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Biotech Process Development Jobs in Lancaster, PA

PSC Biotech

Senior MSAT Engineer

York, PA · On-site

$102K - $141K/yr

... Biotechnology, Related discipline * 7+ years of experience in: * Sterile formulation development * Drug product manufacturing * Pharmaceutical process development * Senior MSAT Engineer * 8+ years ...

PSC Biotech

Senior MSAT Engineer

York, PA · On-site

$102K - $141K/yr

... Biotechnology, Related discipline 7+ years of experience in: Sterile formulation development Drug product manufacturing Pharmaceutical process development Senior MSAT Engineer 8+ years pharmaceutical ...

PSC Biotech

Senior MSAT Engineer

York, PA · On-site

$95K - $120K/yr

... Biotechnology, Related discipline * 7+ years of experience in: * Sterile formulation development * Drug product manufacturing * Pharmaceutical process development * Senior MSAT Engineer * 8+ years ...

PSC Biotech

Senior Process Engineer

York, PA · On-site

$102K - $132K/yr

Process Development & Technology Transfer Lead process transfer activities from clients into ... Benefits Offering a full suite of benefits, PSC Biotech is firmly focused on diligently investing ...

PSC Biotech

Senior Process Engineer

York, PA · On-site

$102K - $132K/yr

Process Development & Technology Transfer * Lead process transfer activities from clients into ... Engineering, Biotechnology, Related Engineering Discipline * 7+ years of pharmaceutical ...

PSC Biotech

Senior Process Engineer

York, PA · On-site

$95K - $120K/yr

Process Development & Technology Transfer * Lead process transfer activities from clients into ... Engineering, Biotechnology, Related Engineering Discipline * 7+ years of pharmaceutical ...

PSC Biotech

Technical Intern - Open Applications

York, PA · On-site

$14.75 - $19/hr

BioTechnique utilizes our team's expertise to create a process design for our clients' products ... and biotech industry across various functions, including: Engineering and Validation Quality ...

PSC Biotech

Technical Intern - Open Applications

York, PA · On-site

$14.75 - $19/hr

BioTechnique utilizes our team's expertise to create a process design for our clients' products ... Business Development The Experience With operations spanning the globe and featuring a multi ...

PSC Biotech

Senior Director of Quality

York, PA · On-site

... development and implementation of training programs Establish and refine QA processes and ... Hybrid Leadership & Strategic Execution - Communicates effectively across PSC Biotech and ...

PSC Biotech

Senior Director of Quality

York, PA · On-site

... development and implementation of training programs * Establish and refine QA processes and ... Hybrid Leadership & Strategic Execution - Communicates effectively across PSC Biotech and ...

PSC Biotech

Senior Director of Quality

York, PA · On-site

$150K - $200K/yr

... development and implementation of training programs * Establish and refine QA processes and ... Hybrid Leadership & Strategic Execution - Communicates effectively across PSC Biotech and ...

PSC Biotech

Manufacturing Associate III

York, PA · On-site

$26 - $32/hr

BioTechnique utilizes our team's expertise to create a process design for our clients' products ... , and Validation. * Assist with training of Manufacturing Associate I's and II's. Requirements

PSC Biotech

Manufacturing Associate III

York, PA · On-site

BioTechnique utilizes our team's expertise to create a process design for our clients' products ... Benefits Offering a full suite of benefits, PSC Biotech is firmly focused on diligently investing ...

Prism Biotech

Biologics Pharma Sales Rep

Lancaster, PA · On-site

$85K - $116K/yr

Additionally, our company provides professional development and industry leading compensation plans ... Promote pharmaceutical products ethically and within compliance based on company's sales process ...

PSC Biotech

Manufacturing Associate III

York, PA · On-site

BioTechnique utilizes our team's expertise to create a process design for our clients' products ... , and Validation. * Assist with training of Manufacturing Associate I's and II's. Requirements

Kenvue Inc.

Manufacturing Engineering Leader

Lititz, PA · On-site

$101K - $126K/yr

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

Prism Biotech, Inc

Biologics Pharma Sales Rep

Lancaster, PA · On-site

$85K - $116K/yr

Additionally, our company provides professional development and industry leading compensation plans ... Promote pharmaceutical products ethically and within compliance based on company's sales process ...

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All JobsBiotech Process Development JobsBiotech Process Development Jobs in Lancaster, PA

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:

Biotech Process Development jobs near you
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 MSAT Engineer

York, PA • On-site

PSC Biotech
Biotechnology Research and Development • 51 - 200 employees
Learn more about PSC Biotechexternal

