Vendor Quality Control Analyst jobs in Somerset, NJ

Johnson & Johnson Family of Companies

Title: Laboratory Technical Writer

Location: Raritan, NJ - 100% Onsite

Duration: 1 year

Benefits on offer for this contract position: Health Insurance, Life insurance, 401K and Voluntary Benefits

Please note that this is a contract role providing services to the Johnson & Johnson Family of Companies through external staffing partners of Kelly OCG. If you are selected for this role, you will be employed by a contract staffing supplier and will not be a member of the Johnson & Johnson Family of Companies.

Summary:

The Technical Writer will plan, execute, and write laboratory investigations/deviations, in coordination with laboratory leads, identifying assignable/root causes and determining effective corrective and preventative actions.

Responsibilities:

• Write and edit detailed SOPs, validation protocols/reports, forms, analytical and technical documents and reports from conception to utilization.
• Provide project and investigation support through data collection, data trending, data review and technical writing of GMP documents (e.g. product/test specific protocols test methods or validation reports), SOPs and other documents associated within QC area.

Qualifications:

• BA/BS degree or higher
• 2 years of QC laboratory experience
• Project management experience is preferred.
• Excellent documentation skills required.
• MS Office Application (Word, Excel, Powerpoint) required.
• Truvault, TrackWise, eLIMS experience preferred.