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Pharma Process Engineer Jobs (NOW HIRING)

Purple Hires Inc

MES Engineer

Greenville, SC · On-site

MES Co-Ordinator/ Engineer Location: Greenville-SC, Cincinnati- OH and St louis - MO (Onsite ... MES Implementation for Chemical, Pharma, Process, Oil & Gas and Food & Beverage Processing ...

PCI Pharma Services

Manufacturing Process Engineer

Bedford, NH · On-site

$72K - $96K/yr

No The Process Engineer is responsible for identifying and mitigating manufacturing issues (i.e ... Minimum of 3-6 years working in a Pharma cGMP environment; equivalent combination of education and ...

PCI Pharma Services

Manufacturing Process Engineer

Bedford, NH · On-site

$72K - $96K/yr

No The Process Engineer is responsible for identifying and mitigating manufacturing issues (i.e ... Minimum of 3-6 years working in a Pharma cGMP environment; equivalent combination of education and ...

Centor

Process Engineer

Millersburg, OH

$80K - $90K/yr

... pharma, biotech and cosmetic industries. The company offers a comprehensive portfolio of ... Process Engineer Reports To: Operations Manager Location: Berlin, Ohio Industry: Packaging ...

JC Automation Corp

PR · On-site

Bachelor's degree in Chemical or Mechanical Engineering * 5+ years of experience in pharma process related areas * Strong knowledge of applicable codes, standards, and regulations governing ...

MGS Mfg. Group, Inc

Process Engineer

Richfield, WI

As a Process Engineer at MGS, you will be responsible for the upkeep of equipment and processes to ... That's why we're the engineering and manufacturing partner of choice for today's leading Pharma ...

EQVAL Group, Inc

Process Engineer

Arecibo, PR · On-site

We are seeking Process Engineers that will supports the development, validation, and implementation ... Pharma, Biotech, or Medical Devices). * Experience with automated manufacturing system and ...

MGS Mfg. Group, Inc

Process Engineer

Richfield, WI

As a Process Engineer at MGS, you will be responsiblefor the upkeep of equipment and processes to ... That's why we're the engineering and manufacturing partner of choice for today's leading Pharma ...

MGS Mfg. Group, Inc

Process Engineer

Richfield, WI

As a Process Engineer at MGS, you will be responsible for the upkeep of equipment and processes to ... That's why we're the engineering and manufacturing partner of choice for today's leading Pharma ...

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Pharma Process Engineer information

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$49.5K

$92K

$142.5K

How much do pharma process engineer jobs pay per year?

As of Aug 22, 2026, the average yearly pay for pharma process engineer in the United States is $92,018.00, according to ZipRecruiter salary data. Most workers in this role earn between $74,500.00 and $103,000.00 per year, depending on experience, location, and employer.

What does a Pharma Process Engineer do?

A Pharma Process Engineer designs, develops, and optimizes manufacturing processes for pharmaceutical products. They ensure that production processes are efficient, safe, and compliant with regulatory standards like Good Manufacturing Practice (GMP). Their work often involves troubleshooting equipment, scaling up production from laboratory to industrial scale, and implementing process improvements to increase yield and product quality. They also collaborate closely with quality assurance and research teams to ensure that all products meet strict safety and efficacy standards.

What are the key skills and qualifications needed to thrive as a Pharma Process Engineer?

To thrive as a Pharma Process Engineer, you need a strong background in chemical engineering or pharmaceutical sciences, often supported by a relevant degree and industry experience. Familiarity with process simulation software (such as Aspen Plus), GMP regulations, and validation protocols is typically required. Strong analytical thinking, problem-solving abilities, and effective communication skills set standout professionals apart in this field. These skills and qualities are important because they ensure safe, efficient, and compliant pharmaceutical manufacturing processes.

What are some common challenges faced by Pharma Process Engineers when optimizing manufacturing processes?

Pharma Process Engineers often encounter challenges such as maintaining strict regulatory compliance while implementing process improvements and ensuring product quality. Balancing efficiency with adherence to Good Manufacturing Practices (GMP) can be complex, especially during scale-up or technology transfer projects. Additionally, collaborating across multidisciplinary teams—including quality assurance, production, and R&D—requires strong communication skills to align objectives and resolve issues quickly. These challenges make adaptability and attention to detail crucial traits for success in the role.

What is the difference between Pharma Process Engineer vs Chemical Process Engineer?

AspectPharma Process EngineerChemical Process Engineer
Required CredentialsBachelor's in Chemical, Pharmaceutical, or related field; GMP certification often preferredBachelor's in Chemical Engineering or related field; Professional Engineer (PE) license optional
Work EnvironmentPharmaceutical manufacturing facilities, labs, cleanroomsChemical plants, refineries, manufacturing sites
Industry UsagePharmaceutical, biotech, healthcareChemical, petrochemical, manufacturing
Common Search/ComparisonYesYes

Both Pharma Process Engineers and Chemical Process Engineers work in manufacturing environments requiring chemical engineering knowledge. Pharma Process Engineers focus on pharmaceutical production, adhering to strict GMP standards, while Chemical Process Engineers work across various chemical industries. Their roles overlap in process design and optimization, but Pharma Process Engineers specialize in drug manufacturing processes.

