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Swiss Responsible Person and GDP Quality Assurance

Rhythmpharmaceuticals · Zurich · Active · JazzHR / ApplyToJob

Job facts

FieldValue
CompanyRhythmpharmaceuticals
TitleSwiss Responsible Person and GDP Quality Assurance
Normalized title-
Department / team-
LocationZurich
Work model-
Employment typeFull Time
Salary-
Statusactive
ATS providerJazzHR / ApplyToJob
Posted / first seen2026-03-11 / 2026-05-30
Changed / last seen2026-05-30 / 2026-06-04

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Linked records

CompanyRhythmpharmaceuticals
Sourcea089d8d0-2598-437f-b618-c2dc9cbdd98b
ATS providerJazzHR / ApplyToJob

Description

Company Overview Rhythm is a global, commercial-stage biopharmaceutical company committed to transforming the lives of patients and their families living with rare neuroendocrine diseases. We develop medicines for previously untreatable or undertreated diseases and provide meaningful support for healthcare providers and patients and their families. We recognize the courage it takes for patients and their caregivers to begin their journey of advocacy to find the answers they need. Their courage inspires us to challenge convention, ask bold questions and seek answers for them. Every day, we strive for excellence through our willingness to learn, adapt and our tenacity to overcome barriers, together. Opportunity Overview This role serves as the Responsible Person (RP) for Switzerland under the Swissmedic Wholesale Distribution License (WDL). The RP is fully accountable for product quality and regulatory compliance under Art. 11 ff of the Medicinal Products Licensing Ordinance (MPLO; SR 812.212.1). In addition to Swiss RP duties, the role provides overall support to the global GDP operations, ensuring alignment and consistency across GDP processes, records, electronic systems, and compliance activities. Responsibilities and Duties The RP must (aligned with Swissmedic and GDP expectations): Maintain an effective QMS, overseeing authorized activities and ensuring accurate, high-quality records. Ensure non-conforming medicinal products, such as expired goods or those failing to meet specifications, are clearly labelled and not released to the market, and that packaging complies with current Swissmedic approvals. Deciding on the final disposition of returned, rejected, recalled, or falsified products. Effectively manage product quality complaints and temperature excursions. Conduct regular self-inspections according to a set schedule, monitor GDP compliance, and implement corrective actions as needed. Approve test reports for finished medicinal products or returning saleable products. Ensure appropriate samples are taken and kept as retention samples. Complete all mock or actual recalls accurately and within the specified time frame. Supplying medicinal products in Switzerland only to customers authorised to distribute them under GDP. Ensure suppliers and subcontracted activities are approved and qualified. Ensure that initial and continuous training programs are implemented and maintained. Act as contact person for Swissmedic. Ensure Swiss-specific assessment and evaluation of APQRs are conducted in accordance with Swissmedic timelines. Conduct Annual Management Reviews. Manage deviations and changes appropriately, and promptly notify Swissmedic of any major change according to Art. 41 of MPLO. Ensure that appropriate Corrective and Preventive Actions (CAPAs) are clearly defined as required and effectively managed throughout their implementation. Ensuring potential risks are thoroughly analyzed and managed effectively. Overall Support for Global GDP Operations The role will: Support global GDP operations by reviewing documents, preparing batch disposition and returns paperwork, and coordinating approval processes within Veeva. Manage temperature excursions and distribution events ensuring all incidents are properly recorded and corrective actions are implemented in line with global GDP standards. Support