1

Biotech Process Development Jobs in Indiana (NOW HIRING)

Responsibilities Essential Functions If applicable, may be accountable for supporting development ... IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for ...

Responsibilities Essential Functions If applicable, may be accountable for supporting development ... IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for ...

Responsibilities Essential Functions If applicable, may be accountable for supporting development ... IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for ...

Responsibilities Essential Functions If applicable, may be accountable for supporting development ... IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for ...

We create intelligent connections to accelerate the development and commercialization of innovative ... IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for ...

Demonstrated knowledge of pharmaceutical manufacturing of biotechnology products, aseptic processing (fill and finish), and process development * Hands-on experience troubleshooting, repairing and ...

next page

Showing results 1-20

Biotech Process Development information

See Indiana salary details

$18

$29

$40

How much do biotech process development jobs pay per hour?

As of May 31, 2026, the average hourly pay for biotech process development in Indiana is $29.96, according to ZipRecruiter salary data. Most workers in this role earn between $26.11 and $33.08 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in Biotech Process Development, and why are they important?

To excel in Biotech Process Development, you need a strong background in bioprocess engineering, molecular biology, and chemistry, typically supported by a degree in biotechnology or related fields. Familiarity with tools such as bioreactors, chromatography systems, and data analysis software, along with certifications in Good Manufacturing Practice (GMP), is highly valuable. Strong problem-solving skills, attention to detail, and effective teamwork distinguish top performers in this role. These competencies are crucial for optimizing processes, ensuring product quality, and driving innovation in the biotech industry.

What are some common challenges faced by professionals in Biotech Process Development, and how are they typically addressed?

Professionals in Biotech Process Development often encounter challenges related to scaling up processes from the laboratory to commercial production, ensuring product consistency, and meeting strict regulatory standards. Addressing these challenges typically involves close collaboration with cross-functional teams such as quality assurance, regulatory affairs, and manufacturing. Continuous process optimization, thorough documentation, and robust validation protocols are essential strategies to overcome these hurdles and ensure successful product development and commercialization.

What is biotech process development?

Biotech process development refers to the design, optimization, and scale-up of manufacturing processes used to produce biological products, such as pharmaceuticals, enzymes, or vaccines. Professionals in this field work to turn laboratory procedures into efficient, large-scale industrial processes that meet regulatory and quality standards. This often involves selecting suitable equipment, optimizing conditions, ensuring reproducibility, and troubleshooting production issues. The ultimate goal is to produce high-quality products safely, consistently, and cost-effectively.

What is the difference between Biotech Process Development vs Biotech Manufacturing Associate?

AspectBiotech Process DevelopmentBiotech Manufacturing Associate
Primary FocusDesigning, optimizing, and scaling up bioprocesses for product developmentExecuting manufacturing processes to produce biopharmaceuticals at scale
Work EnvironmentLaboratories and pilot plant facilitiesProduction floors and manufacturing plants
Required SkillsProcess design, lab techniques, troubleshootingEquipment operation, quality control, adherence to SOPs
Typical CredentialsBSc/MSc in Biotechnology, Chemical Engineering, or related fieldsBSc in Biotechnology, Biology, or related fields

While both roles are essential in biotech, Biotech Process Development focuses on creating and optimizing processes during product development, whereas Biotech Manufacturing Associates handle the day-to-day production to ensure consistent product quality at scale.

What job categories do people searching Biotech Process Development jobs in Indiana look for? The top searched job categories for Biotech Process Development jobs in Indiana are:
What cities in Indiana are hiring for Biotech Process Development jobs? Cities in Indiana with the most Biotech Process Development job openings:

Process Safety Specialist/EHS Coordinator

Arxada

Valparaiso, IN

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 12 days ago


Job description

Process Safety Specialist/EHS Coordinator
Valparaiso, IN (Onsite) | 10-20% Travel to Kalama, WA
Arxada is a global leader in innovative solutions that protect our world. Our groundbreaking technologies, in-depth regulatory know-how, manufacturing and process development help our customers to safeguard nutrition, health and infrastructure efficiently through chemistry and biotechnology that enhance sustainability. We offer a broad portfolio of ingredients and services for multiple end-markets that include Human Health & Nutrition, Home & Personal Care, Professional Hygiene, Paints & Coatings and Wood Protection.
With customers in more than 100 countries, the company achieved sales of CHF 2 billion in 2024. Headquartered in Basel (Switzerland), Arxada employs 3,200 associates across 24 production sites and 14 R&D centers, all committed to our customers' success.]
About the Role
As anProcess Safety Specialist/EHS Coordinatoryou will play a vital role in fostering a strong safety culture at ourValparaiso, Indiana manufacturing site, while also supporting compliance activities at ourKalama, Washington location. This is a handson, onsite role within a chemical manufacturing environment, where your expertise will directly contribute to protecting our people, processes, and communities.
Working collaboratively with site leadership, operations, and employees, you will helpidentify risks, drive proactive safety improvements, and ensure compliance with OSHA and other regulatory requirements. This role is ideal for a selfstarter who is passionate about environmental, health, and safety excellence and motivated to make a real impact every day.
Essential Job Functions
  • Advise site leadership and employees on provisions to minimize safety and occupational health risks.
  • Develop, implement, and enforce OSHA and sitespecific safety policies, including accident and incident reporting processes.
  • Lead and coordinate accident and nearmiss investigations, identifying root causes and recommending corrective actions.
  • Maintain accurate safety records, metrics, and documentation, and ensure audit readiness across both locations.
  • Organize, deliver, and continuously improve EHS and OSHA training programs for site employees.
  • Partner with managers and supervisors to monitor compliance, identify emerging risks, and promote safe work practices.
  • Intervene and take appropriate action in unsafe activities or operations to protect employees and operations.
  • Liaise with regulatory authorities and manage OSHA and safety documentation, including periodic travel (10-20%) to the Kalama, WA site.
Qualifications & Experience
  • Bachelor's degree in Environmental Science, Chemistry, or a related discipline.
  • 2-3 years of experience as an EHS Specialist, Safety Coordinator, or similar role within a manufacturing environment.
  • Strong working knowledge of OSHA regulations, guidelines, and best practices.
  • Demonstrated ability to work independently while collaborating effectively with crossfunctional teams.
  • Experience with safety audits, documentation management, and regulatory recordkeeping.
  • Proven capability in implementing and delivering OSHA and safety training programs.
  • Proficiency in Microsoft Office and strong written and verbal communication skills.
  • Willingness and ability to travel 10-20% as required.

The expected salary range for this role is 69,000- 89,000 annually but specific employee compensation may vary depending on factors including experience, education, training, licensure, certification, location and other jobrelated, nondiscriminatory factors permitted by law.
This role is also eligible to earn a shortterm incentive bonus and the following benefits: 401(k) plan, medical, dental, vision, life, and disability insurance, paid time off, paid holidays and paid sick leave.
[Arxada has world class offering in two distinct areas:
Microbial Control Solutions (MCS)focuses on threats posed by microorganisms to people and planet through five distinct business lines including Professional Hygiene, Home & Personal Care, Wood Protection, Paints & Coatings and Material Protection.
Nutrition, Care & Environmental (NCE),meanwhile, provides materials used to manufacture composites for electronics, aerospace and other markets, as well as vitamins and nutritional ingredients, chemicals and performance intermediates, and raw materials for a wide range of highperformance applications.
Arxada is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a qualified individual with disability, protected veteran status, or any other characteristic protected by law.]
US08