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Pharma Process Engineer jobs near you
Infographic showing various Pharma Process Engineer job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 79% Full Time, 16% Part Time, 3% Contract, and 1% Nights. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $92,018 per year, or $44.2 per hour.

Process Engineer - Pharma

Becton, Dickinson and Company

El Paso, TX • On-site

Full-time

Re-posted 6 days ago

BD rating

7.2

Company rating: 7.2 out of 10

Based on 142 frontline employees who took The Breakroom Quiz

324th of 494 rated machine equipment manufacturers

Job description

We are the people who give possibilities purpose
BD is one of the largest global medical technology companies in the world. Advancing the world of health™ is our Purpose, and it's no small feat. It takes the imagination and passion of all of us-from design and engineering to the manufacturing and marketing of our billions of MedTech products per year-to look at the impossible and find transformative solutions that turn dreams into possibilities.
Job Description
Job Responsibilities:
Responsibilities include but are not limited to:
Process Optimization & Manufacturing Support
  • Provide day-to-day engineering support to pharmaceutical manufacturing operations.
  • Analyze manufacturing processes to identify opportunities for improving efficiency, quality, yield, and cost.
  • Troubleshoot process issues and implement corrective and preventive actions (CAPAs).
  • Monitor process performance through data analysis and key performance indicators (KPIs).
  • Lead root cause investigations related to process deviations, nonconformances, and customer complaints.

Validation & Compliance
  • Support process validation, equipment qualification, and revalidation activities.
  • Develop and execute validation protocols, reports, and technical documentation.
  • Ensure compliance with FDA regulations, cGMP requirements, BD policies, and applicable quality standards.
  • Support internal and external audits, inspections, and regulatory commitments.
  • Maintain manufacturing documentation, standard operating procedures (SOPs), and work instructions.

Continuous Improvement
  • Lead Lean Manufacturing and Continuous Improvement projects.
  • Utilize Six Sigma, DMAIC, and problem-solving methodologies to eliminate waste and improve process capability.
  • Identify and implement productivity, quality, and cost-reduction initiatives.
  • Participate in site transformation and operational excellence programs.

Project Management
  • Support new product introductions, technology transfers, and process changes.
  • Coordinate engineering projects from conception through implementation.
  • Manage timelines, risk assessments, resource requirements, and project documentation.
  • Collaborate with Maintenance, Quality, Operations, Validation, Regulatory Affairs, and Supply Chain teams.

Safety & Quality
  • Promote a strong culture of safety, compliance, and quality.
  • Support risk assessments, process hazard evaluations, and quality improvement initiatives.
  • Ensure all engineering activities are performed following EHS and Quality Management System requirements.

Education and Experience:
  • Bachelor's degree in Chemical Engineering, Industrial Engineering, Mechanical Engineering, Biomedical
  • 3+ years of experience of engineering experience within a pharmaceutical, medical device, biotechnology, or highly regulated manufacturing environment
  • Experience working in FDA-regulated, cGMP, validation, and quality systems.
  • Experience in pharmaceutical manufacturing and aseptic or sterilization processes preferred.
  • Knowledge of process validation, equipment qualification (IQ/OQ/PQ), and risk management methodologies, preferred.
  • Lean Six Sigma Green Belt or Black Belt certification preferred.
  • Experience with SAP, TrackWise, MES, or other manufacturing systems preferred.
  • Knowledge of statistical tools and process capability analysis.
  • Bilingual (English/Spanish) preferred.

Knowledge and Skills:
Technical Skills
  • Strong analytical and problem-solving skills.
  • Experience conducting root cause investigations and implementing CAPAs.
  • Proficiency in Microsoft Office applications and data analysis tools.

Key Competencies
  • Strong problem-solving and analytical skills
  • Detail-oriented with data-driven decision making
  • Ability to manage problem solving and critical thinking
  • Effective communication and collaboration across all levels

Physical Demands:
  • Manufacturing environment with exposure to production areas.

Work Environment:
  • Manufacturing

Why Join Us?
To find purpose in the possibilities, we need people who can see the bigger picture, who understand the human story that underpins everything we do. We welcome people with the imagination and drive to help us reinvent the future of healthcare. At BD, you'll discover a culture in which you can learn, grow and thrive.
We believe that when people connect in person, we learn faster, collaborate more deeply, and build a stronger culture. Join us and enjoy a culture where face-to-face collaboration supports your learning, your progress, and your success.
To learn more about BD visit https://bd.com/careers.
Becton, Dickinson, and Company is an Equal Opportunity Employer. We evaluate applicants without regard to race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, and other legally protected characteristics.
Required Skills
Optional Skills
Primary Work Location
USA TX - El Paso - Northwestern Dr.
Additional Locations
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About BD

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BD is one of the largest global medical technology companies in the world and is advancing the world of health by improving medical discovery, diagnostics and the delivery of care. We have over 65,000 employees and a presence in virtually every country around the world to address some of the most challenging global health issues.

Industry

Medical equipment and supplies manufacturing and manufacturing

Company size

10,000+ Employees

Headquarters location

Franklin Lakes, NJ, US

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