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Biotech Manufacturing Associate Jobs in Indiana (NOW HIRING)

MEDVACON

Aseptic Process Development - CDMO

IN · On-site

... biotech setting Solid foundation in the fundamentals of biochemical engineering, virology and cell biology Pharmaceutical industry experience in technical support of cGMP manufacturing and/or process ...

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Biotech Manufacturing Associate information

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How much do biotech manufacturing associate jobs pay per hour?

As of Aug 16, 2026, the average hourly pay for biotech manufacturing associate in Indiana is $19.83, according to ZipRecruiter salary data. Most workers in this role earn between $15.58 and $22.21 per hour, depending on experience, location, and employer.

What is a biotech manufacturing associate?

Biotech Manufacturing Associates are professionals who work in the production of biotechnology products, such as pharmaceuticals, vaccines, and other biologically derived materials. They are responsible for operating equipment, following strict protocols, and maintaining sterile environments to ensure product quality and safety. Their duties often include preparing materials, monitoring production processes, troubleshooting equipment issues, and documenting all activities according to regulatory standards. This role is essential in ensuring that biotech products are manufactured efficiently and meet both industry and government regulations.

What does a biotech manufacturing associate do?

A biotech manufacturing associate is responsible for producing biological products in a laboratory or manufacturing setting, following strict safety and quality protocols. They operate equipment, prepare materials, monitor processes, and document production activities to ensure compliance with regulatory standards. Strong attention to detail and knowledge of GMP (Good Manufacturing Practice) are essential for this role.

What is the difference between Biotech Manufacturing Associate vs Laboratory Technician?

AspectBiotech Manufacturing AssociateLaboratory Technician
CredentialsHigh school diploma or equivalent; some roles may require associate degreeHigh school diploma or equivalent; some roles may require associate degree or certification
Work EnvironmentManufacturing floor, production lines, cleanroomsLaboratories, research facilities, testing environments
Industry UsageBiotech manufacturing, pharmaceutical productionResearch labs, quality control, testing labs

While both roles support biotech operations, a Biotech Manufacturing Associate primarily works on production and manufacturing processes in a cleanroom environment, focusing on assembling, monitoring, and maintaining manufacturing equipment. In contrast, a Laboratory Technician typically conducts experiments, tests, and quality control procedures in a laboratory setting. Both roles require attention to detail and adherence to safety protocols, but their daily tasks and work environments differ significantly.

What are some common challenges faced by biotech manufacturing associates, and how can they be managed effectively?

Biotech Manufacturing Associates often encounter challenges such as maintaining strict adherence to Good Manufacturing Practices (GMP), troubleshooting equipment malfunctions, and working under tight production deadlines. Effective management of these challenges involves strong attention to detail, proactive communication with cross-functional teams such as quality assurance and engineering, and continuous learning to stay updated on new protocols and technologies. Developing problem-solving skills and embracing a collaborative mindset can also help associates consistently contribute to high-quality production outcomes.

What are the key skills and qualifications needed to thrive as a biotech manufacturing associate?

To thrive as a Biotech Manufacturing Associate, you typically need a background in biology, chemistry, or a related field, along with experience in GMP-regulated environments. Familiarity with bioprocessing equipment, laboratory instrumentation, and documentation systems such as batch records is crucial. Attention to detail, teamwork, and strong problem-solving abilities help you excel in this collaborative and regulated field. These skills ensure the consistent production of safe, high-quality biotech products while maintaining compliance with industry standards.

What are popular job titles related to Biotech Manufacturing Associate jobs in Indiana?

For Biotech Manufacturing Associate jobs in Indiana, the most frequently searched job titles are:

What job categories do people searching Biotech Manufacturing Associate jobs in Indiana look for?

The top searched job categories for Biotech Manufacturing Associate jobs in Indiana are:

What cities in Indiana are hiring for Biotech Manufacturing Associate jobs?

Cities in Indiana with the most Biotech Manufacturing Associate job openings:

Biotech Manufacturing Associate jobs near you
Infographic showing various Biotech Manufacturing Associate job openings in Indiana as of August 2026, with employment types broken down into 1% As Needed, 70% Full Time, 26% Part Time, 1% Temporary, and 2% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $41,242 per year, or $19.8 per hour.

