This is a temporary position.

GENERAL DESCRIPTION:

To inspect the GMP (Good Manufacturing Practices) product within container (vials/ syringes) for defects.  Perform label and packaging activities for finished product.

KEY DUTIES:

• Inspect finished product and empty containers for defects
• Perform daily process activities in compliance with standard operating procedures (SOPs)
• Prepare all process specific and ancillary equipment (i.e. vial coder, vision system) for use in assigned areas
• Assist in writing and implementing area’s process documents
• Operate equipment in compliance with SOPs
• Assure compliance with cGMP requirements (current good manufacturing practices)
• Work non-routine hours as required to maintain production schedule
• Perform label and packaging activities for finished product
• Complete and review associated production records and daily trending logs.
• Ability to pass eye exam and complete inspection certification.
• Assist other manufacturing functions (Formulation, Fill, Materials) as required

SKILLS/ABILITIES:

• Organization and interpersonal Skills (Oral, Written, etc.)
• Good Computer and Database Skills
•  Comprehensive training focused on current Good Manufacturing Practices (cGMP) in the pharmaceutical industry.

PERSONAL ATTRIBUTES:

• Good math skills
• Self-motivated
• Good visual acuity
• Team Oriented
• Effective organization skills and attention to detail
• Ability to work with minimal supervision
• Ability to work flexible hours
• Ability to work hands-on

Requirements

Basic Qualifications:

High School diploma or equivalent.

1 year of manufacturing experience or technical experience.

Preferred Qualification:

Experience in GMP manufacturing facility.

Visual or general inspection experience.