Piper Companies is seeking a Deviation Management Specialist to fill an opportunity with a reputable Pharmaceutical company in Lansdale, PA. Responsibilities for the Deviation Management Specialist * Investigate deviations by assessing product impact, identifying root causes, and implementing corrective/preventative actions. * Author and update GMP documentation, including SOPs, batch records, validation documents, and change controls. * Write quality incident and deviation reports, ensuring thorough analysis and compliance. * Collaborate with cross-functional teams to drive process improvements, resolve investigations, and maintain compliance. Qualifications for the Deviation Management Specialist * 2-4 years of experience in deviation management and investigations within biologics, vaccines, or sterile manufacturing. * Proficient in Change Control processes and technical writing. * Strong communication, leadership, and teamwork abilities. * Skilled in managing projects and meeting deadlines. Compensation for the Deviation Management Specialist * Salary Range is Commensurate with Experience * Long Term Contract (Possible Extension) * Comprehensive Benefits: Medical, Dental, Vision, 401K, PTO, Sick Leave as required by law, and Holidays This job opens for applications on 4/23/2025. Applications for this job will be accepted for at least 30 days from the posting date. Keywords: Deviation, Investigation, Change Control, CAPA, Root Cause, Batch Record, GMP, Good Manufacturing Practice, Validation, Biologics, Vaccines, Pharmaceutical, Quality Assurance, #LI-JM1 #LI-ONSITE