top searched job categories for Aseptic Process Engineer jobs in New York are:
What cities in New York are hiring for Aseptic Process Engineer jobs? Cities in New York with the most Aseptic Process Engineer job openings:

Aseptic Process Expert

Novartis

Morris Plains, NJ

$88K - $132K/yr

Full-time

Medical, Retirement, PTO

Re-posted 21 days ago


Novartis rating

7.5

Company rating: 7.5 out of 10

Based on 17 frontline employees who took The Breakroom Quiz

64th of 86 rated pharmaceutical


Job description

Job Description Summary

Act as Subject Matter Expert for manufacturing aseptic behaviors related to technical training and shopfloor behaviors. Supporting investigation and leading continuous improvement to improve aseptic processing and training within the manufacturing area.


Job Description

365 days a year, we aspire to be the best manufacturer of Cell & Gene therapies to ensure our patients have the treatments they need to live longer, healthier lives.

This role is located on-site in Morris Plains, NJ. Novartis is unable to offer relocation support for this role. Please note the shift for this role is Monday through Friday (9am - 5pm)

Major accountabilities:

Process & Improvements:

• Participate in cross functional aseptic governance and provide insight to aseptic behaviors within manufacturing

Shop Floor Support:

• Provide front line technical and procedural support to manufacturing, working with the shift teams, focusing on manufacturing each batch safely, on time, in compliance with the batch instructions and quality requirements

• Supports updates to and execution of Aseptic operator and process qualification

• Build technical knowledge and culture to empower associates to react appropriately to unplanned situations

Training:

• Support development of strong aseptic training within the Manufacturing Unit

• Owns the Aseptic Training Curriculum and provides the necessary training and support to associates

• Provide training for assigned new processes, technical document execution and products

Audit Support:

• Maintain their processes at inspection readiness level and to provide the necessary

support in any internal or external audit

Deviations, Investigations, and CAPAs:

• Support investigations, Quality Events, CAPAs, and CAPA effectiveness checks related to aseptic process within required timelines

• Ensures all CAPAs are implemented through GMP systems (e.g. MBR revision, training, etc.)

The pay range for this position at commencement of employment is expected to be between $88,000 to $132,000 a year; however, while salary ranges are effective from 1/1/24 through 12/31/24, fluctuations in the job market may necessitate adjustments to pay ranges during this period. Further, final pay determinations will depend on various factors, including, but not limited to geographical location, experience level, knowledge, skills and abilities. The total compensation package for this position may also include other elements, including a sign-on bonus, restricted stock units, and discretionary awards in addition to a full range of medical, financial, and/or other benefits (including 401(k) eligibility and various paid time off benefits, such as vacation, sick time, and parental leave), dependent on the position offered. Details of participation in these benefit plans will be provided if an employee receives an offer of employment. If hired, employee will be in an “at-will position” and the Company reserves the right to modify base salary (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company or individual department/team performance, and market factors.

Minimum Requirements:

  • Bachelor's degree in Biology, Pharmaceutical Technology, Chemistry, Pharmacy or equivalent scientific degree.

  • 3+ years of relevant experience in aseptic GMP manufacturing shop floor is required.

  • Proven understanding of aseptic techniques and cell manufacturing (Pharma, GMP, Regulatory aspects).

  • Previous GxP experience is required.

  • Excellent communication and collaboration skills.

Benefits and rewards: Read our handbook to learn about all the ways we’ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards

Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture

Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network


EEO Statement:

The Novartis Group of Companies are Equal Opportunity Employers who are focused on building and advancing a culture of inclusion that values and celebrates individual differences, uniqueness, backgrounds and perspectives. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, sex, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status. We are committed to fostering a diverse and inclusive workplace that reflects the world around us and connects us to the patients, customers and communities we serve.


Accessibility and reasonable accommodations

The Novartis Group of Companies are committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or to perform the essential functions of a position, please send an e-mail to us.reasonableaccommodations@novartis.com or call +1(877)395-2339 and let us know the nature of your request and your contact information. Please include the job requisition number in your message.


Salary Range

$88,000.00 - $132,000.00


Skills Desired

Change Control, Chemical Engineering, Continual Improvement Process, Efficiency, Employment Discrimination, Flexibility, General Hse Knowledge, Good Documentation Practice, Knowledge Of Capa, Knowledge Of Gmp, Lean Manufacturing, Manufacturing Process, Manufacturing Production, Physics, Process Control, Production Line, Productivity, Risk Management, Root Cause Analysis (RCA), Scheduler, Technology Transfer, Well-Being

What Novartis employees say

Pay

Benefits

Hours and flexibility

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