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Manager Qc Jobs (NOW HIRING)

BeiGene, Inc.

Manager, Quality Control

The Manager, Quality Control (QC), is responsible for the oversight, coordination, and completion of assigned QC reviews, ensuring that clinical and regulatory documents undergo review, copyediting ...

BeiGene USA

Manager, Quality Control

The Manager, Quality Control (QC), is responsible for the oversight, coordination, and completion of assigned QC reviews, ensuring that clinical and regulatory documents undergo review, copyediting ...

TransMedics

Manager Quality Control

Andover, MA · On-site

Overall management of quality control activities; oversee the development and implementation of robust systems and procedures to ensure evaluation, measurement and improvement of processes. * Manage ...

TransMedics

Manager Quality Control

Andover, MA · On-site

Overall management of quality control activities; oversee the development and implementation of robust systems and procedures to ensure evaluation, measurement and improvement of processes. * Manage ...

Anika Therapeutics

Manager, Quality Control

Bedford, MA · On-site

$125 - $150/hr

Manager, Quality Control Regular Full-Time Bedford, MA, Bedford, MA, US 3 days ago Requisition ID: 1757 Salary Range: $122,000.00 To $152,000.00 Annually What You'll Do The Manager, Quality Control ...

Mesa Labs

Manager, Quality Control

San Diego, CA · On-site

$116K - $146K/yr

Job Summary The Manager, Quality Control is responsible for leading and managing the quality control function within Company. This role involves developing and implementing quality control strategies ...

Mesa Labs

Manager, Quality Control

San Diego, CA · On-site

$116K - $146K/yr

Job Summary The Manager, Quality Control is responsible for leading and managing the quality control function within Company. This role involves developing and implementing quality control strategies ...

Gilead

Manager, Quality Control

La Verne, CA · On-site

Manages QC personnel, including organizing and prioritizing daily tasks, performing training, and writing performance reviews. * Oversees overall day-to-day operation of laboratories. * Attends ...

Newrez LLC

Manager - Quality Control

Bethel Park, PA · On-site

The QC Manager plays a key leadership role in developing quality strategies, managing staff, and continuously improving appraisal review processes to maintain integrity and customer confidence.

Kop-Coat, Inc.

Mgr/Quality Control

Attleboro, MA · On-site

The primary result expected from the Quality Manager will be to formulate quality control policies and control quality of laboratory and production efforts by planning, directing, and coordinating ...

Anika

Manager, Quality Control

Bedford, MA · On-site

$125 - $150/hr

What You'll Do The Manager, Quality Control leads daily operations of the analytical testing laboratory, ensuring raw materials, in-process samples, and finished products meet established quality and ...

BeiGene, Ltd.

$125 - $150/hr

Manages QC timelines and communicates with Medical Writers to maintain awareness of expectations, milestones, and deliverables. Able to prioritize tasks, work simultaneously on multiple projects, and ...

New

Curium Pharma

Manager Quality Control

Noblesville, IN · On-site

$125 - $150/hr

The Manager Quality Control will also schedule laboratory testing and provide resource and instrumentation allocation, conducts laboratory investigations, and implements and monitors corrective ...

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Manager Qc information

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$24K

$86.2K

$158K

How much do manager qc jobs pay per year?

As of Sep 8, 2026, the average yearly pay for manager qc in the United States is $86,159.00, according to ZipRecruiter salary data. Most workers in this role earn between $44,000.00 and $136,000.00 per year, depending on experience, location, and employer.

What are the responsibilities of a Manager QC?

A Manager QC (Quality Control Manager) is responsible for overseeing the quality assurance processes within a company to ensure that products meet required standards and specifications. They develop and implement quality control procedures, supervise QC staff, conduct audits, and analyze quality data to identify areas for improvement. Additionally, they collaborate with other departments to resolve quality issues and ensure compliance with industry regulations. Their ultimate goal is to maintain consistent product quality and customer satisfaction.

What skills and qualifications are needed to thrive as a Manager QC?

To thrive as a Manager QC (Quality Control), you need a solid background in quality assurance processes, analytical testing, and industry regulations, typically supported by a degree in science or engineering. Familiarity with quality management systems (like ISO standards), statistical analysis software, and certification such as Six Sigma or ASQ is often required. Strong leadership, problem-solving, and communication skills help drive team performance and handle complex quality issues. These skills are essential for maintaining product standards, ensuring regulatory compliance, and supporting continuous improvement within the organization.

What challenges does a Manager QC face when balancing regulatory compliance with production timelines?

A Manager QC (Quality Control) often faces the challenge of ensuring that all products meet strict regulatory standards while also supporting the company's production goals. This balancing act requires effective communication with production and regulatory teams, as well as proactive planning to anticipate potential bottlenecks. Managers must remain vigilant about documentation and testing, and be prepared to address unforeseen quality issues without causing significant delays. Success hinges on strong leadership, a detail-oriented mindset, and the ability to adapt quickly to changing priorities.

What is the difference between Manager Qc vs Quality Assurance Supervisor?

