Pharma Deviation Investigator & Validation Engineer

Verista, Inc.; Indianapolis (IN); Sur place; USD 69 000 - 103 000; Plein temps

Avantages offerts par ce poste

Health Savings Account

Life Insurance

Disability Insurance

Tuition Reimbursement

Paid Time Off

Résumé du poste

Verista, Inc. in Indianapolis, IN is seeking aDeviation Investigator / CQV to lead deviation investigations, root cause analysis, and CAPA development within the Pharma industry.

The role emphasizes data integrity and regulatory compliance and requires strong technical writing and collaboration with cross-functional teams. Requirements include an engineering/STEM degree, 1–3 years of experience, proficiency with Microsoft Office, and the ability to work onsite in Indianapolis.

Qualifications

• Engineering/STEM degree preferred.
• 1–3 years of experience.
• Deviation investigation remediation and/or quality experience is a plus.
• New college grads with internship experience encouraged to apply.
• Proficiency using PC and Microsoft Office tools.
• Outgoing personality with strong communication abilities.
• Ability to work as part of a team.
• Strong problem-solving and critical thinking skills.
• Excellent technical writing skills.
• Excellent organizational and time management skills.
• Strong attention to detail.
• Strong interpersonal skills and clear communication capabilities.
• Experience with and tolerance for high levels of challenge and change.
• Onsite requirement in Indianapolis, IN.

Responsabilités

• Lead deviation investigations and OOS using structured root cause analysis.
• Author deviation reports and CAPA plans with defensible rationale.
• Draft CAPA plans that are risk-appropriate, measurable, and linked to verified root causes.

Connaissances

Communication skills

Teamwork

Problem solving

Technical writing

Attention to detail

Formation

Undergraduate Engineering degree

Outils

Microsoft Office

Description du poste

Verista, Inc. in Indianapolis, IN is seeking aDeviation Investigator / CQV to lead deviation investigations, root cause analysis, and CAPA development within the Pharma industry.

The role emphasizes data integrity and regulatory compliance and requires strong technical writing and collaboration with cross-functional teams. Requirements include an engineering/STEM degree, 1–3 years of experience, proficiency with Microsoft Office, and the ability to work onsite in Indianapolis.