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Pharma Manufacturing Jobs in Indiana (NOW HIRING)

Catalent, Inc.

Manufacturing Supervisor

Greendale, IN · On-site

$54K - $74K/yr

With strong in-house R&D, quality laboratories, and flexible manufacturing and packaging ... Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or ...

Stark Pharma Solutions Inc

Quality Engineer

Lafayette, IN · On-site

$69K - $89K/yr

Hi, My name is Karthik Mutyala and I'm a Recruitment Manager with Stark Pharma, specializing in ... Support manufacturing process improvements and quality enhancement initiatives * Participate in ...

RADcube

Senior Data Architect

Indianapolis, IN · On-site

$64.25 - $86/hr

Partner with business stakeholders across the pharma value chain (R&D, Manufacturing & Quality, Commercial, Drug Development) to gather and translate requirements into technical specifications

Stevanato Group S.p.A.

Assembly Operator

Fishers, IN · On-site

$15.25 - $18.50/hr

... the pharma industry, operating in 9 countries and exporting its products in 70 countries. Today we are the market leader in the manufacture of cartridges for insulin pen injectors, the world ...

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Stevanato Group S.p.A.

Molding Operator

Fishers, IN · On-site

$15.25 - $18.25/hr

... the pharma industry, operating in 9 countries and exporting its products in 70 countries. Today we are the market leader in the manufacture of cartridges for insulin pen injectors, the world ...

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All JobsPharma Manufacturing JobsPharma Manufacturing Jobs in Indiana

Pharma Manufacturing information

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How much do pharma manufacturing jobs pay per hour?

As of Aug 15, 2026, the average hourly pay for pharma manufacturing 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 are the key skills and qualifications needed to thrive in pharma manufacturing, and why are they important?

To thrive in Pharma Manufacturing, you need a solid background in life sciences or engineering, strong knowledge of Good Manufacturing Practices (GMP), and relevant industry experience. Familiarity with manufacturing equipment, process automation systems, and regulatory compliance certifications (such as GMP or ISO) is typically required. Attention to detail, problem-solving abilities, and effective teamwork are crucial soft skills in this field. These competencies ensure consistent product quality, regulatory compliance, and efficient production processes essential for patient safety and company success.

What is the difference between Pharma Manufacturing vs Pharmaceutical Quality Control?

AspectPharma ManufacturingPharmaceutical Quality Control
Primary FocusProduction of medicines and active pharmaceutical ingredientsInspection and testing of products to ensure quality standards
Work EnvironmentManufacturing plants, production linesLaboratories, quality assurance labs
Required CertificationsGMP training, technical certificationsGMP, quality assurance certifications
Industry UsageUsed by pharmaceutical manufacturers during productionUsed by quality control teams to verify product quality

Pharma Manufacturing involves the actual production of medicines, focusing on manufacturing processes and compliance. Pharmaceutical Quality Control centers on testing and inspecting products to ensure they meet safety and quality standards. Both roles are essential in the pharmaceutical industry but serve different functions within the drug development and production process.

How do you get into pharmaceutical manufacturing?

To enter pharmaceutical manufacturing, candidates typically need a high school diploma or equivalent, with many roles requiring a bachelor's degree in fields like chemistry, biology, or engineering. Relevant skills include attention to detail, knowledge of Good Manufacturing Practices (GMP), and experience with laboratory or production equipment; certifications such as cGMP training can also improve job prospects.

What is pharma manufacturing?

Pharma manufacturing refers to the process of producing pharmaceutical drugs on a large scale. This involves the formulation, production, testing, packaging, and quality assurance of medications to ensure they meet regulatory standards. The industry follows strict guidelines to maintain product safety, efficacy, and consistency. Pharma manufacturing can include both the creation of active pharmaceutical ingredients (APIs) and the final dosage forms like tablets, capsules, or injectables.

What are some common challenges faced in a pharma manufacturing role, and how are they typically addressed?

