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Pharma Manufacturing Jobs in Indiana (NOW HIRING)

Bilfinger

$23.50 - $31.50/hr

... Engineering, Fertigung, Instandhaltung, Turnarounds und digitalen Anwendungen für Branchen wie Energie, Chemie, Pharma und Öl & Gas. Wir sind Ihr Spezialist für Industriegerüstbau ...

Bilfinger

$23.50 - $31.50/hr

... Engineering, Fertigung, Instandhaltung, Turnarounds und digitalen Anwendungen für Branchen wie Energie, Chemie, Pharma und Öl & Gas. Wir sind Ihr Spezialist für Industriegerüstbau ...

ATS Automation

Quality Engineer

Indianapolis, IN

$68K - $88K/yr

Pharma - aseptic handling and filling of liquid and powder APIs, dispensing custom R&D isolators ... Quality Engineering experience in a manufacturing environment preferred.  * Experience with ...

MEDVACON

Aseptic Process Development - CDMO

IN · On-site

... pharma/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 ...

Staffingine LLC

Field Support

Warsaw, IN · On-site

Act as coordinator for resolving incidents related to any application support in manufacturing ... GxP, MES, Pharma Experience, ITIL, Shopfloor Field Support

Compunnel, Inc.

Production Technician

Indianapolis, IN · On-site

$33/hr

This position in the Manufacturing group requires significant training and expertise demonstrated ... Minimum 2 years of pharma experience is mandatory * Aseptic experience is mandatory * Aseptic ...

VIVOS HOLDINGS

QA TECHNICIAN 1

Mooresville, IN

$20.24/hr

Experience in an FDA regulated manufacturing environment (OTC, Pharma, Medical Device, Cosmetic, or Food) is preferred. SKILLS/ABILITIES: Strong attention to detail and organizational skills.

Scismic

Quality Assurance Manager

Indianapolis, IN

Minimum 7+ years of Quality experience in food / pharma industry.Minimum of 5 years of demonstrated leadership position in a Manufacturing PlantEducation: BS Food Science or related requiredProven ...

Scismic

Quality Assurance Manager

Indianapolis, IN

Minimum 7+ years of Quality experience in food / pharma industry.Minimum of 5 years of demonstrated leadership position in a Manufacturing PlantEducation: BS Food Science or related requiredProven ...

Scismic

Quality Assurance Manager

Indianapolis, IN · On-site

Minimum 7+ years of Quality experience in food / pharma industry.Minimum of 5 years of demonstrated leadership position in a Manufacturing PlantEducation: BS Food Science or related requiredProven ...

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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.

Project Director/Site Head, Texas

Novartis Pharmaceuticals Corporation

Indianapolis, IN

$160K - $297K/yr

Full-time

Medical, Life, Retirement, PTO

Re-posted 28 days ago

Job description

Band

Level 6


Job Description Summary

#LI-Onsite
Location: Texas, United States
Build a new site and shape lifechanging medicines from day one. As Project Director/Site Head, you'll lead our Radioligand Therapy (RLT) drug product manufacturing project from design through commercialization-delivering operational readiness, regulatory compliance, and Health, Safety and Environment (HSE) excellence on time and within budget. You'll set strategy, manage risk, and build a capable organization that seamlessly moves from project to steadystate operations, partnering closely across Manufacturing, Quality, Engineering, Supply Chain, Manufacturing Science & Technology, Finance and People & Organizations. You will drive technology transfer, readiness for inspections, and Sales & Operations Planning (S&OP) integration while championing current Good Manufacturing Practice (cGMP) standards and an inclusive, highperforming culture. This is a unique opportunity to create a modern, patientcentric facility in Texas and lead it into its commercial future-so your decisions tangibly accelerate access to therapies for patients and communities.
The selected candidate for this role is expected to assume the position of Site Head following the successful completion of the project phase and the site's designation as a commercial facility.


Job Description

Key Responsibilities:

  • Lead the Texas drug product manufacturing project from design through commercialization.
  • Develop and manage project plans, deliverables, and team performance to meet targets.
  • Align project strategy and execution with senior business stakeholders and cross-functional leaders.
  • Build and transition a capable organization from project phase to commercial operations.
  • Ensure regulatory, quality, and HSE compliance readiness for inspections and audits.
  • Oversee project budget, schedule, and procurement to achieve financial and operational goals.
  • Champion Novartis values, fostering an inclusive, high-performing culture and talent development.

Essential Requirements:

  • Bachelor's degree in Life Sciences, Chemistry, Pharmacy, Engineering, or Management.
  • Minimum 10 years' experience in manufacturing, technical operations, or supply chain management in pharma or life sciences. Management experience outside of Pharma may contribute up to 5 of those years (i.e. Other Manufacturing, Military, Consulting)
  • Proven leadership and change management skills with success in building and managing teams.
  • Ability to work effectively in a global, networked environment.
  • Strong cultural and intercultural awareness.

Desirable Requirements:

  • Experience with Radioligand Therapy manufacturing.
  • Prior involvement in building and leading site organizations or being part of Commercial Readiness Projects.

The salary for this position is expected to range between $160,300 and $297,700 per year.

The final salary offered is determined based on factors like, but not limited to, relevant

skills and experience, and upon joining Novartis will be reviewed periodically. Novartis may change the published salary range based on company and market factors.

Your compensation will include a performance-based cash incentive and, depending on the level of the role, eligibility to be considered for annual equity awards.

US-based eligible employees will receive a comprehensive benefits package that includes health, life and disability benefits, a 401(k) with company contribution and match, and a variety of other benefits. In addition, employees are eligible for a generous time off package including vacation, personal days, holidays and other leaves.

To learn more about the culture, rewards and benefits we offer our people click Thrive Together.


EEO Statement:

The Novartis Group of Companies are Equal Opportunity Employers. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status. We strive to create an inclusive workplace that cultivates bold innovation through collaboration and empowers our people to unleash their full potential.


Accessibility and reasonable accommodations

The Novartis Group of Companies are committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please send an e-mail to tas.nacomms@novartis.com call +1 (877)395-2339 and let us know the nature of your request and your contact information. Please include the job requisition number in your message.
https://www.novartis.com/careers/careers-research/notice-all-applicants-us-job-openings


Salary Range

$160,300.00 - $297,700.00


Skills Desired

Assembly Language, Biotechnology, Change Management, Chemistry, Continual Improvement Process, Cost Reduction, Finance, General Hse Knowledge , Incentive Program, Installations (Computer Programs), Knowledge Of Gmp, Leadership, Lean Manufacturing, Manufacturing Process, Manufacturing Production, Operational Excellence, Productivity, Purchase, Six Sigma

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