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Biotech Quality Control Jobs in New York (NOW HIRING)

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 ...

Valid8 Financial, Inc.

QC Microbiologist

Branchburg, NJ · On-site

$90 - $120/hr

The QC Microbiologist will play a critical role in supporting the environmental and microbiological ... Minimum of 5 years of microbiology laboratory experience in a cGMP pharmaceutical or biotechnology ...

New

Novartis

Quality Facilitator

Morris Plains, NJ · On-site

Change Control Management: Assist in overseeing change control processes, ensuring all ... Pharmaceutical/Biotechnology or Manufacturing Industry: Experience working in industries where ...

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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 Sep 3, 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 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, with an average salary of $88,971 per year, or $42.8 per hour.

Quality Control Analytical Scientist

Lynkx Staffing LLC

Saddle Brook, NJ • On-site

Full-time

Re-posted yesterday

Job description

Quality Control Analytical ScientistAllendale, NJ Lynkx Staffing LLC specializes in placing talented professionals in the Biotechnology, Pharmaceutical and Medical Devices industries in New Jersey. The QC Analytical Scientist will be a member of the Quality Control Department. As a Senior Member of the team the QC Analytical Scientist will be involved in various QC projects and should have a deep understanding of general QC flow and the Product Cycle.
  • Support internal and external customers to ensure that proper and timely execution of all aspects of the clinical analytical method life cycle across clients.
  • Support routine GMP testing as assigned. Mentor and train team members
  • Evaluate corporate and regulatory requirements along with coordination of activities for implementation of these requirements.
  • Write the contents of Analytical Method Transfer and Validation life cycle documentation including master plans, protocols, test methods, and reports.
  • Create validation project plan i.e., timelines and resources and provides status updates to management. Utilize statistical tools for evaluation of method validation and trending data.
  • Identify, evaluate, and implement continuous business process improvements.
  • Perform troubleshooting activities with respect to methods/assays, equipment malfunctions and investigations (Deviations and OOS).
  • Provide support during laboratory investigations.
  • Train QC personnel during method transfer and validation. Provide support during equipment qualification.
  • Consistently produce elevated level of documentation accuracy and clarity according to cGMP documentation practices.
  • Ability to set deadlines and prioritize work for self, group members, and support groups involved. Ability to review/approve work performed by coworkers for accuracy and alignment with procedures.
  • Indirectly may supervise cross functional teams including product development, QA, PMP, and Manufacturing.
REQUIREMENT
  • B.S Analytical Chemistry or other scientific field or MS/Ph.D. in Analytical Chemistry or other scientific field with demonstrated experience in Quality Control laboratories for biotechnology products.
  • 8-10 years of experience in the areas of method development, validation, and transfer.
  • Direct GMP Experience.
  • Proficiency in project management skills and tools.
  • Strong background and in-depth knowledge in analytical chemistry e.g. Flow Cytometry, ELISA, HPLC, CE, PCR, etc.
  • Extensive knowledge and experience of QC assay development, transfer and validation, along with cGMPs.
  • Strong Quality orientation with attention to detail required. Analytical and problem-solving skills required.
  • Excellent communication skills, both written and verbal, with all levels of the organization, including the ability to state opinions clearly, ask questions, seek clarification, communicate facts objectively, challenge when appropriate, and pursue issues to resolution.
  • Excellent presentation skills. Ability to communicate to upper management, across departments and within the immediate QC team.
  • Ability to create and manage work plans and timelines and independently manage competing priorities with limited instruction.
  • Highly motivated individual with good interpersonal skills that have proven effective in managing relationships and negotiating solutions while maintaining a level of approachability with colleagues both internal and external.
  • Must be familiar with GMP lab environment and Aseptic techniques.
Working EnvironmentMust have the ability to work in a team-oriented environment and with clientsMust be able to work during the weekend, holidays, or overtime and as required by the companyMay be exposed to infectious diseases transmittable through human blood, tissues, or bodily fluidsMust utilize proper personal protective equipment (PPE) when handling all human specimens, gases, corrosive chemicals, and liquid nitrogenMust have the ability to work with specialized equipmentMust be able to handle the standard/moderate noise of the manufacturing facilityMay work with hazardous materials and chemicals Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties, or responsibilities that are required of the employee for this job. Duties, responsibilities, and activities may change at any time with or without notice.