Internship Remote Statistical Programmer Jobs in Boca Raton, FL

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.