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Manager Qc Biotech Jobs (NOW HIRING)

Werfen

Manager, Quality Control

Waukesha, WI · On-site

Overview Job Summary The Manager, Quality Control is a key contributor to the Quality Assurance and Regulatory Affairs (QARA) team for the Transplant Technology Center. Reporting to the Sr. Director ...

Centex Materials

Manager -Quality Control

Austin, TX · On-site

Manage Command QC software working with Concrete Production Manager optimizing materials and training personnel. Manage existing and future Quality Control and Process Control Programs. Communicate ...

Werfen

Manager, Quality Control

Waukesha, WI

Overview Job Summary The Manager, Quality Control is a key contributor to the Quality Assurance and Regulatory Affairs (QARA) team for the Transplant Technology Center. Reporting to the Sr. Director ...

Werfen

Manager, Quality Control

Waukesha, WI

Overview Job Summary The Manager, Quality Control is a key contributor to the Quality Assurance and Regulatory Affairs (QARA) team for the Transplant Technology Center. Reporting to the Sr. Director ...

AMRI

Manager, QC Lab Remediation

Rensselaer, NY · On-site

Manager, Quality Control Lab Remediation in Rensselaer, NY Build your future at Curia, where our ... biotech companies to provide life-saving treatments to patients. At Curia, we are on a mission to ...

Curia, Inc.

Manager, QC Lab Remediation

Rensselaer, NY · On-site

Manager, Quality Control Lab Remediation in Rensselaer, NY Build your future at Curia, where our ... biotech companies to provide life-saving treatments to patients. At Curia, we are on a mission to ...

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Manager Qc Biotech information

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$30.5K

$81.3K

$129.5K

How much do manager qc biotech jobs pay per year?

As of Jul 22, 2026, the average yearly pay for manager qc biotech in the United States is $81,324.00, according to ZipRecruiter salary data. Most workers in this role earn between $60,500.00 and $100,000.00 per year, depending on experience, location, and employer.

What is the highest paying job in biotech?

In biotech, senior executive roles such as Chief Scientific Officer (CSO) or Vice President of Research typically have the highest salaries, often exceeding $200,000 annually. These positions require extensive experience, advanced degrees, and leadership skills, and they oversee research and development strategies within biotech companies.

What does a QC specialist do in biotech?

A QC (Quality Control) specialist in biotech is responsible for testing and inspecting products, raw materials, and processes to ensure they meet quality standards and regulatory requirements. They perform laboratory analyses, document results, and may use tools like chromatography or spectrometry, often working under Good Manufacturing Practice (GMP) guidelines. Their role helps ensure the safety, efficacy, and consistency of biotech products.

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 biology jobs pay over $100k?

Manager roles in biotech and pharmaceutical industries, such as Biotech Manager or Quality Control Manager, often pay over $100,000 annually. These positions typically require advanced degrees, industry experience, and skills in regulatory compliance, project management, and laboratory oversight.

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.

Will biotech do well in 2026?

The biotech industry, including roles like Manager Qc Biotech, is expected to continue growing due to ongoing advancements in healthcare and biotechnology. Demand for quality control professionals will likely remain strong as companies focus on regulatory compliance, innovation, and product development in the sector.
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What cities are hiring for Manager Qc Biotech jobs? Cities with the most Manager Qc Biotech job openings:
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Manager Qc Biotech jobs near you
Infographic showing various Manager Qc Biotech job openings in the United States as of July 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $81,324 per year, or $39.1 per hour.
Manager, Quality Control

