Quality Control Technician

Boca Raton, FL - USA

Monthly Salary: Not Disclosed

Posted on: 7 hours ago

Vacancies: 1 Vacancy

Job Summary

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:

Bachelors 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.

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 ex...

Job Title: Quality Control Technician (Quality Engineer Contract)

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:

Bachelors 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