Quality Control Analyst
BioPharma Consulting JAD Group · Fort Worth, TX · 3 days ago
On-siteQuality AssuranceContract
Responsibilities
- Conduct routine and non-routine analyses of raw materials, in-process samples, finished goods, environmental samples, and stability batches
- Perform visual inspections of finished products to verify conformance to specifications
- Monitor testing procedures to ensure all analyses follow established specifications, standard test methods, and approved protocols
- Investigate questionable, out-of-specification, or atypical results and support failure investigations with recommended corrective actions
- Compile laboratory test data, perform trend analyses, and interpret results to determine suitability for release
- Develop, optimize, and qualify new analytical testing methods
- Perform method validations and method transfers in accordance with applicable guidelines and policies
- Prepare or review method transfer documentation, including protocols and technical reports
- Evaluate new technologies, instruments, and analytical approaches; provide recommendations for adoption or improvement
- Write and revise standard operating procedures (SOPs) for quality control processes
- Prepare technical documentation such as deviation reports, testing protocols, trend analyses, and regulatory support data
- Complete all required documentation for testing activities, including data capture forms, equipment logbooks, and inventory records
- Review data generated by contract laboratories to ensure accuracy, completeness, and regulatory compliance
- Calibrate, validate, troubleshoot, and maintain laboratory instruments and equipment
- Identify and resolve equipment issues to minimize downtime and ensure testing continuity
- Receive, inspect, and verify raw materials for compliance with specifications
- Serve as a technical liaison between Quality Control and internal departments, external vendors, and contract laboratories
- Coordinate testing activities with external laboratories and vendors to ensure timely and accurate results
- Participate in internal assessments and audits as required
- Train junior analysts on laboratory procedures, assays, and quality standards
Requirements
- Bachelor's degree in Chemistry, Biology, or a related scientific discipline
- Experience in GMP/GLP environments preferred
- Strong analytical, problem-solving, and documentation skills
- Proficiency with laboratory instrumentation and data systems
- High attention to detail and commitment to quality and compliance
Schedule
Location: Fort Worth, TX (Onsite)
Duration: 12 months contract