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Night Shift Rentschler Biopharma Jobs (NOW HIRING)

Naderi Engineering, Inc.

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Manufacturing Associate

Portsmouth, NH · On-site

$22 - $25.89/hr

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 ...

FUJIFILM Biotechnologies

Position OverviewThis is a night shift position supporting our 2/2/3 schedule from 6pm-6am.The ... By end of 2025, we'll open North America's largest end-to-end CDMO biopharmaceutical manufacturing ...

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How much do night shift rentschler biopharma jobs pay per hour?

As of Aug 14, 2026, the average hourly pay for night shift rentschler biopharma in the United States is $15.21, according to ZipRecruiter salary data. Most workers in this role earn between $12.26 and $16.35 per hour, depending on experience, location, and employer.

What is the difference between Night Shift Rentschler Biopharma vs Night Shift Bioprocess Technician?

AspectNight Shift Rentschler BiopharmaNight Shift Bioprocess Technician
Required CredentialsBiotech degree or equivalent, GMP trainingBiotech or related degree, GMP experience
Work EnvironmentBiopharmaceutical manufacturing, cleanroomsBioprocessing facilities, sterile environments
Employer & Industry UsageRentschler Biopharma, biopharmaceutical industryVarious biotech companies, biopharma sector

Night Shift Rentschler Biopharma and Night Shift Bioprocess Technician roles share similar credentials and work environments, focusing on sterile manufacturing processes in the biopharmaceutical industry. The main difference lies in the specific employer and company branding, with Rentschler Biopharma being a particular employer known for its specialized bioprocessing facilities. Both roles are essential for maintaining continuous production in biotech manufacturing facilities.

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Night Shift Rentschler Biopharma jobs near you
Infographic showing various Night Shift Rentschler Biopharma 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 $31,645 per year, or $15.2 per hour.

Quality Assurance Supervisor - Night Shift

Lonza

Houston, TX • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 24 days ago

Lonza rating

8.3

Company rating: 8.3 out of 10

Based on 42 frontline employees who took The Breakroom Quiz

25th of 86 rated pharmaceutical

Job description

Quality Assurance Supervisor - Night Shift
Location: This is an on-site position located in Pearland, TX.
Available shift: 5:00 pm to 2:00 am Monday through Friday
The Quality Assurance Supervisor - Night Shift will oversee quality assurance activities during the night shift (5:00 PM - 2:00 AM, Monday - Friday) at Lonza Houston Inc., ensuring compliance with all regulatory requirements and internal quality standards for the manufacturing of biopharmaceutical products. This role involves direct supervision of QA personnel and active participation in quality system management to maintain product integrity and safety.
What you will get:
This is a competitive, salary position. In addition, below you will find a comprehensive summary of the benefits package we offer:
• Performance-related bonus.
• Shift differential (15%).
• Medical, dental and vision insurance.
• 401(k) matching plan.
• Life insurance, as well as short-term and long-term disability insurance.
• Employee assistance programs.
• Paid time off (PTO).
Compensation for this role will be determined by the candidate's qualifications, skills, experience, and relevant knowledge.
What you will do:
• Supervise and lead a team of QA personnel, including coaching, mentoring, and conducting performance evaluations.
• Provide QA on-the-floor (QAOTF) support for manufacturing operations and ensure compliance with cGMP requirements.
• Review and approve GMP documentation including batch records, deviations, change controls, CAPAs, and SOPs.
• Support and lead investigations, including deviations, OOS events, and corrective actions.
• Act as QA representative during internal and external audits and regulatory inspections.
• Collaborate cross-functionally with Manufacturing, MSAT, Facilities, and Quality Systems teams.
• Perform QA walkthroughs and provide real-time oversight of production activities to identify and resolve quality issues.
• Ensure training compliance and development of QA staff in alignment with site and regulatory requirements.
• Support gowning requirements (Level 3 / Grade B) and cleanroom activities as needed.
What we are looking for:
• Experience from 5 to 10 years in Quality Assurance within GMP-regulated environments.
• Minimum of Bachelor's degree required in a scientific discipline (life sciences or engineering preferred).
• Previous leadership or supervisory experience, including managing teams and performance evaluations.
• Strong understanding of cGMP principles, regulatory requirements, and quality systems.
• Experience with deviations, investigations, CAPAs, and change control processes.
• Ability to work in a cleanroom environment and perform gowning requirements.
• Demonstrated ability to manage multiple priorities and lead cross-functional teams.
• Strong communication skills, including technical writing and stakeholder engagement.
• Experience with document control systems preferred.
• Knowledge of biologics, viral vectors, or cell and gene therapy manufacturing preferred.
About Lonza:
At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone's ideas, big or small, have the potential to improve millions of lives, and that's the kind of work we want you to be part of.
Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we offer equal employment opportunities to all qualified applicants regardless of race, religion, color, national origin, sex, sexual orientation, gender identity, age, disability, veteran status, or any other characteristic protected by law. If you're ready to help turn our customers' breakthrough ideas into viable therapies, we look forward to welcoming you on board.
Ready to shape the future of life sciences? Apply now.

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