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Entry Level Pharmaceutical Quality Control Jobs (NOW HIRING)

This role offers a comprehensive introduction to the pharmaceutical quality environment, providing ... Understand and analyze QA/QC workflows to create visual process flows and updated Standard ...

QC

Dallas, OR · On-site

$18.75 - $24/hr

Job Level: Entry-level Employment Type: Full Time Annual Salary Range: DOE Reports to: Quality Control Lead Employment Requirements: * Preferred bilingual * Must be able to read and write in English

QC

Dallas, OR · On-site

$15.55 - $17.55/hr

Job Level: Entry-level Employment Type: Full Time Annual Salary Range: DOE Reports to: Quality Control Lead Employment Requirements: * Preferred bilingual * Must be able to read and write in English

QC Chemist

Central Islip, NY · On-site

$65K - $90K/wk

Pharmaceutical Experience Required: 2 to 15 years Compensation: *,000 - *,000 Visa Sponsorship: Not available Remote Option: No Job Overview: We are looking for a dedicated Quality Control Chemist to ...

Our client specializes in pharmaceutical ingredients, Bioscience, Biopharmaceuticals, Custom ... Job Title: QC Specialist II Location: Vacaville, CA, 95688 Duration: 6 Months Job Type: Temporary ...

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Entry Level Pharmaceutical Quality Control information

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$12

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$29

How much do entry level pharmaceutical quality control jobs pay per hour?

As of Sep 2, 2026, the average hourly pay for entry level pharmaceutical quality control in the United States is $20.97, according to ZipRecruiter salary data. Most workers in this role earn between $18.03 and $23.08 per hour, depending on experience, location, and employer.

What is the difference between Entry Level Pharmaceutical Quality Control vs Entry Level Pharmaceutical Quality Assurance?

AspectEntry Level Pharmaceutical Quality ControlEntry Level Pharmaceutical Quality Assurance
Primary FocusTesting and analyzing raw materials, in-process, and finished products to ensure qualityDeveloping, implementing, and maintaining quality systems and procedures
Work EnvironmentLaboratory settings with emphasis on testing and analysisOffice and laboratory settings focusing on documentation and compliance
Required CredentialsTypically a bachelor's in science or related field; certifications like GMP are commonSimilar educational background; GMP knowledge and certifications are also valued

Entry Level Pharmaceutical Quality Control focuses on testing and analyzing products to ensure they meet quality standards, while Entry Level Pharmaceutical Quality Assurance emphasizes establishing and maintaining quality systems and compliance. Both roles require similar educational backgrounds and certifications, but their daily tasks and focus areas differ within the pharmaceutical industry.

What cities are hiring for Entry Level Pharmaceutical Quality Control jobs?

Cities with the most Entry Level Pharmaceutical Quality Control job openings:

What are the most commonly searched types of Pharmaceutical Quality Control jobs?

The most popular types of Pharmaceutical Quality Control jobs are:

What states have the most Entry Level Pharmaceutical Quality Control jobs?

States with the most job openings for Entry Level Pharmaceutical Quality Control jobs include:

Pharmaceutical - Quality Assurance

Integrated Resources INC

San Diego, CA • On-site

Contractor

Re-posted 17 days ago


Job description

Job Description

Job Description:
The individual in this position is responsible for performing day-to-day quality assurance (QA) activities, managing QA processes such as document management, internal audits, instrumentation change control, corrective and preventative actions, and assay validation planning to ensure compliance to GCLP requirements as the Client Oncology Clinical Research Laboratory (POCRL) develops, validates, and performs clinical trial assays. In addition, the position is responsible for providing QA support for clinical trial assay activities, including receipt, accessioning, and internal tracking of clinical trial biospecimens.
RESPONSIBILITIES:
Maintain, troubleshoot, and monitor the effectiveness of the POCRL's Quality Management System (QMS)
Ensure that POCRL activities conform with the requirements of the laboratory QMS
Coordinate creation, approval, implementation, and periodic reviews of Client Standard Operating Procedures for the POCRL according to GCLP guidelines
Review and approve new assay validation plans and reports according to GCLP guidelines with reference to CAP/CLIA regulations for molecular assay validation
Draft, review and approve continuing quality improvement documentation
Maintain laboratory QMS documentation in Client's document management system
Conduct annual QA audits of the POCRL & clinical trial assay processes, document findings, compose and execute Corrective and Preventative Action Plans as appropriate
Coordinate external QA audits as required and advise laboratory director of appropriate corrective actions
Serve as the POCRL's point of contact with clinical Biomarker Assay Specialist groups withing early- and late-clinical development
Ensure that the maintenance/calibration status of POCRL equipment is monitored and current
TECHNICAL SKILLS:
Ability to create and enforce laboratory standard operating procedures
Knowledge of molecular biology and laboratory safety procedures for handling hazardous chemicals and biosafety level 2 biohazard materials
Knowledge of standard molecular biology laboratory equipment
Excellent written and verbal communication skills
Ability to work independently
Ability to interface with clinical research teams
Proficiency with standard office software (Microsoft Office, Adobe Acrobat)
What is the minimum education experience required?:
BS/MS in a biological science, pharmacy, medical technology, or a related field
Medical Technology, MT (ASCP) license or equivalent (preferred)
At least 2 years' experience working in a laboratory setting that included a QMS
Good working knowledge of GCP/GCLP guidelines
Experience working in a GCP/GCLP environment (preferred)

Additional Information

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


Integrated Resources logo

About Integrated Resources

Sourced by ZipRecruiter

Integrated Resources Inc (IRI), based in Edison, NJ, US, is an esteemed player in the staffing solutions industry with a credible presence on their official website irionline.com. Notably, IRI provides a range of professional staffing services including contract, contract-to-hire, and direct hire solutions to a wide spectrum of industries such as healthcare, life sciences, manufacturing, financial, insurance, and others. Since its inception, IRI has been committed to delivering top-talent and optimum solutions to meet its clients' diverse needs.

Industry

Recruiting and staffing services

Company size

51 - 200 Employees

Headquarters location

Edison, NJ, US

Year founded

1996