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Entry Level Pharmaceutical Engineer Jobs (NOW HIRING)

Just In Time Staffing LLC

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Entry Level Manufacturing Engineer

Elgin, IL · On-site

$65K - $82K/yr

Position: Entry- Level Manufacturing Engineer Job Type : Direct Hire Pay: $65,000 - $82,000 ... Experience in food, beverage, pharmaceutical, or other GMP-regulated manufacturing environments.

Barry-Wehmiller

Entry Level Controls Engineer

Abilene, TX · On-site

$80K - $104K/yr

Co-op or project experience with pharmaceutical, consumer products, and high-speed environments ... As a Entry Level Controls Engineer, you will build a meaningful and fulfilling career with the ...

Barry-Wehmiller

Entry Level Controls Engineer

San Antonio, TX · On-site

$75K - $97K/yr

Co-op or project experience with pharmaceutical, consumer products, and high-speed environments ... As a Entry Level Controls Engineer, you will build a meaningful and fulfilling career with the ...

Stark Pharma Solutions Inc

Manufacturing Engineer

Orlando, FL · On-site

$68K - $87K/yr

Manufacturing Engineer Location : Orlando, FL Duration : Long Term Position Overview We are seeking ... pharmaceutical, biotechnology, or medical device industry. This entry-level role is ideal for ...

Acuren Inspection, Inc.

Entry Level NDT Assistant

Tulsa, OK · On-site

$35K - $45K/yr

... engineering, reliability engineering, drones, robotics, V-Deck and condition-based monitoring ... pharmaceutical, aerospace and automotive industries. Acuren employs over 4,000 dedicated ...

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Entry Level Pharmaceutical Engineer information

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$40.5K

$86.4K

$142.5K

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

As of Aug 27, 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 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 the key skills and qualifications needed to thrive as an entry level pharmaceutical engineer?

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 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.

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.

Are entry level pharmaceutical engineers in demand?

Entry level pharmaceutical engineers are in demand due to the ongoing need for drug development, manufacturing, and quality assurance in the pharmaceutical industry. Employers seek candidates with knowledge of process engineering, regulatory standards, and laboratory skills, making this a growing field for new graduates.

Do entry level pharmaceutical engineers make good money?

Entry-level pharmaceutical engineers typically earn a starting salary ranging from $60,000 to $75,000 annually, depending on location and company. With experience, certifications, and advanced skills in process design or quality assurance, salaries can increase significantly. The role often involves working in manufacturing or research environments with standard business hours.

How to get into entry level pharmaceutical engineering?

To enter an entry-level pharmaceutical engineering role, candidates typically need a bachelor's degree in chemical engineering, pharmaceutical sciences, or a related field. Gaining experience through internships, developing skills in process design and quality control, and understanding Good Manufacturing Practices (GMP) can improve job prospects.
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Entry Level Pharmaceutical Engineer jobs near you
Infographic showing various Entry Level Pharmaceutical Engineer job openings in the United States as of August 2026, with employment types broken down into 64% Full Time, and 36% Contract. Highlights an 100% In-person job distribution, with an average salary of $86,381 per year, or $41.5 per hour.

Entry-Level Pharmaceutical Manufacturing Technician

Bend, OR • On-site

Lonza
10K+ employees

8.3

Company rating: 8.3 out of 10

Based on 42 frontline employees who took The Breakroom Quiz

26th of 86 rated pharmaceutical

People enjoy working here

Good employer

Paid breaks

Learn more about Lonzaexternal

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 9 days ago

Job description

The actual location of this job is in Bend, Oregon (USA). Relocation assistance is available for eligible candidates and their families, if needed.
Today, Lonza is a global leader in life sciences operating across five continents. While we work in science, there's no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that's the kind of work we want to be part of.
Lonza Pharma & Biotech has an opening for an experienced Pharmaceutical Manufacturing Technician to join their Early Phase Clinical Manufacturing team. This role offers the outstanding opportunity to contribute to world-class pharmaceutical innovations, while working in a collaborative and inclusive environment. If you are ambitious and driven by the desire to make a meaningful impact, we want you to join our mission to improve lives.
What You Will Get:
  • Shape the future of medicine by building new pharmaceutical products from clinical scale to full manufacturing.
  • Grow your technical skills by taking charge of equipment lifecycles and working with expert teams in quality and engineering.
  • Work in a safe, high-quality cGMP space that values your personal growth and new ideas.
  • Day-One Insurance: Life, disability, and comprehensive health, dental, and vision insurance options
  • 401k Match: 100% match up to 6% of your salary, plus an extra automatic company contribution
  • Tuition reimbursement program
  • Lonza bonus program: Performance-linked variable pay plan that rewards yearly company and individual success

What You Will Do:
Manufacturing Operations
  • Assist in production: Help manufacture clinical trial materials to support new pharmaceutical product development.
  • Follow guidelines: Safely run production equipment and document your work according to standard procedures and Good Documentation Practices (GDP).
  • Learn the equipment: Train to become proficient in assembling, operating, cleaning, and troubleshooting manufacturing machinery.
  • Maintain workspaces: Perform routine cleaning of production areas and assist technicians with equipment maintenance and calibration.
  • Support new projects: Participate in new product transfers and share hands-on feedback with the team.

Technical & Engineering Support
  • Help with setup: Assist engineers with the installation, startup, and testing of new manufacturing equipment.
  • Review process data: Help gather and organize production data to support project goals and team decisions.
  • Spot improvements: Learn the workflow to help identify simple ways to make daily operations smoother and more efficient.

Compliance & Documentation
  • Draft documents: Help write and update simple work instructions, training guides, and basic technical reports.
  • Maintain standards: Ensure all daily tasks strictly follow safety rules and cGMP (Current Good Manufacturing Practice) regulations.
  • Report issues: Assist with basic investigations into equipment or process variations.
  • Communicate clearly: Share daily updates and technical findings clearly with your team members and supervisors.

What We Are Looking For:
  • High School Diploma or GED equivalent.
  • Thrive in fast-paced, collaborative team settings to hit daily production targets.
  • Dedicated to lean principles, quality control, and rapid adaptation to new manufacturing processes.
  • Strictly adhere to OSHA and company safety guidelines while managing hazardous materials and standard operating procedures (SOPs).
  • Fully comfortable operating in controlled environment while wearing required Personal Protective Equipment.
  • Capable of routine heavy lifting, material handling, and active equipment operation.

Join us and be part of a team that drives outstanding pharmaceutical innovations and makes a significant difference in people's lives!
Every day, Lonza's products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically.
People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference.
Lonza is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a qualified individual with disability, protected veteran status, or any other characteristic protected by law.

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