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Pharmaceutical Process Development Jobs (NOW HIRING)

Validation & Engineering Group, Inc

PR

... Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following ... The Process Development Engineer supports the development, validation, and implementation of new ...

Teledyne

Process Development Engineer

Mountain View, CA · Hybrid

$72K - $96K/yr

... pharmaceutical research. We are looking for individuals who thrive on making an impact and want the ... Participate in process development, research, and continuous improvement initiatives * Generate ...

Teledyne FLIR LLC

Process Development Engineer

Goleta, CA · On-site

$90K - $121K/yr

... pharmaceutical research. We are looking for individuals who thrive on making an impact and want the ... As part of process development, hands-on wafer fabrication and characterization of pilot lots is ...

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Pharmaceutical Process Development information

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How much do pharmaceutical process development jobs pay per hour?

As of Aug 10, 2026, the average hourly pay for pharmaceutical 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 the difference between Pharmaceutical Process Development vs Pharmaceutical Manufacturing Technician?

AspectPharmaceutical Process DevelopmentPharmaceutical Manufacturing Technician
Primary FocusDesigning, optimizing, and scaling up manufacturing processes for new or existing drugsOperating equipment, assembling products, and ensuring production runs smoothly
Work EnvironmentLaboratories, R&D facilities, pilot plantsProduction floors, manufacturing plants
Required CredentialsBachelor's degree in pharmacy, chemistry, or related field; experience in process developmentHigh school diploma or equivalent; on-the-job training

Pharmaceutical Process Development focuses on creating and refining manufacturing processes, while Pharmaceutical Manufacturing Technicians handle the day-to-day production tasks. Both roles are essential in the drug development and manufacturing pipeline, but they differ in scope, responsibilities, and work environment.

What are the key skills and qualifications needed to thrive in pharmaceutical process development?

To thrive in Pharmaceutical Process Development, you need a solid background in chemical engineering, pharmaceutical sciences, or a related field, often supported by an advanced degree. Familiarity with process analytical technology (PAT), Good Manufacturing Practice (GMP) standards, and software like MATLAB or SIMCA is typically required. Strong problem-solving, teamwork, and communication skills help professionals navigate complex projects and cross-functional collaborations. These skills are crucial for ensuring efficient, compliant, and innovative drug development processes that meet regulatory requirements and industry standards.

What are the typical challenges faced when transitioning a pharmaceutical process from laboratory scale to full-scale manufacturing?

One of the main challenges in pharmaceutical process development is ensuring that processes developed at laboratory or pilot scale remain robust, efficient, and compliant when scaled up to full manufacturing. Variables such as mixing, temperature control, and material properties can behave differently at larger volumes, potentially impacting product quality or yield. Process developers often work closely with manufacturing, quality assurance, and engineering teams to troubleshoot issues and optimize protocols, making strong cross-functional collaboration skills essential. Addressing regulatory requirements during scale-up is also critical to ensure that the process meets all quality and safety standards.

What is pharmaceutical process development?

Pharmaceutical process development is the series of activities involved in designing, optimizing, and scaling up the manufacturing processes for pharmaceutical products. It includes transforming laboratory procedures into reliable, efficient, and reproducible processes that meet regulatory standards for quality and safety. This phase is crucial for ensuring that medications can be produced consistently and at a larger scale while maintaining product efficacy and compliance with industry regulations.
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What states have the most Pharmaceutical Process Development jobs? States with the most job openings for Pharmaceutical Process Development jobs include:
What job categories do people searching Pharmaceutical Process Development jobs look for? The top searched job categories for Pharmaceutical Process Development jobs are:
Pharmaceutical Process Development jobs near you
Infographic showing various Pharmaceutical Process Development job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 82% Full Time, 14% Part Time, and 3% Contract. Highlights an 91% Physical, 3% Hybrid, and 6% Remote job distribution, with an average salary of $70,060 per year, or $33.7 per hour.

Process Development Engineer

Kuros Biosciences, Inc.

Alpharetta, GA • On-site

Full-time

Posted 27 days ago

Job description

Overview:
The Process Development Engineer supports Kuros' process development engineering activities for the Alpharetta manufacturing facility and broader US Operations objectives. This individual contributor role is responsible for developing, improving, validating, transferring, and sustaining manufacturing processes for Kuros' product portfolio. The engineer will work closely with Operations, Quality, R&D, Supply Chain, Maintenance, and global counterparts to ensure manufacturing processes are safe, scalable, compliant, efficient, and capable of consistently meeting quality, cost, capacity, and customer demand expectations within an ISO 13485 and GMP-regulated environment. This is a full-time, on-site position based out of Alpharetta, GA.
Key Responsibilities:
  • Support process development engineering activities for Kuros' US manufacturing operations, ensuring alignment with production demand, quality objectives, project priorities, and long-term capacity plans.
  • Execute process design, optimization, scale-up, transfer, validation, and lifecycle management activities for new and existing manufacturing processes, including support for product introductions and process transfers from R&D or global manufacturing sites.
  • Develop and support validation and qualification activities for manufacturing equipment, utilities, fixtures, test methods, and processes using appropriate IQ/OQ/PQ, process validation, and risk-based approaches.
  • Create, revise, and maintain manufacturing documentation, including process flow diagrams, BOMs, routings, PFMEAs, control plans, work instructions, SOPs, batch records, validation protocols, validation reports, and engineering change documentation.
  • Partner with Quality to ensure processes, documentation, validation packages, deviations, CAPAs, nonconforming material dispositions, and engineering changes comply with Kuros' quality management system, ISO 13485, GMP, FDA expectations, and applicable regulatory requirements.
  • Perform root cause investigations, failure analysis, and technical problem solving for manufacturing issues, discrepant components, process nonconformances, field feedback, and product performance concerns.
  • Identify and execute continuous improvement initiatives to improve first pass yield, cycle time, throughput, capacity, product reliability, process capability, labor efficiency, safety, and cost using Lean Six Sigma methods such as DMAIC, DMADV, PFMEA, MSA, Gage R&R, Cpk analysis, line balancing, theory of constraints, and waste elimination.
  • Support the design, selection, implementation, commissioning, qualification, and validation of manufacturing equipment, tooling, fixtures, inspection methods, and technology upgrades.
  • Provide technical support for production readiness, process capability, training readiness, standard work, troubleshooting, and day-to-day engineering activities to ensure sustained manufacturing performance.
  • Collaborate cross-functionally with Operations, Quality, R&D, Supply Chain, Maintenance, EH&S, and global Kuros teams to support manufacturing launch, ongoing production, process standardization, and continuous improvement.
  • Collect, analyze, and communicate engineering data and KPIs related to quality, delivery, productivity, validation execution, process capability, project completion, and cost reduction.
  • Support project planning, timeline management, technical risk assessment, and status reporting for assigned process development and manufacturing engineering projects.
  • Promote a safety-first, compliance-driven, data-based, and continuous improvement mindset within manufacturing operations.

