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Gmp Manufacturing Jobs in Indiana (NOW HIRING)

INCOG

Manufacturing Specialist, Filling

Fishers, IN

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 Jul 26, 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 job?

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 the Gmp Manufacturing position, and why are they important?

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 July 2026, with employment types broken down into 79% Full Time, and 21% Contract. Highlights an 100% In-person job distribution, with an average salary of $49,376 per year, or $23.7 per hour.
Manufacturing Specialist, Filling

Manufacturing Specialist, Filling

INCOG BioPharma Services

Fishers, IN • On-site

Full-time

Posted 10 days ago

Job description

Description
Manufacturing Specialist - Filling Summary
INCOG BioPharma is seeking a highly motivated individual with subject matter expert (SME) capabilities in sterile pharmaceutical manufacturing process controls and industrial automation. The Manufacturing Specialist is a key technical role within INCOG BioPharma Operations. 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 efficiently and safely set up and operate various pieces of production equipment within the facility. They 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 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 1st shift position with typical hours from Monday-Friday 7:00AM-3:30PM
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.
  • Perform cleaning and sanitization, equipment preparation, and aseptic filling duties as needed.
  • Safely operate production equipment including setup and changeovers.
  • 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.
  • Collaborate and communicate with cross functional teams.
  • Work flexible hours to ensure production facility coverage.

Special Job Requirements:
  • 3 years of GMP pharmaceutical experience with the operation, cleaning, and maintenance of pharmaceutical filling equipment.
  • Working knowledge of MS Office, MS Word, MS Excel, Windows or equivalent is required.

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.
  • Demonstrated knowledge of pharmaceutical manufacturing of biotechnology products, aseptic processing (fill and finish) general Good Manufacturing Practices (cGMP).
  • 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.
Qualified applicants must be authorized to work in the United States on a full-time basis. INCOG will not provide support for or sponsor work authorization or visas for this role, including but not limited to F-1 CPT, F-1 OPT, F-1 STEM OPT, J-1, H-1B, TN, O-1, E-3, H-1B1, or L-1.
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