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Process Development Associate Biotechnology Jobs

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 ...

Amgen SA

$125 - $150/hr

Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest ... Process Development Senior Associate What you will do Let's do this. Let's change the world. In ...

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How much do process development associate biotechnology jobs pay per hour?

As of Sep 9, 2026, the average hourly pay for process development associate biotechnology in the United States is $33.68, according to ZipRecruiter salary data. Most workers in this role earn between $27.64 and $41.35 per hour, depending on experience, location, and employer.

What is a process development associate biotechnology?

Process Development Associates in Biotechnology are professionals who support the design, optimization, and scale-up of manufacturing processes for biological products such as proteins, vaccines, or cell therapies. They work closely with scientists and engineers to develop efficient, safe, and reproducible methods for producing these products in a laboratory or production setting. Their responsibilities often include running experiments, analyzing data, maintaining detailed records, and troubleshooting issues that arise during process development. This role is crucial in moving products from research to commercial-scale manufacturing, ensuring quality and regulatory compliance.

What are the key skills and qualifications needed to thrive as a process development associate biotechnology?

To thrive as a Process Development Associate in Biotechnology, you need a solid background in biology, chemistry, or bioengineering, often supported by a relevant bachelor's or master's degree. Familiarity with laboratory instrumentation, bioprocessing equipment, and software tools such as LIMS or statistical analysis programs is typically required. Strong problem-solving abilities, attention to detail, and effective teamwork skills distinguish top performers in this role. These competencies ensure the development and optimization of efficient, reproducible bioprocesses critical to successful product development and scale-up.

What are some common challenges faced by a process development associate biotechnology, and how can they be addressed?

Process Development Associates in biotechnology often encounter challenges such as troubleshooting unexpected results during experiments, adapting to rapidly changing project priorities, and ensuring strict compliance with regulatory standards. Effective communication with cross-functional teams, meticulous documentation, and proactive problem-solving are key to overcoming these hurdles. Staying current with industry best practices and being flexible in approach can also contribute to both personal growth and project success in this collaborative, fast-paced environment.

What jobs can you get with a process development associate biotechnology degree?

A process development associate in biotechnology can pursue roles such as process development scientist, manufacturing technician, quality control analyst, or validation specialist. These positions typically require knowledge of bioprocessing, laboratory techniques, and familiarity with regulatory standards like GMP, often involving collaboration in a laboratory or production environment.

What are popular job titles related to Process Development Associate Biotechnology jobs?

For Process Development Associate Biotechnology jobs, the most frequently searched job titles are:

Infographic showing various Process Development Associate Biotechnology job openings in the United States as of September 2026, with employment types broken down into 1% Internship, 1% As Needed, 82% Full Time, 14% Part Time, and 2% Contract. Highlights an 87% Physical, 2% Hybrid, and 11% Remote job distribution, with an average salary of $70,060 per year, or $33.7 per hour.

Aseptic Process Development - CDMO

IN • On-site

MEDVACON
See more jobs at MEDVACONexternal

Full-time

Re-posted 11 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

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