Check with seller Production Operator I Zebulon

  • Location: Zebulon, North Carolina, United States

Site Name: USA - North Carolina - Zebulon
Posted Date: May 20 2020
The purpose of the Production Maker I role is to operate, challenge and clean equipment, per appropriate SOPs and JSAs to deliver high quality products manufactured in a safe way to fulfill the needs of the supply chain. Monitors equipment for excessive rejects. Performs all duties in accordance with regulatory and OSHA requirements.

NOTE: Shift time is TBD. 12 hour shift.

Key responsibilities for this role:

Operates, challenges, and cleans equipment, in accordance with cGMPs, Batch Documentation, SOPs, ZSPs and JSAs, as required.
Monitors equipment for excessive rejects
Performs Basic SAP transactions
Utilizes and continuously improve the GSK Production System standards (i.e. 5s, standard work, problem solving, gemba, process confirmations, and performance management) towards the goal of Zero Accidents, Zero Defects, and Zero Waste.
Records safety, quality and performance data
Utilizes systems/applications required for job performance (i.e. DELTA, myLearning, FreeWeigh, DISY, Active Plant, IP21, etc).
Escalates any problem occurring in the area that affects product quality, safety and other aspects of line performance.
Performs housekeeping/sanitation activities to maintain production areas in ‘inspection ready’ conditions.
Requirements for this role:

Ability to work overtime as needed.
Must be able to wear gloves, eye protection, and protective clothing as required by the specific job role.
Must be able to work inside a manufacturing environment where there may be exposure to noise, moving mechanical parts, and various drug compounds as the specific role mandates
Ability to climb, kneel, stoop, balance, crawl, crouch, reach, sit, stand, walk, push, pull, grasp, feel, talk, hear, lift, and perform repetitive motions as dictated by the specific role
Why you?
Basic Qualifications:
High School diploma.
Basic reading, writing and mathematical skills
Mark 2 or Mark 3 machine experience required.
Previous work experience in a production environment.
Prior experience with cGMP documentation.
Basic computer skills: word processing, spreadsheets, data entry
Experience in using established industry Problem Solving tools, including DMAIC, Kepner-Tregoe, 5Why, Fishbone and other related RCA tools.

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