Quality Batch Record Specialist

at  Infotree Global Solutions

POSITION SUMMARY:

The Project Support Specialist will provide key support to the Quality Organization on various process improvement and project initiatives. These projects are focused on enhancing quality processes and improving operational efficiencies. Key projects may include, but are not limited to, Batch Record Review Process Simplification, Quality KPI-RFT Metrics Acquisition and Evaluation/Reporting, Standardization of the Deviations Tracking System, and Document Control Offload. The role will leverage project management skills, process excellence tools (DMAIC, 5S, Value Stream Mapping), and quality improvement techniques to identify inefficiencies, simplify processes, and support continuous improvement within the quality domain.

CORE ESSENTIAL SKILL SETS:

Candidates must possess the following qualifications to be considered for the role:

• Education: Bachelor’s degree in Engineering, Biology, Chemistry, or a related field from an accredited college or university.
• Experience: Minimum of 1-3 years of relevant experience in the pharmaceutical or manufacturing environment, with a strong focus on cGMP compliance and quality processes.
• Project Management & Process Excellence: Experience with project management and process excellence methodologies (e.g., DMAIC, 5S, Value Stream Mapping).
• Quality & GMP Experience: Solid understanding and experience in quality assurance and GMP (Good Manufacturing Practices) within the pharmaceutical industry.
• Microsoft Tools: Proficiency in Microsoft PowerPoint, Excel, and Visio.

POSITION REQUIREMENTS:

• Bachelor’s degree in Engineering, Biology, Chemistry, or a related field.
• 1-3 years of relevant experience in the pharmaceutical or manufacturing industry, specifically in GMP-compliant environments.
  Job Type: Contract
  Pay: $30.00 - $36.00 per hour

Schedule:

• 8 hour shift
• Monday to Friday

Experience:

• Batch Record: 1 year (Preferred)

Work Location: In perso

• Education: Bachelor’s degree in Engineering, Biology, Chemistry, or a related field from an accredited college or university.
• Experience: Minimum of 1-3 years of relevant experience in the pharmaceutical or manufacturing environment, with a strong focus on cGMP compliance and quality processes.
• Project Management & Process Excellence: Experience with project management and process excellence methodologies (e.g., DMAIC, 5S, Value Stream Mapping).
• Quality & GMP Experience: Solid understanding and experience in quality assurance and GMP (Good Manufacturing Practices) within the pharmaceutical industry.
• Microsoft Tools: Proficiency in Microsoft PowerPoint, Excel, and Visio