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Biotech Process Development Jobs in Indianapolis, IN

MEDVACON

Aseptic Process Development - CDMO

IN · On-site

Our focus is cGMP Quality and Compliance, Validation and Regulatory for pharmaceutical and biotechnology companies. Our leading CDMO client is eager to hire an Aseptic Downstream Process Development ...

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Biotech Process Development information

See Indianapolis, IN salary details

$18

$32

$47

How much do biotech process development jobs pay per hour?

As of Aug 23, 2026, the average hourly pay for biotech process development in Indianapolis, IN is $32.20, according to ZipRecruiter salary data. Most workers in this role earn between $26.44 and $39.52 per hour, depending on experience, location, and employer.

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 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 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 are popular job titles related to Biotech Process Development jobs in Indianapolis, IN?

For Biotech Process Development jobs in Indianapolis, IN, the most frequently searched job titles are:

What job categories do people searching Biotech Process Development jobs in Indianapolis, IN look for?

The top searched job categories for Biotech Process Development jobs in Indianapolis, IN are:

Biotech Process Development jobs near you

Aseptic Process Development - CDMO

MEDVACON

Indianapolis, IN

Full-time

Re-posted 5 days ago

Job description

Company Description

MEDVACON Life Sciences works with many leading pharmaceutical companies to hire consulting, contract and full-time employees to join client organizations.

Our focus is cGMP Quality and Compliance, Validation and Regulatory for pharmaceutical and biotechnology companies.

Our leading CDMO client is eager to hire an Aseptic Downstream Process Development SME for their Indianapolis site.  This is a full-time role directly with the client - an outstanding opportunity to join an innovative company developing brilliant biotechnology.

A successful background will be strong in Lab, Process and Analytical development including working knowledge of cGMPs related to the production of viral therapeutics and the ability to interface successfully with multi-disciplined teams.


Job Description

Direct the development and establishment of processes in GMP. 

Accountable for developing a scalable platform for viral vector production processes that minimizes the risk during Process Development to GMP scale-up. 

Provide technical expertise and leadership in science & technology and requires close collaboration with internal stakeholders.

If you're interested so far - apply!  A member of our talent team will contact you and share comprehensive job details. 

Qualifications

Bachelors Degree

5+ years exp in a cGMP 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 process development, including experience with Contract Development and Manufacturing Organizations

Experience with cell culture technologies, molecular biology, and aseptic processing

Additional Information

Please attach a WORD resume to your submission

All of your information will be kept confidential according to EEO guidelines.

ON-SITE only

This is a FT role and will include a full benefits package

40-hour week

NO AGENCIES please


Apply