AspectManager QcQuality Assurance Supervisor
ResponsibilitiesOversees quality control processes, manages teams, implements quality policiesSupervises QA team, conducts inspections, ensures compliance with standards
CredentialsBachelor's degree in related field, experience in quality management, certifications like CQEBachelor's degree, experience in quality assurance, certifications like CQE or ASQ certifications
Work EnvironmentManagement level, strategic planning, cross-department collaborationOperational level, hands-on inspections, team supervision
Industry UsageManufacturing, pharmaceuticals, food productionManufacturing, electronics, consumer goods

The main difference between a Manager Qc and a Quality Assurance Supervisor lies in scope and level of responsibility. The Manager Qc typically handles strategic oversight and manages multiple teams, while the QA Supervisor focuses on daily supervision and operational tasks. Both roles require similar credentials and are vital in quality management across industries.

Is manager QC a high paying job?

Manager QC roles typically offer higher salaries compared to entry-level quality control positions, with pay varying based on industry, experience, and location. These roles often require strong leadership, technical skills, and certifications, and they tend to be well-compensated in manufacturing, pharmaceuticals, and food industries.

What does a manager QC do?

A manager QC (Quality Control) oversees the inspection and testing of products or processes to ensure they meet quality standards. They develop quality procedures, supervise QC staff, analyze data, and implement improvements to maintain product integrity and compliance with industry regulations.

What cities are hiring for Manager Qc jobs?

Cities with the most Manager Qc job openings:

What are the most commonly searched types of Qc jobs?

The most popular types of Qc jobs are:

What states have the most Manager Qc jobs?

States with the most job openings for Manager Qc jobs include:

What are popular job titles related to Manager Qc jobs?

For Manager Qc jobs, the most frequently searched job titles are:

Manager Qc jobs near you
Infographic showing various Manager Qc job openings in the United States as of August 2026, with employment types broken down into 88% Full Time, 11% Part Time, and 1% Contract. Highlights an 80% Physical, 2% Hybrid, and 18% Remote job distribution, with an average salary of $86,159 per year, or $41.4 per hour.

Manager, Quality Control

Remote

BeiGene, Inc.
Health Care and Social Assistance • 5 - 10K employees
Learn more about BeiGene, Inc.external

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 6 days ago

Job description

BeOne continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our passionate interest in fighting cancer.
General Description:
The Manager, Quality Control (QC), is responsible for the oversight, coordination, and completion of assigned QC reviews, ensuring that clinical and regulatory documents undergo review, copyediting, data verification, and proofreading in a manner that conforms to domestic and/or international regulatory submission and internal document standards, while meeting project timelines. Clinical and regulatory documents include study reports, clinical study protocols or amendments, investigator's brochures, and the clinical sections of INDs, NDAs, MAAs, and other regulatory submission documents. Other documents may include manuscripts, abstracts, posters, briefing documents, responses to health authorities, narratives, and any other documents authored or supported by Global Medical Writing that require a QC review.
This work can be done remotely or from any of BeOne's global offices.
Essential Functions of the Job:
Document Review and Editing:
  • Works effectively within the Global Medical Writing group to produce high-quality, scientifically accurate documents under strict timelines, ensuring consistency between related documents.
  • Applies knowledge of industry standards, regulatory requirements, and internal procedures to ensure document quality and compliance, occasionally requiring prioritization and management of multiple parallel projects.
    • Ensures compliance with Global Medical Writing conventions, processes, and applicable regulatory guidelines.
    • Reviews documents for content completeness, logical consistency, clarity, readability, and adherence to established standards and templates.
    • Identifies gaps, inconsistencies, and missing information and collaborates with document authors to resolve issues before document finalization.
    • Applies knowledge of industry standards, regulatory requirements, and internal procedures to ensure document quality and compliance.

Project and Process Management:
  • Manages team direction and strategy in collaboration with other QC and Global Medical Writing team leaders.
  • Manages QC timelines and communicates with Medical Writers to maintain awareness of expectations, milestones, and deliverables.
  • Able to prioritize tasks, work simultaneously on multiple projects, and complete high-quality documents according to tight timelines and shifting priorities/demands.
  • Partners with document authors and stakeholders to address revision requests and drive efficient resolution of review comments.
  • Contributes to the development, maintenance, and continuous improvement of QC processes, templates, guidance documents, and best practices.

Influence and Training:
  • Engages in trainings that will improve authoring and technical editing skills and expand knowledge of the Global Medical Writing team or other areas of the company (cross-training programs, mentoring programs, etc).
  • Supports onboarding and mentoring of new QC team members and promotes consistency in review practices across the team.
  • Serves as a resource for resolving complex editing, formatting, and quality-related issues.

Qualifications:
  • Demonstrated ability to communicate in clear, concise, and effective English in both written and verbal forms.
  • Experience directly mentoring and managing other team members; completion of management-related training modules or other hands-on management experience; a proven desire to take on management-level responsibilities, including helping to develop team members and effectively assess the performance of at least one direct report.
  • Extensive experience in conducting QC review or copyediting of pharmaceutical industry regulatory documents such as clinical study reports, protocols, and protocol amendments; experience in reviewing or copyediting clinical sections of INDs, MAAs, and NDAs is a plus.
  • A thorough understanding of the general processes of drug/biologics development as well as the key requirements for regulatory submissions as defined in FDA regulations and ICH guidelines.
  • Experience developing and maintaining document templates, style guidance, and process documentation.

