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Manager Biotech Quality Control Jobs in Colorado

STAQ Pharma Inc

Quality Control Technician

Denver, CO · On-site

$24/hr

Support quality management system activities, including document control, training program support ... Pharmaceutical, medical device, biotechnology, laboratory, sterile manufacturing, or regulated ...

Tolmar

Quality Control Planner

Fort Collins, CO · On-site

$39 - $40.50/hr

The QC Planner is responsible for the management, planning and coordination of samples in the QC laboratory. This position will coordinate and communicate across QC and other departments to organize ...

Prescott's, Inc

Quality Control Specialist

Monument, CO · On-site

$60K - $65K/yr

As a Quality Control Specialist, you're the last line of defense between our precision microscopes ... Proficiency in Microsoft Office Suite (Excel) and other quality management software. * Must be able ...

Prescott's, Inc

Quality Control Specialist

Monument, CO · On-site

$60K - $65K/yr

As a Quality Control Specialist, you're the last line of defense between our precision microscopes ... Proficiency in Microsoft Office Suite (Excel) and other quality management software. * Must be able ...

Prescott's, Inc

Quality Control Specialist

Monument, CO · On-site

$60K - $65K/yr

As a Quality Control Specialist, you're the last line of defense between our precision microscopes ... Proficiency in Microsoft Office Suite (Excel) and other quality management software. * Must be able ...

Brannan Companies

Quality Control Technician

Denver, CO

$22 - $24/hr

Quality Control Manager FLSA Status: Full Time Location: Denver Area Plant and Jobsite Locations Position Summary : This position involves the performance and record keeping for quality control tests ...

TotalEnergies

QC Chemist

Grand Junction, CO · On-site

... management of abnormalities or changes against historical norms • Maintain laboratory schedule to ensure QC chemist coverage • Ensure data is available to not delay shipping paperwork • ...

New

Loenbro

QA/QC Manager (Electrical)

Aurora, CO · On-site

Job Title: QA/QC Manager (Electrical) Company: Loenbro, LLC Business Unit/Department: Quality Control Location: Front Range, CO / On-site Reports to: QA/QC Director Employment Type: Full-Time FLSA ...

Loenbro

QA/QC Manager (Electrical)

Aurora, CO · On-site

Job Title: QA/QC Manager (Electrical) Company: Loenbro, LLC Business Unit/Department: Quality Control Location: Front Range, CO / On-site Reports to: QA/QC Director Employment Type: Full-Time FLSA ...

CRH

Quality Control Technician

Canon City, CO · On-site

$18 - $22/hr

Report non-conformance to management, following Quality Control Plan requirements * Investigate, analyze, and recommend action to be taken related to quality control, production, and technical ...

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Manager Biotech Quality Control information

What does a manager biotech quality control do?

A Manager Biotech Quality Control oversees the quality assurance processes within a biotechnology company, ensuring that products meet regulatory standards and internal specifications. They manage teams responsible for testing raw materials, in-process samples, and finished products, and analyze data to identify trends or issues. This role also involves setting quality control policies, training staff, and liaising with regulatory bodies to maintain compliance. Managers in this field play a crucial role in product safety and efficacy, directly impacting the success of biotech products in the market.

What are the key skills and qualifications needed to thrive as a manager biotech quality control?

To thrive as a Manager Biotech Quality Control, you need a strong background in biology or chemistry, extensive knowledge of quality assurance regulations, and typically a bachelor’s or master’s degree in a life science field. Familiarity with laboratory information management systems (LIMS), GMP (Good Manufacturing Practices), and certifications such as ASQ or Six Sigma are highly valued. Leadership, attention to detail, and strong problem-solving and communication skills help you guide teams and ensure compliance. These skills and qualities are critical for maintaining product quality, regulatory adherence, and the overall success of biotech manufacturing operations.

What are the most common challenges faced by a manager biotech quality control, and how are they typically addressed?

Managers in Biotech Quality Control often face challenges such as ensuring regulatory compliance, maintaining rigorous documentation, and managing a team with diverse expertise. Keeping up-to-date with changing industry standards and regulatory requirements is crucial, as is fostering a culture of continuous improvement and clear communication. These challenges are typically addressed through ongoing staff training, implementing robust quality management systems, and close collaboration with other departments like R&D and manufacturing to ensure that quality standards are consistently met.

What is the difference between Manager Biotech Quality Control vs Quality Control Specialist?

AspectManager Biotech Quality ControlQuality Control Specialist
CredentialsBachelor's/Master's in Life Sciences, Quality Certifications (e.g., CQE)Bachelor's in Life Sciences or related field, Quality Certifications preferred
Work EnvironmentOversees QC teams, manages testing processes, and ensures compliancePerforms testing, data analysis, and reports results
Employer & Industry UsageBiotech companies, pharmaceutical firms, contract labsBiotech, pharma, and manufacturing sectors

The Manager Biotech Quality Control typically oversees testing teams and ensures compliance with quality standards, while the Quality Control Specialist focuses on executing tests and analyzing data. Both roles require relevant scientific credentials, but the manager has additional responsibilities in team leadership and process management.

What are popular job titles related to Manager Biotech Quality Control jobs in Colorado?

