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West Pharma Production Operator 12-Hour Shift 
United States, Michigan, Walker 
430526532

28.06.2024

Each shift is a 12-hour shift, with a rotating schedule (commonly referred to as a 2-2-3-2 schedule):

  • Nights - 5:45pm - 6:00am
  • Days - 5:45am - 6:00pm

Essential Duties and Responsibilities:

  • Visually inspects, ensures, and assembles parts in process to quality specifications, being aware of critical visual and dimensional defects and determines acceptability of the parts, based on customer specifications.
  • Assures accuracy of product packaging and tractability as required, including generating labels, the correct labeling of containers, and accurate part count.
  • Operates and maintains production auxiliary equipment utilizing the correct safety precautions.
  • Maintains a clean, orderly and safe workstation and environment at all times.
  • Communicates with Production leadership regarding any unacceptable parts and any malfunctions of the production process within their workstation.
  • Checks part counts by weighing and ensuring that scale(s) are set for accuracy.
  • Follows all applicable SOPs, GMPs, and DOIs.
  • Contributes to continuous process improvement efforts to reduce scrap, cycle times, improve efficiency, and eliminate waste.
  • Supports and contributes in Lean Sigma programs and activities towards delivery of the set target.
  • Provides a “Customer Service” attitude when interacting with internal and external customers while accomplishing work, production, and achieving quality standards.
  • Conforms with and abides by all regulations, policies, work procedures, instruction, and safety rules.
  • Complies with the company’s safety policy at all times
  • Complies with the company’s quality policy at all times
  • Exhibits regular, reliable, punctual and predictable attendance.
  • May be required to work mandatory overtime and/or irregular hours and/or on irregular days to complete assignments and meet business needs.
  • Performs other duties as assigned.

Basic Qualifications:

  • Minimum 18 years of age
  • Able to read and understand procedures, safety sheets, instructions, and policies in English

Preferred Knowledge, Skills and Abilities:

  • Experience: 1-3 years of experience, ideally in manufacturing and/or clean room environment
  • Education: High School Diploma or GED
  • Experience with cGMP practices, ISO, and medical device manufacturing

Travel Requirements:

Physical & Mental Requirements:

  • Medical Device manufacturing requires strict adherence to standards. Working environment is a manufacturing facility, which houses plastic injection molding machines. Must tolerate odors, fumes, particulate and loud noises generated from plastics manufacturing and molding processes.
  • Must work constructively in an environment that may be stressful due to competing resources while at all times maintaining company confidentiality.
  • Must be able to work in a controlled clean room and/or white room environment requiring special gowning. Will be required to follow hygiene and gowning requirements and wear protective clothing over the head, face, hands, feet and body.
  • Ability to stand and sit for extended periods of time
  • Requires occasional bending at the waist, twisting (at the torso and neck), crouching, climbing, kneeling, balancing, reaching (including overhead), pushing, pulling, grasping, holding and manual dexterity
  • Must transport oneself to and from other areas of the facility when necessary
  • Ability to understand verbal or written directions, which may include reading English and understanding symbols and warnings
  • Must have good visual acuity. If specifically necessitated by customer requirements, must be able to see with or without corrective lenses and distinguish color differences for product and safety issues.
  • Must be able to lift a minimum of 25lbs