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Remote Pharmaceutical Quality Control Jobs (NOW HIRING)

Sharecare

Quality Control Specialist - Remote

... leading pharmaceutical brands to drive personalized and value-based care at scale. To learn more ... The Quality Control Specialist is responsible for reviewing electronic medical records and ...

Zantech

Quality Control Manager

San Antonio, TX · On-site +1

Zantech is looking for a talented Quality Control Manager to contribute to the success of our upcoming Information Technology Support Services project for a Remote role, with a 5% to 20% Travel ...

Zantech

Quality Control Manager

Oklahoma City, OK · On-site +1

Zantech is looking for a talented Quality Control Manager to contribute to the success of our upcoming Information Technology Support Services project for a Remote role, with a 5% to 20% Travel ...

Aniesis Pharma

... quality standards. * Maintain comprehensive project documentation compliant with pharmaceutical ... Utilize remote collaboration tools effectively, adhering to data privacy regulations.

Amgen

Associate Quality Control

Thousand Oaks, CA · On-site +1

Associate Quality Control What you will do Let's do this. Let's change the world. In this vital ... Flexible work models, including remote and hybrid work arrangements, where possible Apply now and ...

Danaher

QC Batch Review Technician

Pensacola, FL · On-site +1

$17.75 - $22.75/hr

... pharmaceutical industry. * Build and utilize strong working relationships with other departments ... We recognize the benefits of flexible, remote working arrangements for eligible roles and are ...

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

As of May 29, 2026, the average hourly pay for remote 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 are the key skills and qualifications needed to thrive as a Remote Pharmaceutical Quality Control Specialist, and why are they important?

To thrive as a Remote Pharmaceutical Quality Control Specialist, you need a strong background in chemistry, biology, or pharmaceutical sciences, typically supported by a relevant degree and experience in quality assurance or laboratory settings. Familiarity with laboratory information management systems (LIMS), Good Manufacturing Practice (GMP) guidelines, and regulatory compliance certifications is essential. Attention to detail, strong analytical skills, and effective remote communication set outstanding professionals apart in this field. These skills ensure accurate product testing, regulatory compliance, and seamless collaboration across distributed teams, which are critical for patient safety and product integrity.

What are some common challenges faced by professionals working in remote pharmaceutical quality control roles?

One common challenge in remote pharmaceutical quality control is maintaining clear and consistent communication with on-site teams, especially when reviewing documentation or addressing deviations. Remote professionals may also encounter difficulties accessing physical samples or equipment, requiring strong coordination with in-house staff and effective use of digital tools. Staying updated on evolving regulatory standards and ensuring data security when handling sensitive information are also critical responsibilities. Successful remote quality control specialists often develop strong self-management and collaboration skills to overcome these challenges.

What is a Remote Pharmaceutical Quality Control specialist?

A Remote Pharmaceutical Quality Control specialist is a professional responsible for ensuring that pharmaceutical products meet required quality standards, but works from a location outside of the physical laboratory or manufacturing site. They typically analyze data, review documentation, and monitor compliance with regulations using digital tools and remote access to laboratory information systems. Their role may also include coordinating with on-site teams to address quality issues, conducting virtual audits, and maintaining records for regulatory agencies. Working remotely allows these specialists to contribute to product safety and efficacy while leveraging technology for efficient collaboration.

What is the difference between Remote Pharmaceutical Quality Control vs Remote Pharmaceutical Quality Assurance?

AspectRemote Pharmaceutical Quality ControlRemote Pharmaceutical Quality Assurance
CertificationsQC certifications, GMP trainingQA certifications, GMP compliance training
Work EnvironmentLaboratory testing, sample analysisProcess audits, documentation review
Industry UsageQuality testing roles in pharma companiesProcess and system oversight roles

Remote Pharmaceutical Quality Control focuses on testing and analyzing pharmaceutical samples to ensure product quality, while Remote Pharmaceutical Quality Assurance emphasizes overseeing processes, documentation, and compliance to maintain quality standards. Both roles require similar certifications and are integral to pharmaceutical manufacturing, but they differ in daily tasks and focus areas.

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Remote Pharmaceutical Quality Control jobs near you
Quality Control Technician (Quality Engineer)

Quality Control Technician (Quality Engineer)

Ubertal Inc

Boca Raton, FL • Remote

Contractor

Posted 9 days ago

Job description

Job Title: Quality Control Technician (Quality Engineer – Contract)

Location: 100% Remote (Preferred Eastern or Central Time Zones)
Duration: 12 Months
Schedule: Full-Time, 40 Hours/Week | Standard Business Hours
Conversion: No FTE conversion available
Interview Process: 1 Round

We are seeking an experienced Quality Control Technician with strong validation and quality systems expertise to support documentation, statistical quality control, and regulatory compliance initiatives in a highly regulated pharmaceutical or manufacturing environment.

This role focuses on validation documentation, quality analysis, regulatory compliance, and cross-functional collaboration to ensure systems, products, and processes meet defined reliability and regulatory standards.

Key Responsibilities:

  • Write, review, approve, and execute validation documentation and technical reports for systems, products, and processes

  • Prepare validation protocols, test equipment, and evaluate validation data

  • Conduct statistical quality control analysis of testing results and process anomalies

  • Prepare reports summarizing study results and conformance to acceptance criteria

  • Support development and maintenance of validation programs and Standard Operating Procedures (SOPs)

  • Verify calibration, maintenance, and repair of instruments supporting Quality Systems validation

  • Participate in FMEA, RCA, and CAPA development activities

  • Ensure corrective and preventive measures meet reliability and compliance standards

  • Maintain working knowledge of FDA, CLIA, cGMP, Medical Device Directives, and other applicable regulatory standards

  • Support procedural document management and regulatory audit readiness

  • Communicate cross-functionally regarding validation studies and project deliverables

Required Qualifications:

  • Bachelor’s degree in Science, Engineering, or related field (or equivalent combination of education and relevant experience)

  • Minimum 3 years of quality/validation experience in pharmaceutical manufacturing or a highly regulated industry

  • Strong working knowledge of cGMP principles and regulatory compliance requirements

  • Experience writing and approving validation and technical documentation

  • Experience participating in FMEA, RCA, and CAPA processes

  • Strong analytical, critical thinking, and problem-solving skills

  • Project management skills with ability to manage multiple priorities and tight deadlines

  • Proficiency in Microsoft Office, statistical tools, and electronic quality systems

  • Strong written, verbal, and interpersonal communication skills

  • Ability to maintain confidentiality and demonstrate professional judgment

Preferred Qualifications:

  • ASQ Certification

  • Experience in medical device or regulated laboratory environments

This remote contract opportunity is ideal for a quality professional with deep validation experience, strong regulatory knowledge, and the ability to drive compliance and quality excellence within a regulated pharmaceutical or manufacturing environment.