Manager, Quality Control

Werfen

Waukesha, WI • On-site

Full-time

Posted 6 days ago

Werfen rating

8.7

Company rating: 8.7 out of 10

Based on 27 frontline employees who took The Breakroom Quiz

Job description

Introduction
Werfen is a growing, family-owned, innovative company founded in 1966 in Barcelona, Spain. We are a worldwide leader in specialized diagnostics in the areas of Hemostasis, Acute Care Diagnostics, Transfusion, Autoimmunity, and Transplant. Through our Original Equipment Manufacturing (OEM) business line, we research, develop, and manufacture customized assays and biomaterials. We operate directly in 30 countries, and in more than 100 territories through distributors. Our Headquarters and Technology Centers are located in the US and Europe, and our workforce is more than 7,000 strong.
Our success comes from a specific focus in these rapidly evolving diagnostic areas, our commitment to customers, and our dedication to innovation and quality. We're passionate about providing healthcare professionals the most valuable and complete solutions to improve hospital efficiency and enhance patient care.
Overview
Job Summary
The Manager, Quality Control is a key contributor to the Quality Assurance and Regulatory Affairs (QARA) team for the Transplant Technology Center. Reporting to the Sr. Director Quality Assurance and Regulatory Affairs, this role will be responsible for leading the Quality Control team and all is responsible for all other aspects of the Quality Control Department.
Responsibilities
Key Accountabilities
  • Leads the Quality Control (QC) team, providing strategic direction and day-to-day leadership, including setting clear, challenging, and achieveable SMART goals for the team, aligning individual and department goals with broader business unit strategy, prioritization of work, resource allocation, workforce planning and talent management, including hiring, onboarding, training, performance management to build a high performing team.
  • Partners cross-functionally with Quality Assurance, Regulatory Affairs, Research & Development, Manufacturing Technical Support and Operations to resolve issues, support product development and ensure alignment.
  • Ensures QC team team and site adherence to SOPs, FDA, Regulatory and Compliance (ISO 13485, 21 CFR 820, and MDSAP Requirements) and good manufacturing practices to ensure inspection readiness and audit compliance, while fostering a culture of accountability and quality excellence.
  • Role models and reinforces company values, driving a high performance, collaborative, and inclusive team environment.
  • Drives continuous process improvments and operational efficiency within the department, proactively identifying opportunities to enhance quality, scalability, and effectiveness across QC operations
  • Participates in setting and adherence to the department budget. Coordinates the purchase, training and implementation of new equipment, products, and systems.
  • Sets and tracks department key performance metrics and presents at QRB and MRB.
  • Leads investigation governance within QC, with accountability for OOS, CAPA, and NCR investigations.
  • Authors, updates and reviews SOPs, FORs and TMPs.
  • Represents QC for Validaton Plans, Protocols and PDP projects.
  • Oversees departmental planning and execution, including scheduling, planning, and prioritization of daily work and the QC Stability Program.
  • Participates with technical support issues and coordinates QC resources for investigations.
  • Reviews test results and coordinates QC resources with needed for investigations.
  • Performs other duties and responsibilities as assigned.

Reasonable accommodations may be made to enable individuals with disabilities to perform these essential functions.
Networking/Key relationships
  • Daily interaction with QC Team to support daily activities.
  • Daily interaction with co-workers from Operations to ensure product release priorities.
  • Interaction with Manufacturing Technical Support team in support of product investigations.
  • Interaction with Research and Development to support new products and product improvements.
  • Interaction with Quality Assurance for quality and regulatory compliance.
  • Interaction with Customer Technical Support team in support of customer compaint investigation.

Qualifications
Minimum Knowledge & Experience required for the position:
  • Bachelor's Degree in Medical Technology or a Bachelor's of Science Degree in a related field
  • Minimum 10 years of clinical laboratory experience working with In-Vitro Diagnostics; preferred HLA screening Assay and Elisa products
  • Minimum 5 years of people management experience; preferred people leadership in a clinical setting or GMP environment Strong analytical, communication, and leadership skills
  • Demonstrated leadership skills
  • Excellent verbal and written communication skills
  • Exhibits a disciplined approach to work ensuring thoroughness, consistency, validation, and accuracy in all tasks and work product
  • Management has the discretion of substituting relevant work experience for a degree and/or making exceptions to the years of experience requirement.

Skills & Capabilities:
  • Effective communication
  • Strong leadership
  • Proactive problem-solving
  • Stategic thinking
  • Organizational skills and time management
  • Coaching skills for improvement and problem solving
  • Continous learning and development mindset
  • Conflict resolution
  • Foster a positive and inclusive work environment

Travel requirements:
Up to 5% annually.
Closing
If you are interested in constantly learning and being challenged on a daily basis we encourage you to submit your resume or CV.
Werfen is an Equal Opportunity employer and is committed to a diverse workplace. Werfen strictly prohibits unlawful discrimination, harassment or retaliation based upon an individual's race, color, religion, gender, sexual orientation, gender identity/expression, national origin/ancestry, age, mental/physical disability, medical condition, marital status, veteran status, or any other protected characteristic as defined by applicable state or federal law. If you have a disability and need an accommodation in relation to the online application process, please contact NAtalentacquisition@werfen.com for assistance.
We operate directly in over 30 countries, and in more than 100 territories through distributors. Annual revenue is approximately $2 billion and more than 7,000 employees around the world comprise our Werfen team.
www.werfen.com

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About Werfen

Sourced by ZipRecruiter

Industry

Health care and social assistance

Company size

1,001 - 5,000 Employees

Headquarters location

L'Hospitalet de Llobregat, Barcelona, ES

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