Senior Analyst Quality Control

Johnson & Johnson Innovative Medicine

Nes Ziona, Israel
Not specified (assumed to be onsite given the nature of the role).
Gmp analytical testing
Laboratory management
Gmp compliance
Johnson & Johnson is seeking a Senior Analyst for Quality Control at their Nes Ziona site, focused on hands-on laboratory testing and management within the surgical technology sector. Ideal candidates should possess a strong background in GMP-regulated environments and significant experience with enzymatic/protein assays. The role emphasizes operational excellence, mentoring, and compliance with quality standards

Job Summary

  • This role performs QC analytical testing in accordance with GMP, approved methods, and procedures, and contributes to laboratory management.
  • The position involves developing and supporting implementation of laboratory practices, participating in planning and implementation of changes in analytical methods, tooling, equipment, and test scheduling.
  • The Senior Analyst Quality Control will mentor, coach, and train QC staff through hands-on guidance and knowledge sharing, and support development and tracking of QC metrics.

Matching Summary

Match Score: 85

Johnson & Johnson is seeking a Senior Analyst for Quality Control at their Nes Ziona site, focused on hands-on laboratory testing and management within the surgical technology sector. Ideal candidates should possess a strong background in GMP-regulated environments and significant experience with enzymatic/protein assays. The role emphasizes operational excellence, mentoring, and compliance with quality standards.

Skills & Requirements

Must-have

  • GMP analytical testing
  • laboratory management
  • GMP compliance
  • data integrity
  • troubleshooting skills

Nice-to-have

  • Enzymatic/Protein assays experience
  • operational excellence
  • mentoring and coaching
  • relationship building
  • technologically savvy

Key Requirements

  • B.Sc. in Chemistry, Life Sciences, Biochemistry, Biotechnology, Pharmaceutical Sciences, or related
  • Minimum 2+ years hands-on QC Analyst experience
  • Experience working under GMP
  • High English proficiency

Work Rights

Not specified

Tailored Resume

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