In this visible, hands-on role, you will collaborate daily with Process Development, Clinical Operations, Materials Management, and Quality to turn robust science into reliable manufacturing outcomes.
In this visible, hands-on role, you will collaborate daily with Process Development, Clinical Operations, Materials Management, and Quality to turn robust science into reliable manufacturing outcomes.
In this visible, hands-on role, you will collaborate daily with Process Development, Clinical Operations, Materials Management, and Quality to turn robust science into reliable manufacturing outcomes.
In this visible, hands-on role, you will collaborate daily with Process Development, Clinical Operations, Materials Management, and Quality to turn robust science into reliable manufacturing outcomes.
Validation Engineer I
Rockville, MD · On-site
Incumbents in this role will support in house formulation and process development, author sections of regulatory filing documents, and collaborate cross functionally to ensure timely delivery of ...
Validation Engineer I
Rockville, MD · On-site
Incumbents in this role will support in house formulation and process development, author sections of regulatory filing documents, and collaborate cross functionally to ensure timely delivery of ...
Technical Manager
Frederick, MD · On-site
This role bridges engineering design, materials science, and process development, ensuring our technologies move efficiently from the lab to market-ready systems. Reporting to the Plant GM, the ...
Quick apply
Technical Manager
Frederick, MD · On-site
This role bridges engineering design, materials science, and process development, ensuring our technologies move efficiently from the lab to market-ready systems. Reporting to the Plant GM, the ...
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Process Engineer
Westminster, MD · On-site
$85K - $95K/yr
Process Engineer/Direct Hire Location: Westminster, MD - Onsite position Pay: $85,000/year - $95 ... Works with Battery Design and Mechanical Engineering to transfer new designs from development to ...
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Process Engineer
Westminster, MD · On-site
$85K - $95K/yr
Process Engineer/Direct Hire Location: Westminster, MD - Onsite position Pay: $85,000/year - $95 ... Works with Battery Design and Mechanical Engineering to transfer new designs from development to ...
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Process Engineer
Westminster, MD · On-site
$85K - $95K/yr
Process Engineer/Direct Hire Location: Westminster, MD - Onsite position Pay: $85,000/year - $95 ... Works with Battery Design and Mechanical Engineering to transfer new designs from development to ...
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Process Engineer
Westminster, MD · On-site
$85K - $95K/yr
Process Engineer/Direct Hire Location: Westminster, MD - Onsite position Pay: $85,000/year - $95 ... Works with Battery Design and Mechanical Engineering to transfer new designs from development to ...
Production Technician
Gaithersburg, MD · On-site
$25 - $29/hr
Collaboration is key, and you will work together frequently with Process Development, Clinical Operations, Materials Management, and Quality Teams. Main Duties & Responsibilities: * Author and ...
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Production Technician
Gaithersburg, MD · On-site
$25 - $29/hr
Collaboration is key, and you will work together frequently with Process Development, Clinical Operations, Materials Management, and Quality Teams. Main Duties & Responsibilities: * Author and ...
Process Planner
Frederick, MD · On-site
Development and maintenance of Planning and Production Routings. * Coordinates with Production ... and manufacturing processes (ERP). * Conduct time studies, work measurement, and basic line ...
Process Planner
Frederick, MD · On-site
Development and maintenance of Planning and Production Routings. * Coordinates with Production ... and manufacturing processes (ERP). * Conduct time studies, work measurement, and basic line ...
Process Planner
Frederick, MD · On-site
Development and maintenance of Planning and Production Routings. * Coordinates with Production ... and manufacturing processes (ERP). * Conduct time studies, work measurement, and basic line ...
Process Planner
Frederick, MD · On-site
Development and maintenance of Planning and Production Routings. * Coordinates with Production ... and manufacturing processes (ERP). * Conduct time studies, work measurement, and basic line ...
Experience developing PERL scripts, hardware & software development skills * U.S. citizenship and ability to obtain a Top Secret Security clearance * Strong process scripting experience NICE-TO-HAVES
Experience developing PERL scripts, hardware & software development skills * U.S. citizenship and ability to obtain a Top Secret Security clearance * Strong process scripting experience NICE-TO-HAVES
NIST PREP Postdoc Associate in Metrology of Materials, Surfaces, and Processes for Semiconductor Adv
Gaithersburg, MD · On-site
$70K - $90K/yr
Significant experience, including process development, in semiconductor device fabrication, including wafer cleaning and handling, lithography mask layout, optical or electron beam lithography, RIE ...
NIST PREP Postdoc Associate in Metrology of Materials, Surfaces, and Processes for Semiconductor Adv
Gaithersburg, MD · On-site
$70K - $90K/yr
Significant experience, including process development, in semiconductor device fabrication, including wafer cleaning and handling, lithography mask layout, optical or electron beam lithography, RIE ...
