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Temporary Biopharmaceutical Engineering Jobs (NOW HIRING)

TekWissen LLC

Controls Engineer

Portsmouth, NH · On-site

$85K - $110K/yr

Our client specializes in pharmaceutical ingredients, Bioscience, Biopharmaceuticals, Custom ... Temporary Assignment Work Type: Onsite Summary This is an Automation Engineer / Controls Engineer ...

Extra Resource Staffing

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Construction Project Manager- CSA

West Lafayette, IN · On-site

$130K - $150K/yr

... BioPharma/Pharmaceutical, Mission Critical/Data Centers, or other clean/high-tech construction ... Support temporary facilities, including installation, operation, modification, and eventual ...

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TekWissen LLC

Electrical Engineer

Vacaville, CA · On-site

$35 - $40/hr

Our client specializes in pharmaceutical ingredients, Bioscience, Biopharmaceuticals, Custom ... Temporary Assignment Work Type: Onsite Summary: The Electrical Engineer (Level 2) is responsible ...

TekWissen LLC

Senior Validation Engineer

Portsmouth, NH · On-site

$35 - $45/hr

Our client specializes in pharmaceutical ingredients, Bioscience, Biopharmaceuticals, Custom ... Temporary Assignment Work Type: Hybrid Summary The CSV Engineer will act as an individual ...

TekWissen LLC

MES Engineer

Portsmouth, NH · On-site

$35 - $45/hr

Our client specializes in pharmaceutical ingredients, Bioscience, Biopharmaceuticals, Custom ... Temporary Assignment Work Type: Onsite Summary MES Engineer is responsible for supporting ...

TekWissen LLC

Associate Mechanical Engineer

Vacaville, CA · On-site

$30 - $36/hr

Temporary Assignment Work Type: Onsite Summary The Process Mechanic is responsible for maximizing ... Collaborate with Manufacturing, Engineering, Quality, Technology, and other departments to ensure ...

TekWissen LLC

Automation Systems Engineer

Vacaville, CA · On-site

$30 - $40/hr

Temporary Assignment Work Type: Onsite Summary: We are seeking an Automation Systems Support ... Collaborate with manufacturing, engineering, process science, validation, and quality assurance ...

TekWissen LLC

Quality Assurance Engineer

Tampa, FL · On-site

$25 - $35/hr

Specializing in pharmaceutical ingredients, bioscience, biopharmaceuticals, custom manufacturing ... Temporary Position Work Type: Onsite Summary The QA Engineer is responsible for ensuring the timely ...

TekWissen LLC

QC Validation Specialist

Vacaville, CA · On-site

Job Title: Validation Engineer II / QC Validation Specialist Location: Vacaville, CA, 95688 ... Temporary Assignment Work Type: Onsite Shift: Monday to Friday from 08:00 AM to 04:00 PM Summary

Bilfinger Berger SE

Construction Manager

Green Bay, WI · On-site

$60 - $80/hr

Bilfinger's comprehensive portfolio spans the entire value chain, from consulting & engineering to ... biopharma. With about 31,000 employees, Bilfinger upholds the highest standards of safety and ...

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Temporary Biopharmaceutical Engineering information

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How much do temporary biopharmaceutical engineering jobs pay per year?

As of Sep 5, 2026, the average yearly pay for temporary biopharmaceutical engineering in the United States is $92,956.00, according to ZipRecruiter salary data. Most workers in this role earn between $65,500.00 and $114,000.00 per year, depending on experience, location, and employer.

What is the difference between Temporary Biopharmaceutical Engineering vs Temporary Biopharmaceutical Manufacturing Technician?

AspectTemporary Biopharmaceutical EngineeringTemporary Biopharmaceutical Manufacturing Technician
Required CredentialsBachelor's in Engineering or Life Sciences, relevant certificationsHigh school diploma or associate degree, technical certifications
Work EnvironmentDesign labs, R&D facilities, process development areasManufacturing floors, production lines, quality control labs
Employer & Industry UsageBiotech companies, pharmaceutical firms, contract research organizationsManufacturing plants, biotech production facilities, contract manufacturing organizations

Temporary Biopharmaceutical Engineering roles focus on designing, developing, and optimizing biopharmaceutical processes, often involving R&D and technical analysis. In contrast, Temporary Biopharmaceutical Manufacturing Technicians work directly on production lines, ensuring manufacturing processes run smoothly. Both roles are essential in the biopharmaceutical industry but differ in responsibilities, work environment, and required credentials.

Are temporary biopharmaceutical engineers in demand?

Temporary biopharmaceutical engineers are in demand due to ongoing growth in the biotech and pharmaceutical industries, especially for roles involving process development, manufacturing, and quality assurance. Employers seek candidates with skills in bioprocessing, regulatory compliance, and familiarity with industry tools, making these positions relatively accessible for qualified professionals.

What is a temporary biopharmaceutical engineer?

A temporary biopharmaceutical engineer is a professional hired on a short-term basis to support the development, manufacturing, or quality assurance of biopharmaceutical products. They typically work in laboratory or production environments, utilizing skills in biotechnology, process engineering, and regulatory compliance, often under contract or project-based arrangements.

