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Entry Level Pharmaceutical Engineer Jobs (NOW HIRING)

Fresenius Kabi

Sr Manufacturing Engineer

Melrose Park, IL · On-site

$100K - $130K/yr

Provides manufacturing engineering leadership and mentoring to entry-level Manufacturing Engineers ... Maintains awareness of current pharmaceutical manufacturing needs and standards and communicates ...

LAPORTE L.C.C.

Junior Process Engineer

Atlanta, GA · On-site

Junior Process Engineer LAPORTE is looking for an entry level Process Engineer. Candidate will ... in the pharmaceutical, biotechnology, or food & beverage industries Flexibility to travel to ...

E*Pro, Inc.

Jr. Validation Engineer

Saint Louis, MO · On-site

... Pharmaceutical, Health Care and service industries ensures our services are customized to meet ... Temporary, entry-level position to mitigate expected validation workload Review requirements ...

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Entry Level Pharmaceutical Engineer information

See salary details

$40.5K

$86.4K

$142.5K

How much do entry level pharmaceutical engineer jobs pay per year?

As of Jul 17, 2026, the average yearly pay for entry level pharmaceutical engineer in the United States is $86,381.00, according to ZipRecruiter salary data. Most workers in this role earn between $65,000.00 and $103,500.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as an Entry Level Pharmaceutical Engineer, and why are they important?

To thrive as an Entry Level Pharmaceutical Engineer, you need a bachelor's degree in chemical, biomedical, or pharmaceutical engineering and a solid grounding in process design and regulatory standards. Familiarity with industry-standard software such as AutoCAD, process simulation tools, and GMP (Good Manufacturing Practice) compliance is typically required. Strong analytical thinking, attention to detail, and effective teamwork set top performers apart in this role. These competencies are vital to ensure safe, efficient, and compliant drug manufacturing processes in a highly regulated industry.

What is the difference between Entry Level Pharmaceutical Engineer vs Quality Control Technician?

AspectEntry Level Pharmaceutical EngineerQuality Control Technician
Required CredentialsBachelor's in Pharmaceutical, Chemical, or related field; some roles may require internshipsAssociate's or Bachelor's in Science or related field; certifications like CQE are a plus
Work EnvironmentLaboratories, manufacturing plants, R&D settingsLaboratories, manufacturing facilities, quality assurance departments
Employer & Industry UsagePharmaceutical companies, biotech firms, contract manufacturingPharmaceutical companies, biotech firms, quality assurance labs

Entry Level Pharmaceutical Engineers focus on designing, developing, and improving pharmaceutical manufacturing processes, while Quality Control Technicians primarily test and inspect products to ensure quality standards. Both roles are essential in pharmaceutical production, often working closely but with different core responsibilities.

What does an Entry Level Pharmaceutical Engineer do?

An Entry Level Pharmaceutical Engineer assists in the design, development, and optimization of processes used in the manufacturing of pharmaceutical products. They often work under the supervision of senior engineers to ensure safety, quality, and regulatory compliance in the production of medications. Their responsibilities may include conducting experiments, analyzing data, troubleshooting equipment, and supporting process improvements. This role serves as a foundation for gaining experience in pharmaceutical engineering and understanding industry standards.

What are some common challenges faced by entry level pharmaceutical engineers when transitioning from academia to industry?

Entry level pharmaceutical engineers often find the transition from academia to industry challenging due to the emphasis on strict regulatory compliance, tight project deadlines, and cross-functional teamwork. Unlike academic research, industry projects demand adherence to Good Manufacturing Practices (GMP) and extensive documentation. New hires must quickly adapt to working in multidisciplinary teams alongside professionals from quality assurance, production, and regulatory affairs. Embracing continuous learning and seeking mentorship can help ease this transition and accelerate professional growth.
More about Entry Level Pharmaceutical Engineer jobs
What cities are hiring for Entry Level Pharmaceutical Engineer jobs? Cities with the most Entry Level Pharmaceutical Engineer job openings:
What are the most commonly searched types of Pharmaceutical Engineer jobs? The most popular types of Pharmaceutical Engineer jobs are:
What states have the most Entry Level Pharmaceutical Engineer jobs? States with the most job openings for Entry Level Pharmaceutical Engineer jobs include:
What job categories do people searching Entry Level Pharmaceutical Engineer jobs look for? The top searched job categories for Entry Level Pharmaceutical Engineer jobs are:
Entry Level Pharmaceutical Engineer jobs near you
Infographic showing various Entry Level Pharmaceutical Engineer job openings in the United States as of July 2026, with employment types broken down into 66% Full Time, 17% Part Time, and 17% Contract. Highlights an 100% In-person job distribution, with an average salary of $86,381 per year, or $41.5 per hour.
Manufacturing Engineer I (Entry Level)

Manufacturing Engineer I (Entry Level)

CIS International LLC

Juncos, PR

Full-time

Posted 10 days ago

Job description

Responsibilities may include the following: 

  • Design manufacturing processes, procedures, and production layouts for assemblies, equipment installation, machining, and material handling.
  • Develop and optimize workflow and sequence of operations to improve efficiency and productivity.
  • Design equipment and facility layouts to maximize production capabilities.
  • Adapt machine and equipment designs to meet manufacturing and production requirements.
  • Incorporate inspection and testing requirements into production processes.
  • Evaluate equipment performance and implement corrective actions to resolve issues.
  • Support statistical process control (SPC) and continuous improvement initiatives.
  • Provide engineering support for design concepts and manufacturability.
  • Ensure compliance with FDA, ISO, and GMP regulations.
  • Collaborate with cross-functional teams including Quality, Operations, and R&D.
  • *Other duties may be assigned.*

Requirements:
Education and Experience:

  • Bachelor’s Degree in Engineering (Mechanical, Electrical, Chemical, or related).
  • 0–3 years of experience in manufacturing, engineering, or related roles.
  • Bilingual (English & Spanish).
  • Experience in Computer System Validation (CSV).
  • Experience working in a regulated environment (Medical Devices or Pharmaceutical industry).
  • Basic knowledge of manufacturing processes and equipment.
  • Strong organizational, communication, and technical writing skills.

Preferred Qualifications: 

  • Knowledge of Process Validation (IQ/OQ/PQ)
  • Experience with Statistical Tools (Minitab or equivalent)
  • Familiarity with MES systems (e.g., FactoryWorks)
  • Knowledge of risk management tools (FMEA)
  • *Willing to work 100% On-Site, weekend and other shifts when necessary.*

Skill set

Systems & Tools:

  • Minitab (or equivalent statistical tools)
  • Microsoft Office Suite (Excel, Word, PowerPoint)

Soft Skills:

  • Bilingual Communication (English & Spanish)
  • Problem Solving & Analytical Thinking
  • Organization & Time Management
  • Team Collaboration
  • Attention to Detail
Work Methodology
  • 100% on site job in Juncos- PR
  • Administrative Shift
  • Duration: 6 months (1st contract) with a high possibility of extension based on performance and budget.
  • Professional services Contract
  • Type of industry: Medical devices