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Entry Level Biopharmaceutical Engineering Jobs (NOW HIRING)

ImmunityBio, Inc.

Validation Engineer I

El Segundo, CA · On-site

$98K/yr

... traded biopharmaceutical company with headquarters in Southern California. • Work with a ... (entry-level qualifications) to $98,000 (highly experienced) annually The application window is ...

NKW NantKwest Inc

Validation Engineer I

El Segundo, CA · On-site

$98K/yr

Opportunity to join a publicly traded biopharmaceutical company with headquarters in Southern ... (entry-level qualifications) to $98,000 (highly experienced) annually The application window is ...

ImmunityBio

Validation Engineer I

El Segundo, CA · On-site

$98K/yr

Opportunity to join a publicly traded biopharmaceutical company with headquarters in Southern ... (entry-level qualifications) to $98,000 (highly experienced) annually The application window is ...

ImmunityBio

Validation Engineer I

Mariposa, CA · On-site

$98K/yr

Opportunity to join a publicly traded biopharmaceutical company with headquarters in Southern ... (entry-level qualifications) to $98,000 (highly experienced) annually The application window is ...

Calyx

Clinical Data Programmer I

$52K - $75K/yr

... biopharmaceutical industry bring new, advanced medical treatments to market, faster. We seek to ... Understanding of 21 CFR Part 11 * Entry level SAS programming experience * Experience with EDC (e.g.

Calyx

Clinical Data Programmer I

$51K - $94K/yr

... biopharmaceutical industry bring new, advanced medical treatments to market, faster. We seek to ... OpenClinica, RAVE, Inform, TrialMaster, etc.) * Entry level SQL proficiency • Entry level ...

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Entry Level Biopharmaceutical Engineering information

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$30K

$69.4K

$118K

How much do entry level biopharmaceutical engineering jobs pay per year?

As of Jul 13, 2026, the average yearly pay for entry level biopharmaceutical engineering in the United States is $69,362.00, according to ZipRecruiter salary data. Most workers in this role earn between $51,500.00 and $78,500.00 per year, depending on experience, location, and employer.

What is the difference between Entry Level Biopharmaceutical Engineering vs Entry Level Chemical Engineering?

AspectEntry Level Biopharmaceutical EngineeringEntry Level Chemical Engineering
Required CredentialsBachelor's in Bioengineering, Biotechnology, or related fieldsBachelor's in Chemical Engineering or related fields
Work EnvironmentBiotech labs, pharmaceutical manufacturing facilitiesChemical plants, manufacturing facilities, research labs
Industry UsagePrimarily in biotech and pharmaceutical companiesBroader industry, including chemicals, energy, and materials

Entry Level Biopharmaceutical Engineering focuses on developing and manufacturing biopharmaceutical products, often in biotech labs and pharma companies. Entry Level Chemical Engineering has a broader scope, working in chemical production, energy, and materials industries. Both roles require a bachelor's degree and involve lab and manufacturing environments, but their industry focus and specific applications differ.

More about Entry Level Biopharmaceutical Engineering jobs
What are the most commonly searched types of Biopharmaceutical Engineering jobs? The most popular types of Biopharmaceutical Engineering jobs are:
What job categories do people searching Entry Level Biopharmaceutical Engineering jobs look for? The top searched job categories for Entry Level Biopharmaceutical Engineering jobs are:
Entry Level Biopharmaceutical Engineering jobs near you
Infographic showing various Entry Level Biopharmaceutical Engineering job openings in the United States as of July 2026, with employment types broken down into 36% Locum Tenens, 63% Full Time, and 1% Contract. Highlights an 88% Physical, 2% Hybrid, and 10% Remote job distribution, with an average salary of $69,362 per year, or $33.3 per hour.

