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Gmp Manufacturing Jobs in Indiana (NOW HIRING)

eGenesis

IN

The role supports a unique environment that includes GMP manufacturing operations, research laboratories, animal care operations, veterinary and surgical support areas, maintenance activities, and ...

INCOG

Manufacturing Specialist, Filling

Fishers, IN · On-site

The ideal candidate must have experience in pharmaceuticals and/or biologics, GMP manufacturing, or within highly regulated industries. The Manufacturing Specialist's primary responsibility is to ...

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How much do gmp manufacturing jobs pay per hour?

As of Aug 15, 2026, the average hourly pay for gmp manufacturing in Indiana is $23.74, according to ZipRecruiter salary data. Most workers in this role earn between $19.23 and $27.45 per hour, depending on experience, location, and employer.

What is a GMP manufacturing?

A GMP Manufacturing job involves producing pharmaceutical, biotechnology, or medical device products while following Good Manufacturing Practices (GMP) regulations. Responsibilities typically include operating equipment, maintaining sterile environments, documenting processes, and ensuring product quality and compliance. These roles are essential for maintaining safety and regulatory standards in healthcare-related manufacturing industries.

What are the key skills and qualifications needed to thrive in GMP manufacturing?

To excel in GMP Manufacturing, you need a solid understanding of Good Manufacturing Practices, attention to detail, and experience in regulated production environments, often backed by a degree in life sciences or engineering. Familiarity with quality management systems, batch record documentation, and equipment such as bioreactors or chromatography columns is typically required, and certifications like GMP or Six Sigma can be beneficial. Strong teamwork, communication skills, and the ability to follow precise procedures are essential soft skills for this position. These competencies ensure safe, compliant, and efficient production of pharmaceuticals or biotechnology products within strict regulatory frameworks.

What are some common challenges faced in GMP manufacturing roles?

Employees in GMP Manufacturing often encounter challenges such as maintaining meticulous documentation, adapting to changing regulatory requirements, and adhering to strict cleanliness and safety standards. The production process must be tightly controlled and deviations must be reported and resolved promptly, which requires a high level of diligence and accountability. Additionally, working collaboratively with quality assurance, engineering, and other cross-functional teams can add complexity to daily operations. Overcoming these challenges helps ensure product quality and regulatory compliance, while also providing valuable professional experience in one of the most highly regulated industries.

What are the most commonly searched types of Gmp Manufacturing jobs in Indiana?

The most popular types of Gmp Manufacturing jobs in Indiana are:

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

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

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

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

What cities in Indiana are hiring for Gmp Manufacturing jobs?

Cities in Indiana with the most Gmp Manufacturing job openings:

Gmp Manufacturing jobs near you
Infographic showing various Gmp Manufacturing job openings in Indiana as of August 2026, with employment types broken down into 86% Full Time, 7% Part Time, 4% Contract, and 3% Nights. Highlights an 95% Physical, 2% Hybrid, and 3% Remote job distribution, with an average salary of $49,376 per year, or $23.7 per hour.

Manufacturing Specialist - Filling, 2nd shift

INCOG BioPharma Services

Fishers, IN

Other

Re-posted 18 days ago

Job description

The Manufacturing Specialist is a key technical role within INCOG BioPharma Operations. The ideal candidate must have experience in pharmaceuticals and/or biologics and GMP manufacturing.

The Manufacturing Specialist will be expected to work hands-on, be actively involved in continuous process improvements while taking ownership of the quality and quantity of product produced. The ideal candidate should possess a strong mechanical aptitude with strong trouble shooting skills on filling manufacturing equipment. They should demonstrate mentor and leadership skills to motivate manufacturing personnel, drive timely production activities and inspire problem solving & solution driven thinking.

This is a 2nd shift position with typical hours Monday-Friday from 3:00PM-11:30PM.


Essential Job Functions:

  • Follow production and manufacturing procedures.
  • Perform duties in Grade C, D, and controlled non-classified cleanrooms.
  • Perform aseptic manipulations within Grade A isolators.
  • Safely operate production equipment including setup and changeovers.
  • Lead batch start up activities and execution of production cycles
  • Accurately document data and complete batch records.
  • Execute validation/engineering protocols as needed.
  • Train others in various manufacturing tasks including, but not limited to: fill/finish, sanitization, component and equipment preparation.
  • Maintain production equipment and troubleshoot issues.
  • Support equipment optimization efforts and continuous improvement efforts.
  • Resolve issues that arise in day to day running of operation and providing timely responses and solutions.
  • SME for filling equipment and supporting systems.
  • Participate and/or support process FMEAs to understand process and product risks as a pre-requisite for process validation.
  • Provide technical support to manufacturing activities.
  • Apply Good Engineering Practices (GEP) to drive site engineering and operational excellence.
  • Work flexible hours to ensure production facility coverage.

Special Job Requirements:

  • High School diploma and 7 years of GMP pharmaceutical experience with the installation, operation, cleaning, and maintenance of pharmaceutical GMP equipment.
  • Working knowledge of MS Office, MS Word, MS Excel, Windows or equivalent is required.
  • Must have previous experience with pharmaceutical aseptic processing (fill and finish) cGMP.

Additional Preferences:

  • BS in biological sciences/biotechnology and 1 year of GMP pharmaceutical experience with the installation, operation, cleaning, and maintenance of pharmaceutical GMP equipment.
  • Excellent communication skills.
  • Ability to apply concepts such as fractions, percentages, ratios and proportions to practical situations.
  • Ability to learn and operate a range of industry systems including and not limited to ERP and inventory management systems.

Additional info about INCOG BioPharma Services:

At INCOG BioPharma we have built a world-class CDMO for parenteral injectable drugs. Our culture and priorities are different by design: focused on building long-term value for our customers, we are committed to a service-culture mindset, technical excellence, and a collaborative and team-centered approach to doing business.

If you crave the challenge of creating systems from scratch and believe you have insights for a better way of doing business, which benefits customers by ensuring quality outcomes and accelerating their route to market, we want to hear from you. Unless otherwise specified, all positions are based out of our Fishers, IN offices. Please note, we are a smoke-free campus.

INCOG BioPharma is an Equal Opportunity Employer and prohibits discrimination and harassment of any kind.  All employment decisions at INCOG BioPharma are based on business needs, job requirements and individual qualifications, without regard to race, color, religion or belief, sex (including pregnancy), age, physical disability, sexual orientation, family or parental status, or any other status protected by the laws or regulations in the locations where we operate. We will not tolerate discrimination or harassment based on any of these characteristics.

By submitting your resume and details, you are declaring that the information is correct and accurate.

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