Deviations Investigation Specialist

Kindeva Drug Delivery; Maryland Heights (MO); On-site; USD 85,000 - 115,000; Full time

Job summary

Kindeva Drug Delivery is seeking a Deviations Investigation Specialist to join our Production Operations – Compliance Investigation group. You will lead deviation investigations, assess root causes, and develop CAPAs in collaboration with Quality, Engineering, and Operations.

You will author clear investigation records, perform risk assessments, and ensure compliance with GMP and quality systems while driving continuous improvement across manufacturing processes.

Qualifications

• Bachelor's degree in a related discipline or equivalent combination of education and experience.
• 3+ years in a GMP-regulated manufacturing environment.
• Experience with quality management systems and regulated documentation practices.
• Experience with root cause analysis and structured problem-solving methodologies.
• Strong technical writing, analytical, and communication skills.

Responsibilities

• Lead deviation investigations related to manufacturing and operational events, ensuring timely completion and compliance with site quality systems and GMP requirements.
• Partner with Operations, Quality, Engineering, Validation, and other stakeholders to gather facts, assess impact, establish containment actions, and determine appropriate response plans.
• Facilitate root cause investigations using structured problem‑solving methodologies and data‑driven analysis to identify the most probable causes of events.
• Perform and document risk assessments to evaluate product quality, regulatory, operational, and business impacts.
• Author clear, thorough, and technically sound investigation reports, ensuring conclusions are supported by facts, evidence, and data.
• Develop and support corrective and preventive actions (CAPAs) that address root causes and reduce recurrence.
• Author or support quality system documentation including deviations, CAPAs, risk assessments, change controls, effectiveness checks, and related records as required.
• Analyze investigation data and trends to identify recurring issues and opportunities for continuous improvement.
• Support training, coaching, and collaboration efforts to improve investigation quality, problem‑solving capabilities, and compliance across the organization.

Skills

Root cause analysis

Technical writing

Analytical thinking

Communication skills

Cross-functional collaboration

Problem-solving

Education

Bachelor's degree in Engineering, Chemistry, Biology, Pharmaceutical Sciences, Quality, Business, or related discipline

Job description

Posted Tuesday, July 28, 2026 at 4:00 AM

Our Work Matters

At Kindeva we make products that save lives, ensuring better health and well-being for patients around the world.

The Impact You Will Make

The Deviations Investigation Specialist partners with Operations, Quality, and cross‑functional teams to investigate manufacturing and quality events, determine root cause, assess risk, and support the development of effective corrective and preventive actions. This role leads and facilitates deviation investigations, authors investigation records and risk assessments, and ensures investigations are completed accurately, objectively, and in compliance with applicable GMP and quality system requirements.

The Deviations Investigation Specialist serves as a key resource in identifying systemic issues, improving compliance, and driving sustainable solutions that enhance product quality and manufacturing performance.

Role Responsibilities

• Lead deviation investigations related to manufacturing and operational events, ensuring timely completion and compliance with site quality systems and GMP requirements.
• Partner with Operations, Quality, Engineering, Validation, and other stakeholders to gather facts, assess impact, establish containment actions, and determine appropriate response plans.
• Facilitate root cause investigations using structured problem‑solving methodologies and data‑driven analysis to identify the most probable causes of events.
• Perform and document risk assessments to evaluate product quality, regulatory, operational, and business impacts.
• Author clear, thorough, and technically sound investigation reports, ensuring conclusions are supported by facts, evidence, and data.
• Develop and support corrective and preventive actions (CAPAs) that appropriately address root causes and reduce recurrence.
• Author or support quality system documentation including deviations, CAPAs, risk assessments, change controls, effectiveness checks, and related records as required.
• Analyze investigation data and trends to identify recurring issues and opportunities for continuous improvement.
• Support training, coaching, and collaboration efforts to improve investigation quality, problem‑solving capabilities, and compliance across the organization.

Basic Qualifications

• Bachelor's degree in Engineering, Chemistry, Biology, Pharmaceutical Sciences, Quality, Business, or a related discipline; or equivalent combination of education and experience.
• 3+ years of experience in a GMP‑regulated manufacturing environment.
• Experience authoring, investigating, reviewing, or approving deviations, investigations, or other quality system records.
• Experience with quality management systems and regulated documentation practices.
• Experience utilizing root cause analysis and structured problem‑solving methodologies.
• Strong technical writing, analytical, and communication skills.
• Ability to effectively collaborate with cross‑functional teams and influence outcomes.

Preferred Qualifications

• Experience in pharmaceutical, biotechnology, medical device, or other regulated manufacturing environments.
• Experience supporting aseptic processing, sterile fill‑finish, visual inspection, packaging, or device manufacturing operations.
• Experience authoring or supporting risk assessments, CAPAs, change controls, and effectiveness checks.
• Experience participating in regulatory inspections, customer audits, or internal audits.
• Lean Six Sigma Green Belt, Black Belt, ASQ certification, or similar quality‑related credential.

Kindeva does not accept unsolicited assistance from headhunters or recruitment firms for any of our job openings. Any resumes or candidate profiles submitted to Kindeva employees—regardless of format—without a valid, signed agreement and an approved job order from an authorized signatory in Talent Acquisition will be considered the sole property of Kindeva. No fees will be paid in the event that a candidate is hired as a result of an unsolicited resume or referral.

Equal Opportunity Employer

Kindeva Drug Delivery is an Equal Opportunity/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, gender, age, national origin, disability, Protected Veteran status, sexual orientation, or any other characteristic protected by federal, state or local law.

Job Family D - Production Operations - Compliance Investigation