Sr cGMP Specialist-Quality Control Analytical Radiochemist

Sr. Current Good Manufacturing Practices (cGMP) Specialist

At Houston Methodist, the Sr. Current Good Manufacturing Practices (cGMP) Specialist is responsible for adherence to Standard Operating Procedures (SOPs) and cGMP regulations pertaining to the manufacture of therapeutics and devices. The position oversees compliance with quality operations, reviews procedures, verifies equipment and facility cleanliness, ensures proper gowning, correct material labeling, correct operating parameters for equipment, and proper execution of protocols in accordance with approved SOPs, while guiding junior team members.

As a senior department member, the role actively contributes to the development of policies and procedures for delivering novel products to patients and customers.

Exempt

• Bachelor of Arts or Science degree
• Master’s degree preferred

• Five years of biotechnology or pharmaceutical industry experience with exposure to cGMP manufacturing operations
• Experience performing equipment validation (IQ/OQ/PQ), facility commissioning, internal/external audits, batch record review, and hosting regulatory inspections preferred

• Demonstrates the skills and competencies necessary to safely perform the assigned job, determined through on‑going skills, competency assessments, and performance evaluations
• Proficient in speaking, reading, and writing English necessary to perform essential functions, especially with regard to activities impacting patient or employee safety or security
• Ability to effectively communicate with patients, physicians, family members, and co‑workers in a customer service focused manner and apply positive language principles
• Familiar with quality, compliance, and FDA regulatory requirements for Good Laboratory Practice (GLP) and cGMP auditing procedures
• Proficiency in spreadsheet, word processing, and presentation software
• Ability to work under pressure and balance many competing priorities; highly responsive and solution/action oriented
• Knowledge of regulations applicable to drugs and devices (21 CFR Parts 210/211, Medical Device Regulations, ICH and FDA guidances, etc.) and the ability to apply them based on the phase of the project (GLP, Phase I, Phase II/III, etc.)
• Ability to mentor and coach department personnel
• Demonstrates highly effective communication skills and the ability to lead informal/formal educational sessions to include classroom/seminar instruction in cGMPs and specialized topics related to compliance and best practices

• Provides work direction of authorized core users working in either production or quality control
• Collaborates with cross‑functional teams including research, process development, quality assurance, and quality control
• Works with research team members to assist them with transitioning their research processes to compliant cGMP SOPs and participates in multi‑functional project teams as necessary

• Participates in internal audits and external inspections by Regulatory Agencies and reports findings to direct management
• Responds to calls/alarms off hours and weekends for facility systems and equipment failures
• Serves as technical subject matter expert in support of department functions
• Reviews testing documentation from all cross‑functional departments

• Ensures development, pre‑clinical, and clinical product supply are executed effectively against changing demand schedules and meet quality requirements
• Conducts internal inspections and audits to ensure compliance with Federal Drug Administration (FDA) regulations and cGMP core policies and procedures

• Uses resources efficiently; does not waste supplies. Self‑motivated to independently manage time effectively and prioritize daily tasks

• Participates with the Quality Assurance Manager and/or cGMP Core Director in defining quality policies
• Assists Quality Assurance Manager, cGMP Core Director and/or team members in defining release testing requirements, developing and executing protocols, performing periodic…