Pharma Deviation & CAPA Investigator - Onsite Indy

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

Avantages offerts par ce poste

Life Insurance

Disability Insurance

Health Savings Account

Paid Time Off

Tuition Reimbursement

Parental Leave

Bereavement

Employee Referral Program

Résumé du poste

Verista, based in Indianapolis, IN, seeks a Deviation Investigator / CQV lead to manage deviation investigations, root-cause analysis, CAPA development, and change controls in the Pharma sector. Onsite in Indianapolis, you will collaborate with cross-functional teams to meet regulatory expectations and ensure data integrity.

Requirements include an undergraduate STEM degree, 1-3 years of experience, strong writing and communication skills, and proficiency with MS Office.

Qualifications

• Undergraduate Engineering/STEM degree preferred
• 1-3 years' 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 ability to communicate effectively with peers
• 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 and OOS investigations with root-cause analysis
• Author deviation reports and CAPA plans with defensible rationale
• Draft CAPA plans that are risk-appropriate and linked to verified root causes

Connaissances

Root cause analysis

Technical writing

Communication

Team collaboration

Problem solving

Formation

Undergraduate Engineering/STEM degree

Outils

Microsoft Office

Description du poste

Verista, based in Indianapolis, IN, seeks a Deviation Investigator / CQV lead to manage deviation investigations, root-cause analysis, CAPA development, and change controls in the Pharma sector. Onsite in Indianapolis, you will collaborate with cross-functional teams to meet regulatory expectations and ensure data integrity.

Requirements include an undergraduate STEM degree, 1-3 years of experience, strong writing and communication skills, and proficiency with MS Office.