ZipRecruiter

Log In

1

Temporary Biomedical Chemical Engineering Jobs (NOW HIRING)

Siemens Healthineers

Chemical Engineer

Troy Hills, NJ

$72K - $100K/yr

Performs other duties as assigned or required Qualifications & Experience * BS in Chemical Engineering, Ceramics/Materials Engineering, Biomedical Engineering, or related field * 1+ years of ...

Lonza

MSAT Process Engineer

Portsmouth, NH · On-site

$106K - $137K/yr

Bachelor of Science degree in Biological Sciences or Biomedical/Chemical Engineering. * Senior level experience in biotech industry in process development and process scale up / manufacturing.

Draper

Principal Microfluidics Engineer

Cambridge, MA · On-site

$95 - $245/hr

Requires either a Bachelor's Degree in Bioengineering, Biomedical Engineering, Biochemistry, Chemistry, Cell Biology, Immunology, Microbiology, Molecular Biology, Mechanical Engineering, Chemical ...

previous pagenext page

Showing results 21-40

All Jobstmp JobsScience JobsChemistry JobsChemical Engineer JobsTemporary Biomedical Chemical Engineering Jobs

Temporary Biomedical Chemical Engineering information

See salary details

$41K

$94.8K

$140K

How much do temporary biomedical chemical engineering jobs pay per year?

As of Sep 4, 2026, the average yearly pay for temporary biomedical chemical engineering in the United States is $94,807.00, according to ZipRecruiter salary data. Most workers in this role earn between $74,500.00 and $116,000.00 per year, depending on experience, location, and employer.

What is a temporary biomedical chemical engineer?

Temporary Biomedical Chemical Engineers are professionals who work on short-term or contract assignments within the biomedical and chemical engineering fields. They typically assist with research, product development, process optimization, or equipment maintenance in medical device companies, pharmaceutical firms, or research institutions. These roles are essential for meeting project deadlines or covering staff shortages, and offer valuable experience for those seeking to enter or advance in the biomedical engineering industry.

What are some typical projects or assignments for a temporary biomedical chemical engineer, and how do they contribute to larger team goals?

Temporary Biomedical Chemical Engineers often support ongoing research, product development, or process optimization projects. Assignments can include performing laboratory experiments, analyzing data, assisting with the scale-up of biomedical products, or ensuring regulatory compliance. These roles are highly collaborative, requiring close work with permanent engineers, scientists, and quality assurance teams. By focusing on specific project milestones or short-term objectives, temporary engineers help meet deadlines and maintain workflow continuity during peak periods or staff transitions.

What are the key skills and qualifications needed to thrive as a temporary biomedical chemical engineer, and why are they important?

To thrive as a Temporary Biomedical Chemical Engineer, you need a solid background in chemical and biomedical engineering principles, typically supported by a relevant engineering degree. Familiarity with laboratory instrumentation, CAD software, and regulatory compliance systems such as GMP or FDA guidelines is often required. Strong problem-solving, adaptability, and teamwork skills set candidates apart in dynamic project environments. These skills ensure effective design, testing, and implementation of biomedical solutions while maintaining safety and compliance standards.

What is the difference between Temporary Biomedical Chemical Engineering vs Temporary Biomedical Equipment Technician?

AspectTemporary Biomedical Chemical EngineeringTemporary Biomedical Equipment Technician
CredentialsEngineering degree, certifications in biomedical or chemical engineeringTechnical diploma or certification in biomedical equipment technology
Work EnvironmentLaboratories, research facilities, manufacturing plantsHospitals, clinics, medical device maintenance settings
Employer & IndustryBiotech firms, pharmaceutical companies, research institutionsHospitals, medical device companies, healthcare providers

Temporary Biomedical Chemical Engineers focus on designing, developing, and improving biomedical products and processes, often working in labs or manufacturing. In contrast, Temporary Biomedical Equipment Technicians primarily maintain, repair, and calibrate medical devices in healthcare settings. Both roles require specialized certifications but differ in daily tasks and work environments.

What jobs can you get with a BS in temporary biomedical chemical engineering?

A BS in biomedical chemical engineering can qualify you for roles such as biomedical engineer, process engineer, research associate, or quality control analyst in healthcare, biotech, or pharmaceutical industries. These positions often require knowledge of laboratory techniques, regulatory standards, and engineering principles, and may involve working in labs, manufacturing facilities, or clinical settings.

What cities are hiring for Temporary Biomedical Chemical Engineering jobs?

Cities with the most Temporary Biomedical Chemical Engineering job openings:

What are the most commonly searched types of Biomedical Chemical Engineering jobs?

The most popular types of Biomedical Chemical Engineering jobs are:

What states have the most Temporary Biomedical Chemical Engineering jobs?

States with the most job openings for Temporary Biomedical Chemical Engineering jobs include:

Temporary Biomedical Chemical Engineering jobs near you
Infographic showing various Temporary Biomedical Chemical Engineering job openings in the United States as of June 2026, with employment types broken down into 58% Full Time, 18% Part Time, 12% Temporary, and 12% Contract. Highlights an 99% Physical, and 1% Remote job distribution, with an average salary of $94,807 per year, or $45.6 per hour.

