Deviation Investigations Specialist

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* Job Title:

** Deviation Investigations Specialist

** Location** :
Davie, FL
- ** Must be local and this role is 100% Onsite*
* ** Duration:
** 6 months with possible Temp to perm based on performance

** Pay:**  $35.00/HR.

** Shift:
** Monday - Friday, 8A - 5P. Should be flexible to work other shifts

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** Required Skills** :

- Min 2 years of pharmaceutical industry experience in Deviation Investigations.

- Experience in Deviation Investigations, CAPAs, and FDA Audit exposure.

- This role will focus heavily on internal troubleshooting within the client and require frequent cross-functional collaboration.

- The individual should be confident in navigating conversations across teams, with strong negotiation skills and the ability to communicate effectively and proactively.

- Minimum Master's degree

** POSITION SUMMARY*
* - This position is responsible for leading and performing cGMP investigations supporting Oral Solid Dose (OSD) manufacturing, including complex manufacturing processes and equipment.

- The Investigator authors and coordinates high-quality investigations for events occurring in Production, Engineering, Quality Control (QC) Laboratory, and related support areas, ensuring timely root cause identification, appropriate product impact assessments, and implementation of effective Corrective and Preventive Actions (CAPAs) to maintain compliant supply.

- The role applies scientific and technical judgment to evaluate manufacturing and laboratory data, interviews and observation, equipment/utilities performance, and process parameters to support robust root cause analysis and sustainable remediation for OSD unit operations (e.g.,  blending, granulation, compression, coating, encapsulation, etc.) and associated systems.

** ESSENTIAL AREAS OF RESPONSIBILITY*
* - Lead and/or co-author cGMP investigations for OSD manufacturing and complex operations (deviations/nonconformances/atypical events), ensuring clear problem statements, accurate timelines, and timely closure in the quality system.

- Coordinate event triage and immediate actions, including containment and escalation, and support batch disposition decisions with Operations, Engineering, QC, and QA.

- Collect, organize, and analyze manufacturing, engineering, and laboratory evidence (e.g., batch records, equipment/maintenance logs, MES/SCADA/historian data, calibrations, environmental monitoring, and test results) to establish event sequence and contributing factors.

- Facilitate cross-functional root cause analysis using structured tools (e.g., 5-Why, fishbone, fault tree as applicable) and document technically sound, compliant conclusions and product impact assessments.

- Define, document, and track CAPAs (correction/corrective/preventive actions) with appropriate due dates and effectiveness checks; support on-the-floor verification and implementation to prevent recurrence.

- Prepare clear, complete investigation/CAPA records; support trending and continuous improvement; and participate in audit/inspection readiness by providing evidence packages and responses (while maintaining required training and safe work practices).

** POSITION REQUIREMENTS*
* - Any equivalent combination of education, training and/or experience that fulfills the requirements of the position will be considered.

** Education/Certification/

Experience:

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* - Master's or Ph.D. degree in a scientific or engineering discipline with relevant experience supporting investigations within pharmaceutical manufacturing, engineering, and/or QC laboratories; oral solid dosage (OSD) experience preferred.

- Experience using electronic quality systems and manufacturing/laboratory data systems (e.g., deviation/CAPA systems, MES, LIMS, historian/trending tools, AI tools) to support investigations, trending, and effectiveness monitoring preferred

** Skills/Knowledge/Abilities:*
* - OSD manufacturing and complex process/equipment knowledge sufficient to investigate events across Production, Engineering, and QC (e.g., blending, granulation, compression, coating, encapsulation, and supporting utilities).

- Strong Technical writing and documentation skills (deviations/nonconformances, OOS/OOT as applicable, product…