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Aseptic Jobs in Indiana (NOW HIRING)

Sterling Engineering Inc.

Validation Engineer

Indianapolis, IN · On-site

$75K - $120K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Validation Engineer - VHP / Aseptic Processing / Pharmaceutical Manufacturing Location : Indianapolis, IN or remote in Northeast US Hire Type : Direct Hire Compensation : $75,000 - $120,000 Benefits

Lancesoft INC

Production Technician II

Indianapolis, IN · On-site

$27 - $30/hr

This is a mid-level position in the aseptic filling group within the Manufacturing department. It utilizes those with experience and the training needed to manufacture pharmaceuticals in a strictly ...

Simtra BioPharma Solutions

Process Engineer

Bloomington, IN · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Implement process improvement projects that enhance efficiency, improve quality, and reduce costs for aseptic filling processes, lyophilization, or inspection & packaging processes * Develop user ...

Simtra BioPharma Solutions

Process Engineer

Bloomington, IN · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Implement process improvement projects that enhance efficiency, improve quality, and reduce costs for aseptic filling processes, lyophilization, or inspection & packaging processes * Develop user ...

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Aseptic information

What is an aseptic?

An aseptic job involves maintaining a sterile environment to prevent contamination in industries like pharmaceuticals, biotechnology, and food production. Workers follow strict protocols, including gowning, sanitization, and cleanroom procedures, to ensure product safety. Common roles include aseptic technicians, operators, and quality control specialists. These jobs are crucial in producing sterile medications, medical devices, and other products requiring contamination-free conditions.

What are the typical daily responsibilities for someone working in an aseptic environment?

Aseptic technicians are responsible for preparing, filling, and packaging pharmaceutical or biotechnology products in strictly controlled sterile environments. Daily tasks include gowning up using aseptic techniques, operating filling and sealing machines, monitoring cleanroom conditions, and documenting every process step to comply with regulatory standards. You’ll also be part of routine cleaning, equipment set-up, and frequent inspections to avoid contamination. Collaboration with quality assurance teams and production supervisors is common to ensure all procedures meet Good Manufacturing Practice (GMP) requirements. This role is ideal for individuals who thrive in detail-oriented, process-driven settings and value contributing to patient safety.

What are the key skills and qualifications needed to thrive in the aseptic position, and why are they important?

To thrive as an Aseptic technician, you need a strong understanding of sterile technique, careful attention to cleanliness, and familiarity with Good Manufacturing Practices (GMP), often supported by a high school diploma or associate degree in a science-related field. Experience with autoclaves, laminar flow hoods, and sterile filling equipment, along with training in aseptic gowning and contamination control, is typically required. Strong teamwork, attention to detail, and clear communication help ensure precision and safe operations in highly regulated environments. These skills are crucial for maintaining product safety, complying with industry standards, and supporting smooth production workflows.

What are popular job titles related to Aseptic jobs in Indiana? For Aseptic jobs in Indiana, the most frequently searched job titles are:
What job categories do people searching Aseptic jobs in Indiana look for? The top searched job categories for Aseptic jobs in Indiana are:
What cities in Indiana are hiring for Aseptic jobs? Cities in Indiana with the most Aseptic job openings:
Aseptic jobs near you
Infographic showing various Aseptic job openings in Indiana as of August 2026, with employment types broken down into 66% Full Time, 20% Part Time, 2% Temporary, 8% Contract, and 4% Nights. Highlights an 100% In-person job distribution.

Senior Quality Assurance Representative

Merck Group

Indianapolis, IN • On-site

$69K - $110K/yr

Full-time

Medical, Retirement, PTO

Re-posted 3 days ago

Job description

Work Your Magic with us! Start your next chapter and join MilliporeSigma.
Ready to explore, break barriers, and discover more? We know you've got big plans - so do we! Our colleagues across the globe love innovating with science and technology to enrich people's lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us.
This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US.
Your Role:
This role provides day shift support as quality assurance on-the-floor oversight for manufacturing activities at the facility.
Responsibilities include but are not limited to:
  • Reviews executed documentation to ensure steps are documented and verified at time of execution and that good documentation practices are being followed.
  • Performs and documents line clearances and room release for manufacturing use.
  • Reviews logbooks in manufacturing areas to ensure required activities are being completed and documented.
  • Monitors the formulation and filling processes to ensure cGMP compliance.
  • Provides aseptic core monitoring, acting as a SME for aseptic technique and providing reinforcement of aseptic practices to Manufacturing filling operators. Requires qualification in aseptic gowning and certification as an aseptic processing SME.
  • Observers, reports, and documents operator cleaning and disinfection practices.
  • Documents, reports, and trends observations stemming from Quality Oversight.
  • Documents and reports to management GMP violations, unsafe conditions, or other unusual results or practices.
  • Monday - Friday 8am - 4:30pm.

Physical Attributes:
  • Lift and/or move up to 25 pounds.
  • Wear appropriate Personal Protective Equipment.

Who You Are:
Minimum Qualifications:
  • Bachelors Degree in Biology, Chemistry, or other Life Science Discipline and 2+ years of GMP pharmaceutical industry experience.

OR
  • High School Diploma or GED and 5+ years of GMP pharmaceutical industry experience.

Preferred Qualifications:
  • Experience with computer software applications including Microsoft Excel, Word, and Access.
  • Experience with Quality Management computer systems and SAP.
  • Experience with EU Annex 1 classified areas A, B, C, and D including acceptable aseptic behaviors, practices, and gowning.

Pay Range for this position: $69,200 - $110,900 / year
The offer range represents the anticipated low and high end of the base pay compensation for this position. The actual compensation offered will be determined by factors such as location, level of experience, education, skills, and other job-related factors. Position may be eligible for sales or performance-based bonuses. Benefits offered by the Company include health insurance, paid time off (PTO), retirement contributions, and other perquisites. For more information click here.
RSREMD
What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress!
Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Apply