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Qc Biotech Jobs (NOW HIRING)

QC Inspector

Bothell, WA ยท On-site

$41K - $66K/yr

At least 3 years of experience as a QC inspector in a regulated environment i.e. medical device/ biotechnology/ aerospace industry. Qualifications Minimum Education: Bachelor's degree in a related ...

Who is Omeros? Omeros is an innovative biotechnology company that discovers, develops, and ... Lead Quality Control (QC) activities for clinical and commercial products, including management of ...

Who is Omeros? Omeros is an innovative biotechnology company that discovers, develops, and ... Lead Quality Control (QC) activities for clinical and commercial products, including management of ...

QC Inspector

Bothell, WA ยท On-site

$37K - $66K/yr

At least 3 years of experience as a QC inspector in a regulated environment i.e. medical device/ biotechnology/ aerospace industry. Qualifications Minimum Education: Bachelor's degree in a related ...

Experience working in a GMP-regulated pharmaceutical, biotech, or manufacturing environment * Working knowledge of: * cGMP * SOPs * QC testing and documentation * Environmental Monitoring * Strong ...

... biotechnology and medical devices. This means we have the resources to support you within this ... quality control specifications Set up instruments and conduct sample tests; utilize a variety of ...

Quality Control Inspector

Camarillo, CA ยท On-site

$22 - $24/hr

S. and Europe, we supply global pharmaceutical and biotech companies with the critical tools they ... Job Summary The Quality Control Inspector inspects materials, parts, and products at different ...

QC Microbiologist

Seminole, FL ยท On-site

$23 - $30.25/hr

Quality Control Microbiology Supervisor Overview: Quality Control (QC) Microbiology Supervisor ... Minimum 5 years of hands-on experience in a cGMP pharmaceutical or biotech microbiology laboratory ...

Sr. QC Manager

Waltham, MA ยท On-site

$150 - $170/hr

... biotechnology and clinical systems, including point-of-care (POC) and in vitro diagnostic (IVD ... The Sr. Quality Control Manager will develop and execute comprehensive quality control strategies ...

Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest ... Specialist QC What you will do Let's do this. Let's change the world. In this vital role you will ...

Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest ... Specialist QC What you will do Let's do this. Let's change the world. In this vital role you will ...

$95 - $125/hr

Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest ... Specialist QC What you will do Let's do this. Let's change the world. In this vital role you will ...

Specialist QC

West Greenwich, RI ยท On-site

$95 - $125/hr

Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest ... Specialist QC What you will do Let's do this. Let's change the world. In this vital role you will ...

Bachelor's or Master's Degree in Biology, Immunology or a related Science field * 4 to 6 years of biotech industry experience related to Quality Control * 2 years of experience supervising or leading ...

Lead QC Microbiologist

Lexington, KY ยท On-site

$25.25 - $33.25/hr

Bachelor's degree in Microbiology, Biology, Biotechnology, or a related scientific discipline required. * Five or more years of QC microbiology experience in a pharmaceutical, biotechnology, medical ...

Lead QC Microbiologist

Lexington, KY ยท On-site

$25.25 - $33.25/hr

Bachelor's degree in Microbiology, Biology, Biotechnology, or a related scientific discipline required. * Five or more years of QC microbiology experience in a pharmaceutical, biotechnology, medical ...

Showing results 41-60

Qc Biotech information

See salary details

$30.5K

$81.3K

$129.5K

How much do qc biotech jobs pay per year?

As of Sep 2, 2026, the average yearly pay for 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 a QC Biotech?

A QC (Quality Control) Biotech professional is responsible for ensuring that biotechnology products, such as pharmaceuticals, vaccines, or biologics, meet strict quality and safety standards. They perform laboratory tests, analyze samples, and document results to ensure compliance with regulatory guidelines. QC Biotech professionals play a crucial role in maintaining the integrity of products before they reach the market, working closely with other departments to resolve any quality issues. Their work helps protect patient safety and supports the success of biotech companies.

What are the key skills and qualifications needed to thrive as a QC Biotech?

To thrive as a QC Biotech, you need a solid background in biology, chemistry, and laboratory techniques, usually supported by a degree in life sciences or a related field. Familiarity with analytical instruments such as HPLC, PCR, and ELISA, as well as GMP regulations and LIMS software, is typically required. Attention to detail, strong problem-solving abilities, and effective teamwork are crucial soft skills for this role. These skills and qualities ensure accurate testing, regulatory compliance, and the integrity of biotechnological products.

What are some common challenges faced by QC Biotech professionals and how can they be addressed?

QC Biotech professionals often encounter challenges such as adapting to rapidly changing regulatory standards, troubleshooting complex assay discrepancies, and maintaining precise documentation under tight deadlines. Addressing these challenges requires continuous learning, strong attention to detail, and effective collaboration with cross-functional teams like R&D and manufacturing. Leveraging robust Standard Operating Procedures and clear communication with colleagues can help ensure consistent results and regulatory compliance.

What is the difference between Qc Biotech vs Qc Microbiologist?

AspectQc BiotechQc Microbiologist
Required CredentialsBachelor's in Biology, Biotechnology, or related field; GMP/GxP trainingBachelor's in Microbiology, Biology, or related; microbiology certifications
Work EnvironmentBiotech manufacturing labs, quality control departmentsMicrobiology labs, pharmaceutical or biotech settings
Employer & Industry UsageBiotech companies, pharmaceutical manufacturersPharmaceutical firms, biotech research labs
Common Search & ComparisonYesYes

While both Qc Biotech and Qc Microbiologist roles involve quality testing in biotech and pharmaceutical settings, Qc Biotech focuses on overall product quality, including assays and validation, whereas Qc Microbiologists specialize in microbiological testing and contamination control. The roles often overlap but differ in specific expertise and focus areas.

