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Bioengineering Jobs in New Jersey (NOW HIRING)

Legend Biotech US

Metrology Tech I

Raritan, NJ · On-site

Sc. in Biological/Biochemical Science/Bioengineering related field. Trade / Technical School Certification or Certification in Craft required. Military equivalent of Trade / Technical School ...

MSD

Senior Scientist, Biocatalysis

Rahway, NJ · On-site

D. or Postdoctoral Education in Chemistry, Biochemistry, Bioengineering, Biophysics, Chemical Engineering, Molecular Biology, Synthetic Biology, or a related field; or * M.S. with at least 4 years of ...

Rutgers University

Oral Biology Department Chair

Newark, NJ · On-site

$208 - $254/hr

... bioengineering, and public health. The Chair of Oral Biology will be responsible for the overall administration and strategic leadership of the Department. The successful candidate will be expected ...

Rocket Pharmaceuticals

NJ · On-site

$220 - $293/hr

PhD in chemical engineering, biochemical engineering, bioprocessing, bioengineering, biochemistry, biological sciences, or relevant field of study with 10 years of experience in a biotech ...

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Showing results 21-40

All JobsBioengineering JobsBioengineering Jobs in New Jersey

Bioengineering information

See New Jersey salary details

$44.5K

$68.2K

$98.2K

How much do bioengineering jobs pay per year?

As of Aug 12, 2026, the average yearly pay for bioengineering in New Jersey is $68,248.00, according to ZipRecruiter salary data. Most workers in this role earn between $55,698.00 and $79,149.00 per year, depending on experience, location, and employer.

What is bioengineering?

Bioengineering is an interdisciplinary field that applies principles of biology, engineering, and medicine to develop technologies and devices that improve healthcare and advance biological research. Bioengineers may work on projects such as designing medical devices, developing artificial organs, creating tissue engineering solutions, or improving drug delivery systems. The field blends knowledge from various scientific disciplines to solve complex problems in health and medicine, agriculture, and environmental systems. Bioengineers often collaborate with doctors, researchers, and other engineers to create innovative solutions that benefit society.

What are the key skills and qualifications needed to thrive as a bioengineer, and why are they important?

To thrive as a Bioengineer, you need a solid background in biology, engineering principles, mathematics, and typically a bachelor's or advanced degree in bioengineering or biomedical engineering. Familiarity with CAD software, laboratory instrumentation, and regulatory compliance systems is often required. Strong problem-solving abilities, creativity, and effective communication skills help bioengineers excel in multidisciplinary teams. These skills and qualities are crucial for developing innovative solutions that improve healthcare technologies and biological systems.

Are bioengineers well paid?

Bioengineers typically earn competitive salaries that vary by experience, education, and location. According to industry data, the median annual wage for bioengineers is higher than the national average for all occupations, and those with advanced degrees or specialized skills tend to earn more. The field also offers opportunities for growth in research, development, and healthcare industries.

What are some common interdisciplinary collaborations that a bioengineer can expect in their daily work?

Bioengineers frequently collaborate with professionals from diverse backgrounds, including biologists, medical doctors, chemists, and engineers from other disciplines. These interdisciplinary teams work together to develop innovative medical devices, biomaterials, or diagnostic tools. Effective communication and teamwork are essential, as projects often require integrating biological knowledge with engineering principles. Regular meetings, joint problem-solving sessions, and cross-functional project planning are common, providing bioengineers with valuable exposure to various fields and perspectives.

What is the difference between Bioengineering vs Biomedical Engineering?

AspectBioengineeringBiomedical Engineering
Required CredentialsBachelor's or Master's in Bioengineering or related fieldsBachelor's or Master's in Biomedical Engineering or related fields
Work EnvironmentResearch labs, healthcare companies, biotech firmsHospitals, medical device companies, research institutions
Industry UsageDevelops biological solutions, tissue engineering, genetic researchDesigns medical devices, prosthetics, and healthcare technology

Bioengineering and Biomedical Engineering share many credentials and work environments, often overlapping in research and development roles. However, bioengineering tends to focus more on biological systems and genetic research, while biomedical engineering emphasizes medical devices and healthcare technology. Both fields are integral to advancing healthcare and often collaborate within the biotech and medical industries.

What are popular job titles related to Bioengineering jobs in New Jersey? For Bioengineering jobs in New Jersey, the most frequently searched job titles are:
What job categories do people searching Bioengineering jobs in New Jersey look for? The top searched job categories for Bioengineering jobs in New Jersey are:
What cities in New Jersey are hiring for Bioengineering jobs? Cities in New Jersey with the most Bioengineering job openings:
Bioengineering jobs near you
Infographic showing various Bioengineering job openings in New Jersey as of August 2026, with employment types broken down into 1% Internship, 91% Full Time, 5% Part Time, and 3% Contract. Highlights an 87% Physical, 5% Hybrid, and 8% Remote job distribution, with an average salary of $68,248 per year, or $32.8 per hour.

