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Remote Mass Biologics Quality Control Jobs (NOW HIRING)

Zippy, Inc

Quality Control Analyst

$24.50 - $33/hr

Our remote-first team is spread across cities like Dallas, Houston, Knoxville, Omaha, Philadelphia ... We are seeking a meticulous and experienced Quality Control Analyst to join our team. In this role ...

Clearspeed

Quality Control Data Analyst

$96K - $134K/yr

This is a full-time remote position. Employees must perform all work from a single, approved work ... Complete QC Analyst basic certification training and testing. Following certification, exercises ...

Hui Huliau

Construction Quality Control Manager

OK · Remote

$85K - $113K/yr

The QC Manager is also required to attend all partnering meetings, conduct the QC meetings, perform ... remote work-sharing tools. Must be able to sit, stand, and work at a computer for long periods of ...

W3Global Inc.

Quality Control Inspector

Washington, DC · On-site +1

$90K - $125K/yr

Remote work may be considered for the right candidate, preferably within the Mid-Atlantic region. Most structural steel projects are located between New York and Virginia, so candidates within ...

Advarra

Sr Coordinator, Quality Control

$66K - $116K/yr

Job Overview Summary This role conducts Quality Control (QC) activities on complex IRB and staff ... Familiar with PowerPoint, direct messaging applications such as Slack, remote meeting applications ...

Genstar Capital LLC

$66K - $116K/yr

Job Overview Summary This role conducts Quality Control (QC) activities on complex IRB and staff ... Familiar with PowerPoint, direct messaging applications such as Slack, remote meeting applications ...

Xometry

Virtual Quality Control Inspector

Lexington, KY · On-site +1

The successful candidate will interact with DFM Engineering, Manufacturing, Quality Control, Case ... Previous remote work experience a plus #LI-Hybrid Xometry is an equal opportunity employer. All ...

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How much do remote mass biologics quality control jobs pay per hour?

As of Aug 6, 2026, the average hourly pay for remote mass biologics quality control in the United States is $21.48, according to ZipRecruiter salary data. Most workers in this role earn between $17.31 and $24.04 per hour, depending on experience, location, and employer.
What cities are hiring for Remote Mass Biologics Quality Control jobs? Cities with the most Remote Mass Biologics Quality Control job openings:
What are the most commonly searched types of Mass Biologics Quality Control jobs? The most popular types of Mass Biologics Quality Control jobs are:
What states have the most Remote Mass Biologics Quality Control jobs? States with the most job openings for Remote Mass Biologics Quality Control jobs include:
Remote Mass Biologics Quality Control jobs near you
Infographic showing various Remote Mass Biologics Quality Control job openings in the United States as of July 2026, with employment types broken down into 10% Internship, 1% As Needed, 82% Full Time, 3% Part Time, 3% Contract, and 1% Summer. Highlights an 87% Physical, 6% Hybrid, and 7% Remote job distribution, with an average salary of $44,668 per year, or $21.5 per hour.

Quality Control Technician (Quality Engineer)

Ubertal Inc

Boca Raton, FL • Remote

Contractor

Re-posted 18 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.