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Qc Analyst Ii Jobs (NOW HIRING)

Quality Control Analyst II

Rensselaer, NY ยท On-site

$23.75 - $32/hr

Quality Control Analyst II Location: Rensselaer, NY Shift: This role is an overnight 12-hour rotating shift position . Our client is a global contract development and manufacturing organization (CDMO ...

Quality Control Analyst II

Rensselaer, NY

$23.75 - $32/hr

Quality Control Analyst II in Rensselaer, NY - Nights Build your future at Curia, where our work has the power to save lives Curia is a global contract development and manufacturing organization ...

Quality Control Analyst II

Rensselaer, NY ยท On-site

$23.75 - $32/hr

Quality Control Analyst II in Rensselaer, NY - Nights Build your future at Curia, where our work has the power to save lives Curia is a global contract development and manufacturing organization ...

Quality Control Analyst II

Rensselaer, NY

$23.75 - $32/hr

Quality Control Analyst II in Rensselaer, NY - Nights Build your future at Curia, where our work has the power to save lives Curia is a global contract development and manufacturing organization ...

QC Analyst II

Durham, NC ยท On-site

$23.25 - $31.25/hr

QC Analyst II requires Bachelor's degree as described and 2+ years' experience or Master's Degree with 0+ years' experience. Senior QC Analyst requires Bachelor' degree as described and 4+ years ...

QC Analyst II

Durham, NC ยท On-site

$23.25 - $31.25/hr

QC Analyst II requires Bachelor's degree as described and 2+ years' experience or Master's Degree with 0+ years' experience. Senior QC Analyst requires Bachelor' degree as described and 4+ years ...

Quality Control Analyst II Location: This position is based in our Walkersville, MD office. The typical work schedule is Monday through Friday, 8:00 AM-5:00 PM EST. What you will get: The full-time ...

QC Analyst II (Chemistry)

Rensselaer, NY ยท On-site

$30 - $47/hr

QC Analyst II Albany, NY Pay Range: $30-47/hr Available Shifts: โ€ข 1st Shift - 6am-6:30p on a 2-2-3 rotating schedule (every other weekend) โ€ข 3rd Shift - 6pm-6:30am on a 2-2-3 rotating schedule ...

Quality Control Analyst II

Walkersville, MD ยท On-site

$70K - $81K/yr

Quality Control Analyst II Location: This position is based in our Walkersville, MD office. The typical work schedule is Monday through Friday, 8:00 AM-5:00 PM EST. What you will get: The full-time ...

QC Analyst II

Sellersville, PA ยท On-site

$23.25 - $31.25/hr

For more details, please visit : www.piramalpharmasolutions.com Job Title QC Analyst II The Chemistry Analyst II performs routine analytical testing using Liquid Chromatography (LC) and Gas ...

QC Analyst II

Sellersville, PA ยท On-site

$23.25 - $31.25/hr

For more details, please visit : www.piramalpharmasolutions.com Job Title QC Analyst II The Chemistry Analyst II performs routine analytical testing using Liquid Chromatography (LC) and Gas ...

QC Analyst II

Piscataway, NJ

$24 - $32.25/hr

Description Position Summary The QC Analyst II will be responsible for analytical testing and data verification supporting both late-stage clinical and commercial small molecule and biosimilar ...

QC Analyst II

Piscataway, NJ ยท On-site

$24 - $32.25/hr

Job Type Full-time Description Position Summary The QC Analyst II will be responsible for analytical testing and data verification supporting both late-stage clinical and commercial small molecule ...

Quality Control Analyst II

Brooklyn Park, MN ยท On-site

$25 - $33.50/hr

As a Quality Control Analyst II, you will execute and review routine in-process, drug substance, and stability test methods in a timely manner. You will use a variety of laboratory instrumentation ...

Quality Control Analyst II

Social Circle, GA ยท On-site

$25.75 - $34.75/hr

As a Quality Control Analyst II, you will perform compendial assessments to ensure compliance with current regulatoryrequirements and pharmacopeial standards. You will author and review technical ...

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Qc Analyst Ii information

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How much do qc analyst ii jobs pay per hour?

