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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 ...

System One

QC Analyst - 1st Shift

Bethlehem, PA · On-site

$28 - $35/hr

Onsite - onsite Hours: 7:30am - 5pm, M-F (some weekends, rotates, rare) Overview Pharmaceutical Company in Bethlehem, PA is seeking an experienced QC Analyst to join their team. In this role, you ...

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Pharmaceutical Quality Control information

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How much do pharmaceutical quality control jobs pay per hour?

As of Sep 1, 2026, the average hourly pay for pharmaceutical quality control in the United States is $27.14, according to ZipRecruiter salary data. Most workers in this role earn between $18.99 and $33.65 per hour, depending on experience, location, and employer.

What is a pharmaceutical quality control?

A Pharmaceutical Quality Control (QC) job involves ensuring that medications meet required safety, efficacy, and quality standards before distribution. Professionals in this field conduct tests, analyze raw materials and finished products, and ensure compliance with regulatory guidelines like Good Manufacturing Practices (GMP). They use analytical techniques such as HPLC, spectroscopy, and microbiological testing. QC specialists also document findings, investigate deviations, and collaborate with other departments to resolve quality issues. Their work helps maintain product integrity and patient safety.

What are some typical daily tasks for someone working in pharmaceutical quality control?

A typical day in Pharmaceutical Quality Control involves performing laboratory tests and analyses on raw materials, in-process samples, and finished pharmaceutical products to ensure compliance with safety and regulatory standards. You may prepare and calibrate lab equipment, document test results, review batch records, and assist in investigations of deviations or out-of-specification findings. Additionally, collaboration with production, research, and quality assurance teams is common to maintain continuous improvement and address any quality issues quickly. This role is detail-oriented and often includes both routine testing and problem-solving activities, making each day varied and impactful.

What are the key skills and qualifications needed to thrive in pharmaceutical quality control, and why are they important?

Pharmaceutical Quality Control professionals need a solid background in chemistry, biology, or pharmacy, often supported by a relevant degree and industry knowledge. Familiarity with laboratory instrumentation, Good Manufacturing Practices (GMP), and quality management systems, along with certifications like ASQ or GxP training, is highly beneficial. Attention to detail, strong analytical thinking, and clear communication are key soft skills that drive accuracy and collaboration. These competencies are crucial for ensuring that pharmaceutical products meet strict safety, efficacy, and regulatory standards.

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Pharmaceutical Quality Control jobs near you
Infographic showing various Pharmaceutical Quality Control job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 81% Full Time, 14% Part Time, 3% Contract, and 1% Nights. Highlights an 91% Physical, 1% Hybrid, and 8% Remote job distribution, with an average salary of $56,447 per year, or $27.1 per hour.

Compounding Pharmaceutical QA/QC

VIDRINE PHARMACEUTICAL GROUP LLC

Lake Charles, LA • On-site

Full-time

Posted 28 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.

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