Manufacturing Associate I - Nights
Perrigo Company plc
September 02, 2026
On-site
Covington, OH
Operations
Responsibilities:
- Operates and ensures proper operation of manufacturing equipment.
- Conducts regular in-process checks of quality attributes of materials and products to ensure equipment is operating correctly.
- Assists in recording accurate production and inspection data; completes manufacturing paperwork in compliance with SOPs and cGMPs.
- Performs set ups, changeovers, and cleans the work area throughout the shift.
- Continuously looks for and helps implement improvements to process, productivity, quality, and reduce costs.
- Performs other related duties as assigned.
Qualifications/Requirements:
- High School Diploma or Equivalency required.
- Basic math and reading comprehension; able to read, speak, and comprehend instructions in English (including procedure documents) and proofread alpha/numeric data.
- Ability to follow standard work and SOPs.
- Basic computer skills; may be required to navigate computer-based training systems.
- Effective communication as part of a work team.
- Meets all locally defined training requirements.
- Preferred experience in pharmaceutical/FDA-controlled or other controlled regulatory agencies, or cGMP packaging/manufacturing environment.
- Required to operate and handle material handling equipment.
- Ability to work overtime as required.
Benefits:
- Competitive compensation; benefits for you and your family; career development opportunities.
Application Instructions:
- Click the APPLY button at the bottom of the application; submit all materials (resumes/CVs) in English.
- Operates and ensures proper operation of manufacturing equipment.
- Conducts regular in-process checks of quality attributes of materials and products to ensure equipment is operating correctly.
- Assists in recording accurate production and inspection data; completes manufacturing paperwork in compliance with SOPs and cGMPs.
- Performs set ups, changeovers, and cleans the work area throughout the shift.
- Continuously looks for and helps implement improvements to process, productivity, quality, and reduce costs.
- Performs other related duties as assigned.
Qualifications/Requirements:
- High School Diploma or Equivalency required.
- Basic math and reading comprehension; able to read, speak, and comprehend instructions in English (including procedure documents) and proofread alpha/numeric data.
- Ability to follow standard work and SOPs.
- Basic computer skills; may be required to navigate computer-based training systems.
- Effective communication as part of a work team.
- Meets all locally defined training requirements.
- Preferred experience in pharmaceutical/FDA-controlled or other controlled regulatory agencies, or cGMP packaging/manufacturing environment.
- Required to operate and handle material handling equipment.
- Ability to work overtime as required.
Benefits:
- Competitive compensation; benefits for you and your family; career development opportunities.
Application Instructions:
- Click the APPLY button at the bottom of the application; submit all materials (resumes/CVs) in English.