Quality Consulting Group, LLC

JT371 - SPECIALIST MANUFACTURING

Quality Consulting Group, LLC  •  Juncos, PR (Onsite)  •  10 days ago
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Job Description

QUALITY CONSULTING GROUP, a leader in the 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 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.
  • Initiate, revise, and approve manufacturing procedures.
  • Serve as a document owner.
  • Evaluate, plan, and implement solutions for process improvement opportunities.
  • Provide troubleshooting support.
  • Provide support of timely execution of the process monitoring quarterly reports, Non-Conformance and CAPA.
  • Ensure that all Non-conformances are triaged within the established goal.
  • Responsible for authoring investigation reports.
  • Responsible for execution of corrective actions.
  • Responsible for managing NC/CAPA closure within established goal.
  • Monitor and communicate incidents trends.
  • Review equipment/system Root Cause Analysis investigations and support trend evaluations.
  • Assist with generation of process validation protocols and reports.
  • Participate in the NPI process to assess requirements for documentation, materials, training, and equipment modifications.
  • Assist manufacturing change owner on CCRB packages impacting the process.
  • Participate on the assessment or implementation of special projects or initiatives.


Qualifications:

  • Bachelor's degree in science or engineering.
  • 5 years of Manufacturing Operations experience
  • Experience in handling deviations documentation and Change Control Management
  • Admin Shift | OT based on business needs

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.

Quality Consulting Group, LLC

About Quality Consulting Group, LLC

The Quality Consulting Group is a pharmaceutical, biotechnology, food and medical device specialty consultant that supports the manufacturing industry; services are provided in multiple areas including: Regulatory Compliance, Quality Operations, Validation, Manufacturing, Training and Technical Support. Starting, as individual services provider since 2002, Quality Consulting Group has supported clients implementing the latest standards such as Validation Guidance, ICH Guidelines, and Process Excellence and Risk Management tools.

Quality Consulting Group has provided expertise in such areas as: business, operational, quality, regulatory and manufacturing strategies; organizational structures; management controls; manufacturing and quality systems methodologies and practices; compliance programs; and accuracy reviews; FDA, EMEA and other regulatory matters.

Industry
Consulting & Advisory
Company Size
11-50 employees
Headquarters
San Juan, PR
Year Founded
2011
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