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Entry Level Pharmaceutical Quality Control Jobs (NOW HIRING)

Adecco

QC Scientist I

Cincinnati, OH · On-site

$25/hr

Second shift after completion of first-shift training Position Summary We are seeking a QC Scientist I to join a pharmaceutical Quality Control Analytical Chemistry Laboratory in Cincinnati, OH. This ...

Cipla

Quality Control (QC) Chemist

Fall River, MA · On-site

$65K - $105K/yr

Perform routine and advanced QC testing for pharmaceutical dosage forms, with a strong focus on inhalation products (MDI/DPI systems) * Evaluate critical quality attributes (CQA) such as particle ...

System One

QC Chemist

Cranbury, NJ · On-site

$36 - $40/hr

Job Title : QC Chemist (cGMP / HPLC / Solid Dose) Location : Cranbury, NJ (Onsite) Type : Contract ... Perform batch release and stability testing for pharmaceutical products * Conduct assay ...

System One

QC Chemist

Cranbury, NJ · On-site

$36 - $40/hr

Job Title : QC Chemist (cGMP / HPLC / Solid Dose) Location : Cranbury, NJ (Onsite) Type : Contract ... Perform batch release and stability testing for pharmaceutical products * Conduct assay ...

System One

QC Chemist

Cranbury, NJ · On-site

$36 - $40/hr

Job Title : QC Chemist (cGMP / HPLC / Solid Dose) Location : Cranbury, NJ (Onsite) Type : Contract ... Perform batch release and stability testing for pharmaceutical products * Conduct assay ...

System One

QC Chemist

Cranbury, NJ · On-site

$36 - $40/hr

Job Title : QC Chemist (cGMP / HPLC / Solid Dose) Location : Cranbury, NJ (Onsite) Type : Contract ... Perform batch release and stability testing for pharmaceutical products * Conduct assay ...

System One

QC Chemist

Cranbury, NJ · On-site

$36 - $40/hr

Job Title : QC Chemist (cGMP / HPLC / Solid Dose) Location : Cranbury, NJ (Onsite) Type : Contract ... Perform batch release and stability testing for pharmaceutical products * Conduct assay ...

System One

QC Chemist

Cranbury, NJ · On-site

$36 - $40/hr

Job Title : QC Chemist (cGMP / HPLC / Solid Dose) Location : Cranbury, NJ (Onsite) Type : Contract ... Perform batch release and stability testing for pharmaceutical products * Conduct assay ...

Adecco

QC Scientist I

Greenville, NC

$23 - $24/hr

QC Scientist I Location: Greensville, NC Pay Rate: $23.00-$24.00 per hour Schedule: Monday-Friday ... Conduct validated testing of pharmaceutical finished products, including traditional wet chemistry ...

System One

QC Chemist

Cranbury, NJ · On-site

$36 - $40/hr

Job Title : QC Chemist (cGMP / HPLC / Solid Dose) Location : Cranbury, NJ (Onsite) Type : Contract ... Perform batch release and stability testing for pharmaceutical products * Conduct assay ...

TekWissen LLC

Quality Control Chemist

High Point, NC · On-site

Their global team delivers innovative technologies, convenient procurement solutions, and pharmaceutical services through industry-leading brands. Position: Quality Control Chemist Location: High ...

Alexza Pharmaceuticals

QC Analyst II

Fremont, CA · On-site

$41/hr

Bachelor's Degree in science or related field * 2-5 years relevant experience in a cGMP pharmaceutical QC environment, or at least 1 year with a Master's degree Physical Requirements * Prolonged ...

Astrix Inc

QA Associate (Part Time)

Kalamazoo, MI · On-site

$19 - $20/hr

Pay Rate Low: 19 | Pay Rate High: 20 Position: Entry-Level Quality Assurance Associate (Part-Time) ... that manufacturing and QC activities for the production and testing of active pharmaceutical ...

Piramal Pharma Limited

QC Analyst I

Sellersville, PA · On-site

$23.25 - $31.25/hr

Experience in pharmaceutical, biotechnology, or other regulated laboratory environments ... Quality Control laboratory environment supporting pharmaceutical manufacturing operations.

Piramal Pharma Limited

QC Analyst I

Sellersville, PA

$23.25 - $31.25/hr

Experience in pharmaceutical, biotechnology, or other regulated laboratory environments ... Quality Control laboratory environment supporting pharmaceutical manufacturing operations.

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Entry Level Pharmaceutical Quality Control information

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

As of Sep 1, 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:

Entry Level Pharmaceutical Quality Control jobs near you

Compounding Pharmaceutical QA/QC

VIDRINE PHARMACEUTICAL GROUP LLC

Lake Charles, LA • On-site

Full-time

Posted 29 days ago

Job description

About the Role:

The Compounding Pharmaceutical Quality Assurance professional plays a critical role in ensuring that compounded medications meet the highest standards of safety, efficacy, and regulatory compliance. This position is responsible for overseeing and implementing quality assurance protocols throughout the compounding process, from raw material inspection to final product release. The role requires meticulous attention to detail to identify and mitigate risks, ensuring that all compounded pharmaceuticals adhere to applicable guidelines and industry best practices. The successful candidate will collaborate closely with compounding pharmacists, production teams, and regulatory bodies to maintain continuous quality improvement. Ultimately, this role safeguards patient health by guaranteeing that compounded medications are consistently produced to exacting quality standards.

Minimum Qualifications:

  • Bachelor’s degree in Pharmacy, Pharmaceutical Sciences, Chemistry, or a related scientific discipline.
  • Minimum of 3 years of experience in pharmaceutical compounding quality assurance or a closely related field.
  • In-depth knowledge of USP <795>, USP <797>, USP <800>, and FDA regulations applicable to pharmaceutical compounding.
  • Strong understanding of Good Manufacturing Practices (GMP) and quality management systems.
  • Proven ability to conduct audits, manage documentation, and implement quality control measures.

Preferred Qualifications:

  • Certification in Quality Assurance (e.g., ASQ Certified Quality Auditor or equivalent).
  • Experience working in a sterile compounding environment.
  • Familiarity with electronic quality management systems (eQMS) and laboratory information management systems (LIMS).
  • Advanced degree (Master’s or PharmD) in a relevant field.
  • Experience with risk assessment methodologies and root cause analysis.

Responsibilities:

  • Develop, implement, and maintain quality assurance procedures and documentation specific to pharmaceutical compounding operations.
  • Conduct regular audits and inspections of compounding processes, equipment, and facilities to ensure compliance with USP <795>, <797>, and other relevant standards.
  • Review and approve batch records, compounding formulas, and quality control test results prior to product release.
  • Investigate deviations, non-conformances, and complaints related to compounded products, and coordinate corrective and preventive actions.
  • Train and support compounding staff on quality assurance policies, regulatory requirements, and best practices to promote a culture of quality and compliance.

Skills:

The required skills enable the professional to rigorously evaluate compounding processes and ensure compliance with regulatory standards, which is essential for maintaining product quality and patient safety. Strong analytical and problem-solving skills are used daily to investigate deviations and implement effective corrective actions. Communication skills are vital for training staff and collaborating with cross-functional teams to foster a quality-driven environment. Attention to detail ensures accurate documentation and thorough audits, preventing errors and regulatory non-compliance. Preferred skills such as proficiency with electronic quality management systems enhance efficiency and accuracy in quality assurance activities, while advanced certifications and experience support continuous improvement initiatives.