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Flexible Pharmaceutical Quality Control Jobs (NOW HIRING)

Socket.dev

Pharmaceutical QA Director

Tustin, CA · On-site

$180 - $260/hr

Demonstrated expertise in departmental leadership, quality control, microbiology quality assurance, and process quality assurance within a pharmaceutical manufacturing environment. * Strong knowledge ...

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 ...

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 ...

KVK Tech

Be Seen First

QC Chemist I/II

Newtown, PA · On-site

$56K - $90K/yr

S.-based generic and specialty pharmaceutical manufacturer committed to developing and producing ... What You'll Do The QC Chemist I/II performs analytical testing of raw materials, in-process ...

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 ...

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 ...

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Flexible Pharmaceutical Quality Control information

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How much do flexible pharmaceutical quality control jobs pay per hour?

As of Aug 27, 2026, the average hourly pay for flexible pharmaceutical quality control in the United States is $45.67, according to ZipRecruiter salary data. Most workers in this role earn between $44.47 and $46.88 per hour, depending on experience, location, and employer.

What is the difference between Flexible Pharmaceutical Quality Control vs Pharmaceutical Quality Control Technician?

AspectFlexible Pharmaceutical Quality ControlPharmaceutical Quality Control Technician
CertificationsTypically requires GMP training, quality assurance certificationsGMP certification often required, with specific technical training
Work EnvironmentLaboratories, manufacturing plants, adaptable to different production linesLaboratories, quality control labs, production facilities
Employer & Industry UsageUsed across pharmaceutical companies for flexible testing rolesCommonly employed in QC labs for routine testing

Flexible Pharmaceutical Quality Control professionals perform adaptable testing and quality assurance tasks across various production lines, requiring versatile skills and certifications. Pharmaceutical Quality Control Technicians focus on routine testing within QC labs, often with specific technical certifications. Both roles are essential in maintaining product quality but differ in scope and flexibility.

What cities are hiring for Flexible Pharmaceutical Quality Control jobs?

Cities with the most Flexible 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 Flexible Pharmaceutical Quality Control jobs?

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

Flexible Pharmaceutical Quality Control jobs near you

Compounding Pharmaceutical QA/QC

VIDRINE PHARMACEUTICAL GROUP LLC

Lake Charles, LA • On-site

Full-time

Posted 23 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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