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Remote Quality Control Biotech Jobs in New York (NOW HIRING)

... biotechnology, biologics, cell and gene therapy, or related GMP-regulated environments. * Deep expertise in sterility assurance, contamination control, microbiology, aseptic processing, and quality ...

... biotechnology, biologics, cell and gene therapy, or related GMP-regulated environments. * Deep expertise in sterility assurance, contamination control, microbiology, aseptic processing, and quality ...

Hybrid - onsite and remote Responsibilities * Provide quality engineering support in quality assurance, control, and preventative activities within operations and other business functions. * Develop ...

Order Picker/Filler

Jersey City, NJ · Remote

$16.75 - $19.75/hr

... under your remote control. * Collaborate with on-site staff and provide clear instructions for packing and labeling orders. * Conduct quality control checks remotely, ensuring the accuracy and ...

Hybrid - onsite and remote Overview Advance your quality engineering career with a global medical ... Provide quality engineering support in quality assurance, control, and preventative activities ...

Showing results 41-60

Remote Quality Control Biotech information

What is a remote quality control biotech?

A Remote Quality Control Biotech job involves ensuring the quality, safety, and compliance of biotechnological products and processes while working remotely. Responsibilities may include reviewing data, conducting virtual audits, ensuring regulatory compliance, and collaborating with teams to maintain product integrity. Professionals in this role use digital tools to analyze laboratory results, monitor production processes, and document findings. Strong attention to detail, knowledge of industry regulations, and proficiency in data analysis are essential. This position is critical in maintaining high-quality biotech products while allowing flexibility through remote work.

What skills and qualifications are needed for a remote quality control biotech?

To thrive as a Remote Quality Control Biotech, you generally need a solid background in biology or biotechnology, laboratory techniques, and quality assurance processes, often supported by a relevant degree in life sciences or biotechnology. Familiarity with regulatory standards such as GMP or ISO, data analysis software, and laboratory information management systems (LIMS) is typically required. Strong attention to detail, effective communication, and the ability to work independently are important soft skills in remote settings. These competencies ensure accurate quality assessments, regulatory compliance, and effective collaboration with distributed teams.

What are the most common challenges faced by remote quality control professionals in the biotech industry?

One of the main challenges faced by remote quality control biotech professionals is maintaining effective communication and collaboration with on-site laboratory teams and cross-functional departments. Since much of the data review, reporting, and troubleshooting are performed remotely, it can also be challenging to stay updated with real-time lab processes and quickly resolve discrepancies. To address these issues, many companies use digital collaboration tools, regular virtual meetings, and thorough documentation practices. Adapting to these remote workflows ensures that quality standards are consistently met even from a distance.

What are popular job titles related to Remote Quality Control Biotech jobs in New York?

For Remote Quality Control Biotech jobs in New York, the most frequently searched job titles are:

What cities in New York are hiring for Remote Quality Control Biotech jobs?

Cities in New York with the most Remote Quality Control Biotech job openings:

Infographic showing various Remote Quality Control Biotech job openings in New York as of August 2026, with employment types broken down into 1% As Needed, 85% Full Time, 11% Part Time, 2% Contract, and 1% Nights. Highlights an 91% Physical, 1% Hybrid, and 8% Remote job distribution.

Director, Sterility Assurance

Lonza

Morristown, NJ • On-site

Full-time

Posted 7 days ago


Lonza rating

8.3

Company rating: 8.3 out of 10

Based on 42 frontline employees who took The Breakroom Quiz

24th of 86 rated pharmaceutical


Job description

Today, Lonza is a global leader in life sciences, operating across five continents, Lonza works every day to enable a healthier world. Our greatest scientific solution is talented people working together, devising ideas that help businesses improve lives. In exchange, we empower our employees to own their careers and genuinely make a meaningful difference.
We are seeking an experienced Director, Sterility Assurance to provide global leadership for sterility assurance and contamination control across Lonza's sterile manufacturing network. This highly visible role will drive enterprise-wide strategy, governance, and continuous improvement initiatives to ensure world-class biological contamination control and compliance across sterile drug substance and drug product operations.
Key Responsibilities
Global Sterility Assurance Leadership
  • Develop, implement, and continuously improve biological contamination control strategies addressing viral, bacterial, fungal, mycoplasma, endotoxin, and other adventitious agent risks.
  • Drive and oversee the global sterility assurance strategy, including risk assessment, mitigation planning, gap closure, and sustainable implementation across manufacturing sites.
  • Serve as a global subject matter expert and strategic leader for contamination control and aseptic manufacturing practices.

Risk Management and Site Support
  • Lead global sterility assurance risk assessments and support sites in responding to contamination events, sterility failures, microbiological excursions, and adverse trends.
  • Facilitate root cause investigations and implement effective corrective and preventive actions (CAPAs) across the network.
  • Promote cross-site collaboration, knowledge sharing, and implementation of best practices.

Network Standardization and Continuous Improvement
  • Drive harmonization of sterility assurance standards and contamination control programs across global sites.
  • Establish and improve procedures governing facility and equipment design, process design, material transfer, environmental monitoring, microbiological testing, maintenance, cleaning, disinfection, and segregation controls.
  • Champion continuous improvement initiatives that strengthen contamination control, consistency, and inspection readiness.

New Product Introduction and Technical Expertise
  • Act as the global sterility assurance expert for product development, technology transfer, and new product introductions.
  • Ensure phase-appropriate sterility assurance practices are embedded throughout development and commercial manufacturing programs.
  • Support network expansion projects and new facility start-ups as required.

Capability Building and Regulatory Support
  • Coach and train employees to strengthen understanding of biological risks, contamination control, and aseptic behaviors.
  • Support regulatory inspections, customer audits, GQC audits, mock pre-approval inspections, due diligence activities, and other compliance initiatives as a sterility assurance SME.
  • Monitor evolving industry and regulatory expectations and ensure timely implementation across the network.

What You'll Bring
Education
  • Bachelor's, Master's, or higher degree in Microbiology, Pharmaceutical Sciences, Life Sciences, Biotechnology, Engineering, or a related scientific discipline.
  • Advanced scientific qualifications or certifications are advantageous.

Experience
  • Significant leadership experience within sterile pharmaceutical, biotechnology, biologics, cell and gene therapy, or related GMP-regulated environments.
  • Deep expertise in sterility assurance, contamination control, microbiology, aseptic processing, and quality risk management.
  • Demonstrated experience supporting complex investigations, contamination events, and regulatory inspections.
  • Proven success influencing and leading within global, matrixed organizations.

Skills
  • Expert knowledge of sterile manufacturing regulations and industry standards.
  • Strong understanding of contamination control strategies and microbiological risk assessment.
  • Excellent communication, coaching, and stakeholder management skills.
  • Ability to drive global alignment while balancing site-specific operational needs.
  • Continuous improvement mindset with a passion for scientific excellence and operational effectiveness.

Every Day, Lonza's Products and Services Have a Positive Impact
At Lonza, you will join a purpose-driven organization where your expertise contributes directly to the development and manufacture of therapies that improve and save lives worldwide. We foster a culture of innovation, collaboration, and continuous learning, providing opportunities to make a meaningful impact on a global scale.
Every day, Lonza's products and services have a positive impact on millions of people. For us, this is not only a privilege, but a responsibility we take seriously.
Apply today and help shape the future of sterility assurance across Lonza's global manufacturing network.

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About Lonza

Sourced by ZipRecruiter

Industry

Biotechnology research and development and pharmaceutical and medicine manufacturing

Company size

10,000+ Employees

Headquarters location

Bern, KS, US