West Pharma Quality Technician Nights 

United States, Michigan, Walker 

885479280

Job Summary:

Performs receiving inspections, start-up inspections, in-process and final inspections. Completes documentation & reviews production records. Performs analytical testing on various materials. Troubleshoots and solves technical problems. Programs and operates automated inspection equipment. Prepares shipping documentation & documentation audits.

Essential Duties and Responsibilities:

• • Inspects and release incoming materials. May perform analytical testing, evaluates, records and reports on the chemical and physical properties of various substances and materials to determine product release approval status.
  • Review and approve Batch Production Records from each job.
  • Compose Non-Conformance Report (NCR) Deviations, Document Change Notices (DCN), Out of Specification (OOS), Work Instructions, Incoming Quality Control (IQC) forms and Engineering Change Requests (ECR’s).
  • Assist in the design & drawing reviews and make recommendations for improvements, clarification, and correctness as needed.
  • Assists shift personnel with quality issues and/or measurement techniques.
  • Input incoming lots into expiration/retest database.
  • Maintain expiration/retest date database for incoming materials. Review retest dates and arrange for testing of materials for retest. Review expiration dates and arrange for disposal of expiring materials.
  • Conforms with and abides by all regulations, policies, work procedures, instruction, and all safety rules.

• • Provides a “Customer Service” attitude when interacting with internal and external customers while accomplishing work, production, and achieving quality standards.
  • Maintains a clean, orderly, and safe workstation and environment always.
  • Other duties as assigned.

Basic Qualifications:

• High School or equivalent
• Experience:Less than 3 years of experience.

Preferred Knowledge, Skills, and Abilities:

• Knowledge and experience with FDA and ISO Quality Systems to include SPC and calibrations systems.
• Proficiency with PC and Microsoft Office; Knowledge of QMS Master Control, MeasureLink and other Quality systems is preferred.
• Experience with ISO 9000 standards and GMP’s
• 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.

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.