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Pharmaceutical Process Engineer Jobs in Maryland

Salas O'Brien

Federal Process Engineer

Baltimore, MD · On-site

Federal Process Engineer At Salas O'Brien we tell our clients that we're engineered for impact ... Experience supporting industrial, manufacturing, chemical, energy, pharmaceutical, food and ...

TAI

Senior Process Utilities Engineer

Owings Mills, MD · On-site

$125K - $175K/yr

As a Senior Process (Utilities) Engineer/SME, you will lead the design and coordination of essential process utility systems that support pharmaceutical and biotechnology operations. From developing ...

TAI

Senior Process Utilities Engineer

Owings Mills, MD · On-site

$125K - $175K/yr

As a Senior Process (Utilities) Engineer/SME, you will lead the design and coordination of essential process utility systems that support pharmaceutical and biotechnology operations. From developing ...

Catalent Pharma Solutions

MS&T I

Harmans, MD · On-site

Engineer I, MS&TAbout Site Our FDA-licensed, state-of-the-art CGMP manufacturing facility for Gene ... You will help translate client and Process Development information into cGMP processes. This role ...

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All JobsPharmaceutical Process Engineer JobsPharmaceutical Process Engineer Jobs in Maryland

Pharmaceutical Process Engineer information

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$29

$34

$37

How much do pharmaceutical process engineer jobs pay per hour?

As of Aug 26, 2026, the average hourly pay for pharmaceutical process engineer in Maryland is $34.21, according to ZipRecruiter salary data. Most workers in this role earn between $32.21 and $36.15 per hour, depending on experience, location, and employer.

What does a pharmaceutical process engineer do?

A pharmaceutical process engineer reviews the requirement to produce a pharmaceutical product and develops a process for manufacturing. In this career, your duties vary from employer to employer but usually include tasks such as providing technical specifications for machinery and equipment, working to estimate costs for production, and undertaking a negotiation for the procurement of necessary materials and ingredients. Your responsibilities as a process engineer may include providing analysis of the process to ensure efficiency, safety, and compliance with relevant regulations.

What does a pharmaceutical process engineer do?

A Pharmaceutical Process Engineer is responsible for designing, developing, and optimizing processes used in the manufacturing of pharmaceutical products. They ensure that production methods are efficient, safe, and compliant with regulatory standards. Their work involves troubleshooting process problems, implementing new technologies, and collaborating with other departments to improve product quality and production efficiency. They play a critical role in scaling up laboratory processes to full-scale manufacturing while maintaining product integrity and safety.

What are some common challenges faced by pharmaceutical process engineers when scaling up production from laboratory to manufacturing scale?

Pharmaceutical Process Engineers often encounter challenges when translating lab-scale processes to full-scale manufacturing, such as maintaining product quality, ensuring process consistency, and meeting strict regulatory requirements. Controlling variables like temperature, pressure, and mixing at a larger scale can introduce unforeseen issues that require innovative problem-solving. Collaboration with cross-functional teams—including quality assurance, validation, and production staff—is essential to address these challenges efficiently. Adaptability and attention to detail are crucial in ensuring a smooth and compliant scale-up process.

What are the key skills and qualifications needed to thrive as a pharmaceutical process engineer, and why are they important?

To thrive as a Pharmaceutical Process Engineer, you need a strong background in chemical or process engineering, pharmaceutical manufacturing, and regulatory compliance, typically supported by a relevant engineering degree. Familiarity with process simulation software (such as Aspen Plus), GMP standards, and quality management systems is essential. Attention to detail, problem-solving skills, and effective teamwork are crucial soft skills for optimizing processes and ensuring product quality. These competencies are vital for developing efficient, safe, and compliant pharmaceutical manufacturing processes that meet industry standards.

What is the difference between Pharmaceutical Process Engineer vs Pharmaceutical Manufacturing Technician?

AspectPharmaceutical Process EngineerPharmaceutical Manufacturing Technician
Required CredentialsBachelor's degree in engineering, chemistry, or related field; often includes certifications in process validationHigh school diploma or associate degree; on-the-job training or technical certifications
Work EnvironmentDesign, optimize, and oversee manufacturing processes in labs or production facilitiesOperate equipment, monitor production lines, and ensure quality in manufacturing settings
Employer & Industry UsagePharmaceutical companies, biotech firms, contract manufacturing organizationsPharmaceutical manufacturing plants, biotech production facilities

The main difference is that Pharmaceutical Process Engineers focus on designing and improving manufacturing processes, requiring higher technical credentials, while Pharmaceutical Manufacturing Technicians handle day-to-day production tasks and equipment operation. Both roles are essential in pharmaceutical production but differ in responsibilities and qualifications.

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Pharmaceutical Process Engineer jobs near you
Infographic showing various Pharmaceutical Process Engineer job openings in Maryland as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $71,150 per year, or $34.2 per hour.

