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Manager Qc Biotech Jobs in Rochester, NY (NOW HIRING)

Unifin SAS

QC Chemist Associate

Rochester, NY

Maintains and proposes improvementsto lab quality systems. ESSENTIAL FUNCTIONS / RESPONSIBILITIES ... Distinguishes between training and non-training needs and workswith Supervisor/Manager to recommend ...

Unifin SAS

QC Sampling & Inspection Technician

Rochester, NY · On-site

$18.50 - $23.75/hr

Your role Reporting to the Microbiology Manager , JOB SUMMARY: The QC Sampling & Inspection Technicianperforms sampling and inspection of incoming drug substances, raw materials,and packaging ...

Kodak

Quality Manager

Rochester, NY

This is a Quality Manager position in the printed electronics organization, reporting to the VP, ... Maintain product quality control strategies & develop new strategies as needed, including IQC, in ...

Kodak

Quality Manager

Rochester, NY · On-site

Measurement System Analysis (MSA), Statistical Process Control (SPC), Advanced Product Quality ... quality management within the automotive supply chain. • Ability to translate customer ...

Kodak

Quality Manager

Rochester, NY · On-site

$90K - $115K/yr

Measurement System Analysis (MSA), Statistical Process Control (SPC), Advanced Product Quality ... quality management within the automotive supply chain. • Ability to translate customer ...

Kodak

Quality Manager

Rochester, NY · On-site

$115K/yr

Measurement System Analysis (MSA), Statistical Process Control (SPC), Advanced Product Quality ... quality management within the automotive supply chain. • Ability to translate customer ...

Unifin SAS

QC Chemist Associate

Rochester, NY · On-site

$24 - $31.50/hr

QC Chemist Associate Who we are? As a French pharmaceutical industrial group, we strive to make ... Supervisor/Manager to recommend an appropriate solution toperformance problems. May support ...

Elmira Stamping

Quality Manager

Rochester, NY · On-site

$65K - $75K/yr

As a Quality Manager, you will be responsible for overseeing the quality assurance and quality control processes within our organization. This role is crucial in ensuring that our products meet the ...

Unifin SAS

Associate QC Chemist

Rochester, NY

$23.50 - $31/hr

Maintains and proposes improvements to lab quality systems. ESSENTIAL FUNCTIONS / RESPONSIBILITIES ... Distinguishes between training and non-training needs and works with Supervisor/Manager to ...

Unither Pharmaceuticals

Associate QC Chemist

Rochester, NY

$23.50 - $31/hr

Maintains and proposes improvements to lab quality systems. ESSENTIAL FUNCTIONS / RESPONSIBILITIES ... Distinguishes between training and non-training needs and works with Supervisor/Manager to ...

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Showing results 21-40

All JobsQc Biotech JobsManager Qc Biotech JobsManager Qc Biotech Jobs in Rochester, NY

Manager Qc Biotech information

See Rochester, NY salary details

$30.1K

$80.2K

$127.8K

How much do manager qc biotech jobs pay per year?

As of Aug 7, 2026, the average yearly pay for manager qc biotech 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.

What are the key skills and qualifications needed to thrive as a manager QC Biotech, and why are they important?

To thrive as a Manager QC Biotech, you need a solid background in life sciences, quality control principles, and regulatory compliance, often supported by a relevant degree and experience in biotech or pharmaceutical environments. Familiarity with laboratory information management systems (LIMS), GMP regulations, and analytical instrumentation is crucial. Strong leadership, problem-solving, and communication skills help manage teams and coordinate with cross-functional departments. These skills are vital to ensure product quality, regulatory adherence, and efficient team operations in a highly regulated industry.

What does a manager QC Biotech do?

A Manager QC (Quality Control) Biotech oversees the quality control processes in a biotechnology organization. They are responsible for managing teams that conduct laboratory testing, ensuring products meet regulatory standards, and developing protocols to maintain high-quality results. Their role involves coordinating with other departments, reviewing data, troubleshooting issues, and ensuring compliance with industry regulations such as GMP (Good Manufacturing Practice). Ultimately, they play a crucial part in guaranteeing the safety and effectiveness of biotech products before they reach the market.

What are some typical challenges a manager QC Biotech might face when overseeing quality control in a fast-paced biotech environment?

A Manager QC Biotech often encounters challenges such as maintaining compliance with evolving regulatory standards, managing tight timelines for product release, and ensuring consistent data integrity across multiple projects. Coordinating with cross-functional teams, such as manufacturing and R&D, requires strong communication skills to address unexpected quality issues promptly. Additionally, implementing new technologies and training staff on updated protocols while minimizing disruptions can be demanding but is crucial for continuous improvement and success in the role.
What are popular job titles related to Manager Qc Biotech jobs in Rochester, NY? For Manager Qc Biotech jobs in Rochester, NY, the most frequently searched job titles are:
What job categories do people searching Manager Qc Biotech jobs in Rochester, NY look for? The top searched job categories for Manager Qc Biotech jobs in Rochester, NY are:
Manager Qc Biotech jobs near you
Infographic showing various Manager Qc Biotech job openings in Rochester, NY as of July 2026, with employment types broken down into 50% Internship, and 50% Full Time. Highlights an 100% In-person 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

Re-posted 7 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/