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Quality Control Analyst I Jobs (NOW HIRING)

Unicon Pharma Inc

Quality Control Analyst I

Sunrise, FL · On-site

$23 - $30.75/hr

Quality Control Analyst 5 Months (possible extension) Sunrise, FL Shift Scheduled: Monday to Friday ... i.e. safety glasses, gloves, hearing protection, etc.). Fast paced environment. Able to manage ...

Microbiologics

Quality Control Analyst I

Saint Cloud, MN · On-site

$23.75 - $32/hr

We are currently looking to add a Quality Control Analyst to our Operations team in St. Cloud, MN. This entry-level Lab position is responsible for performing core quality control testing and ...

LGC Group

Quality Control Analyst I

Milford, MA · On-site

$26 - $39/hr

Produce and use control charts. Perform tracking and trend analysis on laboratory data. * Performs quality control duties including, but not limited to; daily temperature log entries, emptying ...

LGC Group

Quality Control Analyst I

Milford, MA

$26.25 - $35.25/hr

Produce and use control charts. Perform tracking and trend analysis on laboratory data. * Performs quality control duties including, but not limited to; daily temperature log entries, emptying ...

LGC Group

Quality Control Analyst I

Milford, MA · On-site

$26.25 - $35.25/hr

Produce and use control charts. Perform tracking and trend analysis on laboratory data. * Performs quality control duties including, but not limited to; daily temperature log entries, emptying ...

LGC Group

Quality Control Analyst I

Milford, MA

$26/hr

Produce and use control charts. Perform tracking and trend analysis on laboratory data. * Performs quality control duties including, but not limited to; daily temperature log entries, emptying ...

Werfen

QC Analyst I

Orangeburg, NY · On-site

$22 - $24/hr

Performs analyses of Clinical Chemistry, Co-Oximeter, Coagulation and/or Microbiology controls and ... Performs automated and manual assays as detailed in departmental/plant SOP's and QC Monographs ...

Werfen

QC Analyst I

Orangeburg, NY · On-site

$22 - $24/hr

Position Summary: Performs analyses of Clinical Chemistry, Co-Oximeter, Coagulation and/or ... Performs automated and manual assays as detailed in departmental/plant SOP's and QC Monographs ...

Werfen

QC Analyst I

Orangeburg, NY · On-site

$22 - $24/hr

Performs analyses of Clinical Chemistry, Co-Oximeter, Coagulation and/or Microbiology controls and ... Performs automated and manual assays as detailed in departmental/plant SOP's and QC Monographs ...

Unicon Pharma Inc.

QC Analyst - Portsmouth, NH

Portsmouth, NH · On-site

$24.50 - $32.75/hr

Job Title: QC Analyst I-Microbial Control Summary: * The Quality Microbial Control Analyst 1 will act as a team member of the Quality Microbial Control department to support production of in-process ...

Saxon Global

Quality Control Analyst I

Frisco, TX · On-site

$22.50 - $30.25/hr

Top 5 Qualifications: 1. Gather and analyze documentation. 2. Assemble audit reports and summarize findings. 3. Review and understand contract language and pricing terms. 4. Pharmacy auditing ...

Legend Biotech US

QC Analyst I/II

Raritan, NJ · On-site

$24.50 - $33/hr

Role Overview The QC Analyst is an exempt level position with responsibilities for performing QC testing related to the manufacturing of cell therapy products for clinical trials and commercial ...

Legend Biotech US

QC Analyst I/II

Raritan, NJ · On-site

$24.50 - $33/hr

Role Overview The QC Analyst is an exempt level position with responsibilities for performing QC testing related to the manufacturing of cell therapy products for clinical trials and commercial ...

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

As of Sep 14, 2026, the average hourly pay for quality control analyst i 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 a Quality Control Analyst I?

A Quality Control Analyst I is an entry-level professional responsible for testing and inspecting products, materials, or processes to ensure they meet specific quality standards and regulatory requirements. They typically work in industries such as pharmaceuticals, manufacturing, or food production. Their duties often include performing routine laboratory tests, documenting results, maintaining laboratory equipment, and reporting any deviations or defects. This role is critical in helping companies maintain product consistency, safety, and compliance with industry regulations.

What are some typical challenges faced by a Quality Control Analyst I in ensuring product consistency across multiple batches?

A common challenge for Quality Control Analyst I is maintaining consistency in product quality across different manufacturing batches, especially when dealing with variations in raw materials, equipment calibration, or environmental conditions. Analysts must be vigilant in following standard operating procedures, accurately documenting test results, and promptly identifying any deviations from quality standards. Effective communication with production and quality assurance teams is essential to quickly resolve issues and prevent recurring problems. Over time, analysts develop a keen eye for detail and learn proactive strategies to address these challenges, contributing to improved processes and product reliability.

