West Pharma Quality Technician 

United States, Arizona, Tempe 

842516105

This position is Wednesday, Thursday, Friday and every other Saturday 5:45 PM - 6:00 AM

Job Summary:

In this role, youassist the 405 QA group with their daily duties including inspection, batch records, document and record control, and shipping requirements. Conduct trainings in NC material identification and disposition.

Essential Duties and Responsibilities:

• Point of QA contact in the 405 WEST location. Organize the QA lab work loads and drive performance across the 4 QA lab shifts.
• Perform and oversee component or product inspection, sampling, analyses following standard methods and procedures, and approval/release.
• Write, review, and revise procedures, work instructions, and any related forms for specific job-related activities.
• Conducts review of batch documentation for GMP Compliance. Works with production personnel to resolve GMP discrepancies. Establishes files for batch documentation.
• Works with databases to collect information and data pertaining to batch documentation.
• Performs QA release of finished product for acceptable materials.
• Disposition NC material in the Bond Room and dispositions NC material per procedures and MRB reviews.
• Assists with the calibration process by recording calibration frequencies, due dates, suppliers, and other calibration duties as required. Maintains organization of calibration activities.
• Store, record and maintain electronic and hard copies of controlled documents and records.
• Performs QA document control functions and upload records in Master Control.
• Coordinates the revision, review, and approval of SOPs and other GMP documents.
• Train existing QA Techs to the material review process for business continuity, provide continued training, as required.
• Support Continuous Improvement program throughout West Phoenix.
• Supports internal / external audits and document control.
• Performs other duties as assigned by the Quality Supervisor or Manager.

Basic Qualifications:

• High School or equivalent Quality, Engineering or related degree.
• Experience:3-5 years of experience.
• Proficiency with PC and Microsoft Office; Knowledge of QMS Master Control, MeasureLink and other Quality systems is preferred.
• Must be able to prioritize and perform position responsibilities accurately and meet required deadlines.
• Strong attention to detail; Strong problem identification/analysis and solving skills with hands-on approach.
• Excellent verbal and written communication skills; Maintain an organized and clean quality Lab.
• Ability to multi-task and prioritize in a fast-paced environment; Ability to interface with all personnel levels.
• Motivated self-starter with ability to work independently on multiple assignments in a team environment.

Preferred Knowledge, Skills and Abilities:

• Knowledge and experience with FDA and ISO Quality Systems to include SPC and calibrations systems.

Travel Requirements:

• Minimal travel may be required.

Physical and Mental Requirements:

• While performing the duties of this job, the associate frequently is required to sit, walk, stand, balance, stoop, kneel, or crouch to support production needs. The associate may lift and/or move up to 25 pounds and occasionally lift and/or move more than 55 pounds.