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Quality Assurance Risk Manager Jobs in Rochester, NY

groteindustries

Quality Assurance Manager

Avon, NY

Creates Quality Assurance guidelines. Leads Quality Management System efforts. Position Duties: - Pursues achievement of company and department goals. - Maintains active communication with immediate ...

Grote Industries

Quality Assurance Manager

Avon, NY · On-site

$105K - $120K/yr

Creates Quality Assurance guidelines. Leads Quality Management System efforts. Position Duties: - Pursues achievement of company and department goals. - Maintains active communication with immediate ...

Unifin SAS

Quality Assurance Manager

Rochester, NY · On-site

Quality Assurance Manager Who we are? As a French pharmaceutical industrial group, we strive to make healthcare solutions that improve and simplify patients' lives accessible to as many people as ...

Unifin SAS

Quality Assurance Manager

Rochester, NY · On-site

Quality Assurance oversight of Deviation Management system. Technical Complaint Management: Investigation, documentation and approval of technical complaints and adverse events. (Adverse events at ...

Baldwin Richardson Foods

QA Analyst

Macedon, NY · On-site

Performs perfect package checks on applicable productions lines and reports any issues to QA management * Verifies food safety preventive controls are in place and operating properly * Supports and ...

Baldwin Richardson Foods

QA Analyst

Williamson, NY · On-site

Performs perfect package checks on applicable productions lines and reports any issues to QA management * Verifies food safety preventive controls are in place and operating properly * Supports and ...

Collabera

Quality Assurance

Rochester, NY · On-site

Reports progress on problem resolution to management. Implements pre-determined improvements to ... Performs work flow analysis and recommends quality improvements. * Escalates software process ...

Safran

Quality Assurance Technician

West Henrietta, NY · On-site

$25 - $30/hr

We're looking for a Quality Assurance Technician to join our growing team in West Henrietta, NY ... Familiarity with quality management systems and tools (ISO9001) * Familiarity with IPC-A-610

Borg & Ide Imaging

RN Supervisor

Rochester, NY · On-site

$88K - $98K/yr

Participate in quality assurance, risk management, and emergency preparedness activities * Collaborate with clinical teams to support efficient scheduling and patient flow * Perform hands-on nursing ...

RadNet

RN Supervisor

Rochester, NY · On-site

$88K - $98K/yr

Participate in quality assurance, risk management, and emergency preparedness activities * Collaborate with clinical teams to support efficient scheduling and patient flow * Perform hands-on nursing ...

RadNet

RN Supervisor

Rochester, NY · On-site

$88K/yr

Participate in quality assurance, risk management, and emergency preparedness activities * Collaborate with clinical teams to support efficient scheduling and patient flow * Perform hands-on nursing ...

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All JobsQuality Assurance Risk JobsQuality Assurance Risk Manager JobsQuality Assurance Risk Manager Jobs in Rochester, NY

Quality Assurance Risk Manager information

See Rochester, NY salary details

$37.5K

$116.5K

$176.6K

How much do quality assurance risk manager jobs pay per year?

As of Aug 23, 2026, the average yearly pay for quality assurance risk manager in Rochester, NY is $116,500.00, according to ZipRecruiter salary data. Most workers in this role earn between $81,900.00 and $142,600.00 per year, depending on experience, location, and employer.

What is the difference between Quality Assurance Risk Manager vs Quality Control Specialist?

AspectQuality Assurance Risk ManagerQuality Control Specialist
CertificationsISO 9001, Six Sigma, CQEISO 9001, Six Sigma, CQE
Work EnvironmentRisk assessment, process improvement, complianceProduct inspection, testing, defect identification
Industry UsageManufacturing, healthcare, aerospaceManufacturing, food production, electronics

The Quality Assurance Risk Manager focuses on identifying and mitigating risks in processes to ensure quality standards are met, often involving risk assessments and compliance. In contrast, the Quality Control Specialist primarily conducts product inspections and tests to detect defects. Both roles require similar certifications and are integral to quality management but differ in scope and focus.

What is quality assurance in risk management?

In the context of a Quality Assurance Risk Manager, quality assurance in risk management involves systematically identifying, assessing, and mitigating potential risks that could impact product quality or operational processes. It includes implementing standards, conducting audits, and using tools like risk assessments to ensure compliance and reduce errors, thereby maintaining product integrity and customer satisfaction.

What cities near Rochester, NY are hiring for Quality Assurance Risk Manager jobs?

Cities near Rochester, NY with the most Quality Assurance Risk Manager job openings:

Quality Assurance Risk Manager jobs near you

Quality Assurance Engineer

Stark Pharma Solutions Inc

Rochester, NY • On-site

Contractor

Re-posted 23 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/