Prepare processing rooms and equipment for R&D, pilot-scale and GMP manufacturing operations. * Execute manufacturing operations in accordance with approved batch records, standard operating ...
Prepare processing rooms and equipment for R&D, pilot-scale and GMP manufacturing operations. * Execute manufacturing operations in accordance with approved batch records, standard operating ...
Development - Development Associate
$60K - $85K/yr
JSSA has an immediate opening for a Development Associate. This position works collaboratively with ... processing the necessary title paperwork and interacting with auction house to manage the pickup ...
Development - Development Associate
$60K - $85K/yr
JSSA has an immediate opening for a Development Associate. This position works collaboratively with ... processing the necessary title paperwork and interacting with auction house to manage the pickup ...
Senior Process Analyst
Kearneysville, WV · On-site
$97K - $123K/yr
Responsibilities As a Senior Process Analyst, you will serve as a primary operational resource for ensuring that applications developed by platform-aligned Product Teams are user-centric ...
Senior Process Analyst
Kearneysville, WV · On-site
$97K - $123K/yr
Responsibilities As a Senior Process Analyst, you will serve as a primary operational resource for ensuring that applications developed by platform-aligned Product Teams are user-centric ...
Development - Development Associate
Rockville, MD · On-site
$60K - $85K/yr
JSSA has an immediate opening for a Development Associate. This position works collaboratively with ... processing the necessary title paperwork and interacting with auction house to manage the pickup ...
Development - Development Associate
Rockville, MD · On-site
$60K - $85K/yr
JSSA has an immediate opening for a Development Associate. This position works collaboratively with ... processing the necessary title paperwork and interacting with auction house to manage the pickup ...
Drive process scale-up and process improvement activities by translating development-scale processes into robust, scalable, and GMP-ready manufacturing operations. GMP Documentation * Author, review ...
Drive process scale-up and process improvement activities by translating development-scale processes into robust, scalable, and GMP-ready manufacturing operations. GMP Documentation * Author, review ...
Drive process scale-up and process improvement activities by translating development-scale processes into robust, scalable, and GMP-ready manufacturing operations. GMP Documentation * Author, review ...
Drive process scale-up and process improvement activities by translating development-scale processes into robust, scalable, and GMP-ready manufacturing operations. GMP Documentation * Author, review ...
Cell Therapy Specialist I
Frederick, MD · On-site
Work as part of a team to execute GMP runs in close collaboration with Process Development and Quality Assist in the development of standard operating procedures, batch records, deviations and change ...
Quick apply
Cell Therapy Specialist I
Frederick, MD · On-site
Work as part of a team to execute GMP runs in close collaboration with Process Development and Quality Assist in the development of standard operating procedures, batch records, deviations and change ...
Technical Manager
Frederick, MD · On-site
Works in conjunction with R&D and sales to develop and approve production trial plans for product changes, machine efficiency tests, and any major adjustments to process recipes. * Supports ...
Technical Manager
Frederick, MD · On-site
Works in conjunction with R&D and sales to develop and approve production trial plans for product changes, machine efficiency tests, and any major adjustments to process recipes. * Supports ...
Engineering Manager
Frederick, MD · On-site
$150K - $165K/yr
Collaborating closely with the Operations Manager, the Engineering Manager will oversee process development in compliance with IPC, ISO, and customer standards, while serving as the technical liaison ...
New
Engineering Manager
Frederick, MD · On-site
$150K - $165K/yr
Collaborating closely with the Operations Manager, the Engineering Manager will oversee process development in compliance with IPC, ISO, and customer standards, while serving as the technical liaison ...
New
Process Development information
See Frederick, MD salary details
$18.88 - $21.64
3% of jobs
$21.64 - $24.40
6% of jobs
$24.40 - $27.16
12% of jobs
$27.63 is the 25th percentile. Wages below this are outliers.
$27.16 - $29.92
23% of jobs
The median wage is $31 / hr.
$29.92 - $32.68
15% of jobs
$32.68 - $35.44
15% of jobs
$36.59 is the 75th percentile. Wages above this are outliers.
$35.44 - $38.20
3% of jobs
$38.20 - $40.96
3% of jobs
$40.96 - $43.72
6% of jobs
$43.72 - $46.48
3% of jobs
$46.48 - $49.24
11% of jobs
$18
$33
$49
How much do process development jobs pay per hour?
As of Aug 8, 2026, the average hourly pay for process development in Frederick, MD is $33.49, according to ZipRecruiter salary data. Most workers in this role earn between $27.50 and $41.11 per hour, depending on experience, location, and employer.
