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.
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.
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