Qualifications:
  • Education:
    • Bachelor's degree in Engineering, Biology, Life Sciences, or a related technical field required.
    • Master's degree in Engineering, Life Sciences, Business Administration, or a related field preferred.
    • Lean Six Sigma Green Belt or Black Belt certification preferred.
  • Experience:
    • 3+ years of experience in manufacturing engineering, process development, process engineering, quality engineering, or a related technical function within an ISO 13485, GMP, FDA-regulated, or similarly regulated environment.
    • Experience participating in cross-functional technical projects, process improvement initiatives, or manufacturing launch activities preferred.
    • Experience supporting process validation, equipment qualification, manufacturing transfer, scale-up, continuous improvement, CAPA, NCR, deviation, and engineering change activities.
    • Medical device, biologics, life sciences, pharmaceutical, or regulated manufacturing experience preferred.
  • Skills:
    • Ability to independently execute technical assignments, manage priorities, and collaborate effectively within cross-functional project teams.
    • Strong technical knowledge of process development, manufacturing process validation, equipment qualification, process control, risk management, and regulated manufacturing documentation.
    • Hands-on experience with IQ/OQ/PQ, process validation, PFMEA, control plans, MSA, Gage R&R, attribute agreement analysis, Cpk analysis, root cause analysis, and corrective action methods.
    • Proficiency in Lean manufacturing and Six Sigma tools, including waste elimination, line balancing, theory of constraints, standard work, visual management, value stream thinking, DMAIC, and DMADV.
    • Strong analytical, troubleshooting, and data-based decision-making skills with the ability to translate technical findings into practical manufacturing improvements.
    • Ability to support multiple technical projects, timelines, priorities, and cross-functional stakeholders in a fast-paced manufacturing environment.
    • Excellent communication skills with the ability to interact effectively with Operations, Quality, R&D, Supply Chain, Maintenance, leadership, vendors, and global partners.
    • Proficiency with data analysis and reporting tools such as Minitab, Power BI, Tableau, or equivalent software.
    • Experience working with ERP, master data, BOMs, routings, and manufacturing system inputs; Microsoft Dynamics 365 experience preferred.
    • Working knowledge of manufacturing KPIs such as first pass yield, NCRs, CAPA effectiveness, process capability, inventory accuracy, throughput, cycle time, scrap, and on-time project execution.

Travel Requirement:
  • Ability to travel domestic and international

Pay Range
$92,000-$105,000 USD
Physical Requirements and Work Conditions
The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of the job. Reasonable accommodations may be made to enable individuals with disabilities to perform these functions.
  • Mobility & Posture: May require occasional sitting, standing, walking, climbing, reaching, bending, or stooping.
  • Lifting/Carrying: May require lifting and carrying items 50 pounds or more, depending on the role.
  • Manual Dexterity: Frequent use of hands and fingers for typing, writing, grasping, and operating office or job-specific equipment.
  • Driving: Some roles may require the ability to operate a motor vehicle for extended periods and maintain a valid driver's license.

Specific requirements may vary by role. Contact an HR representative for details related to the position.
Our credentials
Kuros is a Swiss-headquartered biotech company, listed on the SIX Swiss Stock Exchange since 2016 (under symbol KURN). With additional operations in the Netherlands and the USA, we continue to grow our global team.
To deliver the ideal bone graft, you need the highest quality and quantity of scientific evidence behind it. We believe that this is a key differentiator for Kuros, given the urgent need to advance bone healing.
  • Listing on the SIX Swiss Exchange under the symbol KURN since 2016
  • A commercial & research footprint that spans >20 markets
  • Dozens of clinical and scientific expert Advisers
  • >25 orthobiologics-related patents
  • >400 patients evaluated in Level I, randomized controlled clinical trials
  • >20 well-controlled Level I-IV clinical trials initiated, including 6 that are complete1
  • Published Level I evidence published in Spine

Kuros Biosciences is an equal opportunity employer that is committed to diversity and inclusion in the workplace. We prohibit discrimination and harassment of any kind based on race, color, sex, religion, sexual orientation, national origin, disability, genetic information, pregnancy, or any other protected characteristic as outlined by federal, state, or local laws. Kuros Biosciences complies with GDPR and the California Consumer Privacy Act (CCPA). View our CCPA Notice here.

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