CPCTS Manager — Idorsia Pharmaceuticals
- Location
- Allschwil
- Contract
- full-time
- Posted
- 40 days ago
Role overview
Idorsia 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.
Headquartered 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 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.
- Job Responsibilities
- Lead and manage commercial pharmaceutical artwork projects across the product lifecycle, ensuring timely delivery, quality, compliance and alignment with business priorities.
Main responsibilities
- Job Responsibilities
- Lead and manage commercial pharmaceutical artwork projects across the product lifecycle, ensuring timely delivery, quality, compliance and alignment with business priorities.
- Serve as the primary point of contact for artwork change management associated with product launches, regulatory submissions, market expansions and lifecycle management activities.
- Own the artwork lifecycle from change initiation through creation, review, approval, implementation and market deployment.
- Coordinate artwork development activities, including translations, proofreading, labeling updates and approvals, working closely with Regulatory Affairs, Marketing, Quality, Supply Chain, Manufacturing and external service providers.
- Develop and maintain artwork project plans, timelines, risk assessments, and implementation schedules to ensure successful execution of artwork and associated packaging changes.
- Lead cross-functional artwork governance and approval meetings, ensuring alignment across stakeholders and adherence to global and local regulatory requirements.
- Support commercial packaging activities related to product launches, packaging updates, component changes, serialization and market-specific requirements.
- Manage relationships with artwork agencies, packaging suppliers, and CMOs.
- Ensure artwork and packaging components comply with regulatory requirements, serialization requirements and country-specific labeling regulations.
Application process
- 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.
- We are committed to fostering respect, fairness, and equal opportunities for all job applicants and our employees.
- Please be informed that if you are selected for this position, your employment will be subject to a pre-employment background screening process, of which you would be informed in greater detail in due course.
- Idorsia 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.
- Please note Idorsia operates a strictly controlled list of preferred recruitment partners.
Contacts
- For those partners who have no valid, signed Master Service Agreement in place with Idorsia, all unsolicited resumes, CVs, anonymous profiles, or any other candidate details submitted through our website or to personal e-mail accounts of employees of Idorsia Pharmaceuticals (including any of its subsidiaries, affiliates, or related companies) are considered the property of Idorsia Pharmaceuticals and are not subject to payment of any form of introduction, placement or referral fees.
Company and context
- Excellent analytical, organizational, and problem-solving capabilities.
- Confident, proactive, and capable of influencing stakeholders at all organizational levels.
- Strong interpersonal, communication, and leadership skills.
- Knowledge of other GxP areas such as Pharmacovigilance (GVP), Clinical Quality (GCP), Computerized Systems Validation (CSV), or Data Integrity requirements would be a strong advantage .
- Fluent in English; knowledge of another European language is considered an asset. Work Location: Allschwil, Switzerland Business Area: Technical Operations Global Supply Chain
- Commercial Packaging & Clinical Trial Supply Job Type: Permanent, full time Job ID : 4808
- At Idorsia, we harness the power of difference, authenticity, and inclusion to achieve business success.
Additional details
- Coordinate all artwork-related documentation, specifications, change controls required for successful project delivery. Candidate’s Requirements
- Fluent in English; knowledge of another European language is considered an asset. Work Location: Allschwil, Switzerland Business Area: Technical Operations Global Supply Chain
- Commercial Packaging & Clinical Trial Supply Job Type: Permanent, full time
Notes and original content
- Coordinate all artwork-related documentation, specifications, change controls required for successful project delivery.
- Candidate’s Requirements
- Fluent in English; knowledge of another European language is considered an asset.
- Work Location: Allschwil, Switzerland
- Business Area: Technical Operations
- Global Supply Chain
- Commercial Packaging & Clinical Trial Supply
- Job Type: Permanent, full time
- Job ID : 4808
Questions about this listing
What salary does Idorsia Pharmaceuticals offer for this role?
Idorsia Pharmaceuticals lists CHF 85'500 - 129'500 gross per year for this position in Allschwil. This is the salary published in the original listing (or, when the employer omits a figure, a realistic estimate for the role and sector) — the calculator on this site converts it to your actual net take-home once cross-border tax and social contributions are applied.
Is this a full-time role, and what type of contract does Idorsia Pharmaceuticals offer?
This listing is a full-time position. The contract type shown here comes directly from the employer's original posting; always confirm exact hours, notice period and probation length with Idorsia Pharmaceuticals during the application process, since these details can vary by role even within the same contract category.
Do I need a cross-border work permit for a role in Basel?
EU/EFTA residents living in the border zone of the country adjoining Canton Basel can apply for a G permit; the Swiss employer files it with that canton's migration office after the contract is signed. Border-zone rules and processing times vary by neighbouring country and canton, so confirm the specifics with Basel's cantonal migration office or with HR during the application.
How do I apply for this position at Idorsia Pharmaceuticals?
Use the "Apply now" button on this page — it links directly to Idorsia Pharmaceuticals's original listing at careers.idorsia.com, so your application goes straight to the employer's own applicant-tracking system. Frontaliere Ticino does not collect or forward applications itself.
