Ph3Job Description /h3 pAt Ferring Pharmaceuticals, we help people around the world build families and live better lives. We are entrepreneurial and innovative, with a global team focused on scientific advances in the areas of reproductive and women’s health, gastroenterology and urology. Ferring + You is all about working together and sharing ideas, so that we can bring science to life for patients around the world. /p pOur Technical Operations division develops, manufactures and supplies high-quality products so our patients can live better lives. Creating and delivering life‑changing products means getting it right the first time is a shared responsibility, so our global manufacturing teams work closely together to ensure quality, accuracy and safety at all times. That means a culture of empowerment, where speaking up is valued, and growth and development are constant. /p h3Your Day at Ferring /h3 ul liLead and maintain Deviation Management System in line with Corporate procedures and GMP requirements. /li liOwn and coordinate the self‑inspection program, including annual planning, data analysis, reporting and support to contributors. /li liContribute to Health Authority inspections by leading readiness activities and acting as QMS representative or process expert during inspections. /li liReview and approve quality records, procedures, protocols and reports within the area of expertise. /li liProvide QA oversight for training processes, train new employees on GMP systems and applicable quality processes. /li liSupport regulatory surveillance activities related to Pharmacopoeias, including report review and process improvement. /li liDrive continuous improvement initiatives and support site GxP compliance activities across quality systems. /li /ul h3Qualifications /h3 ul liBachelor’s or Master’s degree in Pharmacy, Life Sciences, Chemistry, Biotechnology or a related scientific discipline. /li liProven experience in Quality Assurance and Quality Management Systems within a GMP‑regulated pharmaceutical or biotechnology environment. /li liStrong knowledge of deviation management, self‑inspections, CAPA and Inspection readiness activities. /li liExperience in drafting, reviewing and approving GMP documentation, procedures, protocols and quality records. /li liAbility to train and support cross‑functional stakeholders on quality systems and compliance expectations. /li liExperience participating in Health Authority inspections and/or supplier audits. /li liStrong analytical skills with the ability to trend data, identify compliance risks and support continuous improvement. /li liExcellent written and spoken English skills, with the ability to draft clear GMP documentation and communicate effectively with cross‑functional and international stakeholders. /li liExperience with Electronic Quality Systems such as TrackWise and Veeva. /li liKnowledge of Pharmacopoeia regulatory surveillance processes. /li liGood knowledge of GMP/GxP requirements, quality systems governance, inspection management, root cause analysis, CAPA processes and quality reporting tools. /li /ul h3Benefits /h3 ul liGet inspired from our commitment to advocate for everyone’s right to build a family, no matter who you are, where you live or who you love. /li liOur inclusive support package – “Building Families at Ferring” provides equal and accessible policies for all employees who wish to start their family journey, ensuring a global standard, irrespective of location and role. /li liParental leave for both birthing and non‑birthing parents. /li liExtended support on family building journey. /li /ul h3Location /h3 pSwitzerland SMP - St Prex /p h3EEO Statement /h3 pWe strive to build and maintain an inclusive and diverse workplace with equal opportunities and mutual respect for all employees regardless of their backgrounds and socioeconomic status. /p /p #J-18808-Ljbffr