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Entry Level Pharmaceutical Engineer Jobs in Raleigh, NC

Actalent

Controls Engineer

Holly Springs, NC

$39.42 - $50/hr

Entry-Level Traveling Controls Engineer Overview: Seeking a Controls Engineer with 1+ year of ... This role supports manufacturing, pharmaceutical, industrial, and data center projects, with ...

BMWC CONSTRUCTORS

Project Engineer I

Raleigh, NC · On-site

$65 - $85/hr

We will train an entry level graduate and/or hire an experienced industrial construction project ... gas, pharmaceutical and biotechnology, and semiconductor. As one of the premier specialty ...

BMWC Constructors

Project Engineer I

Raleigh, NC · On-site

$67K - $86K/yr

... an entry level graduate and/or hire an experienced industrial construction project engineer ... gas, pharmaceutical and biotechnology, and semiconductor. As one of the premier specialty ...

BMWC CONSTRUCTORS

Project Engineer I

Raleigh, NC · On-site

$67K - $86K/yr

We will train an entry level graduate and/or hire an experienced industrial construction project ... gas, pharmaceutical and biotechnology, and semiconductor. As one of the premier specialty ...

BMWC CONSTRUCTORS

Project Engineer I

Raleigh, NC · On-site

$67K - $86K/yr

We will train an entry level graduate and/or hire an experienced industrial construction project ... gas, pharmaceutical and biotechnology, and semiconductor. As one of the premier specialty ...

Applied Industrial Technologies

Planner I

Raleigh, NC · On-site

$22 - $25/hr

This is an ONSITE ENTRY LEVEL position. * This job starts at $22-$25/hour. * This position is not ... Pharmaceutical industry or quality system experience is preferred. PCI is proud to serve ...

Novo Nordisk

Automation Technician I

Clayton, NC · On-site

$35K/yr

Associate's degree in Electronics, Computers, Engineering or a relevant field of study from an ... entry level * Basic understanding of process control systems for Pharmaceutical, Biotech, Food ...

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Entry Level Pharmaceutical Engineer information

See Raleigh, NC salary details

$39.4K

$84K

$138.5K

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

As of Sep 5, 2026, the average yearly pay for entry level pharmaceutical engineer in Raleigh, NC is $83,969.00, according to ZipRecruiter salary data. Most workers in this role earn between $63,200.00 and $100,600.00 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.

What are popular job titles related to Entry Level Pharmaceutical Engineer jobs in Raleigh, NC?

For Entry Level Pharmaceutical Engineer jobs in Raleigh, NC, the most frequently searched job titles are:

What job categories do people searching Entry Level Pharmaceutical Engineer jobs in Raleigh, NC look for?

The top searched job categories for Entry Level Pharmaceutical Engineer jobs in Raleigh, NC are:

Entry Level Pharmaceutical Engineer jobs near you
Infographic showing various Entry Level Pharmaceutical Engineer job openings in Raleigh, NC as of August 2026, with employment types broken down into 90% Full Time, 6% Part Time, and 4% Contract. Highlights an 87% Physical, 5% Hybrid, and 8% Remote job distribution, with an average salary of $83,969 per year, or $40.4 per hour.

Entry Level Validation Engineer

Barry-Wehmiller

Raleigh, NC

$75K - $90K/yr

Full-time

Posted 4 days ago

Job description

About Us:

BW Design Group is a fully integrated architecture, engineering, construction, system integration, and consulting firm committed to helping our clients realize their most critical goals from Strategy to Commercialization. As the only firm born from a manufacturing technology company to become an independent and fully integrated firm, we combine deep domain expertise in the manufacturing environment with an approach that is built to serve the dynamic needs of our clients. Rooted in our distinct culture of Truly Human Leadership, we cultivate the leaders who will define tomorrow and partner with our clients in the food & beverage, life sciences, industrial, and advanced technology industries to build the future of manufacturing and technology.


 

Barry-Wehmiller is a diversified global supplier of engineering consulting and manufacturing technology for the packaging, corrugating, sheeting and paper-converting industries. By blending people-centric leadership with disciplined operational strategies and purpose-driven growth, Barry-Wehmiller has become a $3 billion organization with nearly 12,000 team members united by a common belief: to use the power of business to build a better world.


 

Job Description:

Who You'll Work With

At Design Group,you'llcollaborate with experienced leaders, technical specialists, and subject matter experts to solve complex challenges for some of the world's leading companies.You'lljoin a growing team of more than 1,500 professionals across 45 U.S. offices whereyou'llbe empowered to make an impact, develop yourexpertise, and grow your career.

What You'll Do

In this role,you'llbe responsible forsupporting validation and regulatory compliance activities for pharmaceutical, medical device, and other life sciences projects.You'llwork closely with validation engineers, project teams, clients, vendors, and technical specialists to develop protocols, execute testing, investigate issues, and document results. This position playsan important rolein helping clientsdemonstratethat equipment, utilities, facilities, and automated systems meet quality and regulatory requirements while giving you hands-on experience invalidationengineering and project delivery.

  • Develop and execute validation and FDA compliance documents and protocols for pharmaceutical equipment and automated systems

  • Support manufacturing process design, facility development, and project execution activities

  • Prepare and execute FAT, SAT, IQ, and OQ documentation for equipment and automated systems

  • Assistwith development and execution of quality management system procedures and related compliance documentation

  • Apply applicable requirements from 21 CFR Parts 211 and 820 and ICH Q1, Q8, Q9, and Q10 to project deliverables

  • Conduct investigations and support troubleshooting of validation and compliance issues

  • Prepare clear written validation reports that document testing, results, deviations, and conclusions

  • Coordinate with clients, vendors, engineers, and project teams to support validation planning and execution

  • Support installation, start-up, commissioning, and site-based validation activities

  • Build technicalexpertisein life sciences validation, quality systems, documentation practices, and regulatory compliance

What You'll Bring

Qualifications

  • Bachelor of Science in bioengineering, biomedical engineering, chemical engineering, or a related technical degree

  • Academic, co-op, internship, project, or entry-level experience related to validation, quality, pharmaceutical manufacturing, medical devices, automation, utilities, facilities, or regulated environments

  • Proficiencyusing Microsoft Office and ability to prepare clear technical documentation

  • Ability to organize and execute multiple project responsibilities simultaneously

  • Ability to travel for project requirements, including installation and start-up activities, client and company meetings, trainings, seminars, forums, and conventions

Preferred Qualifications

  • Co-op or project experience with validation of automation, packaging equipment, utilities, or facilities

  • Co-op or project experience in pharmaceutical or medical device environments

  • Exposure to FAT, SAT, IQ, OQ, quality systems, FDA requirements, or technical report writing

Compensation

The approximate pay range for this position is$75,000-$90,000. Please note that the pay range provided is a good faith estimate for the position at the time of posting. Final compensation may vary based on factors including but not limited to background, knowledge, skills, and abilities, as well as geographic location of the position.


 

At Barry-Wehmiller we recognize that people come with a wealth of experience and talent beyond just the technical requirements of a job. If your experience is close to what you see listed here, please still consider applying. We know that our differences often can bring about innovation, excellence and meaningful work-therefore, people from all backgrounds are encouraged to apply to our positions. Please let us know if you require reasonable accommodations during the interview process.

Barry-Wehmiller is an equal opportunity employer. M/F/D/V This organization uses E-Verify.


 

Applicants may be subject to pre-employment screening which may include drug screening, reference checks, employment verifications, background screening and/or skills assessments.


Company:

Design Group

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