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Manager Biotech Quality Control Jobs in New York

RailWorks

Quality Control Manager

Manhattan, NY · On-site

$128K - $155K/yr

Manages the activities of the quality control team to ensure that the work product meets the standards as set forth in the contracts and other specification documents. Primary/Essential ...

FullSteam

Quality Control

East Rutherford, NJ · On-site

$17 - $18/hr

Proficiency in Microsoft Office and quality management systems/software. * Ability to understand and apply quality control procedures and standards. * Strong verbal and written communication skills.

Paris Baguette

Quality Control Manager

New Brunswick, NJ · On-site

$65K - $75K/yr

WHAT WE ARE HUNGRY FOR The position of Quality Control Manager is responsible for auditing Paris Baguette's standards for all our food, baked products, and beverages while ensuring all-around quality ...

Englert Inc.

Quality Control Manager

Perth Amboy, NJ

$100K - $115K/yr

We are actively seeking a dedicated and results-driven Quality Control Manager. In this role, you will be responsible for developing, implementing, and leading the overall quality strategy to ensure ...

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Manager Biotech Quality Control information

What does a manager biotech quality control do?

A Manager Biotech Quality Control oversees the quality assurance processes within a biotechnology company, ensuring that products meet regulatory standards and internal specifications. They manage teams responsible for testing raw materials, in-process samples, and finished products, and analyze data to identify trends or issues. This role also involves setting quality control policies, training staff, and liaising with regulatory bodies to maintain compliance. Managers in this field play a crucial role in product safety and efficacy, directly impacting the success of biotech products in the market.

What are the key skills and qualifications needed to thrive as a manager biotech quality control?

To thrive as a Manager Biotech Quality Control, you need a strong background in biology or chemistry, extensive knowledge of quality assurance regulations, and typically a bachelor’s or master’s degree in a life science field. Familiarity with laboratory information management systems (LIMS), GMP (Good Manufacturing Practices), and certifications such as ASQ or Six Sigma are highly valued. Leadership, attention to detail, and strong problem-solving and communication skills help you guide teams and ensure compliance. These skills and qualities are critical for maintaining product quality, regulatory adherence, and the overall success of biotech manufacturing operations.

What are the most common challenges faced by a manager biotech quality control, and how are they typically addressed?

Managers in Biotech Quality Control often face challenges such as ensuring regulatory compliance, maintaining rigorous documentation, and managing a team with diverse expertise. Keeping up-to-date with changing industry standards and regulatory requirements is crucial, as is fostering a culture of continuous improvement and clear communication. These challenges are typically addressed through ongoing staff training, implementing robust quality management systems, and close collaboration with other departments like R&D and manufacturing to ensure that quality standards are consistently met.

What is the difference between Manager Biotech Quality Control vs Quality Control Specialist?

AspectManager Biotech Quality ControlQuality Control Specialist
CredentialsBachelor's/Master's in Life Sciences, Quality Certifications (e.g., CQE)Bachelor's in Life Sciences or related field, Quality Certifications preferred
Work EnvironmentOversees QC teams, manages testing processes, and ensures compliancePerforms testing, data analysis, and reports results
Employer & Industry UsageBiotech companies, pharmaceutical firms, contract labsBiotech, pharma, and manufacturing sectors

The Manager Biotech Quality Control typically oversees testing teams and ensures compliance with quality standards, while the Quality Control Specialist focuses on executing tests and analyzing data. Both roles require relevant scientific credentials, but the manager has additional responsibilities in team leadership and process management.

What are the most commonly searched types of Biotech Quality Control jobs in New York?

The most popular types of Biotech Quality Control jobs in New York are:

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

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

What job categories do people searching Manager Biotech Quality Control jobs in New York look for?

The top searched job categories for Manager Biotech Quality Control jobs in New York are:

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

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

Manager Biotech Quality Control jobs near you
Infographic showing various Manager Biotech Quality Control job openings in New York as of August 2026, with employment types broken down into 67% Full Time, and 33% Contract. Highlights an 100% In-person job distribution.

