Manufacturing Associate I - Nights
Perrigo Company plc
August 11, 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 required SOPs and cGMPs.
- Performs set ups, changeovers, and cleans the work area throughout the shift to ensure proper clearance of materials.
- Identifies and helps implement improvements to process, productivity, quality, and cost reduction.
- Performs other related duties as assigned.
Qualifications/Requirements:
- High School Diploma or equivalency required.
- Basic math and reading comprehension skills; read/speak/comprehend instructions in English, including procedure documents; proofread alpha and 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.
- Meet all locally defined training requirements.
- Preferred: experience in pharmaceutical, FDA-controlled, other controlled regulatory agency, or cGMP packaging/manufacturing environment.
- Required to operate and handle material handling equipment.
- Ability to work overtime as required.
Benefits:
- Competitive compensation; benefits supporting you and your family; career development opportunities; “Total Rewards” information.
Application Instructions:
- Click the APPLY button at the bottom of the application; submit all application 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 required SOPs and cGMPs.
- Performs set ups, changeovers, and cleans the work area throughout the shift to ensure proper clearance of materials.
- Identifies and helps implement improvements to process, productivity, quality, and cost reduction.
- Performs other related duties as assigned.
Qualifications/Requirements:
- High School Diploma or equivalency required.
- Basic math and reading comprehension skills; read/speak/comprehend instructions in English, including procedure documents; proofread alpha and 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.
- Meet all locally defined training requirements.
- Preferred: experience in pharmaceutical, FDA-controlled, other controlled regulatory agency, or cGMP packaging/manufacturing environment.
- Required to operate and handle material handling equipment.
- Ability to work overtime as required.
Benefits:
- Competitive compensation; benefits supporting you and your family; career development opportunities; “Total Rewards” information.
Application Instructions:
- Click the APPLY button at the bottom of the application; submit all application materials (resumes/CVs) in English.