GDP audits and self‑inspections, including management of records within Veeva eQMS. Support maintenance of global GDP procedures, work instructions, forms, and templates to ensure consistent execution across all Rhythm GDP markets. Contribute to global GDP change control, deviation, CAPA, and quality event administration, ensuring consistent documentation and follow‑up across regions. Coordinate global GDP training activities. Qualifications and Skills Meets requirements to serve as RP under Swissmedic WDL Preferred with 8 +years of relevant industry work experience Broad knowledge of EU GDP Excellent documentation, organizational, and administrative skills Proven experience in managing outsourced GDP activities in a virtual environment In-depth knowledge of the Swiss healthcare system, medical landscape, and current trends in industry Willingness to travel More about Rhythm We are a dynamic and growing global team spanning more than a dozen countries. At Rhythm we are dedicated to transforming the lives of patients living with rare neuroendocrine diseases by rapidly advancing care and precision medicines that address the root cause. Our team is passionate about expanding access to reach more patients and developing novel therapies for other rare neuroendocrine diseases, including congenital hyperinsulinism. At Rhythm Our Core Values Are •      We are committed to advancing scientific understanding to improve patients’ lives •      We are inspired to tackle tough challenges and have the courage to ask bold questions •      We are eager to learn and adapt •      We believe collaboration and ownership are foundational for our success •      We value the unique contribution each individual brings to furthering our mission

Full job record

Job ID4ea2ef3330754609cdbc48b2d4689255124e6707
Org ID73fb8494-6154-4f75-bcac-7c8caae53a03
Source IDa089d8d0-2598-437f-b618-c2dc9cbdd98b
Board IDa089d8d0-2598-437f-b618-c2dc9cbdd98b
Providerjazzhr
Provider Job KeyvItXDErLMo
TitleSwiss Responsible Person and GDP Quality Assurance
Normalized Title—
Statusactive
Activeyes
Location TextZurich
Department—
Team—
Employment Typefull_time
Workplace Type—
Remote Policy—
CountryZurich
Region—
City—
Salary Raw—
Salary Min—
Salary Max—
Salary Currency—
Salary Period—
Source URLhttps://rhythmpharmaceuticals.applytojob.com/apply/vItXDErLMo/Swiss-Responsible-Person-And-GDP-Quality-Assurance
Apply URLhttps://rhythmpharmaceuticals.applytojob.com/apply/vItXDErLMo/Swiss-Responsible-Person-And-GDP-Quality-Assurance
First Seen At2026-05-30 05:59:39Z
Last Seen At2026-06-04 14:30:01Z
Last Checked At2026-06-04 14:30:01Z
Last Changed At2026-05-30 05:59:39Z
Inactive At—
Source Posted At2026-03-11 00:00:00Z
Source Updated At—
Raw Payload Uris3://bluework-jobs-prod-raw-590183727216/raw/provider=jazzhr/board=rhythmpharmaceuticals/date=2026-06-04/2026-06-04T14-30-00-437Z-64bb1c8a7a37bcc562e1926637da330e69f8596b1d4c869230adf3f1b947fc3b.json
Event Fields
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Extensions
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Native Structured
{
  "detail": {
    "url": "https://rhythmpharmaceuticals.applytojob.com/apply/jobs/details/vItXDErLMo?&",
    "heading": "Swiss Responsible Person and GDP Quality Assurance",
    "html_title": "JazzHR » Job Listings",
    "canonical_url": "https://rhythmpharmaceuticals.applytojob.com/apply/vItXDErLMo/Swiss-Responsible-Person-And-GDP-Quality-Assurance",