As of Jul 16, 2026, the average hourly pay for qc analyst ii 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 are the key skills and qualifications needed to thrive as a QC Analyst II, and why are they important?

To thrive as a QC Analyst II, you need a strong background in analytical chemistry, laboratory techniques, and a relevant science degree such as Chemistry or Biochemistry. Familiarity with laboratory information management systems (LIMS), techniques like HPLC, GC, and experience with GMP/GLP regulations and certifications are typically required. Attention to detail, problem-solving, and effective communication are critical soft skills for accurately analyzing data and reporting findings. These skills and qualifications are essential to ensure product quality, regulatory compliance, and efficient laboratory operations in quality control environments.

What are QC Analyst II?

A QC Analyst II is a mid-level quality control professional responsible for conducting laboratory tests to ensure products meet established standards and specifications. They analyze samples, document results, troubleshoot issues with testing equipment, and help maintain compliance with regulatory guidelines. Typically, a QC Analyst II has more experience than an entry-level analyst and may train junior staff or assist in method validation. Their work is essential in industries like pharmaceuticals, biotechnology, and food manufacturing to ensure product safety and quality.

What is the difference between Qc Analyst Ii vs Qc Analyst I?

AspectQc Analyst IQc Analyst II
Required CertificationsTypically less experience, may require basic quality assurance certificationsMore experience, often requires advanced certifications like ASQ CQE or equivalent
Work EnvironmentEntry-level, supervised tasks in laboratory or manufacturing settingsMore independent, complex testing, and data analysis in similar environments
Job ResponsibilitiesPerform routine tests, document results, support quality checksAnalyze data, troubleshoot issues, oversee testing procedures
Employer & Industry UsageCommon in manufacturing, pharmaceuticals, biotechSimilar industries, with increased responsibility and expertise

The main difference between a Qc Analyst I and a Qc Analyst II lies in experience, responsibilities, and certifications. Qc Analyst II roles typically require more expertise, independent work, and advanced certifications, reflecting a higher level of proficiency within the same industry and work environment.

How does a QC Analyst II typically collaborate with other departments in a pharmaceutical or biotech company?

As a QC Analyst II, collaboration with departments such as Quality Assurance, Manufacturing, and Research & Development is frequent and essential. You may be involved in cross-functional meetings to discuss test results, troubleshoot deviations, or help validate new methods or equipment. Effective communication and teamwork are critical, as your data and insights directly impact product release and compliance. These collaborations not only enhance your technical expertise but also provide valuable exposure to broader business processes, supporting career development.
More about Qc Analyst Ii jobs
What cities are hiring for Qc Analyst Ii jobs? Cities with the most Qc Analyst Ii job openings:
What states have the most Qc Analyst Ii jobs? States with the most job openings for Qc Analyst Ii jobs include:
Infographic showing various Qc Analyst Ii job openings in the United States as of July 2026, with employment types broken down into 33% Full Time, and 67% 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 II

Quality Control Analyst II

Mj3 Partners, Inc.

Rensselaer, NY โ€ข On-site

$23.75 - $32/hr

Full-time

Retirement

Re-posted 27 days ago


Job description


Quality Control Analyst II
Location: Rensselaer, NY
Shift: This role is an overnight 12-hour rotating shift position.
Our client is a global contract development and manufacturing organization (CDMO) with over 30 years of experience partnering with pharmaceutical and biotech companies to provide life-saving treatments to patients.
Requirements
Position overview
The Quality Control Analyst II is responsible for performing routine and non-routine analytical chemistry assays of raw materials, in-process samples, finished APIs, and stability samples. This role also participates in special projects, method development/transfers and cleaning study qualifications.
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
Essential job duties
  1. Perform analytical testing for incoming,in-process and final products, and stability samples using equipment suchas balances, pipettes, pH meter, UV/Visible spectrophotometer, TotalOrganic Carbon analyzer, etc.
  2. Perform chromatography (HPLC/GC, UPLC) withminimal qualification and training, wet chemistry assays, analyticalchemistry assays, HPLC, GC, IR, UV, etc. and raw material testing and/orsampling
  3. Back up for QC analytical instrumentmaintenance and calibration
  4. Perform QC general laboratory equipmentmaintenance, laboratory housekeeping and preparation of the laboratory foraudits
  5. Perform or assist with QC methodqualifications, transfers and validations
  6. Perform QC method development
  7. Perform OOS investigations and lab deviationinvestigations
  8. Provide technical support for shiftanalysts
  9. Perform cleaning validation studies
  10. Assist with the evaluation of new equipmentand processes
  11. Assist in the review of QC data and providesummaries to management as needed
  12. Assist QC Management, as needed, in thecompletion of OOS, deviations, and CAPAs investigations for QC
  13. Backup for QC analytical sample receipt forinternal testing, outside laboratory testing, login, processing, shipment,tracking, distribution of test results, and closure

