CPCTS Manager Job Details | Idorsia

ppSelect how often (in days) to receive an alert: /p pIdorsia Ltd is reaching out for more – We have more ideas, we see more opportunities and we want to help more patients. In order to achieve this, we will develop Idorsia into a leading biopharmaceutical company, with a strong scientific core. /p pHeadquartered near Basel, Switzerland – a European biotech-hub – Idorsia is specialized in the discovery, development and commercialization of small molecules to transform the horizon of therapeutic options. Idorsia has a 25-year heritage of drug discovery, a broad portfolio of innovative drugs in the pipeline, an experienced team of professionals covering all disciplines from bench to bedside, and commercial operations in Europe and North America – the ideal constellation for bringing innovative medicines to patients. /p pIdorsia was listed on the SIX Swiss Exchange (ticker symbol: IDIA) in June 2017 and has over 750 highly qualified specialists dedicated to realizing our ambitious targets. /p pWe are looking for a bCPCTS Manager (Artwork Focus) /bto join our Commercial Packaging Clinical Trial Supply Team ! /p h3Job Responsibilities /h3 ul liLead and manage commercial pharmaceutical artwork projects across the product lifecycle, ensuring timely delivery, quality, compliance and alignment with business priorities. /li liServe as the primary point of contact for artwork change management associated with product launches, regulatory submissions, marketexpansions and lifecycle management activities. /li liOwn the artwork lifecycle from change initiation through creation, review, approval, implementation and market deployment. /li liCoordinate artwork development activities, including translations, proofreading, labeling updates and approvals, working closely with Regulatory Affairs, Marketing, Quality, Supply Chain, Manufacturing and external service providers. /li liDevelop and maintain artwork project plans, timelines, risk assessments, and implementation schedules to ensure successful execution of artwork and associated packaging changes. /li liLead cross-functional artwork governance and approval meetings, ensuring alignment across stakeholders and adherence to global and local regulatory requirements. /li liSupport commercial packaging activities related to product launches, packaging updates, component changes,serialization and market-specific requirements. /li liManage relationships with artwork agencies, packaging suppliers, and CMOs. /li liEnsure artwork and packaging components comply with regulatory requirements, serialization requirements and country-specific labeling regulations. /li liTrack and communicate project status, key milestones, risks, and mitigation plans to stakeholders and leadership. /li liCoordinate all artwork-related documentation, specifications, change controls required for successful project delivery. /li /ul h3Candidate’s Requirements /h3 ul liUniversity degree in Pharmacy, Chemistry, Biotechnology, Life Sciences, or another relevant scientific discipline (Master's degree preferred). /li liMinimum 7 years of experience in pharmaceutical Quality Assurance, Compliance, Supplier Quality, Manufacturing Quality, or related GxP functions. /li liDemonstrated experience managing supplier qualification programs and conducting GMP/GDP audits as Lead Auditor. /li liStrong knowledge of pharmaceutical development, manufacturing, packaging, testing, storage, and distribution activities. /li liExcellent knowledge of relevant GMP/GDP regulations and international quality standards, including EU GMP, EU GDP, ICH, PIC/S, WHO, FDA, and ISO requirements. /li liProven ability to independently interpret regulations and implement pragmatic, risk-based compliance solutions. /li liExperience in developing and managing Quality Agreements and external partner oversight programs. /li liStrong project management skills with the ability to manage multiple priorities in a dynamic environment. /li liExcellent analytical, organizational, and problem-solving capabilities. /li liConfident, proactive, and capable of influencing stakeholders at all organizational levels. /liliStrong interpersonal, communication, and leadership skills. /li liKnowledge of other GxP areas such as Pharmacovigilance (GVP), Clinical Quality (GCP), Computerized Systems Validation (CSV), or Data Integrity requirements would be strong advantage. /li liFluent in English; knowledge of another European language is considered an asset. /li /ul h3Business Area /h3 pTechnical Operations - Global Supply Chain - Commercial Packaging Clinical Trial Supply /p h3Job Type /h3 pPermanent, full time /p h3Job ID /h3 p4808 /p pbAt Idorsia, we harness the power of difference, authenticity, and inclusion to achieve business success.br/We encourage all potential candidates with diverse backgrounds of race, color, religion, sexual orientation, gender identity, age, national origin, and disability to submit their job applications. All applicants will receive consideration.br/We are committed to fostering respect, fairness, and equal opportunities for all job applicants and our employees. /b /p pIdorsia Pharmaceuticals Ltd ("Idorsia") is committed to a fair and transparent application process. In order to avoid any conflict of interest in line with Idorsia Code of Business Conduct, which would undermine such a commitment, the applicants must disclose any personal, financial, or other outside interests interfering with the interests of Idorsia. Further, the applicant is obliged to disclose any and all relationships with close or affiliated persons, who are employees of Idorsia or are collaborating with Idorsia in any other contractual relationship. /p /p #J-18808-Ljbffr