20 Best Senior Quality Assurance Analyst jobs (Hiring Now!)

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Quick Apply
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Senior Quality Assurance Analyst - Biotechnology

Vyriad, Inc. - Rochester, MN

Quick Apply

Job Details

Full-time $70,000 - $109,000 a year

Benefits

Relocation assistance
Health insurance
Dental insurance
401(k)
Flexible spending account
Tuition reimbursement
Paid time off
Parental leave
Employee assistance program
Vision insurance
401(k) matching
Professional development assistance
Life insurance

Qualifications

Six Sigma Certification
CGMP
Data analysis skills
Quality management
8 years
Project management
Quality assurance
Bachelor's degree
Certified Quality Auditor
Alignment
Quality control
Manufacturing
Leadership
Communication skills
FDA regulations

Full Job Description

Vyriad is seeking a highly skilled and experienced Senior Quality Assurance Analyst to join our dynamic team. As a senior member of the Quality Assurance department, this role requires a full understanding and knowledge of manufacturing quality system requirements in the biotechnology industry and the ability to independently lead audits, projects, and initiatives. The successful candidate will play a key role in annual audit planning, project management, conflict resolution, and providing guidance to areas navigating compliance challenges.

Senior QA Analyst’s are responsible for oversight of quality and regulatory compliance for the manufacturing of investigational product including review of analytic assay development and testing services, ensuring the quality of our products or services meets the highest standards through continuous monitoring, training, and improvement initiatives. The staff works to identify and reduce regulatory and compliance risks by continuously monitoring and evaluating facility policies and practices to ensure compliance is built into the operational systems. Quality Assurance staff communicate and work effectively with leadership to take necessary actions to mitigate identified risks.

Quality Assurance staff are accountable for the effective implementation of the manufacturing Quality Management System (QMS) and serves as the subject matter expert on the policies, processes, and procedures of the QMS by developing a broad knowledge of the practice, business, and technology as it relates to product biotechnology manufacturing.

In addition to traditional QA responsibilities, this role involves delivering quality training, identifying areas for improvement, designing and implementing quality system enhancements, and fostering innovation within the quality process.

Supervisory Responsibilities

None

Duties and Responsibilities

Full Understanding of Quality System Requirements:

Possess a comprehensive understanding and knowledge of standard quality system requirements.
Stay abreast of industry best practices for biotechnology manufacturing and evolving quality standards.

Regulatory Compliance:

Understand the connections between the quality systems, manufacturing and regulatory requirements.
Ensure compliance with all applicable regulatory standards.

Independent Auditor:

Independently conduct quality system and supplier audits, demonstrating a high level of expertise and attention to detail.
Provide recommendations for continuous improvement based on audit findings.

Annual Audit Planning:

Lead the annual audit planning process, ensuring comprehensive coverage of key areas.
Collaborate with relevant stakeholders to align audit plans with organizational goals.

Project Management:

Lead large projects and initiatives independently, functioning as a project manager.
Ensure successful completion of projects within established timelines.

Conflict Resolution and Compliance Challenges:

Assist areas in navigating conflict and compliance challenges.
Direct root cause and Corrective and Preventive Action (CAPA) investigations as needed.

Project/Assignment Follow-Through:

Demonstrate a commitment to timely and complete follow-through on projects and assignments.
Maintain accountability for project outcomes and deliverables.

Assistance to QA Team Members:

Assist with manufacturing batch record reviews as required.
Assist with testing data and protocol reviews as required.
Perform quality assurance reviews of documents as required.
Assist other QA team members with task completion as needed.
Foster a collaborative and supportive team environment.

Other Responsibilities:

· Provides knowledge and expertise to Vyriad staff on quality concepts and practices.

· Ensures risks are escalated and documented appropriately.

· Maintains control and takes responsibility for third-party service providers (contract manufacturers, contract laboratories, etc.).

· Ensures compliance concerns are prioritized and resources identified.

· Works with staff to ensure compliance with regulatory requirements associated with internal and external assessments and responses to citations.

· Develops regulatory and compliance training program for the intended audience. Maintains program and keeps it up to date.

· Receives, tracks, and responds to customer and regulatory complaints.

· Leads the investigation of events that appear to be associated with regulatory violations. Works with relevant parties to resolve issue and take appropriate corrective and preventive action.

· Conduct routine quality training sessions for staff to ensure understanding and adherence to quality standards.

· Identify areas for improvement within the quality system through the development and analysis of monitoring, measuring, and metrics.

· Design and initiate quality system improvements to address identified areas of improvement and enhance overall quality performance.

· Innovate new and effective ways to meet quality objectives, promote engagement, and drive continuous improvement within the organization.

· Communicate improvement and innovation ideas to leadership, providing recommendations and insights for strategic decision-making.

· Maintain effective communication channels with cross-functional teams to ensure alignment on quality goals and initiatives.

· Collaborate with other departments to integrate quality processes and standards into their workflows as necessary.

· Stay current with industry best practices and technological advancements to enhance the effectiveness of the quality assurance function.

· Provide support during audits and regulatory inspections as needed.

Education and Experience Requirements

· A bachelor’s degree in a science related field is required and a minimum of 8 years’ experience in a manufacturing quality control/quality assurance role.

Required skills and/or qualifications

· Knowledge and experience in FDA current Good Manufacturing Practices for product manufacturing is required. Additional experience with other requirements (ICH, ISO, etc.) is highly desirable.

· Attention to detail-oriented and the ability to work independently and productively with minimal direction.

· Self-motivated and ability to exercise sound judgment.

· Strong analytic skills coupled with critical thinking skills are essential in this role.

· Must have demonstrated capacity to comprehend complex protocols, programs, and situations.

· The ability to exercise good judgment while under pressure and tight deadlines, and strong coping skills are required.

· Must be flexible in adapting to a variety of responsibilities, work assignments, and priorities.

· Extensive experience in quality assurance, with a proven track record in a senior role.

· In-depth understanding of quality system requirements and regulatory standards.

· Strong project management skills and experience leading large initiatives.

· Independent auditor certification and experience preferred.

· Strong understanding of quality management principles, methodologies, and tools.

· Proven experience in delivering quality training sessions to diverse audiences.

· Proficiency in data analysis and interpretation to drive quality improvements.

· Excellent problem-solving skills with the ability to identify root causes and implement effective solutions.

· Strong communication and interpersonal skills, with the ability to effectively engage with stakeholders at all levels.

· Demonstrated ability to work independently with minimal supervision while maintaining alignment with organizational goals.

· Experience with quality management systems (QMS) and regulatory requirements is preferred.

· Certifications such as Six Sigma, Lean, or Certified Quality Auditor (CQA) are a plus.

Physical Requirements

· Prolonged periods of sitting at a desk and working on a computer.

· Must be able to lift up to 15 pounds at times.

COPYRIGHT © Vyriad, Inc.. This information is intended for use by Vyriad, Inc., and affiliated employees only. It is confidential and no part of it may be transmitted in any form by electronic, mechanical, photocopying, or any other means to anyone outside Vyriad, Inc. without prior permission.

Job Type: Full-time

Pay: $70,000.00 - $109,000.00 per year

Benefits:

401(k)
401(k) matching
Dental insurance
Employee assistance program
Flexible spending account
Health insurance
Life insurance
Paid time off
Parental leave
Professional development assistance
Relocation assistance
Tuition reimbursement
Vision insurance

Compensation package:

Performance bonus

Experience level:

8 years

Schedule:

Day shift
Monday to Friday

Ability to Relocate:

Rochester, MN 55901: Relocate before starting work (Required)

Work Location: In person

Quick Apply

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