Manufacturing Associate

M-F 8AM-5PM Shift.

Responsibilities:

• Operate production equipment efficiently.
• Clean production and packaging rooms according to Standard Operating Procedures (SOPs).
• Maintain, clean, and operate production machinery in accordance with SOPs.
• Adhere to the instructions provided in the Batch Manufacturing Document during production processes.
• Accurately document production operations in the Batch Manufacturing Document.
• Record cleaning and operational details in the Equipment Log Book.
• Log room usage, including cleaning and usage details, in the Room Log Book.
• Ensure compliance with FDA cGMP (Current Good Manufacturing Practice) requirements throughout all activities.

Skills:

• 1-3 years of experience in solid dose production, API production, or other pharmaceutical manufacturing.
• Strong understanding of FDA cGMP requirements.