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Biotech Process Development Jobs (NOW HIRING)

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... biotechnology process development. - Analysis of experiments through analytical techniques including HPLC, light scattering, and spectroscopy. - Data interpretation and presentation, manuscript ...

NJ · On-site

$220 - $293/hr

This role involves leading process development and manufacturing efforts to support pipeline ... The ideal candidate will hold a PhD with extensive experience in a biotech setting, specifically in ...

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Biotech Process Development information

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$18

$33

$49

How much do biotech process development jobs pay per hour?

As of Aug 20, 2026, the average hourly pay for biotech process development 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 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.

More about Biotech Process Development jobs

What cities are hiring for Biotech Process Development jobs?

Cities with the most Biotech Process Development job openings:

What states have the most Biotech Process Development jobs?

States with the most job openings for Biotech Process Development jobs include:

Infographic showing various Biotech Process Development job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 83% Full Time, 14% Part Time, and 2% Contract. Highlights an 90% Physical, 3% Hybrid, and 7% Remote job distribution, with an average salary of $70,060 per year, or $33.7 per hour.

Associate Director, Process & Analytical Development

Lonza

Walkersville, MD • On-site, Remote

$155K - $181K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 2 days ago

New


Lonza rating

8.3

Company rating: 8.3 out of 10

Based on 42 frontline employees who took The Breakroom Quiz

25th of 86 rated pharmaceutical


Job description

Associate Director, Process & Analytical Development

Location: This position is currently remote. A future transition to an on-site location on the U.S. East-Coast/Mid-West is anticipated as the project progresses, with an expected timeline in 2027. This is a full-time role with a Monday-Friday schedule from 8:00 a.m. to 5:00 p.m.

What you will get:

The full-time base annual salary for this position is expected to range between $155,700 to $181,650. In addition, below you will find a comprehensive summary of the benefits package we offer:

  • Performance-related bonus.

  • Medical, dental and vision insurance.

  • 401(k) matching plan.

  • Life insurance, as well as short-term and long-term disability insurance.

  • Employee assistance programs.

  • Paid time off (PTO).

Compensation for this role will be determined by the candidate's qualifications, skills, experience, and relevant knowledge.

What will you do:

The Associate Director, Process & Analytical Development (ADPD) provides strategic and operational leadership for analytical development, process development, and project-specific manufacturing activities within the ADPD organization. This role is accountable for ensuring the organization consistently delivers services and products safely, compliantly, on time, in full, and within budget while supporting ADS business objectives and long-term growth strategies.

This position will initially operate remotely and transition to the future U.S. ADPD center of gravity as the organization continues to expand.

  • Lead, coach, and develop a high-performing Process & Analytical Development team, fostering a culture of accountability, collaboration, safety, continuous improvement, and operational readiness.

  • Define the strategic direction of the ADPD organization through long-range planning, portfolio prioritization, resource allocation, and performance management.

  • Drive organizational readiness and capability development to support future manufacturing operations and business growth.

  • Serve as a key contributor to the Sales & Operations Planning (S&OP) process, ensuring capabilities, capacity, and organizational structures align with customer demand and business objectives.

  • Ensure the successful execution of all development and manufacturing activities while meeting safety, quality, compliance, and business requirements.

  • Maintain ownership of operational budgets and resources to ensure efficient and effective organizational performance.

  • Drive Lean maturity and continuous improvement initiatives across the organization, establishing a culture focused on operational excellence and performance.

  • Lead the execution of strategic initiatives that support business objectives and organizational growth within the ADPD function.

Additional Responsibilities:

  • Partner closely with R&D and technical organizations to support the deployment of new technologies and innovative development approaches.

  • Serve as a subject matter expert during product acquisition, technology transfer, and process development activities.

  • Support facility startup, operational readiness, validation, and manufacturing scale-up initiatives.

  • Collaborate with Engineering, Manufacturing, Quality, MSAT, Automation, EH&S, Finance, and HR to ensure successful project execution and organizational alignment.

  • Establish strong governance and communication practices that enable effective decision-making and risk management.

  • Build organizational capability and succession plans to support future operational requirements.

  • Drive adoption of digital tools, automation solutions, and data-driven decision-making practices.

What we are looking for:

  • Master's degree in engineering, Life Sciences, Pharmaceutical Sciences, Chemistry, Biochemistry, or a related scientific discipline.

  • Minimum of 10 years of progressive leadership experience in pharmaceutical, biotechnology, process development, analytical development, or manufacturing operations.

  • Deep understanding of small molecule and bioconjugate technologies.

  • Significant experience within GMP-regulated pharmaceutical or biotechnology environments.

  • Proven leadership experience supporting facility startups, technology transfers, validation programs, operational readiness initiatives, or large-scale capital projects.

  • Strong knowledge of pharmaceutical manufacturing operations, GMP requirements, process development, analytical development, and commercialization activities.

  • Experience supporting greenfield and brownfield facility expansion projects and cross-functional project governance.

  • Demonstrated expertise in small molecule drug substance manufacturing processes and technologies.

  • Proven ability to influence cross-functional stakeholders including Engineering, Quality, Manufacturing, MSAT, Automation, EH&S, Finance, and Human Resources.

  • Strong strategic and practical problem-solving capabilities with the ability to translate business requirements into operational solutions.

  • Excellent executive communication and presentation skills, with experience reporting risks, operational readiness, and business performance to senior leadership.

  • Demonstrated success building teams, developing organizational capability, and preparing organizations for operational growth.

  • Knowledge of Lean Manufacturing, Six Sigma methodologies, digital systems, automation technologies, and data integrity principles.

  • Ability to thrive in a dynamic environment and effectively manage ambiguity, evolving priorities, and multiple stakeholder groups.

  • Strong leadership presence with a track record of delivering results through collaboration, innovation, and accountability.

About Lonza

At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone's ideas, big or small, have the potential to improve millions of lives, and that's the kind of work we want you to be part of.

Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we offer equal employment opportunities to all qualified applicants regardless of race, religion, color, national origin, sex, sexual orientation, gender identity, age, disability, veteran status, or any other characteristic protected by law. If you're ready to help turn our customers' breakthrough ideas into viable therapies, we look forward to welcoming you on board.

Ready to shape the future of life sciences? Apply now.


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