    "description_html": "<span style=\"font-size:12pt;\"><span style=\"line-height:normal;\"><span style=\"font-family:Aptos, sans-serif;\"><b><span style=\"font-size:11pt;\"><span style=\"font-family:Calibri, sans-serif;\">Company Overview</span></span></b></span></span></span><br><span style=\"font-size:12pt;\"><span style=\"line-height:normal;\"><span style=\"font-family:Aptos, sans-serif;\"><span style=\"font-size:11pt;\"><span style=\"font-family:Calibri, sans-serif;\">Rhythm is a global, commercial-stage biopharmaceutical company committed to transforming the lives of patients and their families living with rare neuroendocrine diseases. We develop medicines for previously untreatable or undertreated diseases and provide meaningful support for healthcare providers and patients and their families. We recognize the courage it takes for patients and their caregivers to begin their journey of advocacy to find the answers they need. Their courage inspires us to challenge convention, ask bold questions and seek answers for them. Every day, we strive for excellence through our willingness to learn, adapt and our tenacity to overcome barriers, together.</span></span><br><br><b><span style=\"font-size:11pt;\"><span style=\"font-family:Calibri, sans-serif;\">Opportunity Overview</span></span></b><br><span style=\"font-size:11pt;\"><span style=\"font-family:Calibri, sans-serif;\">This role serves as the <b>Responsible Person (RP)</b> for Switzerland under the Swissmedic Wholesale Distribution License (WDL). The RP is fully accountable for product quality and regulatory compliance under Art. 11 ff of the Medicinal Products Licensing Ordinance (MPLO; SR 812.212.1).</span></span></span></span></span><br><br><span style=\"font-size:12pt;\"><span style=\"line-height:normal;\"><span style=\"font-family:Aptos, sans-serif;\"><span style=\"font-size:11pt;\"><span style=\"font-family:Calibri, sans-serif;\">In addition to Swiss RP duties, the role provides overall support to the global GDP operations, ensuring alignment and consistency across GDP processes, records, electronic systems, and compliance activities.</span></span></span></span></span><br><br><span style=\"font-size:12pt;\"><span style=\"line-height:normal;\"><span style=\"font-family:Aptos, sans-serif;\"><b><span style=\"font-size:11pt;\"><span style=\"font-family:Calibri, sans-serif;\">Responsibilities and Duties</span></span></b></span></span></span><br><span style=\"font-size:12pt;\"><span style=\"line-height:normal;\"><span style=\"font-family:Aptos, sans-serif;\"><b><span style=\"font-size:11pt;\"><span style=\"font-family:Calibri, sans-serif;\">The RP must (aligned with Swissmedic and GDP expectations):</span></span></b></span></span></span><ul><li class=\"MsoListBulletCxSpFirst\"><span style=\"font-size:12pt;\"><span style=\"line-height:normal;\"><span><span style=\"font-family:Aptos, sans-serif;\"><span style=\"font-size:11pt;\"><span style=\"font-family:Calibri, sans-serif;\">Maintain an effective QMS, overseeing authorized activities and ensuring accurate, high-quality records.</span></span></span></span></span></span></li><li class=\"MsoListBulletCxSpMiddle\"><span style=\"font-size:12pt;\"><span style=\"line-height:normal;\"><span><span style=\"font-family:Aptos, sans-serif;\"><span style=\"font-size:11pt;\"><span style=\"font-family:Calibri, sans-serif;\">Ensure non-conforming medicinal products, such as expired goods or those failing to meet specifications, are clearly labelled and not released to the market, and that packaging complies with current Swissmedic approvals.</span></span></span></span></span></span></li><li class=\"MsoListBulletCxSpMiddle\"><span style=\"font-size:12pt;\"><span style=\"line-height:normal;\"><span><span style=\"font-family:Aptos, sans-serif;\"><span style=\"font-size:11pt;\"><span style=\"font-family:Calibri, sans-serif;\">Deciding on the final disposition of returned, rejected, recalled, or falsified products.</span></span></span></span></span></span></li><li class=\"MsoListBulletCxSpMiddle\"><span style=\"font-size:12pt;\"><span style=\"line-height:normal;\"><span><span style=\"font-family:Aptos, sans-serif;\"><span style=\"font-size:11pt;\"><span style=\"font-family:Calibri, sans-serif;\">Effectively manage product quality complaints and temperature excursions.</span></span></span></span></span></span></li><li class=\"MsoListBulletCxSpMiddle\"><span style=\"font-size:12pt;\"><span style=\"line-height:normal;\"><span><span style=\"font-family:Aptos, sans-serif;\"><span style=\"font-size:11pt;\"><span style=\"font-family:Calibri, sans-serif;\">Conduct regular self-inspections according to a set schedule, monitor GDP compliance, and implement corrective actions as needed.