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

In this role, you will ensure quality control for manufactured parts in accordance with established ... management and production personnel in a timely manner. This position also provides day-to-day ...

Position Description The Quality Control Inspector is responsible for performing the final ... Cleaning of assigned work area, and additional duties as delegated by management including but not ...

Position Description The Quality Control Inspector is responsible for performing the final ... Cleaning of assigned work area, and additional duties as delegated by management including but not ...

Asphalt Quality Control Technician AMAT Manchester, New York, United States Job ID: 520889 The ... Please complete your online profile and it will be sent to the hiring manager. Our system allows ...

Asphalt Quality Control Technician AMAT Walworth, New York, United States Job ID: 526533 The ... Please complete your online profile and it will be sent to the hiring manager. Our system allows ...

Job Summary The QC tech role is vital to the successful delivery of quality asphalt, and aggregate ... Please complete your online profile and it will be sent to the hiring manager. Our system allows ...

Job Summary The QC tech role is vital to the successful delivery of quality asphalt, and aggregate ... Please complete your online profile and it will be sent to the hiring manager. Our system allows ...

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

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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 Jul 26, 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 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.
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:
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 Control Supervisor

$36 - $42/hr

Other

Posted 4 days ago


Job description

Description

POSITION SUMMARY

We are looking for a Quality Control Supervisor to join our team. In this role, you will ensure quality control for manufactured parts in accordance with established company and customer standards. You will perform inspections, verify product conformance to engineering drawings and specifications, document inspection results, and communicate quality findings to management and production personnel in a timely manner. This position also provides day-to-day leadership and oversight of quality inspection activities to ensure consistent execution of quality standards, employee development, and departmental performance.


Uses a variety of inspection instruments (calipers, micrometers, CMMs, height gauges, optical comparators, etc.) and calculations to determine conformity to engineering drawings and specifications.

  • Performs visual inspections under magnification to determine conformity to customer and company standards.
  • Reviews certifications from suppliers and vendors to verify compliance with engineering and customer requirements.
  • Maintains accurate inspection records and quality documentation using company databases and quality management systems.
  • Coordinates inspection activities to ensure work is completed efficiently, accurately, and in accordance with production priorities.
  • Communicates inspection findings, nonconformances, and quality concerns to production, engineering, and management in a timely manner.
  • Assists in root cause investigations and supports corrective and preventive action activities.
  • Supports continuous improvement initiatives to improve product quality, reduce defects, and enhance inspection processes.
  • Ensures compliance with company quality procedures, customer requirements, AS9100 standards, and applicable regulatory requirements.
SUPERVISORY RESPONSIBILITIES
  • Provides day-to-day leadership, direction, and work assignments for Quality Control Inspectors and Technicians.
  • Trains, mentors, and develops team members on inspection methods, quality standards, equipment operation, and documentation requirements.
  • Monitors employee performance provides coaching and constructive feedback, and conducts performance evaluations.
  • Partners with Human Resources to address attendance, performance, and employee relations issues through coaching and corrective action when appropriate.
  • Ensures employees comply with all safety requirements, company policies, quality procedures, and regulatory standards.
  • Plans and prioritizes departmental workload to support production schedules and customer delivery commitments.
  • Participates in recruiting, interviewing, onboarding, and training new Quality team members.
  • Promotes a culture of accountability, continuous improvement, teamwork, and customer focus.
  • Tracks departmental performance metrics and implements improvements to increase quality, efficiency, and productivity.
  • Collaborates with Production, Engineering, Manufacturing, and Supply Chain to resolve quality issues and drive process improvements.

WORK ENVIRONMENT:

The performance of this position will require exposure to the manufacturing areas where all areas require the use of personal protective equipment such as safety glasses, hearing protection, steel toe shoes, and other mandatory safety equipment.

For the most part, ambient temperatures with typical plant lighting and manufacturing equipment are present throughout the facility.


PHYSICAL DEMANDS:

Sit or stand as needed.

Walking primarily on a level surface for periodic periods throughout the day.

Reaching above shoulder height, below the waist, or lifting as required to reach documents or store materials throughout the workday.

Proper lifting techniques required.

Ability and comfortability to work in small confine spaces while following proper safety protocol. 

Ability to accomplish the physical requirements of the position with or without reasonable accommodation.


SAFETY AND POLICY PRACTICES:

Each employee must be knowledgeable of standard safety policies and procedures and adhere to the same while supporting the goals and objectives of the organization and recognizing the Company's need to achieve its business objectives. Each employee is responsible for complying with company hazardous waste disposal procedures.

ITAR REQUIREMENTS:

To conform to U.S. export control regulations, applicant should be eligible for any required authorizations from the U.S. Government.


AFFIRMATIVE ACTION:

ADDMAN Engineering is proud to be an Equal Opportunity Employer of Minorities, Women, Protected Veterans, and Individuals with Disabilities. All terms and conditions of employment will be administered without regard to an individual's sex, gender identity, sexual orientation, race, color, religious creed, national origin, physical or mental disability, protected veteran status, or any other characteristic protected by applicable law.

NOTE: This job description is intended to describe the general level of work being performed. This job description is not intended to be all-inclusive. The duties of this position may change from time to time, and the employee may perform other related duties to meet the ongoing needs of the organization. ADDMAN Engineering reserves the right to add, delete or modify these duties and responsibilities at its discretion. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions of this position. Employment is at-will, and nothing in this job description is intended to create or imply a contractual relationship or alter the at-will status of the employee.

Requirements

SKILL REQUIREMENTS:

  • Commitment to a safety culture where safety is the first consideration before starting any task.
  • Proficient with the use of manual inspection equipment.
  • Experience programming and/or operating CMMs using PC-DMIS is preferred, but not required.
  • Selects and uses appropriate inspection equipment and techniques.
  • Interpret drawings and specifications.
  • Determines acceptability of quality of work.
  • Meets time and quality standards.
  • Seeks out additional duties when it is needed.
  • Brings up potential problems with suggested solutions.
  • Promotes a positive environment through what is said and by setting an example.

QUALIFICATIONS:

  • Graduate of related two-year vocational school program and two years related work experience and/or training; or equivalent combination of education and experience is preferred, but not required.
  • Able to work in a dynamic environment with changing priorities to exceed customer expectations.
  • Works independently, has a strong work ethic, is self-motivated and able to complete tasks with minimal supervision. 
  • Ability to work on cross-functional teams to support the core business, ensuring quality products are delivered on time.
  • Computer aptitude (Outlook, PowerPoint, Word, and Excel).
  • Ability to read, write, and communicate in the English language.
  • Must be a team player and willing to learn new skills and concepts.
  • Eligible to work in the United States without company sponsorship. 
PREFERRED QUALIFICATIONS (Optional)
  • Previous experience supervising or leading quality personnel in an aerospace, precision machining, or advanced manufacturing environment.
  • Working knowledge of AS9100, ISO 9001, GD&T, and blueprint interpretation.
  • Experience with CMM programming or advanced metrology equipment preferred.
  • Strong leadership, communication, and problem-solving skills.