What are the key skills and qualifications needed to thrive as a Quality Control Analyst I, and why are they important?

To thrive as a Quality Control Analyst I, you need a solid background in laboratory techniques, analytical testing, and a relevant science degree such as chemistry or biology. Familiarity with laboratory information management systems (LIMS), chromatographic instruments (like HPLC), and adherence to regulatory standards such as GMP is typically required. Attention to detail, problem-solving, and strong organizational skills help ensure accuracy and reliability in data analysis and reporting. These competencies are essential to maintain product quality, comply with industry regulations, and support efficient laboratory operations.

What is the difference between Quality Control Analyst I vs Quality Control Technician?

AspectQuality Control Analyst IQuality Control Technician
Required CredentialsBachelor's degree in science or related fieldAssociate's degree or equivalent experience
Work EnvironmentLaboratories, manufacturing facilitiesProduction lines, labs, manufacturing sites
Employer & Industry UsagePharmaceutical, biotech, food industriesManufacturing, pharmaceutical, food sectors
Common Search & ComparisonYesYes

The main difference between a Quality Control Analyst I and a Quality Control Technician lies in their educational requirements and scope of responsibilities. The Analyst I typically holds a bachelor's degree and performs analytical testing, data analysis, and reporting. The Technician often has an associate's degree or equivalent and focuses on sample preparation, equipment operation, and routine testing. Both roles are essential in quality assurance within manufacturing and lab environments, but the Analyst I generally has a broader analytical role with more emphasis on data interpretation.

How much does a quality control analyst earn?

A Quality Control Analyst I typically earns between $40,000 and $55,000 annually, depending on location, industry, and experience. Entry-level roles may start lower, while those with certifications or specialized skills can earn higher salaries.

What cities are hiring for Quality Control Analyst I jobs?

Cities with the most Quality Control Analyst I job openings:

What states have the most Quality Control Analyst I jobs?

States with the most job openings for Quality Control Analyst I jobs include:

What are popular job titles related to Quality Control Analyst I jobs?

For Quality Control Analyst I jobs, the most frequently searched job titles are:

Quality Control Analyst I jobs near you
Infographic showing various Quality Control Analyst I job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 81% Full Time, 13% Part Time, 4% Contract, and 1% Nights. Highlights an 84% Physical, 1% Hybrid, and 15% Remote job distribution, with an average salary of $58,065 per year, or $27.9 per hour.

Quality Control Analyst I

Sunrise, FL • On-site

Unicon Pharma Inc
Recruiting and Staffing Services • 11 - 50 employees
Learn more about Unicon Pharma Incexternal

