Job Overview

CMIC CMO USA

is seeking a full-time Production Intern to support manufacturing and packaging operations within a pharmaceutical cGMP environment. This position will provide hands-on experience in operations planning, customer coordination, quality systems, documentation, data analysis, and continuous improvement. This is a full-time internship with the opportunity for conversion to a regular full-time employee based on performance and business needs. Key Responsibilities Support day-to-day Operations activities to facilitate the efficient execution of manufacturing and packaging processes. Coordinate and contribute to operational activities in support of business objectives and departmental priorities. Assist with production planning, schedule management, operational readiness, and performance monitoring. Facilitate effective communication and coordination among internal stakeholders to support Operations strategies and initiatives. Support customer-related activities through the coordination of information, schedules, priorities, and operational deliverables. Engage with cross-functional teams to align customer requirements with operational execution. Contribute to quality system activities, including change management, corrective and preventive actions (CAPAs), investigations, and documentation reviews. Support compliance with applicable regulatory guidelines, cGMP standards, and Good Documentation Practices. Participate in the development, review, and maintenance of technical and operational documentation. Apply scientific and technical knowledge to support operational decision-making and problem-solving. Analyze operational data and contribute to process monitoring, statistical analysis, and performance improvement initiatives. Participate in continuous improvement programs focused on operational excellence, quality, compliance, customer satisfaction, and efficiency. Support projects and initiatives that enhance manufacturing and packaging performance across the organization. Qualifications Master's degree in Pharmaceutical Sciences, preferably Pharmaceutics, Chemistry, or a related scientific discipline. Strong technical writing, documentation, and analytical skills. Proficiency in Microsoft Office applications and enterprise systems. Strong understanding of pharmaceutical manufacturing operations, preferably within an Oral Solid Dosage (OSD) environment. Knowledge of pharmaceutical quality systems, applicable regulatory guidelines, and cGMP principles. Knowledge of statistical methods and Statistical Process Control (SPC) concepts. Strong communication, organizational, and interpersonal skills. Ability to collaborate effectively with customers, internal stakeholders, and cross-functional teams. Ability to work effectively in a collaborative and dynamic environment.

Pay:

$19.00 - $20.00 per hour Expected hours: 40.0 per week

Benefits:

Paid time off Application Question(s): Are you able to work a fulltime 40 hour per week schedule? Do you require sponsorship?

Work Location:

In person