Job description

Responsibilities

• Follow Master Batch Records for the packaging of controlled, oral solid dose (OSD) and other dosage forms when required.
• Perform weight checks for incoming and dispensed materials ensuring compliance with established procedures. Operates scales including set-up, verification, leveling and challenging.
• Identify, report, and resolve quality issues.
• Safely and in compliance with batch records and SOPs, set up, operate, and clean packaging equipment.
• Perform in-process testing and inspections as required by Master Batch Record (weighing, tablet thickness, tablet hardness, friability, visual inspection, etc.).
• Clean and sanitize packaging equipment including walls, floors, and ceilings per SOPs.
• Report accidents and unsafe conditions or unusual circumstances to supervisor.
• Complete accurate and timely documentation. Follow good documentation practices in accordance with GMP.
• Process labeling and components correctly; transferring, counting, FIFO, returns, etc. during packaging processes.
• Actively participate in Production team and Site communication meetings.
• Maintain regular and punctual attendance; work overtime as required.
• Support GMP investigations and events.
• Identify and report potential GMP impacting situations.
• Contribute to Standard Operating Procedure (SOP) writing in your technical area.

Required

• High School Diploma or equivalent.
• Minimum of one – five years pharmaceutical industry experience preferred or an equivalent combination of education, demonstrated mechanical skill, and experience in a similar industry.

Job Type: Contract

Schedule:

• Overtime

Ability to commute/relocate:

• Wilson, NC 27893: Reliably commute or planning to relocate before starting work (Required)

Experience:

• Manufacturing: 1 year (Preferred)

Work Location: One location

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