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Pfizer Senior Process Development Scientist Jobs

kindeva

Senior Process Development Engineer

Lexington, KY · On-site

$103K - $133K/yr

As a Senior Process Development Engineer, you will lead and coordinate the transfer of ... Apply scientific and statistical methods to analyze and diagram production processes * Lead ...

Pfizer

Senior Associate Scientist

Chesterfield, MO

$68K - $114K/yr

By leveraging cutting-edge design and process development capabilities, you will help accelerate ... Pfizer compensation structures and benefit packages are aligned based on the location of hire. The ...

Abbott

Sr Process Development Engineer

Santa Clara, CA · On-site

$122K - $158K/yr

... scientists. The Opportunity This position works out of our Santa Clara, CA location in the SH ... As the Sr Process Development Engineer, you will serve as the primary engineering personnel ...

Gilead

Sr Scientist, Process Development

Foster City, CA · On-site

$106K - $145K/yr

... development timelines and strengthen process understanding. We are seeking a Senior Scientist with expertise in purification automation, high-throughput experimentation, mechanistic modeling, and ...

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Pfizer Senior Process Development Scientist information

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How much do pfizer senior process development scientist jobs pay per year?

As of Jun 7, 2026, the average yearly pay for pfizer senior process development scientist in the United States is $110,545.00, according to ZipRecruiter salary data. Most workers in this role earn between $91,500.00 and $125,000.00 per year, depending on experience, location, and employer.

What is the difference between Pfizer Senior Process Development Scientist vs Pfizer Process Development Scientist?

AspectPfizer Senior Process Development ScientistPfizer Process Development Scientist
Required ExperienceTypically 5+ years in process development, leadership skills1-3 years, focused on executing development tasks
ResponsibilitiesLeading projects, mentoring, process optimizationSupporting process development activities, data collection
Work EnvironmentSenior-level projects, cross-functional teamsExecution-focused, laboratory and pilot plant work
CertificationsAdvanced degrees often preferred, industry certificationsRelevant degrees, entry to mid-level certifications

The Pfizer Senior Process Development Scientist role involves leading projects, mentoring junior staff, and overseeing process optimization, requiring more experience and leadership skills. In contrast, the Pfizer Process Development Scientist focuses on executing development tasks and supporting ongoing projects. Both roles are essential in drug development, but the senior position emphasizes strategic oversight and team leadership.

What are some common challenges faced by a Pfizer Senior Process Development Scientist and how are they addressed?

A Pfizer Senior Process Development Scientist often encounters challenges such as optimizing complex bioprocesses for scalability, ensuring regulatory compliance, and managing cross-functional project timelines. These scientists work closely with multidisciplinary teams—including analytical, quality, and manufacturing groups—to troubleshoot process deviations and implement improvements. Staying current with technological advances and maintaining thorough documentation are key strategies to address these challenges, ensuring robust and efficient process development for new pharmaceuticals.

What are the key skills and qualifications needed to thrive as a Pfizer Senior Process Development Scientist, and why are they important?

To thrive as a Pfizer Senior Process Development Scientist, you need a strong background in chemical engineering, biochemistry, or a related field, often supported by an advanced degree and experience in pharmaceutical process development. Expertise with process analytical technologies (PAT), data analysis software, and familiarity with regulatory compliance systems such as cGMP are typically required. Strong problem-solving, project management, and cross-functional communication skills help you lead teams and drive innovation. These skills are crucial to efficiently develop robust pharmaceutical processes, ensure product quality, and support regulatory approvals.

What does a Pfizer Senior Process Development Scientist do?

A Pfizer Senior Process Development Scientist is responsible for designing, optimizing, and scaling up manufacturing processes for pharmaceutical products. They collaborate with cross-functional teams to ensure that drug development processes are efficient, safe, and compliant with regulatory standards. Their work involves conducting experiments, analyzing data, troubleshooting process issues, and implementing new technologies to improve product quality and production efficiency. This role is critical in bringing new medicines from the laboratory to large-scale production while maintaining high standards of quality and safety.
Infographic showing various Pfizer Senior Process Development Scientist job openings in the United States as of May 2026, with employment types broken down into 1% Locum Tenens, 95% Full Time, 2% Part Time, and 2% Contract. Highlights an 93% Physical, 2% Hybrid, and 5% Remote job distribution, with an average salary of $110,545 per year, or $53.1 per hour.

Senior Process Development Engineer

kindeva

Lexington, KY

$103K - $133K/yr

Other

Posted 11 days ago

Kindeva rating

6.8

Company rating: 6.8 out of 10

Based on 6 frontline employees who took The Breakroom Quiz

Job description

Our Work Matters

At Kindeva we make products that save lives, ensuring better health and well-being for patients around the world.

The Impact You Will Make:

Join a rapidly expanding pharmaceutical CDMO where your work directly enhances the scalability and efficiency of life-changing treatments. As a Senior Process Development Engineer, you will lead and coordinate the transfer of pharmaceutical products and manufacturing processes between R&D and commercial manufacturing sites. You’ll ensure processes are scalable, robust, and compliant with regulatory standards. Your expertise will shape systems, equipment, and SOPs while supporting the production of finished pharmaceutical products.

Responsibilities:

Technology Transfer

  • Plan and execute technology transfer activities for drug products or devices from R&D to manufacturing or between commercial sites
  • Author and/or review tech transfer documentation (e.g., process descriptions, gap assessments, risk assessments, readiness assessments, protocols)
  • Translate lab-scale processes into commercial manufacturing processes

Process Optimization & Troubleshooting

  • Support scale-up activities and resolve technical issues during manufacturing
  • Work with R&D to adapt and optimize processes for commercial equipment
  • Implement process improvements to enhance product quality, yield, and efficiency

Documentation & Compliance

  • Ensure all tech transfer activities are documented per regulatory requirements
  • Support regulatory submissions and inspections/audits
  • Draft production documentation including batch records and protocols
  • Support validation and qualification efforts (process, equipment, cleaning)

Cross-Functional Collaboration

  • Serve as technical liaison between engineering, R&D, manufacturing, QA, and regulatory
  • Coordinate with customers, vendors, and external partners

Training & Support

  • Train manufacturing staff on transferred processes
  • Facilitate knowledge transfer and review development history
  • Troubleshoot and escalate risks with proposed mitigation strategies
  • Ensure effective and compliant transfer of knowledge, data, and technology

Problem Solving

  • Apply scientific and statistical methods to analyze and diagram production processes
  • Lead structured problem-solving to identify root causes and develop solutions
  • Drive Risk Management tools like Fault Tree Analysis and FMEA
  • Address diverse technical problems requiring informed judgment and adaptive techniques
  • Provide technical leadership and guidance to others as a subject matter expert

Qualifications:

Minimum Qualifications Required

  • BS in engineering/related degree or equivalent experience
  • 5+ years of related experience with a bachelor’s degree; or 3 years with a master’s degree, or PhD.
  • Previous work experience in GMP pharmaceutical manufacturing and technical transfers
  • Working knowledge of cGMP, GAMP5, and regulatory requirements

Preferred Qualifications

  • Experience working with nasal spray products/devices or related drug-delivery technologies
  • Strong technical and nontechnical communication skills
  • Experience supporting client/regulatory audits and follow-up responses
  • Extensive technical writing experience

Join our One Team mission of manufacturing more tomorrows. Your expertise will help ensure better health and well-being for patients worldwide.

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