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Biotech Process Development Jobs in Lancaster, PA

... development, equipment optimization, automation initiatives, reliability programs, and cross ... Support equipment, process, facility, utility, automation, and operational improvement initiatives.

... development, equipment optimization, automation initiatives, reliability programs, and cross ... Support equipment, process, facility, utility, automation, and operational improvement initiatives.

... development, equipment optimization, automation initiatives, reliability programs, and cross ... Support equipment, process, facility, utility, automation, and operational improvement initiatives.

... development, equipment optimization, automation initiatives, reliability programs, and cross ... Support equipment, process, facility, utility, automation, and operational improvement initiatives.

... development, equipment optimization, automation initiatives, reliability programs, and cross ... Support equipment, process, facility, utility, automation, and operational improvement initiatives.

... development, equipment optimization, automation initiatives, reliability programs, and cross ... Support equipment, process, facility, utility, automation, and operational improvement initiatives.

... development, equipment optimization, automation initiatives, reliability programs, and cross ... Support equipment, process, facility, utility, automation, and operational improvement initiatives.

Contribute in the development of tool to estimate utilization and cost for life cycle of a project ... Experience in an FDA regulated Biotech/Pharmaceutical industry * Experience in working in an FTE ...

Showing results 21-40

Biotech Process Development information

See Lancaster, PA salary details

$18

$32

$48

How much do biotech process development jobs pay per hour?

As of Sep 10, 2026, the average hourly pay for biotech process development in Lancaster, PA is $32.73, according to ZipRecruiter salary data. Most workers in this role earn between $26.88 and $40.19 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 Lancaster, PA?

For Biotech Process Development jobs in Lancaster, PA, the most frequently searched job titles are:

What job categories do people searching Biotech Process Development jobs in Lancaster, PA look for?

The top searched job categories for Biotech Process Development jobs in Lancaster, PA are:

What cities near Lancaster, PA are hiring for Biotech Process Development jobs?

Cities near Lancaster, PA with the most Biotech Process Development job openings:

Infographic showing various Biotech Process Development job openings in Lancaster, PA as of June 2026, with employment types broken down into 5% As Needed, 67% Full Time, 18% Part Time, 5% Temporary, and 5% Contract. Highlights an 86% Physical, 2% Hybrid, and 12% Remote job distribution, with an average salary of $68,088 per year, or $32.7 per hour.

Senior Engineering Professional, Manufacturing & Technical Operations

Lititz, PA • On-site

Kenvue
Toiletries Manufacturing • 10K+ employees

$90K - $127K/yr

Full-time

PTO

Posted 8 days ago


Key responsibilities

  • Support engineering projects throughout the project lifecycle, from planning and design through implementation and operational readiness.

  • Collaborate with cross-functional teams including Engineering, Manufacturing, Quality, Validation, Automation, Supply Chain, and Operations.

  • Contribute to the development, execution, and maintenance of engineering and technical programs that support operational excellence and compliance.


Kenvue rating

9.1

Company rating: 9.1 out of 10

Based on 6 frontline employees who took The Breakroom Quiz


Job description

Kenvue is currently recruiting for a:

Senior Engineering Professional, Manufacturing & Technical Operations

What we do

At Kenvue, we realize the extraordinary power of everyday care. Built on over a century of heritage and rooted in science, we’re the house of iconic brands - including NEUTROGENA®, AVEENO®, TYLENOL®, LISTERINE®, JOHNSON’S® and BAND-AID® that you already know and love. Science is our passion; care is our talent.

Who We Are

Our global team is ~ 22,000 brilliant people with a workplace culture where every voice matters, and every contribution is appreciated.  We are passionate about insights, innovation and committed to delivering the best products to our customers. With expertise and empathy, being a Kenvuer means having the power to impact millions of people every day. We put people first, care fiercely, earn trust with science and solve with courage – and have brilliant opportunities waiting for you! Join us in shaping our future–and yours. For more information, click here.

Role reports to:

Sr Manager Engineering and Automation

Location:

North America, United States, Pennsylvania, Lititz

Work Location:

Fully Onsite

What you will do

We are continuously building a network of experienced engineering professionals to support current and future opportunities across our manufacturing and technical operations environments. This evergreen position is designed for individuals who are passionate about delivering engineering excellence, driving continuous improvement, supporting complex projects, and ensuring operational readiness in regulated manufacturing settings.

Successful candidates may contribute to a variety of initiatives involving equipment, facilities, utilities, manufacturing processes, automation, compliance, and operational improvement programs across multiple locations and business functions.

Key Responsibilities
  • Support engineering projects throughout the project lifecycle, from planning and design through implementation and operational readiness.
  • Collaborate with cross-functional teams including Engineering, Manufacturing, Quality, Validation, Automation, Supply Chain, and Operations.
  • Contribute to the development, execution, and maintenance of engineering and technical programs that support operational excellence and compliance.
  • Review, develop, and maintain technical documentation, procedures, protocols, reports, and related records.
  • Participate in risk assessments, troubleshooting efforts, investigations, and continuous improvement initiatives.
  • Support qualification, validation, commissioning, equipment lifecycle management, and process improvement activities as applicable.
  • Ensure adherence to company standards, industry regulations, and applicable quality requirements.
  • Provide technical guidance and subject matter expertise to project teams and business partners.
  • Assist in project planning, resource coordination, execution tracking, and reporting activities.
  • Support internal and external audits, inspections, and compliance initiatives when required.
  • Contribute to the development and implementation of best practices that improve efficiency, reliability, quality, and operational performance.
QualificationsRequired
  • Bachelor's degree in Engineering, Science, or a related technical discipline.
  • Several years of experience supporting engineering, manufacturing, technical operations, project execution, quality, validation, automation, or related functions.
  • Experience working within regulated manufacturing environments.
  • Strong problem-solving, analytical, and decision-making skills.
  • Ability to manage multiple priorities and work effectively in cross-functional teams.
  • Strong written and verbal communication skills.
Preferred
  • Experience supporting pharmaceutical, medical device, consumer health, biotechnology, food, or other highly regulated industries.
  • Knowledge of Good Manufacturing Practices (GMP) and related quality systems.
  • Experience with capital projects, equipment lifecycle management, process improvement, commissioning, qualification, validation, automation, or operational excellence initiatives.
  • Professional certifications in project management, quality, engineering, or continuous improvement methodologies are a plus.

What’s in it for you

Annual base salary for new hires in this position ranges:

$90,100.00 - $127,200.00

This takes into account a number of factors including work location, the candidate’s skills, experience, education level & other job-related factors.

  • Competitive Benefit Package*

  • Paid Company Holidays, Paid Vacation, Volunteer Time & More!

  • Learning & Development Opportunities

  • Kenvuer Impact Networks

  • This list could vary based on location/region

*Note: Total Rewards at Kenvue include salary, bonus (if applicable) and benefits. Your Talent Access Partner will be able to share more about our total rewards offerings and the specific salary range for the relevant location(s) during the recruitment & hiring process.

Kenvue is proud to be an Equal Opportunity Employer. All qualified applicants will receive consideration for employment based on merit without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.

If you are an individual with a disability, please check our Disability Assistance page for information on how to request an accommodation.


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