Specialist Quality Assurance - Drug Product

BioPharma Consulting JAD Group; Juncos (PR); In loco; USD 39.000 - 50.000; Tempo pieno

Descrizione del lavoro

BioPharma Consulting JAD Group seeks a Specialist Quality Assurance to support the Drug Product Quality Assurance team at a manufacturing site in Juncos, Puerto Rico. The role provides QA oversight of manufacturing, packaging and inspection operations to ensure cGMP compliance and adherence to site procedures.

Key responsibilities include approving master production records, change controls, deviations, CAPAs, and leading site audits.

Mansioni

• Review and approve master production records, process validation protocols and reports.
• Represent Quality on incident triage teams and New Product Introduction (NPI) teams.
• Approve change controls, planned incidents, nonconformance investigations and CAPA records.
• Lead investigations and site audits; own site quality program procedures.
• Review risk assessments and support automation, facilities and environmental programs.
• Review and approve work orders and EMS/BMS alarms; approve environmental characterization reports and release of sanitary utility systems.
• Act as designee for the QA manager on the local change control review board.
• Provide lot disposition and authorize lots for shipment.

Descrizione del lavoro

We are seeking a Specialist Quality Assurance to support the Drug Product Quality Assurance technical team at a biopharmaceutical manufacturing site in Juncos, Puerto Rico. Working under minimal supervision, this role provides Quality oversight of manufacturing, packaging and inspection operations, ensuring compliance with cGMP and site quality procedures.

Key Responsibilities

• Review and approve master production records, process validation protocols and reports.
• Represent Quality on incident triage teams and New Product Introduction (NPI) teams.
• Approve change controls, planned incidents, nonconformance investigations and CAPA records.
• Lead investigations and site audits; own site quality program procedures.
• Review risk assessments and support automation, facilities and environmental programs.
• Review and approve work orders and EMS/BMS alarms; approve environmental characterization reports and release of sanitary utility systems.
• Act as designee for the QA manager on the local change control review board.
• Provide lot disposition and authorize lots for shipment.

Education (one of the following)

• Doctorate degree; OR
• Master's degree + 2 years of directly related experience; OR
• Bachelor's degree + 4 years of directly related experience; OR
• Associate's degree + 8 years of directly related experience; OR
• High school diploma/GED + 10 years of directly related experience

Preferred Qualifications

• GMP manufacturing experience in Quality Assurance, including review and approval of change controls, deviations, CAPAs, protocols, reports and procedures
• Experience supporting packaging and/or inspection operations
• Strong knowledge of Good Documentation Practices (GDP) and electronic quality systems
• Ability to collaborate effectively with Manufacturing, Engineering and Process Development
• Bilingual English/Spanish communication skills

Key Skills

• Project management and strong organizational skills; ability to initiate and lead cross-functional teams
• Strong knowledge of manufacturing, distribution, QA, validation and process development processes
• Ability to interact with regulatory agencies and evaluate compliance issues
• Advanced data trending and evaluation; strong Microsoft Office skills
• Excellent written and oral communication, facilitation and presentation skills

• Contract position: approximately 5 months (October 2026 – March 2027), with possible extension
• Shift: Administrative shift
• Days: Monday to Friday, 8 hours/day (40 hours/week)
• On-site in Juncos, Puerto Rico