</span></span></span></span></span></span></li><li class=\"MsoListBulletCxSpMiddle\"><span style=\"font-size:12pt;\"><span style=\"line-height:normal;\"><span><span style=\"font-family:Aptos, sans-serif;\"><span style=\"font-size:11pt;\"><span style=\"font-family:Calibri, sans-serif;\">Approve test reports for finished medicinal products or returning saleable products.</span></span></span></span></span></span></li><li class=\"MsoListBulletCxSpMiddle\"><span style=\"font-size:12pt;\"><span style=\"line-height:normal;\"><span><span style=\"font-family:Aptos, sans-serif;\"><span style=\"font-size:11pt;\"><span style=\"font-family:Calibri, sans-serif;\">Ensure appropriate samples are taken and kept as retention samples.</span></span></span></span></span></span></li><li class=\"MsoListBulletCxSpMiddle\"><span style=\"font-size:12pt;\"><span style=\"line-height:normal;\"><span><span style=\"font-family:Aptos, sans-serif;\"><span style=\"font-size:11pt;\"><span style=\"font-family:Calibri, sans-serif;\">Complete all mock or actual recalls accurately and within the specified time frame.</span></span></span></span></span></span></li><li class=\"MsoListBulletCxSpMiddle\"><span style=\"font-size:12pt;\"><span style=\"line-height:normal;\"><span><span style=\"font-family:Aptos, sans-serif;\"><span style=\"font-size:11pt;\"><span style=\"font-family:Calibri, sans-serif;\">Supplying medicinal products in Switzerland only to customers authorised to distribute them under GDP.</span></span></span></span></span></span></li><li class=\"MsoListBulletCxSpMiddle\"><span style=\"font-size:12pt;\"><span style=\"line-height:normal;\"><span><span style=\"font-family:Aptos, sans-serif;\"><span style=\"font-size:11pt;\"><span style=\"font-family:Calibri, sans-serif;\">Ensure suppliers and subcontracted activities are approved and qualified.</span></span></span></span></span></span></li><li class=\"MsoListBulletCxSpMiddle\"><span style=\"font-size:12pt;\"><span style=\"line-height:normal;\"><span><span style=\"font-family:Aptos, sans-serif;\"><span style=\"font-size:11pt;\"><span style=\"font-family:Calibri, sans-serif;\">Ensure that initial and continuous training programs are implemented and maintained.</span></span></span></span></span></span></li><li class=\"MsoListBulletCxSpMiddle\"><span style=\"font-size:12pt;\"><span style=\"line-height:normal;\"><span><span style=\"font-family:Aptos, sans-serif;\"><span style=\"font-size:11pt;\"><span style=\"font-family:Calibri, sans-serif;\">Act as contact person for Swissmedic.</span></span></span></span></span></span></li><li class=\"MsoListBulletCxSpMiddle\"><span style=\"font-size:12pt;\"><span style=\"line-height:normal;\"><span><span style=\"font-family:Aptos, sans-serif;\"><span style=\"font-size:11pt;\"><span style=\"font-family:Calibri, sans-serif;\">Ensure Swiss-specific assessment and evaluation of APQRs are conducted in accordance with Swissmedic timelines.</span></span></span></span></span></span></li><li class=\"MsoListBulletCxSpMiddle\"><span style=\"font-size:12pt;\"><span style=\"line-height:normal;\"><span><span style=\"font-family:Aptos, sans-serif;\"><span style=\"font-size:11pt;\"><span style=\"font-family:Calibri, sans-serif;\">Conduct Annual Management Reviews.</span></span></span></span></span></span></li><li class=\"MsoListBulletCxSpMiddle\"><span style=\"font-size:12pt;\"><span style=\"line-height:normal;\"><span><span style=\"font-family:Aptos, sans-serif;\"><span style=\"font-size:11pt;\"><span style=\"font-family:Calibri, sans-serif;\">Manage deviations and changes appropriately, and promptly notify Swissmedic of any major change according to Art. 41 of MPLO.</span></span></span></span></span></span></li><li class=\"MsoListBulletCxSpMiddle\"><span style=\"font-size:12pt;\"><span style=\"line-height:normal;\"><span><span style=\"font-family:Aptos, sans-serif;\"><span style=\"font-size:11pt;\"><span style=\"font-family:Calibri, sans-serif;\">Ensure that appropriate Corrective and Preventive Actions (CAPAs) are clearly defined as required and effectively managed throughout their implementation.