Manager Manufacturing Operations

Lynkx Staffing LLC

Saddle Brook, NJ • On-site

Full-time

Re-posted 9 days ago

Job description

Manager Manufacturing OperationsAllendale, NJ Lynkx Staffing LLC specializes in placing talented professionals in the Life Sciences, Biotechnology, Pharmaceutical and Medical Devices industries in New Jersey. The Primary Processing Unit (PPU), Manager, Manufacturing Operations is responsible for efficient capacity utilization of site resources to meet customer demand. They will partner with support functions to deliver on customer demands. This leader is accountable for the management of client projects at the site and for delivery of results within project scope, agreed timelines, contract requirements, revenue targets, as well as compliance and regulatory requirements. The Manager, Manufacturing Operations is responsible for profit and loss within their PPU and will deliver on revenue. This role will also drive individual and team development to ensure a prepared and empowered workforce to become the provider of choice for the industry.
  • Meet client process demands through planning, scheduling, manufacture and delivery.
  • of clinical cell therapy products according to established procedures, regulations and contract.
  • Ensures manufacturing documentation is closed out in a timely manner in accordance with applicable regulations and per contract.
  • Ensures capacity availability of resources (room/equipment/staff) to perform clinical manufacture for clients per contract.
  • Ensures process hours are charged - tracked to meet contract and revenue targets.
  • Accountable for maintaining a mechanism to work with clients to troubleshoot problems, suggests improvements and determines & advocates for value-add projects.
  • Assures manufacturing space is kept in a clean, validated state in compliance with company procedures, GMP and applicable regulations
  • Ensures on the job training program and resources for new associate (proficiency) training and cross training of existing staff.
  • Ensures a safe work environment for employees.
  • Ensures department staff compliance with corporate and site-specific HR policies, safety and business policies and practice.
  • Approves job specific curriculum for the training and professional development of department staff.
  • Holds regular staff and 1:1 meetings to emphasize corporate culture, maintain morale, and provides a forum for staff development and discussion.
  • Responsible for the profit and loss for the PPU
  • Deliver on revenue
  • Assures compliance with budget
  • Liaison with support groups – supply chain, training, quality systems, and business development
  • Partners with clients along with Project Management and team leadership; drives the account management and liaison with the clients
  • Sets team expectations and goals and delivers the business direction for the PPU
  • Sets KPIs & ROIs targets and assures PPU metrics are maintained and tracked monthly.
  • Coordinates with PPU leadership and team meetings and determines PPU strategy development
  • Accountable for driving the spirit of continuous improvement
  • Collaborates with Business Development to ensure compliance and contract requirements
  • Carries out supervisory responsibilities in accordance with the organization's policies and applicable laws. Responsibilities include interviewing, hiring, and training employees; planning, assigning, and directing work; appraising performance; rewarding and disciplining employees; addressing complaints and resolving problems. Directly supervises the following roles: Associate Manager, Manufacturing, Manufacturing Associates, Lead Manufacturing Associates, Production Support Associates, Technical Trainers, Compliance Investigators
REQUIREMENTS
  • Bachelor's degree (ie Biology, Biotechnology, Bioengineering, Chemical Engineering).
  • 5-7 years of cGMP environment, aseptic processing, mammalian cell culture, cell processing, cryopreservation experience.
  • 5-7 years of leadership experience or equivalent combination of experience.
  • Strong business acumen
  • Deep understanding of cGMP and cGLP
  • Working knowledge of financial operations and budget development
  • Relevant IT skills (Visio, Microsoft Project and Excel)
  • Ability to think strategically and tactically (detail-oriented)
  • Strong collaborative and influencing skills and ability to work well in a cross-functional, matrixed environment
  • Analytical and problem-solving skills
  • Strong written and oral communication skills
  • Meeting management/facilitation skills/teamwork
  • Ability to multi-task team is essential
  • Flexible and able to adapt to company growth and evolving responsibilities
  • Drive to create and maintain order in a fluid technically complex environment
  • Integrity, accountability and strong dedication to regulatory compliance
  • Continuous improvement mindset
  • List required training that must be completed by incumbent in order to fulfill the responsibilities for this role. Examples can include aseptic techniques, gowning qualifications, manager training, GMP, etc.
  • Must have the ability to work in a team-oriented environment and with clients
  • Must be able to work during the weekend, holidays and as required by the company
  • May be exposed to infectious diseases transmittable through human blood, tissues, or bodily fluids
  • Must utilize proper personal protective equipment (PPE) when handling all human specimens, gases, corrosive chemicals, and liquid nitrogen
  • Must have the ability to work in the cleanroom environment for extended period of time
  • Must have the ability to work with specialized equipment
  • May work with hazardous materials and chemicals
  • Environment requires gowning, hair net, safety glasses, gloves, and foot coverings.
Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties, or responsibilities that are required of the employee for this job. Duties, responsibilities, and activities may change at any time with or without notice.