What are the key skills and qualifications needed to thrive as a process development professional, and why are they important?
To thrive in Process Development, you need a strong background in engineering, chemistry, or a related scientific field, often with a bachelor's or advanced degree. Familiarity with process simulation software, statistical analysis tools, and industry-specific quality standards or certifications like Six Sigma is typically required. Analytical thinking, problem-solving abilities, and effective cross-functional communication are crucial soft skills for success in this role. These skills and qualifications are vital for designing efficient, scalable processes that improve productivity and ensure product quality.
What is the difference between Process Development vs Process Engineering?
| Aspect | Process Development | Process Engineering |
|---|---|---|
| Focus | Designing and optimizing new processes for products or manufacturing | Implementing, maintaining, and improving existing processes |
| Work Stage | Early-stage process creation and testing | Scaling up, troubleshooting, and sustaining processes |
| Skills & Certifications | Chemical/biochemical engineering, lab skills, process modeling | Process optimization, quality control, engineering principles |
Process Development primarily focuses on creating and refining new processes, while Process Engineering emphasizes implementing and maintaining those processes in production. Both roles require similar technical backgrounds but differ in their stage of involvement within the product lifecycle.
What is process development?
Process development is the systematic approach of designing, optimizing, and scaling up manufacturing or business processes to improve efficiency, quality, and cost-effectiveness. It typically involves taking a concept or product from the laboratory or pilot stage to full-scale production, ensuring that the process is robust, reproducible, and compliant with industry standards. Professionals in process development work closely with research, engineering, and production teams to identify improvements and troubleshoot issues during scale-up.
What are the main challenges faced by professionals in process development, and how are they typically addressed?
Professionals in Process Development often encounter challenges such as scaling laboratory processes to full production, troubleshooting unexpected technical issues, and ensuring process consistency while meeting regulatory requirements. These challenges are typically addressed by collaborating closely with cross-functional teams—including R&D, Quality Assurance, and Manufacturing—to share expertise and implement robust validation protocols. Continuous learning, strong project management skills, and adaptability are important for overcoming these hurdles and ensuring successful process implementation.
What are the most commonly searched types of Process Development jobs in Frederick, MD? The most popular types of Process Development jobs in Frederick, MD are:
What cities near Frederick, MD are hiring for Process Development jobs? Cities near Frederick, MD with the most Process Development job openings:
Full-time
Medical, Dental, Vision, Retirement, PTO
Posted 17 days ago
AstraZeneca rating
8.4
Based on 45 frontline employees who took The Breakroom Quiz
22nd of 86 rated pharmaceutical
Job description
Associate Specialist (Cell Therapy Manufacturing)
Introduction to role
Are you ready to bring precision and initiative to the start-up of a new cell therapy manufacturing facility-seeing your work translate into clinical trials that could change patients' lives? Join a team producing next-generation cell therapy products at a pivotal moment as our first clinical batches move from process development into cGMP operation.
In this visible, hands-on role, you will collaborate daily with Process Development, Clinical Operations, Materials Management, and Quality to turn robust science into reliable manufacturing outcomes. You will help build the documentation, run sophisticated automated equipment in Grades A and B cleanrooms, and lead by example on the floor to keep every batch on track. Can you picture yourself owning a "right first time" mindset and guiding a shift handover that keeps a critical lot moving?
Accountabilities
Essential Skills/Experience
Desirable Skills/Experience
Why AstraZeneca
Here, your work sits close to the decision point and the patient impact. You will operate at the forefront of science with high visibility, shaping end deliverables across therapy areas and collaborating with unexpected teams in the same room to unleash bold thinking. We balance ambition with support-leaders empower you to improve, experiments are celebrated for what they teach, and resilient minds find inventive paths through a heavily regulated environment. You will expand your skills as you apply advanced technologies to complex problems, contribute to enterprise-recognized work, and bring courage and curiosity to challenges that truly matter. We value kindness alongside ambition, and we back people who speak up, share opinions, and turn critique into better solutions.
Step into this high-exposure manufacturing role and help deliver transformative cell therapies to patients-take the next step today and show us how your precision and initiative will raise our standards!
The annual base pay for this position ranges from $65,082 to $97,622. Our positions offer eligibility for various incentives-an opportunity to receive short-term incentive bonuses, equity-based awards for salaried roles and commissions for sales roles. Benefits offered include qualified retirement programs, paid time off (i.e., vacation, holiday, and leaves), as well as health, dental, and vision coverage in accordance with the terms of the applicable plans.
Date Posted
03-Aug-2026
Closing Date
04-Aug-2026
Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and employees. In furtherance of that mission, we welcome and consider applications from all qualified candidates, regardless of their protected characteristics. If you have a disability or special need that requires accommodation, please complete the corresponding section in the application form.