</span></span></span></span></span></span></li><li class=\"MsoListBulletCxSpMiddle\"><span style=\"font-size:12pt;\"><span style=\"line-height:normal;\"><span><span style=\"font-family:Aptos, sans-serif;\"><span style=\"font-size:11pt;\"><span style=\"font-family:Calibri, sans-serif;\">Ensuring potential risks are thoroughly analyzed and managed effectively.</span></span></span></span></span></span></li></ul><br><span style=\"font-size:12pt;\"><span style=\"line-height:normal;\"><span style=\"font-family:Aptos, sans-serif;\"><b><span style=\"font-size:11pt;\"><span style=\"font-family:Calibri, sans-serif;\">Overall Support for Global GDP Operations</span></span></b></span></span></span><br><span style=\"font-size:12pt;\"><span style=\"line-height:normal;\"><span style=\"font-family:Aptos, sans-serif;\"><b><span style=\"font-size:11pt;\"><span style=\"font-family:Calibri, sans-serif;\">The role will:</span></span></b></span></span></span><ul><li class=\"MsoListBulletCxSpMiddle\"><span style=\"font-size:12pt;\"><span style=\"line-height:normal;\"><span><span style=\"font-family:Aptos, sans-serif;\"><span style=\"font-size:11pt;\"><span style=\"font-family:Calibri, sans-serif;\">Support global GDP operations by reviewing documents, preparing batch disposition and returns paperwork, and coordinating approval processes within Veeva.</span></span></span></span></span></span></li><li class=\"MsoListBulletCxSpMiddle\"><span style=\"font-size:12pt;\"><span style=\"line-height:normal;\"><span><span style=\"font-family:Aptos, sans-serif;\"><span style=\"font-size:11pt;\"><span style=\"font-family:Calibri, sans-serif;\">Manage temperature excursions and distribution events ensuring all incidents are properly recorded and corrective actions are implemented in line with global GDP standards. </span></span></span></span></span></span></li><li class=\"MsoListBulletCxSpMiddle\"><span style=\"font-size:12pt;\"><span style=\"line-height:normal;\"><span><span style=\"font-family:Aptos, sans-serif;\"><span style=\"font-size:11pt;\"><span style=\"font-family:Calibri, sans-serif;\">Support GDP audits and self‑inspections, including management of records within Veeva eQMS.</span></span></span></span></span></span></li><li class=\"MsoListBulletCxSpMiddle\"><span style=\"font-size:12pt;\"><span style=\"line-height:normal;\"><span><span style=\"font-family:Aptos, sans-serif;\"><span style=\"font-size:11pt;\"><span style=\"font-family:Calibri, sans-serif;\">Support maintenance of global GDP procedures, work instructions, forms, and templates to ensure consistent execution across all Rhythm GDP markets.</span></span></span></span></span></span></li><li class=\"MsoListBulletCxSpMiddle\"><span style=\"font-size:12pt;\"><span style=\"line-height:normal;\"><span><span style=\"font-family:Aptos, sans-serif;\"><span style=\"font-size:11pt;\"><span style=\"font-family:Calibri, sans-serif;\">Contribute to global GDP change control, deviation, CAPA, and quality event administration, ensuring consistent documentation and follow‑up across regions.</span></span></span></span></span></span></li><li class=\"MsoListBulletCxSpLast\"><span style=\"font-size:12pt;\"><span style=\"line-height:normal;\"><span><span style=\"font-family:Aptos, sans-serif;\"><span style=\"font-size:11pt;\"><span style=\"font-family:Calibri, sans-serif;\">Coordinate global GDP training activities.