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Quality Control Analyst Bioassay Jobs (NOW HIRING)

QC Analyst

Vacaville, CA · On-site

$56K - $93K/yr

The Quality Control (QC) Analyst will act as a team member of the Quality Control department to support production of in-process, drug substance, drug product, raw materials, and stability lots for ...

QC Analyst

Raleigh, IL · On-site

$22.75 - $30.75/hr

QC Analyst At Guerbet, we build lasting relationships so that to enable people to live better . This is Our Purpose. We are a global leader in medical imaging, offering an extensive portfolio of ...

QC Analyst

Vacaville, CA · On-site

$56K - $93K/yr

The Quality Control (QC) Analyst will act as a team member of the Quality Control department to support production of in-process, drug substance, drug product, raw materials, and stability lots for ...

QC Analyst

Raleigh, IL

$22.75 - $30.75/hr

QC Analyst At Guerbet, we build lasting relationships so that to enable people to live better . This is Our Purpose. We are a global leader in medical imaging, offering an extensive portfolio of ...

QC Analyst

Orangeburg, NY · On-site

$21 - $23/hr

Job Title: QC Analyst Location: Orangeburg, NY Type: Contract Compensation: $21-$23/hour Work Model: Onsite - onsite Hours: 2:00 pm -10:30 pm Responsibilities * Perform analyses of Clinical Chemistry ...

Quality Control Analyst

Winchester, KY · On-site

$20.75 - $27.75/hr

Quality Control Analyst Position Summary * Typical working hours are Monday-Friday 3 PM - 11:30 PM. * This position is 100% on-site in Winchester, Kentucky. Catalent's Winchester location is the ...

Quality Control Analyst

Winchester, KY · On-site

$20.75 - $27.75/hr

Quality Control Analyst Position Summary * Typical working hours are on E shift (6 AM- 6 PM Saturday - Monday, every other Tuesday from 6 AM - 2:30 PM) * This position is 100% on-site in Winchester ...

The company is looking for a Sr. QC Associate to join the team. This is an amazing opportunity to ... analytical platforms, including chromatography, potency/bioassays, microbiology, raw materials ...

QC Analyst

Orangeburg, NY · On-site

$21 - $23/hr

Job Title: QC Analyst Location: Orangeburg, NY Type: Contract Compensation: $21-$23/hour Work Model: Onsite - onsite Hours: 2:00 pm -10:30 pm Responsibilities * Perform analyses of Clinical Chemistry ...

QC Analyst

Orangeburg, NY · On-site

$23/hr

Job Title: QC Analyst Location: Orangeburg, NY Type: Contract Compensation: $21-$23/hour Work Model: Onsite - onsite Hours: 2:00 pm -10:30 pm Responsibilities * Perform analyses of Clinical Chemistry ...

QC Analyst

Orangeburg, NY · On-site

$23/hr

Job Title: QC Analyst Location: Orangeburg, NY Type: Contract Compensation: $21-$23/hour Work Model: Onsite - onsite Hours: 2:00 pm -10:30 pm Responsibilities * Perform analyses of Clinical Chemistry ...

QC Analyst

Orangeburg, NY · On-site

$21 - $23/hr

Job Title: QC Analyst Location: Orangeburg, NY Type: Contract Compensation: $21-$23/hour Work Model: Onsite - onsite Hours: 2:00 pm -10:30 pm Responsibilities * Perform analyses of Clinical Chemistry ...

Quality Control Analyst

Winchester, KY · On-site

$20.75 - $27.75/hr

Quality Control Analyst Position Summary * Typical working hours are on E shift (6 AM- 6 PM Saturday - Monday, every other Tuesday from 6 AM - 2:30 PM) * This position is 100% on-site in Winchester ...

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Quality Control Analyst Bioassay information

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$16

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$41

How much do quality control analyst bioassay jobs pay per hour?

As of Jul 2, 2026, the average hourly pay for quality control analyst bioassay in the United States is $27.92, according to ZipRecruiter salary data. Most workers in this role earn between $23.08 and $31.01 per hour, depending on experience, location, and employer.

What is the difference between Quality Control Analyst Bioassay vs Quality Control Analyst Microbiology?

AspectQuality Control Analyst BioassayQuality Control Analyst Microbiology
Required CredentialsBachelor's in Life Sciences, certifications in bioassay techniquesBachelor's in Microbiology or related, microbiology certifications
Work EnvironmentLaboratories performing bioassay testing for biologicsMicrobiology labs testing for contamination and sterility
Industry UsagePharmaceuticals, biotech, biologics manufacturingPharmaceuticals, healthcare, biotech industries

While both roles involve laboratory testing in the pharmaceutical industry, the Quality Control Analyst Bioassay focuses on biological activity testing of biologics, whereas the Quality Control Analyst Microbiology specializes in detecting microbial contamination. Understanding these differences helps employers and candidates identify the right role based on skills and industry needs.

