Pharma Deviation Investigator — Process & QA

Spectraforce Technologies, Inc.; Clayton (NC); On-site; USD 34,000 - 47,000; Full time

Job summary

Spectraforce Technologies, Inc. in Clayton, NC is seeking a Deviation Investigator for a 12-month assignment, with a shift from 8 to 5. You will work with production and QA to investigate deviations, establish quick containment, and perform root cause analysis to prevent recurrence.

Qualifications include an Associate's degree in technology or equivalent, plus manufacturing experience (pharma preferred) and strong written communication. GMP knowledge and system familiarity are considered a plus.

Qualifications

• Associate's degree in technology required
• Minimum of two years manufacturing experience, preferably in a pharmaceutical environment
• Minimum of one year manufacturing experience in a pharmaceutical environment preferred
• Excellent written communication skills required
• GMP knowledge preferred
• System knowledge preferred
• Manufacturing experience preferred
• Pharmaceutical manufacturing experience a plus

Responsibilities

• Work directly with production and QA to support deviation investigations, quick containments and root cause analysis
• Ensure compliance with standards
• Identify process needs and improvement opportunities for routine to minimally complex matters
• Perform process confirmations to ensure compliance and process improvements
• Responsible for reviewing BPRs as necessary
• Follow all safety & environmental requirements in the performance of duties
• Other duties, as assigned

Skills

Deviation investigation or QA

Systematic problem solving

Pharma experience

Education

Associate's degree in technology

High School Diploma with 2 years manufacturing experience

Job description

Spectraforce Technologies, Inc. in Clayton, NC is seeking a Deviation Investigator for a 12-month assignment, with a shift from 8 to 5. You will work with production and QA to investigate deviations, establish quick containment, and perform root cause analysis to prevent recurrence.

Qualifications include an Associate's degree in technology or equivalent, plus manufacturing experience (pharma preferred) and strong written communication. GMP knowledge and system familiarity are considered a plus.