</span></span></span></span></span></span></li></ul><br><span style=\"font-size:12pt;\"><span style=\"line-height:normal;\"><span style=\"vertical-align:baseline;\"><span style=\"font-family:Aptos, sans-serif;\"><span style=\"font-size:11pt;\"><span style=\"font-family:Calibri, sans-serif;\"><b>Qualifications and Skills</b></span></span></span></span></span></span><ul><li class=\"MsoListBulletCxSpFirst\"><span style=\"font-size:12pt;\"><span style=\"line-height:normal;\"><span><span style=\"font-family:Aptos, sans-serif;\"><span style=\"font-size:11pt;\"><span style=\"font-family:Calibri, sans-serif;\">Meets requirements to serve as RP under Swissmedic WDL</span></span></span></span></span></span></li><li class=\"MsoListBulletCxSpMiddle\"><span style=\"font-size:12pt;\"><span style=\"line-height:normal;\"><span><span style=\"font-family:Aptos, sans-serif;\"><span style=\"font-size:11pt;\"><span style=\"font-family:Calibri, sans-serif;\">Preferred with 8 +years of relevant industry work experience</span></span></span></span></span></span></li><li class=\"MsoListBulletCxSpMiddle\"><span style=\"font-size:12pt;\"><span style=\"line-height:normal;\"><span><span style=\"font-family:Aptos, sans-serif;\"><span style=\"font-size:11pt;\"><span style=\"font-family:Calibri, sans-serif;\">Broad knowledge of EU GDP </span></span></span></span></span></span></li><li class=\"MsoListBulletCxSpMiddle\"><span style=\"font-size:12pt;\"><span style=\"line-height:normal;\"><span><span style=\"font-family:Aptos, sans-serif;\"><span style=\"font-size:11pt;\"><span style=\"font-family:Calibri, sans-serif;\">Excellent documentation, organizational, and administrative skills</span></span></span></span></span></span></li><li class=\"MsoListBulletCxSpMiddle\"><span style=\"font-size:12pt;\"><span style=\"line-height:normal;\"><span><span style=\"font-family:Aptos, sans-serif;\"><span style=\"font-size:11pt;\"><span style=\"font-family:Calibri, sans-serif;\">Proven experience in managing outsourced GDP activities in a virtual environment</span></span></span></span></span></span></li><li class=\"MsoListBulletCxSpMiddle\"><span style=\"font-size:12pt;\"><span style=\"line-height:normal;\"><span><span style=\"font-family:Aptos, sans-serif;\"><span style=\"font-size:11pt;\"><span style=\"font-family:Calibri, sans-serif;\">In-depth knowledge of the Swiss healthcare system, medical landscape, and current trends in industry</span></span></span></span></span></span></li><li class=\"MsoListBulletCxSpMiddle\"><span style=\"font-size:12pt;\"><span style=\"line-height:normal;\"><span><span style=\"font-family:Aptos, sans-serif;\"><span style=\"font-size:11pt;\"><span style=\"font-family:Calibri, sans-serif;\">Willingness to travel</span></span></span></span></span></span></li></ul><br><span style=\"font-size:12pt;\"><span style=\"line-height:115%;\"><span style=\"font-family:Aptos, sans-serif;\"><i><span style=\"font-size:10pt;\"><span style=\"background:#FFFFFF;\"><span style=\"line-height:115%;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">More about Rhythm</span></span></span></span></span></i></span></span></span><br><span style=\"font-size:12pt;\"><span style=\"line-height:115%;\"><span style=\"font-family:Aptos, sans-serif;\"><i><span style=\"font-size:10pt;\"><span style=\"line-height:115%;\"><span style=\"font-family:Calibri, sans-serif;\">We are a dynamic and growing global team spanning more than a dozen countries. At Rhythm we are dedicated to transforming the lives of patients living with rare neuroendocrine diseases by rapidly advancing care and precision medicines that address the root cause. Our team is passionate about expanding access to reach more patients and developing novel therapies for other rare neuroendocrine diseases, including congenital hyperinsulinism. </span></span></span></i></span></span></span><br><br><span style=\"font-size:12pt;\"><span style=\"line-height:115%;\"><span style=\"font-family:Aptos, sans-serif;\"><i><span style=\"font-size:10pt;\"><span style=\"background:#FFFFFF;\"><span style=\"line-height:115%;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">At Rhythm Our Core Values Are</span></span></span></span></span></i></span></span></span><br><span style=\"font-size:12pt;\"><span style=\"line-height:115%;\"><span style=\"font-family:Aptos, sans-serif;\"><i><span style=\"font-size:10pt;\"><span style=\"background:#FFFFFF;\"><span style=\"line-height:115%;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">•      