What jobs can you get with a temporary biopharmaceutical engineering degree?

A temporary biopharmaceutical engineering degree can qualify you for roles such as process engineer, manufacturing technician, quality control analyst, or research associate in biopharmaceutical companies. These positions often require knowledge of GMP regulations, laboratory skills, and familiarity with bioprocessing tools and equipment.
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Temporary Biopharmaceutical Engineering jobs near you
Infographic showing various Temporary Biopharmaceutical Engineering job openings in the United States as of August 2026, with employment types broken down into 92% Full Time, 4% Part Time, 3% Contract, and 1% Nights. Highlights an 86% Physical, 4% Hybrid, and 10% Remote job distribution, with an average salary of $92,956 per year, or $44.7 per hour.

(CW) Manufacturing Associate (Temporary/Contract) Night Shift

BioMarin Pharmaceutical Inc.

Novato, CA

Temporary, Other

Posted 8 days ago

BioMarin Pharmaceutical rating

7.8

Company rating: 7.8 out of 10

Based on 8 frontline employees who took The Breakroom Quiz

50th of 86 rated pharmaceutical

Job description

Who We Are
BioMarin is a leading rare disease biotechnology company focused on genetically defined conditions.
Guided by our purpose to develop medicines that make a profound impact on people’s lives, our global teams have delivered a portfolio of therapies since our founding in 1997. Our revolutionary treatments for conditions like achondroplasia (the most common form of dwarfism), PKU (phenylketonuria), CLN2, a form of Batten disease, and a number of forms of MPS (mucopolysaccharidosis) offer new possibilities for patients and families who previously had few, if any, available options. More recently, with the close of the Amicus acquisition, our portfolio has expanded to include therapies for Fabry disease and Pompe disease, expanding our ability to reach more people living with rare genetic conditions.
Our success comes from our unwavering commitment to excellence, our deep understanding of patient needs, our scientific expertise, and our world-class manufacturing capabilities. At the heart of BioMarin is a dedicated team of the brightest minds in the industry working together to deliver innovative therapies to patients and families around the world.
About Technical Operations
BioMarin’s Technical Operations group is responsible for creating our drugs for use in clinical trials and for scaling production of those drugs for the commercial market. These engineers, technicians, scientists and support staff build and maintain BioMarin’s cutting-edge manufacturing processes and sites, provide quality assurance and quality control to ensure we meet regulatory standards, and procure the needed goods and services to support manufacturing and coordinating the worldwide movement of our drugs to patients.

Onsite Night Shift Temporary

Duties
PROCESS KNOWLEDGE: Understanding of process theory and equipment operation. Ability to learn biopharmaceutical manufacturing processes including mammalian cell culture, depth filtration, tangential flow filtration, column chromatography, centrifugation, protein purification, and formulation of bulk drug substance. Support initiatives for process optimization. Identify and elevate processing issues and support solutions. Gain experience with automation systems (LIMS, MES, PI, etc.).
TECHNICAL DOCUMENTATION: Provide feedback and/or suggested changes to operational procedures. Assist in the incorporation of new technologies, practices, and standards into procedures. Capable of writing and reviewing process documents.
QUALITY AND COMPLIANCE: Understanding of cGMPs as related to Commercial Operations. Ability to utilize Quality systems (Deviations, CAPAs, Change Requests, Action/Alert Reports, etc.).
BUSINESS: Ability to participate on projects and contribute to outcomes. Capability to learn and support new business systems (Track wise, ERP, etc.). Support trending of defined department metrics.
WORK ENVIRONMENT/PHYSICAL DEMANDS
• Consists of strenuous, repetitive work. The following list of physical movements may be used on a daily basis: bending, reaching, climbing stairs and ladders, kneeling and making numerous equipment connections using hands.
• Independently have the ability to regularly lift, dispense, push and/or pull items with an average weight of 25 pounds.
• May require work around loud equipment. • The use of personal protective equipment will be required.
• Requires various shift based work and off hours.
Skills
• Strong communication skills—verbal and written
• Ability to work in a team environment which includes good conflict resolution and collaboration
• Displays good initiative to identify areas for improvement and implement solutions
Education
-Bachelor’s degree in science related area or engineering
-Associate’s degree in science related area or Biotech certificate with 2+ years of experience in a biotech manufacturing environment or other regulated industryReason for Request:


Note: This description is not intended to be all-inclusive, or a limitation of the duties of the position. It is intended to describe the general nature of the job that may include other duties as assumed or assigned.
Equal Opportunity Employer/Veterans/Disabled
An Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability.
Ireland Safety Responsibility Support the organisation’s commitment to environmental protection, injury prevention, and continual improvement of EHS management systems. Actively contribute to a safe and environmentally responsible workplace by identifying hazards, reporting incidents and participating in EHS initiatives and training.
Ireland Safety Responsibility
Support the organisation’s commitment to environmental protection, injury prevention, and continual improvement of EHS management systems. Actively contribute to a safe and environmentally responsible workplace by identifying hazards, reporting incidents and participating in EHS initiatives and training.

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