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Entry Level Bioengineering Jobs in Camden, NJ (NOW HIRING)

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Entry Level Bioengineering information

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How much do entry level bioengineering jobs pay per hour?

As of Sep 6, 2026, the average hourly pay for entry level bioengineering in Camden, NJ is $20.12, according to ZipRecruiter salary data. Most workers in this role earn between $16.49 and $22.55 per hour, depending on experience, location, and employer.

What is an entry level bioengineer?

Entry level bioengineering jobs are positions designed for individuals who have recently graduated with a degree in bioengineering or a related field. These roles typically involve assisting in research, product development, quality control, or laboratory work within industries such as healthcare, pharmaceuticals, biotechnology, or medical devices. Entry level bioengineers may work alongside experienced engineers and scientists to design, test, or improve biological systems and medical devices. These positions often provide on-the-job training and opportunities for professional growth.

What does an entry level bioengineer do?

As an entry-level bioengineer, you'll typically contribute to projects such as developing medical devices, conducting laboratory experiments, or analyzing biological data. Your daily responsibilities may include assisting with research, running tests, collecting and interpreting data, and preparing reports for senior engineers or project managers. You’ll often work as part of a multidisciplinary team, collaborating closely with scientists, clinicians, and other engineers. This collaborative environment provides valuable learning opportunities and exposure to various aspects of bioengineering, helping you build foundational skills for career growth.

What are the key skills and qualifications needed to thrive as an entry level bioengineer?

To thrive as an Entry Level Bioengineer, you need a solid background in biology, engineering principles, and mathematics, typically supported by a bachelor's degree in bioengineering or a related field. Familiarity with CAD software, laboratory instrumentation, and data analysis tools like MATLAB or Python is commonly required. Strong problem-solving abilities, teamwork, and effective communication skills help you excel in collaborative research and development environments. These skills are essential for innovating and delivering solutions that advance healthcare technology and improve patient outcomes.

What are some entry-level bioengineering jobs available?

Entry-level bioengineering jobs include roles such as biomedical engineering technician, research assistant, or laboratory technician, often requiring a bachelor's degree in bioengineering or related fields. These positions typically involve supporting research, device testing, or manufacturing processes and may require familiarity with lab equipment and basic data analysis. Opportunities are available in healthcare, medical device companies, and research institutions.

What jobs can I get with entry level bioengineering?

Entry-level bioengineers can work in roles such as research assistants, laboratory technicians, or quality control specialists in healthcare, biotech, or medical device companies. These positions often require knowledge of biology, engineering principles, and proficiency with tools like CAD software or lab equipment, and may involve data analysis and compliance with safety standards.
Entry Level Bioengineering jobs near you
Infographic showing various Entry Level Bioengineering job openings in Camden, NJ 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 $41,843 per year, or $20.1 per hour.

Entry Level Validation Engineer

Barry-Wehmiller

Philadelphia, PA • On-site

$75K - $90K/yr

Full-time

Posted 5 days ago

Key responsibilities

  • Support validation and regulatory compliance activities for pharmaceutical, medical device, and other life sciences projects.

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

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

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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