RNA-LNP Process Development Lab Manager - Group Leader

Eurofins

Boston, MA • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 14 days ago

Eurofins rating

7.5

Company rating: 7.5 out of 10

Based on 181 frontline employees who took The Breakroom Quiz

64th of 121 rated laboratories

Job description

Company Description
The work we do at Eurofins Professional Scientific Services matters, and so do our employees. At Eurofins PSS, we put a focus on your professional growth. We provide our employees the ability to break into the biopharmaceutical industry and grow from the bottom up. We have the supportive teams and tools available to invest in you while also affording you work-life balance and a competitive benefits package.
Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies.
If you're looking for a rewarding career, a place to call home, apply with us today!
Job Description
We are seeking an RNA-LNP Lab Manager / Group Leader to support an LNP and RNA Process Development and Technology Transfer team. The successful candidate will supervise laboratory operations of a team conducting studies focused on the process development and tech transfer of LNP drug products, mRNA drug substances, and gRNA drug substances. Additionally, they will be responsible for overseeing GLP sample management for process development studies across multiple programs. The successful candidate will have a passion for driving efficient lab operations through excellence in lab operations, raw material and sample inventory management, and coordination of partner analytical testing and results communication.
Technical Responsibilities:
  • Support continuous improvement initiatives related to lab operations.
  • Build and maintain process development specific raw material, consumable, and sample management inventory systems.
  • Submit analytical samples with partner analytical organizations and track results return.
  • Order supplies and equipment as needed. Coordinate, receive, and inventory deliveries.
  • Maintain detailed inventory records in an electronic lab notebook (ELN).
  • Coordinate and ensure routine maintenance and upkeep of laboratory equipment used in process development.
  • Build and maintain equipment maintenance program for Agilent HPLC, AKTA Avant preparative liquid handling, and capillary gel electrophoresis (CGE) systems.
  • Work closely with collaborators in Process Development, Tech Transfer, Facilities, Laboratory Operations, IT, and Safety teams as needed.
  • Author lab maintenance protocols, SOPs, provide updates to the weekly lab operations meeting, and track and analyze lab efficiency metrics.
  • Collaborate with cross-functional teams including analytical development and manufacturing

Leadership & Team Management Responsibilities:
  • Lead, manage, and develop a team of process development scientists.
  • Serve as a proactive and effective point of contact for client and internal teams.
  • Participate in new hire interviews and onboarding processes
  • Disseminate administrative communications and promote company vision
  • Ensure adherence to highest quality and efficiency standards in laboratory operations
  • Perform administrative tasks to support team member growth and development
  • Balance technical work with team leadership responsibilities
  • Foster morale, collaboration, and teamwork with the group

Qualifications
Minimum Required Qualifications:
  • B.S. degree in biological sciences, chemistry, or biomedical/chemical engineering (or related field) with 5+ years of relevant pharmaceutical, CRO, or biotech experience. M.S. degree in biological sciences, chemistry, or biomedical/chemical engineering (or related field) with 3+ years of relevant pharmaceutical, CRO, or biotech experience. PhD with 2+ years of relevant pharmaceutical, CRO, or biotech experience.
  • Prior laboratory supervisory or team lead experience.
  • Excellent writing and communication skills; ability to understand and communicate scientific information.
  • Experience with the operation and maintenance of equipment commonly used in the process development of nucleic acids (experience with Atka Avant chromatography systems and Agilent HPLC systems is strongly preferred).
  • Strong commitment to laboratory safety protocols.
  • Attention to detail, analysis of data and troubleshooting abilities.
  • Proven ability to manage multiple workstreams in parallel and adapt to changing priorities.
  • Self-motivated with the ability to identify and solve problems proactively.
  • Strong work ethic and excitement for leading an integrated operations team.
  • Authorization to work in the United States indefinitely without restriction or sponsorship.

Preferred Qualifications:
  • Experience building laboratory inventory management systems is strongly preferred.
  • Knowledge of nucleic acid (mRNA, gRNA), LNP, and/or biologics process development.
  • Knowledge of analytical methods used for nucleic acid and/or biologics process development, including HPLC, CGE, or ELISA experience.

Additional Information
The position is full-time, Monday-Friday, 8am-5pm with overtime as needed. Candidates living within a commutable distance of Boston, MA are encouraged to apply.
Excellent full-time benefits include:
  • Comprehensive medical coverage, dental, and vision options
  • Life and disability insurance
  • 401(k) with company match
  • Paid vacation and holidays
  • Eligibility for yearly goal-based bonus & merit-based increases
  • Compensation: $100,000 to $115,000 per year based on education and related experience:

Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

What Eurofins employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom

Eurofins logo

About Eurofins

Sourced by ZipRecruiter

Industry

Scientific research and development services, biotechnology research and development and environmental consulting services

Company size

10,000+ Employees

Headquarters location

Leacock, PA, US

View All Eurofins Jobs

Apply