Associate Process Equipment and Reliability Engineer

WuXi Biologics

Cranbury, NJ • On-site

$55K - $88K/yr

Full-time

Posted 15 days ago

Job description

Job Title - Associate Process Equipment and Reliability Engineer
Work Location - Cranbury NJ
Job Summary
The Associate Process Equipment and Reliability Engineer will support the safe, reliable, and compliant operation of process and utility equipment within a biopharmaceutical manufacturing facility. This entry-level position, under the guidance of senior engineers and engineering leadership, provides opportunities to develop foundational knowledge in equipment engineering, maintenance, reliability practices, and cGMP-regulated manufacturing environments. The Associate Engineer will assist with equipment monitoring, maintenance activities, technical documentation, troubleshooting, and continuous improvement initiatives, while building technical competency in biopharmaceutical manufacturing systems and reliability engineering principles.
Job Responsibilities
  • Assist in monitoring equipment performance and identifying basic equipment issues or reliability concerns.
  • Support troubleshooting activities for process and utility equipment under the direction of senior engineers.
  • Participate in equipment investigations and help collect information to support root cause analysis and CAPA activities.
  • Gather and organize equipment performance data, maintenance records, and operational metrics.
  • Support reliability assessments by maintaining accurate records and reporting equipment observations.

Maintenance & Asset Management
  • Assist with preventive maintenance and predictive maintenance program activities.
  • Support maintenance planning efforts through data collection and documentation updates.
  • Maintain accurate equipment records and documentation within CMMS and asset management systems.
  • Assist with development and revision of maintenance procedures, work instructions, and SOPs.
  • Learn and apply basic reliability engineering concepts, including Failure Modes and Effects Analysis (FMEA) and Reliability-Centered Maintenance (RCM).

Process Equipment Familiarization
  • Gain exposure to upstream, downstream, and fill/finish equipment (e.g., bioreactors, chromatography skids, filtration systems, CIP/SIP systems, autoclaves).
  • Work with operations, maintenance, and senior engineers to understand process-equipment interactions.
  • Support commissioning, qualification, and validation activities for new or modified equipment as assigned.

Compliance & Documentation
  • Develop familiarity with biopharmaceutical manufacturing equipment including upstream, downstream, and fill/finish systems, CIP/SIP systems, autoclaves, and utility equipment.
  • Support equipment inspections, maintenance observations, and engineering assessments.
  • Work closely with Operations, Maintenance, Validation, Quality, and Engineering teams to understand equipment and process interactions.
  • Participate in commissioning, qualification, and validation activities as assigned.

Continuous Learning & Improvement
  • Participate in training programs focused on process equipment, reliability engineering, maintenance practices, and regulatory compliance.
  • Support continuous improvement projects aimed at improving equipment reliability, reducing downtime, and enhancing operational efficiency.
  • Develop technical and professional skills through mentorship and on-the-job learning opportunities.
  • Collaborate with cross-functional teams to support operational excellence initiatives.

Qualifications
  • Bachelor's degree in Mechanical Engineering, Chemical Engineering, Bioprocess Engineering, Electrical Engineering, or related engineering discipline.
  • 0-2 years of engineering experience. Internship, co-op, research experience, or exposure to pharmaceutical, biotechnology, manufacturing, or regulated industries is preferred but not required.
  • Basic understanding of engineering principles and equipment systems.
  • Strong analytical, problem-solving, and organizational skills.
  • Demonstrated willingness to learn and develop technical expertise in equipment reliability and maintenance engineering.
  • Effective written and verbal communication skills.
  • Ability to work collaboratively within cross-functional teams.
  • Exposure to CMMS systems, data analysis tools, or reliability methodologies is a plus.
  • Familiarity with cGMP or regulated manufacturing environments is desirable but not required.
  • Ability to work in a self-motivated, flexible, organized, and detail-oriented manner.
  • Must be able to wear required PPE and work safely within manufacturing and utility areas.
  • Ability to stand, walk, and sit for extended periods.
  • Ability to occasionally lift to 50 pounds.
  • Occasional evening conference calls and limited local or international travel may be required.

The anticipated salary range for this position $55,000 - $88,000
The job description does not intend to list all the duties and responsibilities assigned to this position. An employee holding this position would be required to perform other job-related duties/responsibilities based on their expertise and the company's business needs.

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