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.
PDN-9b01fc25-ed64-42ef-b451-924d5027fccd
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