Process Engineering - Life Sciences - Division Manager

TAI

Owings Mills, MD • On-site

Full-time

Medical, Dental, Vision, Life, PTO

Posted 14 days ago

Job description

About the Role:
Lead and shape the future of TAI's Process Engineering - Life Sciences Division. As Division Manager, you'll guide a talented team of engineers and designers, oversee complex project delivery, and drive the strategic growth of a high performing division. This position places you at the center of developing innovative process solutions for pharmaceutical and biotech clients, blending technical direction, operational oversight, and hands on subject matter expertise. You'll influence project outcomes, strengthen client relationships, and collaborate across disciplines to elevate engineering standards and deliver impactful results in a rapidly evolving industry.
About TAI:
TAI brings together engineering, construction, systems integration, on-site services, and technical services - combining proven execution with trusted expertise to support clients across the entire project lifecycle. Team members at TAI are capable, well-rounded, flexible, and optimistic. We have found that the best employees are the ones who recognize the importance of what they do and the ones who let that guide them in the actions they take. More than any skill, we seek people who make decisions that support the common good. We work for our clients, and we work for one another.
Here's a glimpse into your day to day:
  • Oversee and manage divisional operations, ensuring compliance with corporate standards and policies.
  • Provide strong leadership and deep, practical process life sciences and GMP process engineering knowledge.
  • Bring knowledge and creativity to the position as well as having the discipline to drive results and follow established fundamental processes.
  • Responsible for quality, budget, and schedule performance of divisional operations.
  • Responsible for staff management, engagement, training, mentoring and career growth.
  • Responsible for project resource management and ensuring projects are staffed with personnel having appropriate qualifications to perform assigned tasks.
  • Responsible for ensuring quality control policies are being adhered to.
  • Responsible for conducting annual and quarterly employee reviews and completion of HR documentation.
  • Responsible for business development support, including site walks and engineering design scope and fee development, with a focus on pharmaceutical manufacturing and facility design opportunities, providing early engineering input on process design, equipment selection, and GMP compliance as needed.
  • Responsible for relationship management of existing clients.
  • Responsible for relating to employees and clients in a mature and professional manner.
  • Responsible for compliance with corporate safety policies and procedures.
  • Responsible for coordination and collaboration with other division managers for engineering processes and standards.
  • Responsible for functioning as Subject Matter Expert (SME) for process life science projects.
  • Responsible for researching applicable regulatory codes, industry guidelines and standards.
  • Responsible for interpreting codes and collaborating with other design professionals as needed.
  • Responsible for preparing detailed engineering analysis, studies, and reports.

You'll be a perfect fit if you have:
  • Bachelor's degree from an accredited university in Chemical Engineering, Mechanical Engineering, or related engineering field.
  • Master's degree in biotechnology or similar focus is preferred.
  • Professional Engineering Licensure.
  • NCEES Model Law Engineer is preferred.
  • NCEES Records holder is preferred.
  • Minimum 13 years of process engineering experience within the life sciences/ pharmaceutical industry. This includes experience with pharmaceutical manufacturing and equipment, FDA and EU regulations, and cGMP guidelines.
  • Minimum 5 years of applicable design experience within a consulting engineering firm. Applicable design experience includes creating construction documents and specifications for life sciences/pharmaceutical projects involving process and/or utility systems and equipment.
  • Minimum 5 years of experience developing PFD's, P&ID's, equipment and piping specifications.
  • Ability to act as Subject Matter Expert (SME) for life sciences process and/or utility systems.
  • Knowledge and experience with pharmaceutical process validation and quality control is preferred.
  • Understanding of pharmaceutical safety protocols and risk management processes is preferred.
  • Experience with the following equipment and related systems (design experience preferred):
    • Proficiency with GMP process utilities, including USP purified water, Water for Injection, Process/Biowaste, process gases and liquid nitrogen.
    • Familiarity with process equipment, including bioreactors, mixers, chromatography systems, filtration skids, single-use equipment, viral inactivation, incubators, washers, sterilizers, and controlled temperature units (-20C freezers, -80C freezers, and cryogenic freezers).
    • Proficiency with Process Flow Diagrams (PFDs), P&IDs, and piping specifications.
    • Proficiency with User Requirement Specifications (URS).
    • Developing GMP Equipment lists.
    • Determining process utility requirements.
    • Sizing, specification and layout of process utility equipment.
    • Planning, organizing, and preparing GMP process layouts for pharmaceutical and cell therapy manufacturing facilities is preferred.
    • Support for commissioning and qualification of equipment, utility systems and facilities, including IQ, OQ, and PQ is preferred.
  • Ability to perform field work
  • Willingness to travel to client sites.
  • Willingness to work in the office at least two days per week.
  • Ability to gather and organize information and documentation.
  • Ability to multitask.
  • Ability to mentor staff.
  • Excellent verbal and written communication skills, a positive work attitude, and willingness to learn new skills.

Compensation and Benefits:
  • Pay: $140,000-185,000 annually (depending on experience)
  • Eligible for overtime pay
  • Annual Profit Sharing Bonus (variable)
  • PTO and Paid Holidays
  • Health Benefits: Employee through family level coverage for medical, dental, and vision insurances. Company funded life and long-term disability insurances. Short Term Disability, FSA, HSA, EAP, and supplemental life insurances (employee - family) are also available!
  • 401(k)with employer match

Other Offerings:
  • The opportunity to make a real impact on a variety of industry-leading projects.
  • The ability to balance your work and family activities.
  • Flexible work schedule
  • Work in a dynamic and collaborative environment that values creativity and innovation.
  • A chance to learn and grow alongside some of the brightest minds in engineering.
  • Professional Development, Tuition Reimbursement, and Association Membership Reimbursements.

Discover what makes TAI a top-20 manufacturing partner, according to Engineering News-Record (ENR), and one of the top-50 fastest-growing private companies in the Baltimore Business Journal. Learn more about us at www.tai.inc/.

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