Senior Specialist, Lead Investigator

Resilience; Ohio; On-site; USD 90,000 - 120,000; Full time

Job summary

Resilience, Inc. is hiring a Senior Specialist, Lead Investigator in Ohio to drive complex investigations from initiation to closure. You will define scope, coordinate with QA, Manufacturing, and R&D, and ensure timely, compliant root-cause analysis and CAPA actions.

The role emphasizes strong communication and regulatory understanding. The position requires a Bachelor's in a related field, 5+ years of regulated manufacturing experience, and proven ability to manage multiple investigations in a

Qualifications

• Experience in Pharmaceutical Manufacturing or similar regulated industry.
• Familiarity with cGMP documentation practices and regulatory requirements.
• Ability to present findings clearly and lead investigations to closure.
• Ability to manage multiple investigations with timelines and accountability.
• Strong written, verbal, and presentation skills.

Responsibilities

• Plan and conduct organized investigations with defined scope, strategy, and timeline.
• Author investigation reports detailing scope, root cause, and corrective actions.
• Collaborate with cross-functional teams to develop investigation strategy and CAPA actions.
• Communicate status and outcomes to stakeholders; escalate as needed.

Skills

Investigation management

Cross-functional collaboration

Written/verbal communication

Problem solving

Regulatory awareness

Education

Bachelor's degree in Science/Engineering

Tools

CAPA system

Lean problem-solving tools

Job description

.Senior Specialist, Lead Investigator page is loaded## Senior Specialist, Lead Investigatorlocations: USA - OH - West Chestertime type: Full timeposted on: Posted Todayjob requisition id: R-107411A career at Resilience is more than just a job - it's an opportunity to change the future.Resilience is a technology-focused biomanufacturing company that's changing the way medicine is made. We're building a sustainable network of high-tech, end-to-end manufacturing solutions to better withstand disruptive events, serve scientific discovery, and reach those in need.For more information, please visitThe Senior Specialist, Lead Investigator is responsible for performing investigations and driving each event to conclusion by working with others. The Lead Investigator ensures the investigation outcome and root cause analysis are completed in a timely, effective, and compliant manner. The speed and rigor demonstrated by the Lead Investigator will drive a culture that prevents unplanned deviations through a robust and proactive investigation process.# **Job Responsibilities****Investigation Management & Execution*** Conducts organized investigations with a well-defined scope, strategy, and timeline, documenting status and progress of the investigation.* Authors reports that document the investigation of issues, including definition, scope, product impact, root cause, and corrective actions to prevent the recurrence of the issue.* Utilizes the appropriate and approved investigation tools necessary to drive the team to root cause.* Prioritizes work to aid in timely decisions and completion of investigations. Escalates issues as appropriate.**Root Cause & Cross-Functional Collaboration*** Seeks and leverages the skills and technical expertise of internal and external resources to improve the speed and rigor of investigations.* Collaborates with a cross-functional team to determine:+ Communication strategy so all stakeholders have appropriate information.+ Investigation strategy including a clear and actionable problem statement.+ Investigation tools.+ Investigation action plan and timing.+ Root cause.+ CAPA action plan and effectiveness checks.## **Education & Experience****Minimum Qualifications*** Experience in Pharmaceutical Manufacturing and/or other similar regulated industry.* Familiarity with cGMP documentation practices and applicable regulatory requirements.* Ability to quickly assess and assimilate technical data and conduct a thorough investigation; ability to present findings, conclusions, and complex information in a clear, concise, and logical manner.* Ability to manage multiple concurrent investigations, monitoring progress against objectives and timelines to drive timely closure.* Excellent written, verbal, and presentation skills, including technical and investigation report writing.* Ability to work in a fast-paced and rapidly changing environment.* Ability to prioritize work activities to meet customer needs and deadlines.* Ability to take accountability with excellent follow up and follow through; owns issues through the full cycle investigation process.* Exercises independent judgment to advance investigations with minimal direction; coaches others and builds cross-functional alignment on root cause and corrective-action decisions.**Preferred Qualifications*** Bachelor's degree, preferably in Science, Engineering, or other related technical discipline. Relevant work experience will be considered in lieu of a degree.* 5+ years of experience in a pharmaceutical or other regulated manufacturing environment, including quality investigations and deviation management.* Understanding of the internal core business processes.* Adept at identifying and understanding the critical factors in order to generate appropriate solutions.* Multiple site or function experience* Familiar with Lean problem-solving tools# **Physical & Work Environment*** Work is performed in a combination of office, laboratory, and cGMP manufacturing environments.* This position may also include the following conditions: sitting, standing, walking, repetitive motion, and / or wearing personal protective equipment.* May require specific visual skills such as interpreting sounds and associated meanings at volume levels consistent with interpersonal or group conversations; interpreting letters and numbers when viewed on a computer screen, monitor, reports and other documents; identifying and distinguishing colors# **Work Schedule****Schedule: 8 hours - Monday- Friday**The work schedule listed reflects the employee's expected schedule at the time of hire. The Company reserves the right to modify work schedules at any time, including requiring overtime, with or without notice, based on business needs, operational requirements, or other considerations. Nothing in this description creates a guarantee of specific hours, days, or shift assignments.***Sponsorship or support for work authorization, including visas, is not available for this position.***Resilience is an Equal Employment Opportunity Employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender perception or identity, national origin, age, marital status, protected veteran status, disability status, physical or mental disability, genetic information, or characteristic, or other non-job-related characteristics or other prohibited grounds specified in applicable federal, state, and local laws. Requests for reasonable accommodation can be made at any stage of the recruitment process.