More about Quality Control Analyst Bioassay jobs
What cities are hiring for Quality Control Analyst Bioassay jobs? Cities with the most Quality Control Analyst Bioassay job openings:
What states have the most Quality Control Analyst Bioassay jobs? States with the most job openings for Quality Control Analyst Bioassay jobs include:
What job categories do people searching Quality Control Analyst Bioassay jobs look for? The top searched job categories for Quality Control Analyst Bioassay jobs are:
Infographic showing various Quality Control Analyst Bioassay job openings in the United States as of June 2026, with employment types broken down into 60% Full Time, 20% Temporary, and 20% Contract. Highlights an 100% In-person job distribution, with an average salary of $58,065 per year, or $27.9 per hour.
Quality Control Analyst

$24.25 - $32.50/hr

Full-time

Posted 6 days ago


Mallinckrodt rating

8.0

Company rating: 8.0 out of 10

Based on 8 frontline employees who took The Breakroom Quiz

37th of 73 rated pharmaceutical


Job description

Company Description
Who We Are:
Mallinckrodt Pharmaceuticals is a multibillion dollar specialty pharmaceutical company focused on our mission: Managing Complexity. Improving Lives. We provide medicines to address unmet patient needs, stemming from 150 years of using our unique strengths, experience and expertise to help improve people's lives. Discover how our rich history of innovation and patient-centered solutions has helped influence our vision for the future.
What We Do:
Our strong ability to master and manage complexity is the key component in making high-quality products that provide value for patients. Mallinckrodt's growing portfolio of specialty pharmaceuticals help treat a wide variety of health conditions. We invest in areas such as autoimmune and rare diseases; immunotherapy and neonatal respiratory critical care therapies; analgesics and hemostasis products. To see what sets Mallinckrodt apart, take a look at our distinctive approach to solving complex challenges with unique solutions.
What We Believe In:
People throughout the world count on Mallinckrodt products every day to help them lead healthier lives. That's why we proudly stand by the three values we have held for 150 years: to produce quality products with the utmost integrity and unparalleled service in order to better serve the patients, customers and communities in which we live and work. Explore the roles of our dedicated employees and our commitment to responsibility.
At Mallinckrodt Pharmaceuticals, our five Cultural Hallmarks guide our work and serve as a foundation for our success. Employees are Accountable, Competitive, Collaborative, High Performing and Trustworthy.Our Culture
  • ACCOUNTABLE - We are each personally responsibility for ensuring Mallinckrodt's success
  • COMPETITIVE - We value breakthrough thinking that leads to industry leadership
  • COLLABORATIVE - We work together to create solutions
  • HIGH PERFORMING - We deliver on our commitments
  • TRUSTWORTHY - We consistently model our values

Job Description
The Quality Control (QC) Analyst will work both independently and within a team to perform daily analysis of in-process samples, finished product and raw materials via established test methods while following cGMP and GDP in the QC laboratory. Typical analysis consists of pH, Osmolality, ELISA, PCR, sterility, UV/Vis spectroscopy and other general chemical and bioanalytical assays.
Principal Responsibilities
  • Conducts routine analysis of in-process samples, finished products, and raw materials according to standard operating procedures (SOPs) and Master Specifications.
  • Utilizes proper aseptic technique during the execution of analysis.
  • Performs stability testing according to established schedules.
  • Documents and investigates any OOS results.
  • Follows cGMP and GDP to perform all tasks.
  • Documents and assesses data against established specifications.
  • Perform inventory, stock and clean QC laboratories.
  • Perform QC review of data records.

Department specific/Non-essential responsibilities:
  • Assist with calibrating and maintaining laboratory equipment.
  • May perform training of new and existing QC team on established methods and procedures
  • May provide technical expertise for method optimization, verification, qualification, and validation.
  • May develop and qualify testing methods and SOPs.
  • May assist with or lead QC projects for process improvements.
  • May draft reports, plans and protocols.
  • May revise and updates SOPs.
  • Additional duties as assigned.

Qualifications
Experience / Skills:
  • Bachelor's degree in a scientific discipline or equivalent and a minimum of three years' related experience required.
  • Knowledge of cGMP is required.
  • Must possess skills and knowledge of general chemical and bioanalytical test methods.
  • Knowledge of ELISA, PCR, UV/Vis spectroscopy, cell culture and aseptic technique is preferred.

Competencies:
  • Attention to detail: able to organize and maintain data and information.
  • Ability to work in a controlled environment with gowning/PPE requirements.
  • Ability to learn through observation and hand's on experience.
  • Ability to work independently in a fast-paced, team oriented organization.
  • Strong written and verbal communication skills.

Additional Information
Organizational Relationship/Scope:
  • Reports to Quality Control leadership team.
  • Work is performed within a team of QC Analysts.
  • Regular communication with QC, manufacturing, technical operations among others.

Working Conditions:
  • 70% laboratory and manufacturing environment
  • 30% normal office and meeting room conditions
  • Must be able to perform work while aseptically gowned with the appropriate PPE

All your information will be kept confidential according to EEO guidelines.

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