Introduction to role
Are you ready to bring precision and initiative to the start-up of a new cell therapy manufacturing facility-seeing your work translate into clinical trials that could change patients' lives? Join a team producing next-generation cell therapy products at a pivotal moment as our first clinical batches move from process development into cGMP operation.
In this visible, hands-on role, you will collaborate daily with Process Development, Clinical Operations, Materials Management, and Quality to turn robust science into reliable manufacturing outcomes. You will help build the documentation, run sophisticated automated equipment in Grades A and B cleanrooms, and lead by example on the floor to keep every batch on track. Can you picture yourself owning a "right first time" mindset and guiding a shift handover that keeps a critical lot moving?
Accountabilities
- GMP Documentation Excellence: Author and execute manufacturing batch records, work instructions, and SOPs with a "right first time" mindset; maintain bills of materials; reconcile batches promptly; document all activities to meet cGMP requirements; assist with deviations, non-conformances, and OOS investigations. Your rigor reduces errors, speeds release, and strengthens audit readiness.
- Aseptic Equipment Operations: Monitor, clean, prepare, and operate automated cell processing, cell expansion, and filling equipment in Grades A and B cleanrooms. Your care and consistency protect product quality and patient safety.
- Training and Knowledge Transfer: Train personnel on aseptic processing, equipment operation, cGMPs, documentation, and technical theory. By elevating team capability, you increase throughput and reliability.
- Document Review and Continuous Improvement: Review batch records, SOPs, and logbooks for completeness, clarity, and accuracy; submit edits for revision as needed. Your attention to detail drives procedural clarity and repeatability.
- Tech Transfer and Process Development: Participate in tech transfer activities; support development of platform processes; contribute to study and experiment designs; modify or improve processes and systems when appropriate. Your input helps mature processes from concept to cGMP readiness.
- Floor Leadership and Problem Solving: Provide technical instruction; allocate administrative tasks; assign work to manufacturing staff; lead activities on the manufacturing floor; communicate product status at shift change; troubleshoot processing and equipment issues. Your leadership keeps operations aligned, responsive, and efficient.
- Safety and Compliance Stewardship: Ensure a safe work environment in accordance with AstraZeneca standards. Your vigilance fosters a strong safety culture.
- Flexibility: Weekend work may be required. Your adaptability ensures continuity of critical manufacturing runs.
Essential Skills/Experience
- Bachelor's degree in life sciences, engineering, or a related field with 0-3 years of general cGMP manufacturing experience or a Master's degree in life sciences, engineering, or a related field with 0-2 years of general cGMP manufacturing experience
- Basic knowledge in biologics manufacturing process, cell culture and/or vector products.
- Technical proficiency in aseptic technique and working with manufacturing equipment in open and closed systems.
- Working knowledge of automated manufacturing equipment and/or process analytical technologies.
- Proficiency in Microsoft Word, Excel and data analysis.
Desirable Skills/Experience
- Previous manufacturing or process development experience with cell therapy or vector products.
- Dynamic individual with the ability to communicate and engage others.
- Independent and self-starting. Ability to work with minimal supervision.
- Demonstrate flexibility and willingness to change ways of working/identify opportunities to improve processes within cGMP clinical manufacturing environment.
Why AstraZeneca
Here, your work sits close to the decision point and the patient impact. You will operate at the forefront of science with high visibility, shaping end deliverables across therapy areas and collaborating with unexpected teams in the same room to unleash bold thinking. We balance ambition with support-leaders empower you to improve, experiments are celebrated for what they teach, and resilient minds find inventive paths through a heavily regulated environment. You will expand your skills as you apply advanced technologies to complex problems, contribute to enterprise-recognized work, and bring courage and curiosity to challenges that truly matter. We value kindness alongside ambition, and we back people who speak up, share opinions, and turn critique into better solutions.
Step into this high-exposure manufacturing role and help deliver transformative cell therapies to patients-take the next step today and show us how your precision and initiative will raise our standards!
The annual base pay for this position ranges from $65,082 to $97,622. Our positions offer eligibility for various incentives-an opportunity to receive short-term incentive bonuses, equity-based awards for salaried roles and commissions for sales roles. Benefits offered include qualified retirement programs, paid time off (i.e., vacation, holiday, and leaves), as well as health, dental, and vision coverage in accordance with the terms of the applicable plans.
Date Posted
03-Aug-2026
Closing Date
04-Aug-2026
Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and employees. In furtherance of that mission, we welcome and consider applications from all qualified candidates, regardless of their protected characteristics. If you have a disability or special need that requires accommodation, please complete the corresponding section in the application form.
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