Deviation Investigation Support

For the past 25 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. ProPharma partners with its clients through an advise-build-operate model across the complete product lifecycle.

With deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners’ most high-profile drug and device programs. This will be a 15-month contract, beginning in Q4 2026 through the end Q4 2027.

The deviation writers will be involved in meetings with site representatives for deviation events, collaborating with SMEs as needed, and providing deviation investigation support with updates as needed.

The deviation writers will go through training with the company and be responsible for: Completion of training on time Presence and engagement at meetings Clear communication of progress on deviation records Ownership of deviation records through approval including but not limited to the following activities: Thorough root cause investigation, including process background, event overview, creation of CAPA(s) and effectiveness checks.

Set-up deviation review board when applicable Route deviation records for review and approval Requirements The deviation writers should have a background in Quality Control Laboratories, experience in root cause investigation, and CAPA creation. Personnel are expected to have excellent communication, technical writing skills, and time management skills to ensure timely and high-quality deviation writing and timely approval. Additional skills such as experience with systems such as Veeva QMS, MODA, and SmartLab would be helpful in ensuring their success in this space.

LabVantage experience is a plus. 5+ years of relevant experience #LI-EB3 #Quality Control #Deviations We celebrate our differences and strive to create a workplace where each person can be their authentic self. We are committed to diversity, equity, and inclusion. Employees are encouraged to unleash their innovative, collaborative, and entrepreneurial spirits. With a holistic approach as an Equal Opportunity Employer, we provide a safe space where all employees feel empowered to succeed. All applications to roles at ProPharma are personally reviewed by a member of our recruitment team.

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• 5+ years experience in Quality Control Laboratories with root cause investigation and CAPA creation
• Excellent communication, technical writing, and time management skills
• Familiarity with Veeva QMS, MODA, SmartLab; LabVantage experience is a plus