Education Required:
  • BA/BS degree; Masters, PhD/PharmD, or other graduate-level degree is a plus.
  • At least 5+ years of relevant industry experience as a QC editor/specialist, medical writer, or technical copyeditor. Management experience is preferred.

Supervisory Responsibilities:
  • Manages and supervises staffing and performance management, including, but not limited to, hiring, training, coaching, and conducting performance reviews for direct reports, if applicable.

Computer Skills:
  • Technical expertise in Microsoft Word, Adobe Acrobat, and electronic document management systems; proficiency in Microsoft Outlook, Excel, and PowerPoint.
  • Proficiency in navigating Microsoft Windows.
  • Proficiency or familiarity with SharePoint and Veeva Vault is preferred.

Other Qualifications:
  • Effective Communication: Communicates critical information to key stakeholders with clarity, precision, and conviction. Proactively escalates questions/issues to appropriate stakeholders at an early stage. Takes part in discussions with different viewpoints, and proactively provides value-added inputs.
  • Embracing Change: Always seeking and open to new opportunities and changes. Be able to execute new and different solutions when faced with new challenges. Embraces change and quickly alters course in response to new challenges. Leads change efforts management within the department and across functions.
  • Creating Innovation: Anticipates the need for and adopts new methods and practices. Generates innovative ideas and new approaches for addressing a range of work areas; encourages others to generate ideas.
  • Thinking Strategically: Understands how concepts (eg, strategic review, lean writing) relate to the future objectives and aims of the department, and identifies the principles for new concepts. Leads (part of) the establishment of clear and effective strategies for the department, and contributes to the establishment of clear and effective strategies for cross-functions, based on an in-depth understanding of industry trends and company mission.
  • Mentoring: Provides feedback related to individual and department to support ongoing development and overall department performance as needed. Finds opportunities to individually coach others, providing specific insights and tips to enhance skills, knowledge, or work performance.

Travel: N/A
Global Competencies
When we exhibit our values of Patients First, Driving Excellence, Bold Ingenuity and Collaborative Spirit, through our twelve global competencies below, we help get more affordable medicines to more patients around the world.
  • Fosters Teamwork
  • Provides and Solicits Honest and Actionable Feedback
  • Self-Awareness
  • Acts Inclusively
  • Demonstrates Initiative
  • Entrepreneurial Mindset
  • Continuous Learning
  • Embraces Change
  • Results-Oriented
  • Analytical Thinking/Data Analysis
  • Financial Excellence
  • Communicates with Clarity

Salary Range: $111,100.00 - $151,100.00 annually
BeOne is committed to fair and equitable compensation practices. Actual compensation packages are determined by several factors that are unique to each candidate, including but not limited to job-related skills, depth of experience, certifications, relevant education or training, and specific work location. Packages may vary by location due to differences in the cost of labor. The recruiter can share more about the specific salary range for a preferred location during the hiring process. Please note that the listed range reflects the base salary or hourly range only. Non-Commercial roles are eligible to participate in the annual bonus plan, and Commercial roles are eligible to participate in an incentive compensation plan. All Company employees have the opportunity to own shares of BeOne Medicines Ltd. stock because all employees are eligible for discretionary equity awards and to voluntarily participate in the Employee Stock Purchase Plan. The Company has a comprehensive benefits package that includes Medical, Dental, Vision, 401(k), FSA/HSA, Life Insurance, Paid Time Off, and Wellness.
We are proud to be an equal opportunity employer. BeOne does not discriminate on the basis of race, religion, color, sex, gender identity, sexual orientation, age, disability, national origin, veteran status or any other basis covered by appropriate law. All employment is decided on the basis of qualifications, merit, and business need. In order to ensure reasonable accommodation for individuals protected by Section 503 of the Rehabilitation Act of 1973, the Vietnam Era Veterans' Readjustment Assistance Act of 1974, Title I of the Americans with Disabilities Act of 1990, and any other applicable federal, state or local laws, applicants who require reasonable accommodation in the job application process may contact accommodationsus@beonemed.com.
BeiGene logo

About BeiGene

Sourced by ZipRecruiter

BeiGene (NASDAQ: BGNE; HKEX: 06160; SSE: 688235) is a global, science-driven biotechnology company focused on developing innovative and affordable medicines to improve treatment outcomes and access for patients worldwide. With a broad portfolio of more than 40 clinical candidates, we are expediting development of our diverse pipeline of novel therapeutics through our own capabilities and collaborations. We are committed to radically improving access to medicines for two billion more people by 2030. BeiGene has a growing global team of over 8,200 colleagues across five continents. For more information, please visit www.beigene.com .

Industry

Health care and social assistance

Company size

5,001 - 10,000 Employees

Headquarters location

Cambridge, MA, US

Year founded

2010

Social media

Twitter

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