JT004 - MANUFACTURING PROCESS TECHNICIAN NS

New albany, OH

Temporary

Biopharmaceutical

Mid Level

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

Responsibilities:

Under limited supervision, performs manufacturing processes according to Standard Operating Procedures.
Perform initial review of manufacturing procedures and batch records
Train Manufacturing Operators and Associate Manufacturing staff on process theory
Draft and revise complex documents such as MPs, SOPs, technical reports, validation documents, and investigation reports
Audit critical records
Propose corrective actions for Quality incidents
Assist with and plan implementation of routine process improvements
Collaborate with other departments to execute planned improvements
Identify and propose solutions to complex problems
Perform data analysis (e.g., SPC, CPV) on critical process parameters
Serve as a lead for equipment and process operations
Support the generation and review of manufacturing procedures and related documentation
Troubleshoot processes and assess performance through monitoring
Support training activities
Participate in NC CAPA processes by conducting process assessments, joining cross-functional investigations, defining/implementing CAPAs, and reporting on incident trends
Assist in generating, reviewing, and executing process validation protocols
Support new product introductions and product life cycle activities
Initiate and implement Level 1 and Level 2 Change Control records
Material loading and movement through SAP
Operating Equipment and documenting issues and exceptions
Support any continuous Improvement projects
Equipment cleaning

Qualifications:

High School diploma with experience
1 to 3 years of manufacturing experience preferably in a FDA regulated environment.
Pharma experience a plus
Candidates may be needed to stand for prolonged periods when necessary.
Operations/GMP knowledge
Ability to operate Advanced Equipment safely
Documentation and Communication Skills
Night shift - 2:30pm - 11pm - Monday - Friday (may vary)

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.

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