JT716 - SPECIALIST MANUFACTURING

Quality Consulting Group, LLC; Juncos (PR); On-site; USD 65,000 - 90,000; Full time

Job summary

Quality Consulting Group, LLC is seeking a motivated professional to join our team in Puerto Rico/USA. You will support manufacturing quality systems, manage change controls, and assist with investigations while collaborating across functions to ensure compliant operations.

The role emphasizes documentation, training support, and hands-on process improvements, aligning with regulatory expectations and continuous improvement initiatives.

Qualifications

• Bachelor's degree in Life Sciences, Biology, Chemistry, and/or Engineering.
• Manufacturing Operation experience (not quality).
• Document Management, create new documents, review and approval of documents.
• Administrative Shift.

Responsibilities

• Support the execution of manufacturing/quality systems, including non-conformances, process validation, procedures, training, and new product introductions.
• Apply process, operational, scientific expertise, basic compliance knowledge, and analytical skills to support manufacturing operations.
• May serve as primary production process owner for process support systems and assist with ownership on complex systems.
• Own change controls for manufacturing process changes and ensure proper documentation.
• Support investigations, root cause analysis, corrective/preventive actions, and regulatory inspection readiness.
• Contribute to risk assessments and microbial assessment evaluations.
• Assist in training material generation and provide training on technical aspects of processes.
• Provide on-floor troubleshooting and cross-functional collaboration across teams.
• Design and coordinate functional tests, water tests, and run simulations during major changes or campaigns; generate protocols.
• Assist and guide Master Batch Record creation/revisions and assess process modifications.
• Review performance data and develop solutions for process improvements.

Skills

Manufacturing operations experience

Document management

Administrative shift

Education

Bachelor's degree in Life Sciences/ Biology/ Chemistry/ Engineering

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 to a world-class manufacturing industry in Puerto Rico & USA.

Responsibilities:

• Support the execution of manufacturing/quality systems such as non-conformances, process validation, procedures, training, and new product introductions.
• Apply process, operational, scientific expertise, basic compliance knowledge, and analytical and troubleshooting skills to support manufacturing operations.
• May serve as primary production process owner for process support systems and assist with process ownership responsibilities on more complex process systems.
• Own change controls for manufacturing process changes
• Support major/trend deviation investigations throughout the whole lifecycle including Root Cause Analysis investigation, determination of Corrective/Preventive Actions, authoring process investigation reports, and presenting within regulatory inspections.
• Support Risk Assessments exercises and Microbial assessment evaluations.
• Led commercial campaign readiness and effectively communicate and collaborate with cross function areas.
• Assist in the generation of training materials and assist in providing training on scientific or technical aspects of the process.
• Provide commercial support when needed and assist on the floor troubleshooting.
• Design, coordinate, and support execution of functional tests, water tests, and other runs to challenge process and operations during major changes, or campaign readiness. Generate technical protocols as needed.
• Assist and provide guidance during MBR (Master Batch Record) creation/revisions.
• Perform assessment to support process, automation, or equipment modification or implementation of special projects
• Initiate, revise, and approve standard manufacturing procedures. Ensure all procedures reflect current operations. Serve as a document owner.
• Assess process performance and review of performance data. Evaluate, plan, and implement solutions for process improvement opportunities.
• Complete assessments for CAPA applicability requests from other plants/sites
• Complete assessment for new or changes in BOM's (Bill of Materials)
• Serves as a peer-recognized specialist in at least one area, with overall responsibility for determining methodologies in that area.

Qualifications:

• Bachelor's degree in Life Sciences, Biology, Chemistry, and/or Engineering.
• Manufacturing Operation experience(not quality)
• Document Management, create new documents, review and approval of documents.
• Administrative Shift

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.