QUALITY ASSURANCE SPECIALIST
LGM Pharma
Key Responsibilities
All suitably qualified candidates will receive consideration for employment based on objective work-related criteria and without regard for the following: age, disability, ethnic origin, gender, marital status, race, religion, responsibility of dependents, sexual orientation, or gender identity or other characteristics in accordance with the applicable governing laws.
- Execute routine on-site activities relevant to quality operations, including receiving and quarantine, storage and segregation, environmental and temperature-controlled storage, order picking, packing, and shipment, returns and reverse logistics.
- Ensure warehouse activities comply with approved SOPs, GDP requirements, and regulatory expectations.
- Revise and/or author SOPs, forms, and controlled documents
- Execute receiving records, Certificates of Analysis (CoAs), lot traceability records, and distribution documentation.
- Execute quality release activities for APIs prior to distribution, as applicable to LGM Pharma's regulatory model.
- Assist with investigations related to warehouse deviations and nonconformances, temperature excursions, shipping errors or damage, inventory discrepancies, product quality complaints, product handling complaints, and other discrepancies as assigned
- Collaborate with SCD Quality Program Management to ensure timely initiation, investigation, and closure of deviations and CAPAs.
- Monitor warehouse environmental controls, including:
- Temperature and humidity monitoring
- Alarm response and excursion management
- Mapping, qualification, and requalification activities
- Participate in the qualification and maintenance of (not all inclusive) warehouse storage areas, temperature-controlled equipment, data loggers, equipment, and monitoring systems.
- Assist with change controls impacting warehouse activities, layout, equipment, or processes and ensure changes are implemented in a controlled and compliant manner.
- Represent QA in risk assessment activities related to storage, handling, and distribution activities.
- Collaborate with quality colleagues to ensure warehouse personnel are GMP/GDP trained, qualified, and compliant with role-based training requirements.
- Support onboarding, retraining, and periodic GMP refreshers.
- Execute backroom activities during FDA inspections and audits
- Ensure warehouse documentation and practices are always inspection-ready.
- Support responses to audit findings and FDA Form 483 observations related to warehouse operations.
- Partner closely with Warehouse Operations, Supply Chain, Logistics, Supplier Quality, and Quality Systems.
- Support vendor oversight related to 3PLs, couriers, and transportation providers.
- Track and trend quality operations metrics related to warehouse operations, such as: Temperature excursions, deviation rates, shipping errors, documentation timeliness, etc.
- Execute continuous improvement initiatives to enhance compliance, efficiency, and reliability.
- Escalate quality risks and compliance issues to QA management
- Other duties as assigned
- Bachelor's degree in Business Administration, Chemistry, Engineering, or a related discipline.
- Equivalent experience may be considered in lieu of a degree.
- 2-4 years of quality experience in the pharmaceutical industry.
- 2+ years supporting warehouse, distribution, or GMP operations.
- Experience with API distribution, GMP/pharmaceutical warehousing, or 3PL oversight required.
- Hands-on experience with GDP and warehouse quality operations required.
- Strong working knowledge of:
- 21 CFR Parts 210 & 211, 21 CFR Part 11, ICH Q7, Q9, Q10
- GDP principles for pharmaceutical distribution
- FDA inspection expectations for API distribution facilities
- Data integrity and documentation practices
- DEA requirements for controlled substances (if applicable)
- Strong understanding of warehouse operations and quality oversight .
- Ability to assess operational risk and make sound quality decisions.
- Strong investigation, root cause analysis, and CAPA skills.
- Excellent communication skills for working with operations teams.
- Ability to work effectively in a hands-on, GMP warehouse environment .
- Proficient with QMS/eQMS systems and warehouse documentation
All suitably qualified candidates will receive consideration for employment based on objective work-related criteria and without regard for the following: age, disability, ethnic origin, gender, marital status, race, religion, responsibility of dependents, sexual orientation, or gender identity or other characteristics in accordance with the applicable governing laws.
Vacancy posted 1 day ago
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