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Biotech Manufacturing Jobs in Indiana (NOW HIRING)

The job opportunity is for one of our clients specializing in biotechnology product development ... Manufacturing Associate Location: Indianapolis, IN, 46221 Duration: 12 Months Job Type: Temporary ...

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Biotech Manufacturing information

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How much do biotech manufacturing jobs pay per hour?

As of Sep 7, 2026, the average hourly pay for biotech 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 is biotech manufacturing?

Biotech manufacturing is the process of producing products using biological systems or living organisms, such as bacteria, yeast, or mammalian cells. This field is crucial for making pharmaceuticals, vaccines, enzymes, and other biological products on a large scale. Biotech manufacturing involves a combination of biology, chemistry, and engineering to ensure products are made efficiently, safely, and to high quality standards. It is a key part of the biotechnology industry and is vital for developing new medical treatments and therapies.

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

To excel in Biotech Manufacturing, a background in biology, chemistry, or engineering with knowledge of GMP (Good Manufacturing Practices) is typically required. Familiarity with bioprocessing equipment, laboratory information management systems (LIMS), and relevant certifications such as Six Sigma or ASQ is often expected. Attention to detail, problem-solving abilities, and strong teamwork skills help professionals stand out in this environment. These competencies are crucial for ensuring safe, efficient, and compliant production of biotechnological products.

What are some common challenges faced in biotech manufacturing, and how can new team members prepare for them?

In biotech manufacturing, common challenges include maintaining strict quality standards, adhering to complex regulatory requirements, and troubleshooting equipment or process issues. New team members can prepare by familiarizing themselves with Good Manufacturing Practices (GMP), developing strong attention to detail, and being proactive in learning about the latest industry protocols. Teamwork is essential, as much of the work involves cross-functional collaboration with quality assurance, engineering, and research departments to ensure smooth production and compliance.

What is the difference between Biotech Manufacturing vs Biotech Quality Control?

AspectBiotech ManufacturingBiotech Quality Control
CredentialsTypically requires a degree in biotech, biology, or chemistrySimilar credentials, often with additional certifications in quality assurance
Work EnvironmentProduction floors, laboratories, cleanroomsLaboratories, testing facilities, quality assurance labs
Employer & Industry UsageManufacturing plants, biotech companies, pharmaceutical firmsQuality assurance departments within biotech and pharma companies
Common Search & ComparisonBiotech Manufacturing vs Biotech Quality Control

Biotech Manufacturing focuses on producing biotech products, involving process development and production. Biotech Quality Control emphasizes testing and ensuring product quality, often working closely with manufacturing but with a focus on compliance and standards.

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

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

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

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

Infographic showing various Biotech Manufacturing job openings in Indiana as of August 2026, with employment types broken down into 87% Full Time, 7% Part Time, 4% Contract, and 2% Nights. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution, with an average salary of $41,242 per year, or $19.8 per hour.

Biotech Manufacturing Technician (Wed-Sat) (West Lebanon, NH, US)

Biopharma Careers

West Lebanon, IN • On-site

$60 - $80/hr

Other

Medical, Dental, Vision, Retirement, PTO

Posted 4 days ago


Job description

About the Department

Site New Hampshire, located in West Lebanon, is where Novo Nordisk’s life‑saving treatments are brought to life. Our manufacturing facility produces a global supply of our hemophilia and growth hormone product lines, as well as our next generation of cutting‑edge medications.

What we offer you:
  • Leading pay and annual performance bonus for all positions
  • 36Paid days off including vacation, sick days & company holidays
  • Health Insurance, Dental Insurance, Vision Insurance
  • Guaranteed 8% 401K contribution plus individual company match option
  • 14weeks Paid Parental Leave
  • Free access to Novo Nordisk-marketed pharmaceutical products
The Position

Our team of Manufacturing Technicians is looking for a new colleague to join them as soon as possible! Our department consists of several teams working hard to manufacture our life‑saving medicine. This role will be joining our team responsible for the recovery and purification process of Active Pharmaceutical Ingredients (API) for the medicine we produce.