One of the most common challenges in pharma manufacturing is maintaining strict compliance with regulatory standards while ensuring product quality and consistency. Employees must adhere to Good Manufacturing Practices (GMP) and undergo regular audits, which can be demanding but also offer valuable learning experiences. Additionally, adapting to new technologies and process changes is essential, as the industry is constantly evolving. Strong teamwork and clear communication with quality assurance, engineering, and R&D departments help address these challenges and maintain smooth operations.

Is pharmaceutical manufacturing a good job?

Pharmaceutical manufacturing is a stable career that offers opportunities for growth and competitive wages. It requires attention to detail, adherence to safety protocols, and often involves working in cleanroom environments with specialized equipment. Certifications such as Good Manufacturing Practice (GMP) are valuable for advancement in this field.

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

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

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

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

What cities in Indiana are hiring for Pharma Manufacturing jobs?

Cities in Indiana with the most Pharma Manufacturing job openings:

Pharma Manufacturing jobs near you
Infographic showing various Pharma Manufacturing job openings in Indiana as of August 2026, with employment types broken down into 88% Full Time, 6% Part Time, 1% Temporary, 3% Contract, and 2% Nights. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $41,242 per year, or $19.8 per hour.

Manufacturing Engineer with CNC

Noblesoft Technologies

Warsaw, IN • On-site

$70K - $89K/yr

Contractor

Re-posted 22 days ago

Job description

    
Title: Manufacturing Engineer with CNC
Location: Warsaw, IN
 
JD as below
 
Focus: Ensure IQ/OQ/PQ, calibration, traceability, and compliance with GMP/ISO standards in a regulated MedTech environment.
Aim: Ensure robust, reproducible manufacturing processes and maintain inspection-ready documentation.

Key Responsibilities
 
  • Develop and execute validation activities for CNC machines (e.g., mills, lathes, multi-axis CNCs) and associated tooling/work holding.
  • Create and maintain validation documentation, including IQ (Installation Qualification), OQ (Operational Qualification), and PQ (Performance Qualification) protocols and reports.
  • Lead Master Validation Plan, risk assessments (FMEA), and ensure alignment with regulatory requirements (ISO 13485, GMP, 21 CFR Part 820).
  • Collaborate with Manufacturing, Quality Assurance, Regulatory Affairs, and Equipment Engineering to qualify new machines and implement change controls.
  • Design, execute, and document calibration, metrology, and gauge R&R activities; ensure traceability of measurement equipment.
  • Analyze process data (statistical methods, capability studies like Cp/Cpk, Gage R&R) to demonstrate repeatability, accuracy, and process control.
  • Generate, review, and approve validation reports; ensure closure of deviations, CAPAs, and non-conformances.
  • Support supplier qualification and acceptance tests for CNC-related components and tooling.
  • Provide training and knowledge transfer to operators and maintenance staff on validated CNC processes.
  • Ensure compliance with documentation control, record retention, and audit readiness; participate in internal/external audits.
  • Maintain equipment lifecycle documentation (maintenance plans, calibration schedules, firmware/software updates) and ensure alignment with change management processes.
  • Support manufacturing investigations and root-cause analyses related to CNC processes and equipment performance.

Required Qualifications
 
  • Education: Bachelor’s degree in mechanical engineering, Manufacturing Engineering, Biomedical Engineering, or related discipline.
  • Experience: 3–7 years in CNC manufacturing and equipment validation in a regulated environment (MedTech, pharma, or healthcare devices).
  • Regulatory & Standards: Strong knowledge of ISO 13485, GMP, and 21 CFR Part 820; familiarity with risk management (ISO 14971) and validation concepts (IQ/OQ/PQ).
  • Technical Skills:
  • Proficiency in developing and executing IQ/OQ/PQ protocols.
  • Experience with metrology, calibration, and measurement system analysis.
  • Knowledge of CNC machines, CAM software, and basic CNC programming concepts.
  • Statistical tools experience (Minitab, JMP, or similar) for process capability studies.
  • Document control and eQMS systems experience (e.g., MasterControl, ETQ, etc.).
  • Communication: Strong written and verbal communication; ability to write clear validation documentation and present findings to cross-functional teams.