$102K - $141K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 14 days ago

Job description


BioTechnique is a sterile injectable full service CDMO providing cytotoxic and therapeutic sterile injectable fill-finish services.From IND applications through commercial scale production, we provide formulation and compounding, fill-finish, and lyophilization services for a wide variety of liquid injectables. BioTechnique utilizes our team's expertise to create a process design for our clients' products that best suits their needs.
The Experience
With operations spanning the globe and featuring a multi-cultural team, BioTechnique is passionate about bringing the best and brightest together in an effort to form something truly special. When you make the decision to join our team, you will be offered the ability to feel inspired in your career, explore your professional passions, and work alongside a group of people who will value and nurture your talents.
We are firm believers in coaching and developing the next generation of industry leaders and influencers. As such, you will not only be offered a compensation and benefits structure that rewards you, but also be provided with the tools that will help you grow and learn.
At BioTechnique, it's about more than just a job-it's about your career and your future.
Your Role
BioTechnique is seeking a Senior MSAT Engineer to support formulation development, compounding process design, technology transfer, scale-up, and commercial manufacturing readiness for sterile injectable products.
The successful candidate will serve as the technical lead for drug product formulation and compounding activities, supporting products ranging from early clinical development through commercial manufacturing. This role will work closely with clients, Manufacturing, Quality, Validation, Process Engineering, and Regulatory teams to ensure formulations are robust, scalable, and suitable for aseptic manufacturing.
This position requires strong expertise in sterile formulation development, compounding operations, biologics handling, process characterization, and GMP manufacturing.
Formulation Development & Technical Transfer
  • Lead formulation assessment and process transfer activities from client organizations.
  • Review development reports, formulation histories, and manufacturing records.
  • Support development and optimization of sterile injectable formulations.
  • Evaluate formulation robustness, manufacturability, and scale-up risks.
  • Develop formulation and process transfer documentation.
  • Collaborate with clients to establish manufacturing strategies for clinical and commercial production

Compounding Process Development
    • Develop and optimize compounding processes for sterile drug products.
    • Establish mixing strategies, hold times, filtration approaches, and process parameters.
    • Support formulation scale-up from laboratory to GMP manufacturing.
    • Identify critical process parameters (CPPs) and critical quality attributes (CQAs).
    • Author process descriptions and manufacturing instructions.
    • Evaluate process performance and support continuous improvement initiatives.

Aseptic Manufacturing Support
  • Provide technical support during:
    • Solution preparation
    • Compounding operations
    • Sterile filtration
    • Aseptic filling
    • Lyophilized product manufacturing
  • Support engineering runs and manufacturing campaigns.
  • Troubleshoot processing deviations and formulation-related challenges.
  • Investigate batch failures, yield losses, or process excursions.

Process Characterization & Scale-Up
  • Design and execute process characterization studies.
  • Support:
    • Mixing studies
    • Hold time studies
    • Filtration studies
    • Product recovery studies
    • Process robustness evaluations
  • Evaluate manufacturing scalability and process capability.
  • Generate data supporting process validation and commercialization.

Technology Transfer & Client Support
  • Serve as technical SME during client onboarding and transfer activities.
  • Support preparation of:
    • Technology Transfer Plans
    • Gap Assessments
    • Risk Assessments
    • Process Transfer Reports
  • Participate in client meetings and technical reviews.
  • Provide scientific guidance throughout development and manufacturing campaigns.

Lyophilization Support
  • Support formulation development for lyophilized products.
  • Collaborate with Lyophilization Development teams on:
    • Formulation optimization
    • Reconstitution performance
    • Product stability considerations
  • Support cycle transfer and scale-up activities.

Regulatory & Compliance Support
  • Ensure activities comply with:
    • FDA cGMP requirements
    • EU GMP Annex 1
    • ICH Guidelines
    • USP Standards
  • Support investigation activities, CAPAs, and client audits.
  • Provide technical documentation for regulatory submissions when required.

Requirements
  • Bachelor of Science in: Chemical Engineering, Pharmaceutical Sciences, Biochemistry, Biotechnology, Related discipline
  • 7+ years of experience in:
    • Sterile formulation development
    • Drug product manufacturing
    • Pharmaceutical process development
    • Senior MSAT Engineer
  • 8+ years pharmaceutical industry experience
  • Strong experience supporting sterile injectable products
  • Must be authorized to work in the U.S.
  • No C2C at this time.

Benefits
Offering a full suite of benefits, PSC Biotech™ is firmly focused on diligently investing in our employees who enable our company to fulfill our mission and achieve success. We want to promote balance, so you not only enjoy your work, but also have the time and resources to live your life happy and healthy.
  • Medical, Dental, and Vision - PSC pays 100% of all qualifying employee medical premiums and 50% for qualifying dependents
  • Insurance options for Employee Assistance Programs, Basic Life Insurance, Short/Long Term Disability and more.
  • 401(k) and 401(k) matching
  • PTO, Sick Time, and Paid Holidays
  • Education Assistance
  • Pet Insurance
  • Fitness Benefits (Membership discounts and other perks/services at qualifying gyms like Anytime Fitness, 24-Hour Fitness, and more)
  • Financial Perks and Discounts

Equal Opportunity Employment Statement
PSC is committed to a policy of Equal Employment Opportunity with respect to all employees, interns, and applicants for employment. Consistent with this commitment, our policy is to comply with all applicable federal, state and local laws concerning employment discrimination. Accordingly, the Company prohibits discrimination against qualified employees, interns and applicants in all aspects of employment including, but not limited to: recruitment, interviewing, hiring (or failure or refusal to hire), evaluation, compensation, promotion, job assignment, transfer, demotion, training, leaves of absence, layoff, benefits, use of facilities, working conditions, termination and employer-sponsored activities and programs,including wellness, social and recreational programs. Employment decisions will be made without regard to an applicant's, employee's, or intern's actual or perceived: race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), national origin, age (40 or older), disability, genetic information, or any other status protected by law.
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