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Pharmaceutical Process Engineer Jobs in Hanover, MD

Quality Agents, LLC

Process Engineer

Rockville, MD · On-site

Quality Agents, LLC offers validation and quality expertise to the pharmaceutical and biotechnology industries. We are seeking a detail-oriented and collaborative Process Engineer to support ...

Valspec

Process Validation Engineer

Rockville, MD

$70 - $80/hr

Process Engineer -- Upstream / Downstream / Clean Utilities (Consultant) -- Contract Engagement ... pharmaceutical or biotech GMP manufacturing environment. * Hands-on experience in at least one of:

CAMRIS

Automation and Controls Engineer

Silver Spring, MD · On-site

$92K - $117K/yr

PBF is a one-of-a-kind cGMP-compliant pharmaceutical manufacturing facility engaging in next ... Partner with process engineers and manufacturing staff to automate unit operations and integrate ...

CAMRIS

Automation and Controls Engineer

Silver Spring, MD · On-site

$92K - $117K/yr

PBF is a one-of-a-kind cGMP-compliant pharmaceutical manufacturing facility engaging in next ... Partner with process engineers and manufacturing staff to automate unit operations and integrate ...

LifeSprout

R&D Engineer

Baltimore, MD · On-site

Perform process development activities to improve product performance, manufacturability ... Pharmaceutical Sciences, or a related technical field; advanced degree preferred. * 2+ years of ...

Workforce Genetics

R&D Engineer

Baltimore, MD · On-site

$80K - $100K/yr

Perform process development activities to improve product performance, manufacturability ... Science, Pharmaceutical Sciences, or a related technical field; advanced degree preferred.

Quality Agents, LLC

Automation Engineer

Rockville, MD · On-site

Quality Agents, LLC offers validation and quality expertise to the pharmaceutical and biotechnology ... The ideal candidate has experience with PLCs, SCADA, building management systems (BMS), and process ...

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All JobsPharmaceutical Process Engineer JobsPharmaceutical Process Engineer Jobs in Hanover, MD

Pharmaceutical Process Engineer information

See Hanover, MD salary details

$30

$35

$38

How much do pharmaceutical process engineer jobs pay per hour?

As of Aug 4, 2026, the average hourly pay for pharmaceutical process engineer in Hanover, MD is $35.07, according to ZipRecruiter salary data. Most workers in this role earn between $33.03 and $37.07 per hour, depending on experience, location, and employer.

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.

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 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 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 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.
More about Pharmaceutical Process Engineer jobs
What are popular job titles related to Pharmaceutical Process Engineer jobs in Hanover, MD? For Pharmaceutical Process Engineer jobs in Hanover, MD, the most frequently searched job titles are:
Pharmaceutical Process Engineer jobs near you
Infographic showing various Pharmaceutical Process Engineer job openings in Hanover, MD as of July 2026, with employment types broken down into 96% Full Time, 1% Part Time, and 3% Contract. Highlights an 87% Physical, 5% Hybrid, and 8% Remote job distribution, with an average salary of $72,943 per year, or $35.1 per hour.

Process Engineer

Quality Agents, LLC

Rockville, MD • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 27 days ago

Job description

Quality Agents, LLC offers validation and quality expertise to the pharmaceutical and biotechnology industries.
We are seeking a detail-oriented and collaborative Process Engineer to support manufacturing and technical operations in a dynamic biotech environment. This role plays a key part in optimizing existing processes, implementing new technologies, and ensuring consistent, compliant production of clinical and commercial biologics.
The ideal candidate brings hands-on experience in biotech or pharmaceutical process engineering, with a focus on upstream, downstream or cell therapy operations.


Key Responsibilities


Support the design, scale-up, optimization, and validation of biopharmaceutical manufacturing processes.
Assist in tech transfer activities for new products or process changes.
Develop and revise process documentation including batch records, SOPs, and protocols.
Investigate and troubleshoot process deviations, equipment issues, and production challenges.
Analyze process data and identify opportunities for improvement in yield, efficiency, or quality.
Collaborate cross-functionally with QA, QC, Manufacturing, and Engineering teams.
Support commissioning, qualification (IQ/OQ/PQ), and validation activities for equipment and systems.
Ensure all work aligns with GMP and regulatory requirements.


Minimum Requirements:


B.S. or M.S. in Chemical Engineering, Biochemical Engineering, or related field.
3+ years of experience in a biotech, pharmaceutical, or GMP-regulated environment.
Familiarity with upstream (cell culture/fermentation) or downstream (purification) processes.
Experience with process monitoring, root cause analysis, and continuous improvement initiatives.
Working knowledge of industry guidelines (GMP, ICH, FDA).
Strong communication, organization, and problem-solving skills.


Quality Agents offers a full suite of benefits for full-time employees including:
Health, dental and vision insurance
Life, AD&D and Disability Insurance
Health savings account for participants in our health plan
401k retirement plan
Paid time off
Paid holidays


Quality Agents accepts applications on an on-going basis in order to build a talent pool of potential candidates. These applications remain open for consideration, as positions become available, for one (1) year from the date of application. After that time, or if your application information changes, please submit your application again.

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