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Night Shift Biopharmaceutical Engineering Jobs (NOW HIRING)

Bechtel

Night Shift Manager

NV · On-site

$144K - $220K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

... engineering and building the facility. We are also managing procurement of about $1 Billion in ... In this role, you will manage the Night Shift operations and direction of project construction ...

Actalent

Fractionation Lab Technician (Night Shift)

Boca Raton, FL · On-site

$18 - $24/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Perform production operations related to fractionation and biopharmaceutical manufacturing in a ... About Actalent Actalent is a global leader in engineering and sciences services and talent ...

Lonza

Quality Assurance Supervisor - Night Shift

Houston, TX · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... biopharmaceutical products. This role involves direct supervision of QA personnel and active ... Minimum of Bachelor's degree required in a scientific discipline (life sciences or engineering ...

Lonza

Quality Assurance Supervisor - Night Shift

Pearland, TX · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... biopharmaceutical products. This role involves direct supervision of QA personnel and active ... Minimum of Bachelor's degree required in a scientific discipline (life sciences or engineering ...

New

Lonza

Quality Assurance Supervisor - Night Shift

Houston, TX · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... biopharmaceutical products. This role involves direct supervision of QA personnel and active ... life sciences or engineering preferred). • Previous leadership or supervisory experience ...

Naderi Engineering, Inc.

Be Seen First

Manufacturing Associate

Portsmouth, NH · On-site

$22 - $25.89/hr

  • Medical

  • Dental

  • Vision

B Night Shift - 12-Hour Rotating Schedule Hours: 6:30 PM - 6:30 AM (18:30-06:30) Schedule ... biopharmaceutical manufacturing environment. This position will support key upstream activities ...

CCS INC

Construction Manager - Night Shift

Manhattan, NY · On-site

$100 - $110/hr

  • Medical

  • Dental

  • Vision

Regular Night Shift hours shall be 8 hrs/day from 5pm to 3 am, 5 days/week. During the scheduled ... Knowledge and experience in performing inspection and resident engineering activities in active ...

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Night Shift Biopharmaceutical Engineering information

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How much do night shift biopharmaceutical engineering jobs pay per hour?

As of Aug 14, 2026, the average hourly pay for night shift biopharmaceutical engineering in the United States is $33.06, according to ZipRecruiter salary data. Most workers in this role earn between $26.44 and $38.22 per hour, depending on experience, location, and employer.
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Night Shift Biopharmaceutical Engineering jobs near you
Infographic showing various Night Shift Biopharmaceutical Engineering job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 72% Full Time, 21% Part Time, 4% Contract, and 2% Nights. Highlights an 99% Physical, and 1% Remote job distribution, with an average salary of $68,760 per year, or $33.1 per hour.

Manufacturing Associate II (Night Shift)

KBI Biopharma, Inc.

Durham, NC

$24 - $31.25/hr

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 17 days ago

KBI Biopharma rating

6.5

Company rating: 6.5 out of 10

Based on 6 frontline employees who took The Breakroom Quiz

Job description

Position Summary

This position operates on a night shift 2-2-3 schedule. The Manufacturing Associate I/II (Manufacturing Associate) is responsible for performing upstream or downstream processing of bulk intermediates and/or bulk drug substances for biopharmaceutical products. The Manufacturing Associate must follow written, approved procedures and forms to ensure all work is conducted "Right First Time" (RFT) following Good Manufacturing Practice (GMP), including good documentation practices, and/or Good Laboratory Practice (GLP). As needed, the Manufacturing Associate will work individually or on teams to author standard operating procedures (SOPs) or Master Batch Records (MBRs); write corrective and preventive actions (CAPAs); and specify, commission, and qualify new equipment.

The Manufacturing Associate will be responsible for upstream unit operations (seed expansion, bioreactor operations, cell culture harvest). The Manufacturing Associate will have a working knowledge of upstream processing equipment (incubators, biosafety cabinets, bioreactors, cell counters, blood gas analyzers, metabolite testing equipment). Additionally, the manufacturing associate will have knowledge of general bioprocessing equipment such as filters, filter integrity testers, balances, pumps, pH/conductivity meters, and disposable technologies (disposable bags, sterile tubing welders, tubing sealers). Following task execution, the Manufacturing Associate will review the executed production records and logbooks to ensure GxP compliance.

The Manufacturing Associate will execute daily tasks and maintain strict accordance with manufacturing records, SOPs, and GMP. Staff will maintain a sense of ownership of the production processes, the manufacturing environment, and the facility. Staff will work cross-functionally with QA, MS&T, facilities, engineering, supply chain, IT, AFS, and other key departments to ensure startup and ongoing manufacturing operations are successful, reliable, and compliant. A proven Manufacturing Associate will demonstrate the following qualities: learning agility, orientation toward action, results driven, team player, strong attention to detail, and superior integrity and accountability.

Position Responsibilities

  • Manufacture bulk intermediates and drug substances per manufacturing batch records in compliance with quality, company policies, and current regulations
  • Perform operations in a cleanroom environment, applying controls to ensure aseptic processing, including gowning and cleaning procedures
  • Document each task involving manufacturing records and logbooks following GDP at the time of execution
  • Utilize and perform maintenance on equipment per applicable SOP
  • Ensure all materials are issued and accounted for during the execution of a record
  • Demonstrate, apply, and ensure understanding of cGMP and how it applies to specific tasks and responsibilities
  • Participate and be accountable for workplace organization

Position Requirements

  • Manufacturing Associate II- Bachelor's degree in a related scientific or engineering discipline and 2-5 years' experience in related cGMP manufacturing operations; or high school diploma and 4-6 years' experience, or equivalent
  • Basic knowledge of upstream processing- cell culture or fermentation
  • Experience in single-use platform technology is preferred

*Please note: this is a night shift opportunity and will be eligible for a shift differential on top of listed salary*

Salary Range: $24-$31.25/hour

Salary range provided per current averages and expectations. The salary and job title for this opening will be based on the selected candidate's qualifications and experience and may be outside this range. KBI has a robust total rewards strategy which includes an annual bonus structure for all employees, medical, dental, and vision coverage, paid PTO and holidays, Sabbatical program, 401K matching with 100% vesting in 60 days and employee recognition programs.

KBI Biopharma is committed to providing a safe and healthy workplace. Any employee entering a KBI site located in the US must inform KBI Biopharma of their vaccination status and must submit their vaccination status. All vaccinated employees are required to provide proof of their COVID-19 vaccination, with a COVID-19 vaccination which has been granted FDA approval or Emergency Use Authorization.

KBI Biopharma, Inc. is an EEO/AA employer and actively seeks to diversify its work force. Therefore, all qualified applicants, regardless of race, color, national origin, religion, gender, gender identity, sexual orientation, age, disability or veteran status, are strongly encouraged to apply.

I understand that neither the completion of this application nor any other part of my consideration for employment establishes any obligation for KBI Biopharma, Inc. to hire me. If I am hired, I understand that either KBI Biopharma, Inc. or I can terminate my employment at any time and for any reason, with or without cause and without prior notice. I understand that no representative of KBI Biopharma, Inc. has the authority to make any assurance to the contrary.

I attest with my signature below that I have given to KBI Biopharma, Inc. true and complete information on this application. No requested information has been concealed. I authorize KBI Biopharma, Inc. to contact references provided for employment reference checks. If any information I have provided is untrue, or if I have concealed material information, I understand that this will constitute cause for the denial of employment or immediate dismissal.

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