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Job Requirements of MS&T Specialist – Deviations Investigator:
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Employment Type:
Contractor
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Location:
Davie, FL (Onsite)
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MS&T Specialist – Deviations Investigator
Careers Integrated Resources Inc
Davie, FL (Onsite)
Contractor
Job Title: MS&T Specialist – Deviations Investigator (Contract)
Location: Davie, FL (100% Onsite – Local candidates only)
Duration: 6 Months (Potential for Temp-to-Perm)
Shift: Monday – Friday | 8:00 AM – 5:00 PM
Position Summary
We are seeking a highly motivated MS&T Specialist – Deviations Investigator to support cGMP investigations within Oral Solid Dose (OSD) pharmaceutical manufacturing. This role will focus on leading and supporting deviation investigations, performing root cause analysis, and driving CAPA implementation to ensure compliant and continuous manufacturing operations.
The ideal candidate will be hands-on in troubleshooting, comfortable working cross-functionally, and capable of navigating complex technical discussions across Production, Engineering, Quality, and QC teams.
Key Responsibilities
- Lead and support deviation investigations, non-conformances, and atypical events in a cGMP environment
- Perform root cause analysis using structured tools (e.g., 5-Why, Fishbone)
- Collaborate cross-functionally with Manufacturing, Engineering, QA, and QC teams to resolve issues
- Analyze manufacturing and laboratory data (batch records, equipment logs, etc.) to determine root causes
- Develop and track Corrective and Preventive Actions (CAPAs) and ensure effectiveness
- Support batch disposition decisions and ensure product quality compliance
- Maintain clear and compliant documentation aligned with Good Documentation Practices (GDP)
- Participate in continuous improvement initiatives and support audit readiness
Required Qualifications
- Minimum Master’s degree in a scientific or engineering discipline (e.g., Chemistry, Biology, Chemical Engineering, Pharmaceutical Sciences)
- Experience in pharmaceutical manufacturing environment (cGMP)
- Strong experience in deviation investigations, CAPA, and root cause analysis
- Knowledge of Oral Solid Dose (OSD) processes (e.g., granulation, compression, coating, blending) preferred
- Familiarity with quality and manufacturing systems (e.g., MES, LIMS, eQMS)
Core Skills & Competencies
- Strong troubleshooting and analytical skills in a manufacturing setting
- Excellent cross-functional collaboration and communication skills
- Ability to navigate complex discussions, influence stakeholders, and drive resolution
- Strong negotiation and interpersonal skills
- Ability to manage multiple priorities and work independently in a fast-paced environment
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