JT657 - SPECIALIST QA

Quality Consulting Group, LLC; Juncos (PR); On-site; USD 70,000 - 95,000; Full time

Job summary

Quality Consulting Group, LLC is seeking a talented QA professional to join our team in the pharmaceutical and biotech manufacturing sector in Puerto Rico and the USA. You will perform batch record reviews, ensure GMP/GDP documentation integrity, and support manufacturing operations with SAP-based inventory activities.

The role requires strong data integrity practices, risk-based thinking, and the ability to convey complex information clearly in cross-functional meetings.

Qualifications

• Bachelor's degree required in a related field.
• Experience in GMP-regulated pharmaceutical/biotech manufacturing preferred.
• Familiarity with batch record review and GDP/GMP documentation.

Responsibilities

• Support Quality and Manufacturing operations through batch record review and documentation compliance.
• Review manufacturing documentation for GDP, data integrity, traceability, and procedural compliance.
• Utilize SAP for inventory management and manufacturing support.
• Engage in DAI meetings and quality forums to present information and escalate risks.
• Communicate risks, priorities, pending items, and decisions clearly across shifts.

Skills

Batch Record Review

GMP/GDP Documentation

SAP Inventory Management

PAX / eBR

Data Integrity

Risk-based thinking

Present information in meetings

Communication of risks

Education

Bachelor's Degree in related area

Tools

SAP Inventory Management

PAX / Electronic Batch Records (eBR)

Job description

QUALITY CONSULTING GROUP, a leader inthe pharmaceutical, biotech, medical devices, and manufacturing industry, is looking for a talented, highly motivated and enthusiastic to join our team. In this role, you’ll work with a highly enthusiastic team, contributing in a world-class manufacturing industry in Puerto Rico & USA.

Responsibilities:

• Supporting Quality and Manufacturing operations through accurate Batch Record Review, documentation compliance, electronic systems management, inventory control, and timely operational decision-making.
• Perform comprehensive Batch Record Review to ensure completeness, accuracy, compliance, and adherence to approved procedures and GMP requirements.
• Review manufacturing documentation for Good Documentation Practices (GDP), data integrity, accuracy, traceability, and procedural compliance.
• Utilize SAP for inventory-related activities, including material verification, inventory transactions, reconciliation, status review, and manufacturing support.
• Demonstrate experience with PAX / Electronic Batch Record (eBR) systems to review, assess, and support electronic manufacturing documentation and workflows.
• Participate actively in DAI meetings and other operational or Quality forums by presenting relevant information, identifying risks, communicating pending items, and supporting timely decisions.
• Evaluate operational situations and apply appropriate decision-making and risk-based thinking, escalating issues when required based on potential impact to product quality, compliance, operations, or patient safety.
• Support the assessment and communication of Quality events, documentation discrepancies, process concerns, and operational issues.
• Work effectively under pressure while maintaining accuracy, compliance, and appropriate prioritization of critical activities.
• Manage assigned responsibilities independently and with minimal supervision, demonstrating ownership, accountability, and appropriate follow-through.
• Collaborate effectively with Quality, Manufacturing, Supply Chain, Warehouse, and other cross-functional teams.
• Maintain strong communication across shifts and functions to ensure critical information, pending activities, risks, and decisions are clearly transferred.
• Organize complex information and communicate it clearly, concisely, and accurately, enabling management and cross-functional teams to make informed decisions.
• Identify potential issues proactively and demonstrate a solution-oriented and continuous-improvement mindset.

Qualifications:

• Bachelor's Degree in related area
• Experience in GMP-regulated pharmaceutical or biotechnology manufacturing, capable of combining Quality compliance, operational knowledge, electronic systems expertise, and sound judgment.
• Batch Record Review
• GMP / GDP Documentation
• SAP Inventory Management
• PAX / Electronic Batch Records (eBR)
• Manufacturing and Quality Systems
• Inventory reconciliation and material traceability
• Quality event assessment and escalation
• Data Integrity principles
• Risk-based thinking
• Ability to present information during DAI and operational meetings
• Clear communication of risks, priorities, pending items, and decisions
• Ability to translate complex operational information into concise, actionable messages for different levels of the organization

Quality Consulting Group, LLC is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, genetic information, national origin, protected veteran status, disability status, or any other characteristic protected by law.