More about Qc Biotech jobs

What cities are hiring for Qc Biotech jobs?

Cities with the most Qc Biotech job openings:

What are the most commonly searched types of Qc Biotech jobs?

The most popular types of Qc Biotech jobs are:

What states have the most Qc Biotech jobs?

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

Infographic showing various Qc Biotech job openings in the United States as of August 2026, with employment types broken down into 1% Internship, 1% As Needed, 88% Full Time, 6% Part Time, 3% Contract, and 1% Nights. Highlights an 93% Physical, 3% Hybrid, and 4% Remote job distribution, with an average salary of $81,324 per year, or $39.1 per hour.

QC Inspector

UNAVAILABLE

Bothell, WA โ€ข On-site

$41K - $66K/yr

Full-time

Medical, Dental, Life, Retirement, PTO

Re-posted 2 days ago


Job description

Overviewย As one of the world's leading analytical instrumentation companies, Bruker covers a broad spectrum of advanced solutions in all fields of research and development. All our systems and instruments are designed to improve safety of products, to accelerate time-to-market, and to support industries in successfully enhancing quality of life. We have been driving innovation in analytical instrumentation for over 60 years now. Today, more than 8,500 employees distributed across 90 locations around the world continue to delight our customers with innovative solutions.

Bruker Nano, one of Bruker's four operating segments, provides customers in academic and governmental institutions, life science, materials, and applied industries with the tools to determine the characteristics of matter and visualize the structure of molecules. Divisions within BNANO include Bruker AXS, Bruker Nano Analytics, Bruker Nano Surfaces and Metrology, Fluorescence Microscopy, and Canopy.

The Quality Control Inspector (QCII) is primarily responsible for Quality Control inspections of all Bruker Spatial Biology incoming raw materials, components and sub-assemblies received at our facilities per inspection plan meeting applicable material specifications. QCII is also responsible for all finished instrumentation testing of all final assembled instruments per inspection plan.ย ย Responsibilities

The scope of this position is includes performing all necessary quality control checks, including FAI's and associated reports (First Article Inspection & Reports),ย using appropriate testing procedures and test instrumentation supported with appropriate documentation for all Bruker Spatial Biology products to manage quality risk and provide oversight over manufacturing processes. This position reports into the Sr. Quality Manager which is part of Quality organization and support associated tasks and activities coordinated and integrated with production and inventory control. The individual ensures consistent implementation, improvement, and compliance to the Bruker Spatial Biology, ISO 13485 and ISO 9001 Quality Management Systems.

Responsibilities:

  • Perform timely incoming and final quality control inspections to support Manufacturing and Operations quality for all Bruker Spatial Biology instruments following approved and active Incoming Specifications
  • Update incoming inspection specifications and procedures as required, in collaboration with other cross-functional departments.
  • Record non conformances and support in conducting root cause investigations.
  • Manage nonconforming (or potentially nonconforming) material through disposition.
  • Perform lot validation testing while monitoring and adjusting testing frequencies.
  • Support review and updating of SOPs relating to Quality Control Procedures.
  • Collaborate with Manufacturing, Manufacturing Engineering, New Product Introduction, Procurement, Quality, and Supply Chain partners as well as vendors on the above activities.
  • Basic application of statistical tools and methods
  • Participates in FDA/ISO inspections and customer audits and maintain ongoing audit readiness
  • Perform other relevant duties as may be assigned by management
  • Act as Quality ambassador providing decisive approach for implementation to manage Quality Management System with various tasks, projects, as required

Skills and Abilities:

  • Analytical decision-making skills to apply logical or Quality control thinking principles to operations using pragmatic approaches.
  • Demonstrates working knowledge of ISO 9001, ISO 13485 quality system and/or FDA 21 CFR 820 quality regulations as applicable to products.
  • Analytical and creative problem-solving skills that include experience in leading and or participating on process improvement/lean projects.
  • Excellent written and oral communication skills
  • Ability to work independently and collaboratively in cross-functional teams
  • Ability to multi-task with demonstrated problem solving skills in a fast paced complex environment

Specialized Knowledge:

  • GD&T and CMM skills is preferred
  • At least 3ย years of experience as a QC inspector in a regulated environment i.e. medical device/ biotechnology/ aerospace industry.
Qualifications

Minimum Education:ย Bachelor's degree in a related field strongly preferred OR High school STEM or technical diploma or equivalent BS in technical discipline, real world hands-on regulated industry experience may also be considered.

Minimum Experience :ย 3-5 years quality-related experience in biotech, the pharmaceutical or consumer regulated device industry.

At Bruker, base salary is part of our total compensation. The estimated base salary range for this full-time position is between $41,500 and $66,000 provides an opportunity to progress as you grow and develop within a role. The base salary for the role will depend on a several job-related factors, including, but not limited to education, training, experience, the geographic location of the successful candidate, skills, competencies, job-related knowledge and travel requirements for this position. Full-time employees may also be eligible for a performance-related incentive in addition to a full range of benefits including 401(k) with company match, an employee stock purchase plan, medical and dental plans, life insurance, short-term and long-term disability insurance, employee assistance program and paid time off including vacation, sick time and holidays, and more.

Bruker is an equal-opportunity employer. We evaluate qualified applicants without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, and other legally protected characteristics.

Certain positions at Bruker require compliance withย export control laws and as a result, all interviewed candidates for all positions will be screened pre-interview to determine theirย eligibility in light of export control restrictions

Employment Type: OTHER