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Biotech Quality Control Jobs in New York (NOW HIRING)

ClifyX

QC and LIMS

Springfield, NJ · On-site

Minimum 3 years of experience in an IT support role within a pharmaceutical, biotechnology, or regulated laboratory environment. * Proven experience with GMP regulations, QC software (e.g., LIMS, CDS ...

Tris Pharma

QC Analytical Chemist

Monmouth Junction, NJ · On-site

$90K/yr

... pharmaceutical, biotechnology or academic settingAnticipated salary range: $60-65k/yr. QC ... Analytical Chemist I -Bachelor's Degree in Chemistry or related science field and minimum 1-5 years ...

PSG Global Solutions

Quality Control Analyst

Summit, NJ

$25.50 - $34.25/hr

... biotechnology and medical companies. As specialists in recognising talent we pride ourselves on not just finding the best people for our client partners but on our ability to spot the best and ...

Novartis

Site QC Head (Associate Director)

Millburn, NJ · On-site

$226K/yr

BSc in Chemistry, Biology, Pharmacy, Biotechnology, Biomedical Engineering, or related experience. Advanced Degree is preferred. * 10+ years' experience in Quality Control, Quality Assurance, Quality ...

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Biotech Quality Control information

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$33.4K

$89K

$141.7K

How much do biotech quality control jobs pay per year?

As of Aug 23, 2026, the average yearly pay for biotech quality control in New York is $88,971.00, according to ZipRecruiter salary data. Most workers in this role earn between $66,200.00 and $109,400.00 per year, depending on experience, location, and employer.

What is a biotech quality control?

A Biotech Quality Control (QC) job involves ensuring that biological products, processes, and facilities meet regulatory and quality standards. QC professionals conduct testing, analyze data, and document results to verify product safety and efficacy. They work with laboratory techniques such as PCR, HPLC, and microbiological testing. The role is critical in maintaining compliance with industry regulations like GMP and FDA guidelines.

What does a biotech quality control do?

On a daily basis, a Biotech Quality Control professional performs routine testing and analysis of raw materials, intermediates, and finished products to ensure they meet established specifications. This involves preparing samples, operating analytical equipment, maintaining accurate records, and documenting results in compliance with regulatory guidelines. Quality Control staff also collaborate closely with production, quality assurance, and research teams to troubleshoot issues and support process improvements. Regular internal audits and participation in team meetings are common, making communication and teamwork key parts of the job.

What are the key skills and qualifications needed to thrive in biotech quality control?

To excel in Biotech Quality Control, candidates typically need a background in biology, chemistry, or related sciences, with strong knowledge of laboratory techniques and regulatory requirements. Familiarity with laboratory information management systems (LIMS), Good Manufacturing Practices (GMP), and common analytical instruments such as HPLC or PCR is highly valued. Attention to detail, problem-solving abilities, and effective communication are crucial soft skills for this role. These competencies are vital for ensuring that biotech products consistently meet quality and compliance standards essential for patient safety and regulatory approval.

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 Biotech Quality Control jobs in New York?

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

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

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

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

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

Biotech Quality Control jobs near you
Infographic showing various Biotech Quality Control job openings in New York as of August 2026, with employment types broken down into 87% Full Time, and 13% Part Time. Highlights an 100% In-person job distribution, with an average salary of $88,971 per year, or $42.8 per hour.

HTP Analytical QC Associate Scientist

GenScript Biotech

Piscataway, NJ

$60K - $75K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 3 days ago

New

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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