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Biotech Quality Control Jobs in Rochester, NY (NOW HIRING)

Arxada

Lab Technician

Rochester, NY

$53/hr

... and biotechnology that enhance sustainability. We offer a broad portfolio of ingredients and ... Support quality control processes by identifying deviations and collaborating on root cause ...

New

Arxada

Controls Technician

Rochester, NY · On-site

$31 - $40/hr

... and biotechnology that enhance sustainability. We offer a broad portfolio of ingredients and ... optimizing control systems that drive safe and high-quality production. This is an exciting ...

Arxada

Controls Technician

Rochester, NY

$31 - $40/hr

... and biotechnology that enhance sustainability. We offer a broad portfolio of ingredients and ... optimizing control systems that drive safe and high-quality production. This is an exciting ...

Iff

Reliability Engineer

Rochester, NY · On-site

$101K - $127K/yr

Serve as owner of the site's Mechanical Integrity and Quality Assurance (MIQA) Program, ensuring ... Experience supporting reliability programs within food, ingredients, chemical, biotechnology, or ...

New

Arxada

Chemical Operator

Rochester, NY · On-site

$26 - $27/hr

... and biotechnology that enhance sustainability. We offer a broad portfolio of ingredients and ... Take process and product samples and perform basic quality checks (e.g., pH, concentration) to ...

Arxada

Chemical Operator

Rochester, NY

$26 - $27/hr

... and biotechnology that enhance sustainability. We offer a broad portfolio of ingredients and ... Take process and product samples and perform basic quality checks (e.g., pH, concentration) to ...

All JobsBiotech Quality Control JobsBiotech Quality Control Jobs in Rochester, NY

Biotech Quality Control information

See Rochester, NY salary details

$30.1K

$80.2K

$127.8K

How much do biotech quality control jobs pay per year?

As of Jul 10, 2026, the average yearly pay for biotech quality control in Rochester, NY is $80,239.00, according to ZipRecruiter salary data. Most workers in this role earn between $59,700.00 and $98,700.00 per year, depending on experience, location, and employer.

Does QA or QC pay more?

In biotech quality control, Quality Assurance (QA) roles typically pay slightly more than Quality Control (QC) positions due to their broader responsibilities in process oversight and compliance. Both roles require attention to detail and knowledge of industry regulations, but QA positions often involve more strategic planning and documentation, which can influence salary differences.

What are the typical daily responsibilities of someone working in Biotech Quality Control?

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.

How to become a biotech quality control specialist?

To become a biotech quality control specialist, candidates typically need a bachelor's degree in biology, chemistry, or a related field. Relevant skills include knowledge of laboratory techniques, quality assurance processes, and familiarity with regulatory standards like GMP. Certifications such as ASQ CQE or training in laboratory management can enhance job prospects.

What is the highest paying job in biotech?

In biotech quality control, senior roles such as Director of Quality Assurance or Vice President of Quality typically have the highest salaries, often exceeding six figures. These positions require extensive experience, leadership skills, and knowledge of regulatory standards like GMP and ISO.

What is a Biotech Quality Control job?

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 are the key skills and qualifications needed to thrive in the Biotech Quality Control position, and why are they important?

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 does quality control do in biotech?

In biotech, quality control (QC) involves testing and inspecting products, raw materials, and processes to ensure they meet safety, efficacy, and quality standards. QC teams use analytical techniques and documentation to identify deviations and maintain compliance with regulatory requirements such as GMP. This role is essential for ensuring product consistency and regulatory approval.
What are popular job titles related to Biotech Quality Control jobs in Rochester, NY? For Biotech Quality Control jobs in Rochester, NY, the most frequently searched job titles are:
What job categories do people searching Biotech Quality Control jobs in Rochester, NY look for? The top searched job categories for Biotech Quality Control jobs in Rochester, NY are:
Biotech Quality Control jobs near you
Infographic showing various Biotech Quality Control job openings in Rochester, NY as of July 2026, with employment types broken down into 1% Locum Tenens, 1% As Needed, 86% Full Time, 7% Part Time, 1% Temporary, and 4% Contract. Highlights an 82% Physical, 2% Hybrid, and 16% Remote job distribution, with an average salary of $80,239 per year, or $38.6 per hour.

Quality Assurance Engineer

Stark Pharma Solutions Inc

Rochester, NY • On-site

Contractor

Posted 9 days ago

Job description

Hi,

My name is Sravani Dasari from Stark Pharma Solutions Inc. We are hiring talent for our client and are currently working on a Quality Assurance Engineer position. Please send me your updated resume if you have relevant experience and are interested in this opportunity. The detailed job description is as follows.

Job Title: Quality Assurance Engineer
Location: New York
Duration: Long Term

Position Overview

We are seeking an experienced Quality Assurance Engineer to support quality assurance activities within a pharmaceutical, biotechnology, or medical device manufacturing environment. This role will focus on ensuring product quality, regulatory compliance, and continuous process improvement by supporting quality systems, inspections, audits, documentation, and CAPA activities. The ideal candidate will have strong knowledge of FDA regulations, GMP, ISO standards, and quality management systems while collaborating with cross-functional teams to maintain the highest quality standards.

Key Responsibilities

• Perform quality inspections, manufacturing audits, and process reviews to ensure compliance with quality standards.

• Review batch records, device history records, and quality documentation for accuracy and regulatory compliance.

• Ensure compliance with FDA regulations, GMP, ISO 13485, and company quality management systems.

• Investigate quality issues, non-conformances, deviations, and customer complaints, and support CAPA activities.

• Participate in internal audits, supplier audits, and regulatory inspections while ensuring audit readiness.

• Collaborate with Manufacturing, Engineering, Regulatory Affairs, Validation, and Quality Control teams to improve product quality and manufacturing processes.

• Develop, review, and maintain quality procedures, SOPs, work instructions, and technical documentation.

• Support risk assessments, root cause analysis, change control, and continuous improvement initiatives.

• Monitor quality metrics and analyze trends to identify opportunities for process improvement and operational excellence.

• Ensure compliance with company quality policies and applicable regulatory requirements throughout the product lifecycle.

Required Qualifications

• Bachelor's Degree in Engineering, Biotechnology, Life Sciences, Chemistry, Biology, or a related scientific discipline.

• 2–5 years of Quality Assurance experience within pharmaceutical, biotechnology, medical device, or other regulated manufacturing environments.

• Strong knowledge of FDA regulations, GMP, ISO 13485, CAPA, Quality Management Systems (QMS), and regulatory compliance requirements.

• Experience performing quality inspections, manufacturing audits, documentation review, and quality investigations.

• Hands-on experience with deviations, non-conformances, root cause analysis, CAPA, and change control processes.

• Familiarity with quality documentation, batch record review, SOP development, and document control systems.

• Experience supporting internal audits, supplier audits, and regulatory inspections.

• Strong analytical, problem-solving, technical documentation, and organizational skills.

• Excellent communication and cross-functional collaboration skills with the ability to work effectively in a regulated environment.

• Experience working within pharmaceutical, biotechnology, or medical device manufacturing facilities is highly preferred.

• Knowledge of statistical quality tools, risk management methodologies, Lean Manufacturing, or Six Sigma is an added advantage.

I am actively connecting with professionals for current and upcoming opportunities. If you are open to exploring new roles or would like to stay informed about relevant positions, please send me your updated resume along with the best number and time to reach you.

Please follow Stark Pharma Solutions on LinkedIn for the latest job updates: https://www.linkedin.com/company/99455976/