HTP Analytical QC Associate Scientist

GenScript Biotech

Piscataway, NJ • On-site

$60K - $75K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 11 days ago

Job description

HTP Analytical QC Associate Scientist

Piscataway, New Jersey, United States

About GenScript

Founded in 2002 in New Jersey, GenScript Biotech Corporation accelerates innovation in biotech and healthcare by providing researchers and companies with the building blocks needed to develop groundbreaking treatments and products. Guided by its mission to Make People and Nature Healthier Through Biotechnology, and its role as a well-recognized biotechnology company, GenScript has a team of approximately 6,165 employees and has served more than 200,000 customers across over 100 countries and regions.

Genscript is seeking a motivated and detail-oriented HTP Analytical QC Associate Scientist to join our dynamic US Protein Department in Piscataway, New Jersey.

The estimated salary range is $60,000 - $75,000, depending on experience.

Reporting to: Supervisor of HTP Platform Employment Type: Full-time

Role Description:

We are seeking a detail-oriented and proactive Associate Scientist to join our High-Throughput Protein Analytical QC Laboratory. This role is responsible for performing analytical characterization and quality control testing of recombinant proteins generated from high-throughput production workflows.

The successful candidate will play a critical role in ensuring protein identity, purity, and overall quality through robust analytical methodologies. This position operates in a data-driven and quality-focused environment where accuracy, reproducibility, and data integrity are essential. The ideal candidate will have hands-on experience with protein analytical techniques and familiarity with laboratory data management systems such as ELN, LIMS, or equivalent platforms.

Key Responsibilities:

  • Perform routine and non-routine analytical and QC testing to evaluate protein identity, purity, and quality attributes.
  • Execute a range of protein characterization assays, including:
  • HPLC / UPLC (e.g., SEC, RP, IEX)
  • Capillary Electrophoresis (CE, iCE/cIEF)
  • SDS-PAGE
  • Western blot
  • LC-MS
  • Endotoxin assays
  • Prepare samples, reagents, buffers, and standards in accordance with established protocols and assay requirements.
  • Perform sample preparation workflows, including use of automated liquid handling systems where applicable.
  • Analyze, interpret, and document experimental data in ELN, LIMS, or equivalent systems, ensuring compliance with data integrity standards (e.g., ALCOA+ principles).
  • Support method troubleshooting and optimization, ensuring assay robustness, reproducibility, and consistency across runs.
  • Maintain laboratory instruments and ensure proper calibration and performance, supporting compliance with quality and safety standards.
  • Collaborate with cross-functional teams (e.g., protein production, process development) to support project timelines and deliverables.
  • Contribute to continuous improvement initiatives, including method refinement, workflow efficiency, and data quality enhancement.

    • Qualifications:

    • BS or MS in Biochemistry, Analytical Chemistry, Biotechnology, or a related field with 2+ years of relevant experience in protein analytical characterization or QC.
    • Hands-on experience with protein analytical techniques such as HPLC/UPLC, CE, SDS-PAGE, Western blot, LC-MS, or endotoxin assays.
    • Familiarity with protein characterization workflows, including purity, aggregation, and identity analysis.
    • Experience with laboratory data systems (ELN, LIMS, or similar) and strong documentation practices.
    • Strong attention to detail and commitment to data integrity, accuracy, and reproducibility.
    • Experience in a CRO/CDMO or regulated QC environment is preferred.

    Benefits include medical, dental, and vision insurance as well as a 401(k) retirement plan with a company match that vests fully on day one. We offer paid parental leave after just three (3) months of employment, and a paid time off policy that includes vacation time, personal time, sick time, floating holidays, and company holidays. Additional benefits include flexible spending and health savings accounts, life and AD&D insurance, short- and long-term disability coverage, legal assistance, and supplemental plans such as pet, critical illness, accident, and hospital indemnity insurance. We also provide commuter benefits, well-being initiatives, and peer-to-peer recognition programs; demonstrating our ongoing commitment to building a culture where our people feel empowered, supported, and inspired to do their best work.

    GenScript USA Inc/ProBio Inc. is a proud equal opportunity/affirmative action employer committed to attracting, retaining, and maximizing the performance of a diverse and inclusive workforce. It is the Company's policy to ensure equal employment opportunity without discrimination or harassment based on race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity or expression, age, disability, national origin, marital or domestic/civil partnership status, genetic information, citizenship status, uniformed service member or veteran status, or any other characteristic protected by law.

    GenScript USA Inc./ProBio Inc. maintains a drug-free workplace.

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