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Qc Biotech Jobs (NOW HIRING)

QC Inspector

Bothell, WA · 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. Minimum Education: Bachelor's degree in a related field strongly ...

QC Analyst III

Piscataway, NJ · On-site

$24 - $32.25/hr

Bachelor's degree in biotechnology, biochemistry, chemistry, or related field with a minimum of 10 years of experience in a pharmaceutical/biotech QC laboratory. Alternatively, master's degree in ...

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 ...

QC Analyst III

Piscataway, NJ · On-site

$24 - $32.25/hr

... in biotechnology, biochemistry, chemistry, or related field with a minimum of 10 years of ... QC laboratory. Alternatively, master's degree in above areas with 8 years of experience in a ...

QC Inspector

Bothell, WA · 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 ...

QC Inspector

Bothell, WA · 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 ...

QC Analyst II

Piscataway, NJ · On-site

$24 - $32.25/hr

... biotech QC laboratory. Experience: • Previous experience in a cGMP laboratory. • Strong ... background in small molecule and protein chemistry and experience troubleshooting analytical ...

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 Analyst II

Piscataway, NJ · On-site

$24 - $32.25/hr

Bachelor's degree in biotechnology, biochemistry, chemistry, or related field with a minimum of 8 years of experience in a pharmaceutical/biotech QC laboratory. Alternatively, Master's degree in ...

Quality Control Technician

Minneapolis, MN

$19.50 - $25/hr

The Quality Control Technician works hands-on with porcine tissues, prepares and processes ... Interest in working in a biotech environment with opportunities for advancement to Technician II ...

Experience in the medical device or biotechnology industry with a technical background is preferred. * Knowledge of Good Manufacturing Practices (GMP) and quality control principles in a regulated ...

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Qc Biotech information

See salary details

$30.5K

$81.3K

$129.5K

How much do qc biotech jobs pay per year?

As of Jun 30, 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 are the key skills and qualifications needed to thrive as a QC Biotech, and why are they important?

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 is a QC Biotech professional?

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 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.

What is QC in biotech?

QC in biotech refers to Quality Control, which involves testing and inspecting products, raw materials, and processes to ensure they meet regulatory standards and quality specifications. QC professionals use techniques like laboratory testing, data analysis, and documentation to maintain product safety and efficacy throughout manufacturing. Certification in laboratory practices and attention to detail are important in this role.

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 jobs pay 500,000 a year in the US?

In biotech and related fields, senior executive roles such as Chief Scientific Officer, Vice President of R&D, or Chief Executive Officer can earn $500,000 or more annually, especially in large companies or with significant stock options and bonuses. High-level roles often require advanced degrees, extensive experience, and leadership skills, with compensation packages including salary, bonuses, and equity. These positions are typically found in established biotech firms, pharmaceutical companies, or biotech divisions of large corporations.

What is the highest paying job in biotech?

In biotech, senior roles such as Biotech Executive, Director of Research, or Vice President of R&D tend to be the highest paying positions, often earning six-figure salaries. These roles typically require extensive experience, advanced degrees, and leadership skills, and may involve overseeing multiple projects or departments within biotech companies.

Which pays more, QA or QC?

In biotech, QA (Quality Assurance) roles often have higher salaries than QC (Quality Control) positions due to their focus on process improvement and compliance management. QA jobs typically require more experience and may involve oversight, documentation, and regulatory knowledge, which can lead to higher pay. However, salaries vary based on experience, certifications, and company size.
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 June 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.
QC Inspector

$41K - $66K/yr

Full-time

Medical, Dental, Life, Retirement, PTO

Posted 27 days ago


Bruker rating

7.4

Company rating: 7.4 out of 10

Based on 17 frontline employees who took The Breakroom Quiz


Job description

 
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.
 
 

The scope of this position is includes performing all necessary quality control checks, including FAI's and associated reports (First Article Inspection & Reports), 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 3 years of experience as a QC inspector in a regulated environment i.e. medical device/ biotechnology/ aerospace industry.

Minimum Education: 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 : 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 with export control laws and as a result, all interviewed candidates for all positions will be screened pre-interview to determine their eligibility in light of export control restrictions


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