For Manager Biotech Quality Control jobs in Colorado, the most frequently searched job titles are:

What job categories do people searching Manager Biotech Quality Control jobs in Colorado look for?

The top searched job categories for Manager Biotech Quality Control jobs in Colorado are:

What cities in Colorado are hiring for Manager Biotech Quality Control jobs?

Cities in Colorado with the most Manager Biotech Quality Control job openings:

Manager Biotech Quality Control jobs near you
Infographic showing various Manager Biotech Quality Control job openings in Colorado as of August 2026, with employment types broken down into 1% As Needed, 80% Full Time, 15% Part Time, 3% Contract, and 1% Nights. Highlights an 88% Physical, 3% Hybrid, and 9% Remote job distribution.

Quality Control Microbiology Analyst

Agilent

Frederick, CO • On-site

$27.15 - $42.43/hr

Full-time

This job post has expired 1 day ago. Applications are no longer accepted.

Agilent Technologies rating

8.2

Company rating: 8.2 out of 10

Based on 41 frontline employees who took The Breakroom Quiz

89th of 540 rated manufacturers

Job description

Job Description
The world's most revolutionary biopharma companies are partnering with Agilent Technologies to advance the next frontier of medicine. Agilent continues to invest in capacity and expansion of its Colorado operations. Join our team of professionals dedicated to the development and commercialization of nucleic acid therapeutics for life changing, lifesaving medicines.
We are seeking a detail-oriented and experienced Quality Control Microbiology Analyst to join our growing Quality team. In this role, you will support product release, stability testing, environmental monitoring, and cleaning verification activities under cGMP and GLP conditions. You'll play a key part in ensuring the quality and safety of pharmaceutical products while maintaining strict compliance with FDA, ICH, and international regulatory standards.
Key Responsibilities
  • Conduct routine and non-routine microbiological and analytical testing in accordance with Standard Operating Procedures (SOPs) and current Good Manufacturing Practices (cGMPs)
  • Perform testing for Active Pharmaceutical Ingredients (APIs), final drug products, and in-process samples
  • Review and interpret data to ensure compliance with product specifications; troubleshoot and escalate abnormalities as necessary
  • Conduct environmental monitoring, cleaning verification, and stability testing
  • Ensure laboratory equipment is functioning properly and initiate corrective actions as needed
  • Maintain thorough and accurate documentation following Good Documentation Practices (GDP)
  • Communicate effectively with project managers and internal stakeholders regarding test results, timelines, and any issues
  • Participate in the continuous improvement of laboratory processes, procedures, and quality systems
  • Collaborate cross-functionally to meet project timelines and operational goals

Wednesday-Saturday Shift. 9a.m.-7p.m.
Qualifications
Required:
  • Secondary Education with QC experience
  • Knowledge of analytical equipment and instrumentation

Desired:
  • Bachelor's of Science (Microbiology, Life Sciences, or related field)
  • One year of experience in a Quality Control laboratory setting, preferably in the pharmaceutical or biotechnology industry
  • Knowledge of cGMP guidelines as well as international regulations
  • Knowledge of FDA regulations and guidelines
  • Personal leadership skills and fosters working in a team environment
  • Knowledge of and skills in using computer software and hardware applications, including Microsoft Word and Excel
  • Familiarity with a wide range of microbiological and analytical techniques below is preferred:
    • Bacterial Endotoxin Testing (LAL Analysis)
    • Bioburden Testing (Membrane Filtration)
    • Total Organic Carbon (TOC) Testing
    • Compressed Gas Monitoring
    • Environmental Monitoring
    • UV Analysis
    • USP <61> testing

Additional Details
This job has a full time weekly schedule. Applications for this job will be accepted until at least July 7, 2026 or until the job is no longer posted.
The full-time equivalent pay range for this position is $27.15 - $42.43/hr plus eligibility for bonus, stock and benefits. Our pay ranges are determined by role, level, and location. Within the range, individual pay is determined by work location and additional factors, including job-related skills, experience, and relevant education or training. During the hiring process, a recruiter can share more about the specific pay range for a preferred location. Pay and benefit information by country are available at: https://careers.agilent.com/locations
Agilent Technologies, Inc. is an Equal Employment Opportunity and merit-based employer that values individuals of all backgrounds at all levels. All individuals, regardless of personal characteristics, are encouraged to apply. All qualified applicants will receive consideration for employment without regard to sex, pregnancy, race, religion or religious creed, color, gender, gender identity, gender expression, national origin, ancestry, physical or mental disability, medical condition, genetic information, marital status, registered domestic partner status, age, sexual orientation, military or veteran status, protected veteran status, or any other basis protected by federal, state, local law, ordinance, or regulation and will not be discriminated against on these bases. Agilent Technologies, Inc., is committed to creating and maintaining an inclusive in the workplace where everyone is welcome, and strives to support candidates with disabilities. If you have a disability and need assistance with any part of the application or interview process or have questions about workplace accessibility, please email [email protected] or contact +1-262-754-5030. For more information about equal employment opportunity protections, please visit www.agilent.com/en/accessibility.
Travel Required:
Occasional
Shift:
Day
Duration:
No End Date
Job Function:
Quality/Regulatory

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