$23 - $30.75/hr

Contractor

Re-posted 22 days ago

Job description

Quality Control Analyst
5 Months (possible extension)
Sunrise, FL
Shift Scheduled: Monday to Friday 8am 5 pm
Core essential skill sets candidates must have to be considered for the role:
o Bachelor's degree, preferably in Chemistry or Microbiology, or equivalent education/experience
o Minimum of two years experience in a Quality Control in CGMP pharmaceutical, biotechnology or environmental laboratory
o Experience to Labware LIMS V7 and laboratory auditing processes
o Microbiology testing experience on Environmental Samples for surface and air, Purified Water Samples, and RM/FP Microbial Limit Test following USP
o Computer proficiency with comprehensive working knowledge of MS Office products, Learning Management Systems (LMS)
o Ability to communicate effectively with excellent written and oral communication skills for scientific and/or technical ideas
o Acts independently and proactively to recommend methods and procedures for problem resolution
o Self-directed with ability to organize and prioritize work
o Understand Data Integrity (ALCOA+) and laboratory documentation practices
Screenings:
1. Basic Background
2. 11 Panel Drug + Fentanyl
3. Medical Screenings:
a) Vision Screenings - Far, Near, Depth, and Peripheral
b) Vital Signs
c) Whisper Test
d) Lifting Assessment: max 25 pounds
POSITION SUMMARY
This position performs testing of raw materials and drug products, maintenance and calibration of analytical
instruments, prepares standard and sample solutions and maintains appropriate records.
ESSENTIAL AREAS OF RESPONSIBILITY
All areas of responsibility listed below are essential to the satisfactory performance of this position by any
incumbents with reasonable accommodation if necessary. Any non-essential functions are assumed to be included
in other related duties or assignments.
Carries out responsibilities in accordance with the organization's policies, procedures, and state, Federal and
local laws.
Complies with all safety rules and regulations.
Perform analysis on raw materials, finish goods, API, and control substances
Ensures that balances are reviewed and calibrated.
Perform peer review of laboratory testing as required.
Responsible for Wet Chemistry testing (such as LOD, PH, titration, etc.)
Work within a team to meet productions, validation, stability, and request deadlines.
Participates in troubleshooting of analytical test methods and laboratory instruments.
Responsible for completing all training requirements and maintaining 100% compliance with all assignments.
Responsible for maintaining work areas and performing job functions in a safe and efficient manner in
accordance with company policies and procedures, Good Manufacturing Practices (cGMP's), and Standard
Operating Procedures (SOP's) instructions.
Responsible for performing additional related duties as assigned.
POSITION REQUIREMENTS
Any equivalent combination of education, training and/or experience that fulfills the requirements of the position
will be considered.
Education/Certification/Experience:
Requires a Bachelor's degree, preferably in Chemistry or Microbiology, or equivalent education/experience
with a minimum of two years relevant progressive experience in a Quality Control Laboratory environment.
Requires working knowledge of cGMP, DEA and other applicable industry regulatory requirements as they
relate to the production of pharmaceutical products and associated quality systems.
Labware LIMS and/or Empower preferred experience preferred.
Microbiology testing experience preferred.
Skills/Knowledge/Abilities:
Solid understanding of the principles of analytical chemistry as it applies to HPLC, GC, FTIR, UV-Vis and other
general analytical techniques.
Computer proficiency with comprehensive working knowledge of MS Office products, Learning Management
Systems (LMS), ERP systems such as SAP or Oracle and manufacturing/quality systems such as LIMS, Trackwise
and Qdocs.
Ability to effectively communicate scientific and/or technical ideas in writing.
Ability to communicate effectively with excellent written and oral communication skills.
Ability to interact positively and collaborate with co-workers, management and other internal stakeholders.
Self-directed with ability to organize and prioritize work.
Detail oriented with the ability to identify errors and/or inconsistencies while performing tasks.
Business, scientific and personal computer hardware and software applications.
Skill levels in MS Office including proficiency in Word, PowerPoint, Excel and SharePoint.
Must be able to maintain the highest levels of confidentiality, integrity and discretion.
Excellent verbal, written, and interpersonal skills required.
Problem Solving:
Works on problems of moderate scope where evaluation of contributing factors requires analysis of situation
or data.
Exercises judgment within broadly defined practices and policies and selects methods and techniques for
obtaining solutions.
Selects methods, techniques, and evaluation criteria for obtaining results.
Acts independently and proactively to recommend methods and procedures for problem resolution.
Able to identify solutions to general problems through collaboration and creativity.
PHYSICAL REQUIREMENTS
Frequent:
Sitting for extended periods at workstation or mobile equipment.
Standing for extended periods at workstation or equipment.
Using fingers to perform activities such as picking, pinching or typing.
In accordance with the Americans with Disabilities Act, it is possible that requirements may be modified to reasonably accommodate disabled
individuals. However, no accommodations will be made which may pose serious health or safety risks to the employee or others or which impose an undue
hardship on the Company.
The requirements and responsibilities in this position description do not create an employment contract and are not meant to be all-inclusive. The incumbent
is responsible to ensure compliance with all laws, regulations, codes, standards and company policies relevant to this position. This document in no way
states or implies that only the duties described above are to be performed by the incumbent. The incumbent will be expected to follow instructions and
perform duties as required by his or her supervisor and understand that aspects of their position may be changed by the Company on an as-needed basis.
Occasional:
Walking to move short distances quickly and frequently.
Twisting/Reaching turning at waist and extending hands and/or arms in any direction.
Grasping applying pressure to an object with the fingers and palm.
Repetitive Motions (frequent motions of the wrists, hands and/or fingers).
Lifting Rising from lower to upper and/or moving objects horizontally up to 25 lbs.
Visual Acuity:
Close visual acuity to perform activities such as computer work, preparing and analyzing data, extensive
reading, and visual inspection involving small defects, small parts and/or operation of machines (including
inspection), using measurement devices and/or assembly or fabrication of parts at a distance close to the
eyes.
WORKING ENVIRONMENT:
Exposure to fumes, odors, dusts, mists or gasses (for non-office).
Exposure to moving mechanical parts or moving equipment.
Exposure to low to moderate to loud noise levels.
May be required to wear personal protective equipment (PPE) as needed for assigned area and/or process
(i.e. safety glasses, gloves, hearing protection, etc.).
Fast paced environment.
Able to manage multiple priorities and ensure appropriate follow-ups.
Highly organized and excellent time and project management skills with the ability to juggle a wide range.
Ability to work under pressure and meet deadlines