Quality Specialist

3 weeks ago


Somerset, United States Inteldot Full time

Inteldot has over 14 years in the life science industry with allocations a cross Puerto Rico, United Sates, Europe and Japan. This is a great opportunity for one of our leading clients in .

Conduct detailed reviews of deviation and investigation reports.
Provide feedback, comments, and edits on the reports.
Identify and document what actions need to be taken based on the findings in the reports.
Ensure reports comply with GMP standards.
Collaborate with other team members to maintain consistent quality and compliance.

Strong understanding of Good Manufacturing Practices (GMP).
Experience in reviewing and analyzing deviation and investigation reports.
Familiarity with control systems/automated systems (DCS); expertise is not required, but a working knowledge is essential.
Detail-oriented with excellent analytical and communication skills.
Must be able to work onsite in Central New Jersey.

2-3 months, with the potential for extension based on project needs.


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