We are committed to advancing scientific understanding to improve patients’ lives</span></span></span></span></span></i></span></span></span><br><span style=\"font-size:12pt;\"><span style=\"line-height:115%;\"><span style=\"font-family:Aptos, sans-serif;\"><i><span style=\"font-size:10pt;\"><span style=\"background:#FFFFFF;\"><span style=\"line-height:115%;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">•      We are inspired to tackle tough challenges and have the courage to ask bold questions</span></span></span></span></span></i></span></span></span><br><span style=\"font-size:12pt;\"><span style=\"line-height:115%;\"><span style=\"font-family:Aptos, sans-serif;\"><i><span style=\"font-size:10pt;\"><span style=\"background:#FFFFFF;\"><span style=\"line-height:115%;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">•      We are eager to learn and adapt</span></span></span></span></span></i></span></span></span><br><span style=\"font-size:12pt;\"><span style=\"line-height:115%;\"><span style=\"font-family:Aptos, sans-serif;\"><i><span style=\"font-size:10pt;\"><span style=\"background:#FFFFFF;\"><span style=\"line-height:115%;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">•      We believe collaboration and ownership are foundational for our success<br>•      </span></span></span></span></span></i></span></span></span><span style=\"font-size:12pt;\"><span style=\"line-height:115%;\"><span style=\"font-family:Aptos, sans-serif;\"><i><span style=\"font-size:10pt;\"><span style=\"background:#FFFFFF;\"><span style=\"line-height:115%;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">We value the unique contribution each individual brings to furthering our mission</span></span></span></span></span></i></span></span></span><br> ",
    "description_text": "Company Overview\n Rhythm is a global, commercial-stage biopharmaceutical company committed to transforming the lives of patients and their families living with rare neuroendocrine diseases. We develop medicines for previously untreatable or undertreated diseases and provide meaningful support for healthcare providers and patients and their families. We recognize the courage it takes for patients and their caregivers to begin their journey of advocacy to find the answers they need. Their courage inspires us to challenge convention, ask bold questions and seek answers for them. Every day, we strive for excellence through our willingness to learn, adapt and our tenacity to overcome barriers, together.\n Opportunity Overview\n This role serves as the Responsible Person (RP) for Switzerland under the Swissmedic Wholesale Distribution License (WDL). The RP is fully accountable for product quality and regulatory compliance under Art. 11 ff of the Medicinal Products Licensing Ordinance (MPLO; SR 812.212.1).\n In addition to Swiss RP duties, the role provides overall support to the global GDP operations, ensuring alignment and consistency across GDP processes, records, electronic systems, and compliance activities.\n Responsibilities and Duties\n The RP must (aligned with Swissmedic and GDP expectations): Maintain an effective QMS, overseeing authorized activities and ensuring accurate, high-quality records.\n Ensure non-conforming medicinal products, such as expired goods or those failing to meet specifications, are clearly labelled and not released to the market, and that packaging complies with current Swissmedic approvals.\n Deciding on the final disposition of returned, rejected, recalled, or falsified products.\n Effectively manage product quality complaints and temperature excursions.\n Conduct regular self-inspections according to a set schedule, monitor GDP compliance, and implement corrective actions as needed.\n Approve test reports for finished medicinal products or returning saleable products.\n Ensure appropriate samples are taken and kept as retention samples.\n Complete all mock or actual recalls accurately and within the specified time frame.