FREE ACCESS
5,000–10,000 jobs/day
See all jobs on Scoutfield
Search thousands of fresh jobs every day.
Discover
- Fresh listings
- Fast filters
- No subscription required
Create a free account and start exploring right away.
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in quality control processes, including sample submission, documentation review, and compliance with ISO 17025 and cGMP standards. Proficient in data management and reporting, with strong analytical skills to support laboratory operations and cross-functional collaboration.
Highest-signal resume keywords
Quality Control ExperienceISO 17025 ComplianceProficiency in Microsoft OfficeFamiliarity with cGMPAnalytical Skills
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Sample SubmissionData EntryQuality Trending ReportsCertificates of AnalysisLaboratory AuditsSOP FamiliarityMathematical SkillsAnalytical TerminologyDocumentation ReviewTechnical Support
Soft Skills
CollaborationCommunication SkillsTraining Ability
Tools & Technologies
AS400SharePointExcelWordPowerPointPLM/PQMSAP
Industry Keywords
Good Documentation PracticesCurrent Good Manufacturing PracticesQuality Lab ServicesNestlé GLPNestlé QMS
About the role
Key responsibilities & impact- Submit samples routinely to QC laboratories
- Provide daily and weekly management updates on samples undergoing QC testing
- Communicate out-of-specification failures to the Quality Analyst for MRB review
- Support cross-functional teams with laboratory target releases and facility audits
- Escalate priorities to QC management and correspond with internal and external stakeholders
- Provide status updates on sample submissions, handling, control, and data entry
- Process raw material, bulk, contract bulk, and special sample submissions
- Perform electronic transactions to release material
- Coordinate re-sampling and resolve missing documentation or specification information
- Support annual facility audits
- Create and maintain quality trending reports, informational spreadsheets, and laboratory logs
- Review supplier certificates of analysis, QA/QC reports, and quality documents
- Draft certificates of analysis for authorized review
- Provide information for customer complaint testing investigations
- Coordinate outside laboratory samples and results
- Create purchase orders and manage laboratory supply receipts and invoices
- Train and provide technical support to the Quality Coordinator group
- Lead continual improvement initiatives
- Follow Quality Lab Services principles, ISO 17025, SHE principles, Nestlé GLP, and Nestlé QMS
- Work with technical and scientific personnel on analytical issues, testing requirements, and new product specifications
Requirements
What you’ll need- Associate's or Bachelor's Degree preferred
- At least three years of relevant quality experience strongly preferred
- Proficient computer skills, including Microsoft Office
- Proficient basic mathematical and analytical skills
- Familiarity with SOPs (Standard Operating Procedures), GDPs (Good Documentation Practices), and cGMPs (Current Good Manufacturing Practices)
- Proficiency with AS400, SharePoint, Excel, Word, PowerPoint, PLM/PQM, and SAP
- Ability to read and understand chemistry and microbiology terminology and documentation
- Familiarity with GMP and Good Documentation Practices
- Good English verbal and written skills
- Ability to work collaboratively within teams
- Position is not eligible for Visa Sponsorship
Benefits
Comp & perks- Performance-based incentives
- 401k with company match
- Healthcare coverage
- Benefits supporting physical, financial, and emotional wellbeing
- Dynamic career paths
- Robust development opportunities
- Opportunities to learn from talented colleagues around the globe
- Reasonable accommodations during the recruitment experience