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 defectsPerform 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 areasAssist in writing and implementing area's process documentsOperate equipment in compliance with SOPsAssure compliance with cGMP requirements (current good manufacturing practices)Work non-routine hours as required to maintain production schedulePerform label and packaging activities for finished productComplete 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 requiredSKILLS/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 skillsSelf-motivatedGood visual acuityTeam OrientedEffective organization skills and attention to detailAbility to work with minimal supervisionAbility to work flexible hoursAbility to work hands-onRequirements

　　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