Education, experience, certification and licensures Required
โ€ข Bachelor's degree in Chemistry or related field
โ€ข Minimum 3-5 years' experience in pharmaceutical industry environment or equivalent combination of education and experience
Preferred
โ€ข Experience working in cGMP or GLP pharmaceutical industry environment
Knowledge, skills and abilities
  1. Excellent verbal and written communicationskills, including the ability to effectively present information andrespond to questions from groups of managers, clients, customers, and thegeneral public
  2. Ability to meet deadlines and work underpressure with limited supervision
  3. Strong time management and organizationalskills with the ability to multi-task and manage multiple projectsindependently
  4. Ability to read, analyze, and interpretgeneral business periodicals, professional journals, technical procedures,or governmental regulations
  5. Ability to write reports, businesscorrespondence, and procedure manuals
  6. Ability to apply advanced mathematicalconcepts such as exponents, logarithms, quadratic equations, andpermutations
  7. Ability to apply mathematical operations tosuch tasks as frequency distribution, determination of test reliabilityand validity, analysis of variance, correlation techniques, samplingtheory, and factor analysis
  8. Ability to define problems, collect data,establish facts, and draw valid conclusions
  9. Ability to interpret an extensive variety oftechnical instructions in mathematical or diagram form and deal withseveral abstract and concrete variables
  10. Proficient use of computer software,including Microsoft Office Suite and instrument manufacture-based systems
  11. Knowledgeable in FDA GMPs (21 CFR, 211, 820,and/or 600); ISO 9001 and 13485 a plus

Our client proudly offers
  • Generous benefit options (eligible first dayof employment)
  • Paid training, vacation and holidays(vacation accrual begins on first day of employment)
  • Career advancement opportunities
  • Education reimbursement
  • 401K program with matching contributions
  • Learning platform
  • And more!

Physical requirements
The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
While performing the duties of this job, the employee is regularly required to stand; walk; or sit; use hands to finger, handle, or feel; and talk or hear. The employee frequently is required to reach with hands and arms. The employee is occasionally required to climb or balance; and stoop, kneel, crouch, or crawl. The employee must occasionally lift and/or move up to 50 pounds. Specific vision abilities required by this job include close vision, and ability to adjust focus.
Work environment
The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
While performing the duties of this job, the employee has the potential of being exposed to fumes or airborne particles and toxic or caustic chemicals (wearing proper Personal Protective Equipment will be required in these situations). The employee is occasionally exposed to wet and/or humid conditions; moving mechanical parts; high, precarious places; outside weather conditions; and risk of electrical shock (always being aware of one's environment and taking proper precautions is required). The noise level in the work environment is usually moderate.
Employee will be responsible for generating hazardous waste for treatment, storage and disposal. Affected employee will need to be familiar with the applicable training requirements included in the Resources, Conservation and Recovery Act. Employee will understand waste labeling, secondary containment, chemical compatibility, storage time limits, container size and quantity limits, container integrity when waste is left unattended and improper disposal of hazardous materials.
The above statements are intended to describe the general nature and level of work performed by people assigned to this classification. They are not intended to be construed as an exhaustive list of all job duties performed by the personnel as classified. Management reserves the right to revise or amend duties at any time.
Pay Range:$63,000 - $79,000
All interested applicants must apply online. Please be aware of scammers. Our client will only send offer letters and requests for sensitive personal information from a company email address. Our client is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability. Our client is an E-Verify employer.