Nestlé Health Science is looking to ensure products are being produced in a manner that meets all current Good Manufacturing Practices (cGMPs) and Product Specification criteria, enabling improved first pass quality and adherence to cGMPs on the production floor at all times.
Requirements
- Prior Quality Assurance experience in manufacturing environment required
- Prior experience working with manufacturing equipment preferred
- Prior experience with QA Systems and software’s like Oracle, AS400, PQM, Captiva, etc preferred
- MS Office programs (Outlook, Excel, Word, etc.)
Responsibilities
- Perform in-process testing verifications of manufacturing/packaging data to confirm consistency in testing methodology and test data.
- Submit daily Analytical and Micro samples to QC for appropriate testing.
- Conduct approval of pre-start-up activities including line/room clearance, and initial equipment checks.
- Consistently review in-process batch documentation to ensure real-time compliance to product specifications, good documentation practices, company SOPs and cGMPs.
- Discuss errors directly with line personnel so corrections can be made if required.
- Follows and ensures all associate safety rules, SOPs, GDPs, and cGMPs guidelines.
- Performs daily compliance Audit and Gemba walk for all applicable areas.
Other
- Must have basic proficiency of English language to comply with verbal and written directions, signs, policies and procedures.
- This position will work the evening shift: 3pm-11:30pm, Monday - Friday.
- Physical ability to repetitively lift, stand, climb, bend, etc… within a manufacturing environment.
- Ability to write simple correspondence
- Basic mathematical skills
- Must be able to respond to verbal and written instructions
- Highly organized and attentive to details
- Ability to work collaboratively in team environment
