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Biotech Process Development Jobs in Bennington, VT

Biotech Process Development information

See Bennington, VT salary details

$18

$32

$47

How much do biotech process development jobs pay per hour?

As of Aug 20, 2026, the average hourly pay for biotech process development in Bennington, VT is $32.48, according to ZipRecruiter salary data. Most workers in this role earn between $26.63 and $39.86 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.

Infographic showing various Biotech Process Development job openings in Bennington, VT as of August 2026, with employment types broken down into 1% As Needed, 80% Full Time, 15% Part Time, and 4% Contract. Highlights an 93% Physical, 2% Hybrid, and 5% Remote job distribution, with an average salary of $67,564 per year, or $32.5 per hour.

Director Biotech Production

Regeneron Pharmaceuticals, Inc

Saratoga Springs, NY • On-site

$172.20 - $286.90/hr

Other

Posted 15 days ago


Regeneron rating

8.4

Company rating: 8.4 out of 10

Based on 43 frontline employees who took The Breakroom Quiz

22nd of 86 rated pharmaceutical


Job description

Build our future together

At Regeneron, we use science and innovation to develop life‑changing medicines for people with serious diseases. We are seeking a Director, Biotech Production to join our core manufacturing leadership team, supporting the startup of our new biologics drug substance facility in Saratoga Springs, New York in an on‑site role.

In this role, you will lead manufacturing readiness for facility start‑up—spanning staffing, training, equipment commissioning, and operational readiness—while setting the operating standards for the plant and connecting floor‑level work to global IOPS goals, in close collaboration with Facilities, Process Development, Quality, and Regulatory teams.

This position offers the opportunity to contribute to a fast‑growing, science‑driven organization making a meaningful difference to patients worldwide.

When & where
  • Location: Saratoga Springs, New York, United States
  • Work model/flexibility: On‑site
  • Shift Requirements: May require off‑shift availability and on‑call support as part of the manufacturing leadership team
Discover your role
  • Leads the manufacturing team through facility start‑up, setting the operating standards for a brand‑new biologics plant
  • Directs manufacturing of recombinant proteins according to approved protocols, regulations, and schedules across 2,000L and 10,000L bioreactor suites
  • Translates corporate objectives into strategy, connecting floor‑level performance to global IOPS goals
  • Guides validation activities and equipment commissioning/qualification to ensure operational readiness
  • Partners across Facilities, Process Development, Quality, and Regulatory to keep production running smoothly
  • Builds and develops a high‑performing team, embracing the ambiguity that comes with standing up a new site
  • Tracks and trends key metrics to keep operations safe, compliant, and efficient
  • Thrives on ownership, taking accountability for team performance and results from day one
This role requires
  • Bachelor's in a physical or biological science or chemical engineering and 12+ years of biopharmaceutical/biotech work in a GMP production facility with 8-10 years (MA/MS), or 4-7 years (PhD) of biopharmaceutical/biotech work in a GMP production facility
  • Demonstrated experience leading operational start‑up for a clinical and commercial biologics manufacturing facility
  • Experience working with industrial systems such as SCADA, DCS, MES, and PAT technologies; experience implementing these systems from an operational perspective is preferred
  • Familiarity with other Industry 4.0 technologies and strategies is a plus
  • Gowning and Physical Requirements: requires regular presence on the production floor and entry into classified/controlled environments requiring gowning

We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.

Salary Range (annually)

$172,200.00 - $286,900.00

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