The technicians are continuously working with our teams of engineers, scientists, process associates, facilities support, QA and other stakeholders to improve and simplify our processes. The Manufacturing Technician can expect a dynamic and fast‑paced day centered around production activities on our shopfloor. The shopfloor is fully gowned and a clean manufacturing environment (more details in the essential functions).

We are looking for a team player who is curious, energetic, and who likes staying engaged. In this job you will get a chance to develop your production skills via training, experience, and on the job training. And we want our technicians to be encouraged to engage in optimization of our standards & structures on a daily basis. We expect you to be eager to learn and have a can‑do attitude when it comes to collaboration, have agility in your day‑to‑day work tasks, and be able to adapt to changes with a positive mindset. You will be supervised by your Sr. Manager who will provide direction, support and coaching as you go through your development as a Tech.

This role is based onsite at our West Lebanon, NH bioproduction facility with our Back End Days Manufacturing team, the work schedule for this is as follows:

Week 1: 7AM-7PM Thursday, Friday, Saturday

Week 2: 7AM-7PM Wednesday, Thursday, Friday, Saturday

The first 3-4 weeks will be training in our 'bootcamp' for Manufacturing Technicians. Schedule will be Monday-Friday 8AM-430PM, until the transition to Back End Days schedule.

Relationships

Reports to: Sr. Manager, API Manufacturing

Essential Functions
  • Product manufacturing and product manufacturing support activities
  • Completion of routine documentation associated with the manufacture of product
  • Support in‑process activities and product development when instructed by supervisor
  • Incorporate pre‑planned process improvements/cost reduction program into manufacturing
  • Perform area equipment and process validations in accordance with validation procedures
  • Perform in‑process product testing in accordance with standard procedures
  • Working in the cleanroom areas may require wearing: hairnet, beard cover, frocks/coveralls, shoe covers, snood, face mask, sterile gloves, and to follow GMP processes at all times. Examples of prohibited materials in cleanroom areas may include (but are not limited to): food/drink/gum, jewelry, cosmetics, nail acrylics, perfume/cologne, and personal cell phones
  • Support manufacturing activities in other departments as instructed by supervisor
  • Performs all job duties and responsibilities in a compliant and ethical manner and in accordance with all applicable healthcare laws, regulations and industry codes
  • Incorporates the Novo Nordisk Way and 10 Essentials in all activities and interactions with others
Qualifications

Education and Certifications:

  • High School diploma or Associates Degree or equivalent with a minimum of three (3) years experience, relevant manufacturing preferred or
  • Bachelors’ Degree in a science discipline with zero (0) years’ experience

Knowledge, Skills, and Abilities:

  • Knowledge of cGMP operations preferable
  • The ability to understand and execute established written instructions is essential
Physical Requirements
  • 0-10% overnight travel required. The ability to climb, balance, stoop, reach, stand and walk. The ability to push, lift, grasp, finger and feel. The ability to speak, listen, and understand verbal and written communication. Repetition including substantial movement of wrists, hands, and or fingers.
  • Lifting up to 10 pounds of force occasionally to lift, carry, push, pull, or otherwise move objects.
  • Visual acuity to perform close activities such as: reading, writing, and analysing; and to determine the accuracy, neatness and thoroughness of work assigned or to make general observations.
  • The working environment includes a variety of physical conditions including: noise, close proximity to moving parts and equipment and exposure to chemicals; atmospheric conditions including: odours, fumes and dust.
We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.

At Novo Nordisk, we're not chasing quick fixes – we're creating lasting change for long‑term health. For over 100 years, we've been driven by a single purpose: to defeat serious chronic diseases and help millions of people live healthier lives. This dedication fuels our constant curiosity and inspires us to push the boundaries of what's possible in healthcare. We embrace diverse perspectives, seek out bold ideas, and build partnerships rooted in shared purpose. Together, we're making healthcare more accessible, treating and defeating diseases, and pioneering solutions that create change spanning generations. When you join us, you become part of something bigger – a legacy of impact that reaches far beyond today.

Novo Nordisk is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, protected veteran status or any other characteristic protected by local, state or federal laws, rules or regulations.

If you are interested in applying to Novo Nordisk and need special assistance or an accommodation to apply, please call us at 1-855-411-5290. This contact is for accommodation requests only and cannot be used to inquire about the status of applications.

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