Sr Mfg Equipment Maintenance Technician - 2nd Shift

Thermo Fisher Scientific

Indianapolis, IN • On-site

Full-time

Re-posted 29 days ago

Thermo Fisher Scientific rating

7.7

Company rating: 7.7 out of 10

Based on 426 frontline employees who took The Breakroom Quiz

199th of 540 rated manufacturers

Job description

Work Schedule
Second Shift (Afternoons)
Environmental Conditions
Able to lift 40 lbs. without assistance, Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc... allowed, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)
Job Description
About Thermo Fisher Scientific
When you're part of Thermo Fisher Scientific, you'll do challenging work that makes a real-world impact. Our Clinical Trials Division supports the development and delivery of life-changing therapies by ensuring high-quality, compliant manufacturing and packaging operations.
Time/Shift Hours:
10-hour Shift
Monday - Thursday
2:45pm - 1:30AM
Position Summary
The Equipment Maintenance Technician III is a senior-level technical role technical role responsible for maintaining, troubleshooting, and optimizing automated manufacturing and packaging equipment in a GMP-regulated environment. This role supports equipment reliability, regulatory compliance, and operational efficiency to ensure uninterrupted production of clinical trial materials.
This position requires hands-on technical expertise, the ability to work independently on routine and moderately complex issues, and effective collaboration with cross-functional teams including Engineering, Quality, and Manufacturing.
Key Responsibilities
Equipment Maintenance & Reliability
  • Perform preventive, predictive, and corrective maintenance on automated manufacturing and packaging equipment.
  • Troubleshoot and repair mechanical, electrical, pneumatic, and control system issues.
  • Support root cause analysis (RCA) and implement corrective and preventive actions (CAPAs).
  • Ensure equipment uptime and reliability meet operational performance targets.

Technical Troubleshooting & Systems Support
  • Diagnose and resolve issues involving PLC-controlled systems (Allen-Bradley, Siemens), HMIs, robotics (Fanuc preferred), and vision systems (Cognex).
  • Interpret electrical schematics, mechanical drawings, and system diagrams to support troubleshooting and repairs.
  • Escalate complex issues as needed while contributing to timely resolution.

Production Support
  • Support equipment setup, changeovers, and line clearance activities in compliance with GMP requirements.
  • Configure equipment for different products, packaging formats, and batch requirements.
  • Provide real-time technical support during production to minimize downtime.

Compliance & Documentation
  • Maintain accurate documentation in accordance with cGMP and Good Documentation Practices (GDP).
  • Support deviation investigations, audits, and regulatory inspections.
  • Follow Environmental Health & Safety (EHS) procedures, including lockout/tagout (LOTO).

Continuous Improvement
  • Participate in Lean Manufacturing and continuous improvement initiatives.
  • Identify opportunities to improve equipment performance, reduce downtime, and enhance product quality.
  • Support Engineering in equipment upgrades, qualifications, and process improvements.

Collaboration
  • Partner with Manufacturing, Quality, Engineering, and Validation teams to ensure safe and compliant operations.
  • Communicate technical issues, risks, and solutions effectively.

Qualifications
Education
  • Associate degree or technical certification in Mechatronics, Industrial Maintenance, Automation, or a related field, or equivalent experience.

Experience
  • 2-4 years of experience in equipment maintenance within a manufacturing environment; pharmaceutical, biotech, or medical device experience preferred.
  • Experience supporting automated manufacturing or packaging equipment.

Technical Skills
  • Experience troubleshooting PLC systems (Allen-Bradley and/or Siemens).
  • Familiarity with robotics (Fanuc preferred) and vision systems (Cognex preferred).
  • Strong mechanical and electrical troubleshooting capabilities.
  • Ability to read and interpret technical documentation (schematics, diagrams, manuals).

Soft Skills
  • Strong problem-solving and analytical abilities.
  • Ability to work independently and within a team environment.
  • Effective communication skills.
  • Attention to detail with a focus on quality and compliance.

Physical & Work Environment Requirements
  • Ability to lift up to 50 lbs and perform physical tasks such as standing, bending, and reaching.
  • Work performed in GMP-controlled environments, including cleanrooms requiring gowning.
  • Flexibility to work shifts, weekends, or overtime as needed to support production.

Why Join Us?
  • Work on impactful projects that support patient health worldwide
  • Opportunities for career growth and technical development
  • Collaborative and safety-focused work environment
  • Competitive compensation and benefits package

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