\n Supplying medicinal products in Switzerland only to customers authorised to distribute them under GDP.\n Ensure suppliers and subcontracted activities are approved and qualified.\n Ensure that initial and continuous training programs are implemented and maintained.\n Act as contact person for Swissmedic.\n Ensure Swiss-specific assessment and evaluation of APQRs are conducted in accordance with Swissmedic timelines.\n Conduct Annual Management Reviews.\n Manage deviations and changes appropriately, and promptly notify Swissmedic of any major change according to Art. 41 of MPLO.\n Ensure that appropriate Corrective and Preventive Actions (CAPAs) are clearly defined as required and effectively managed throughout their implementation.\n Ensuring potential risks are thoroughly analyzed and managed effectively.\n Overall Support for Global GDP Operations\n The role will: Support global GDP operations by reviewing documents, preparing batch disposition and returns paperwork, and coordinating approval processes within Veeva.\n Manage temperature excursions and distribution events ensuring all incidents are properly recorded and corrective actions are implemented in line with global GDP standards.\n Support GDP audits and self‑inspections, including management of records within Veeva eQMS.\n Support maintenance of global GDP procedures, work instructions, forms, and templates to ensure consistent execution across all Rhythm GDP markets.\n Contribute to global GDP change control, deviation, CAPA, and quality event administration, ensuring consistent documentation and follow‑up across regions.\n Coordinate global GDP training activities.\n Qualifications and Skills Meets requirements to serve as RP under Swissmedic WDL\n Preferred with 8 +years of relevant industry work experience\n Broad knowledge of EU GDP\n Excellent documentation, organizational, and administrative skills\n Proven experience in managing outsourced GDP activities in a virtual environment\n In-depth knowledge of the Swiss healthcare system, medical landscape, and current trends in industry\n Willingness to travel\n More about Rhythm\n We are a dynamic and growing global team spanning more than a dozen countries. At Rhythm we are dedicated to transforming the lives of patients living with rare neuroendocrine diseases by rapidly advancing care and precision medicines that address the root cause. Our team is passionate about expanding access to reach more patients and developing novel therapies for other rare neuroendocrine diseases, including congenital hyperinsulinism.\n At Rhythm Our Core Values Are\n •      We are committed to advancing scientific understanding to improve patients’ lives\n •      We are inspired to tackle tough challenges and have the courage to ask bold questions\n •      We are eager to learn and adapt\n •      We believe collaboration and ownership are foundational for our success\n•      We value the unique contribution each individual brings to furthering our mission",
    "jsonld_jobposting": {
      "url": "https://rhythmpharmaceuticals.applytojob.com/apply/vItXDErLMo/Swiss-Responsible-Person-And-GDP-Quality-Assurance",
      "@type": "JobPosting",
      "title": "Swiss Responsible Person and GDP Quality Assurance",
      "@context": "http://schema.org/",
      "datePosted": "2026-03-11",
      "description": "<span style=\"font-size:12pt;\"><span style=\"line-height:normal;\"><span style=\"font-family:Aptos, sans-serif;\"><b><span style=\"font-size:11pt;\"><span style=\"font-family:Calibri, sans-serif;\">Company Overview</span></span></b></span></span></span><br><span style=\"font-size:12pt;\"><span style=\"line-height:normal;\"><span style=\"font-family:Aptos, sans-serif;\"><span style=\"font-size:11pt;\"><span style=\"font-family:Calibri, sans-serif;\">Rhythm is a global, commercial-stage biopharmaceutical company committed to transforming the lives of patients and their families living with rare neuroendocrine diseases. We develop medicines for previously untreatable or undertreated diseases and provide meaningful support for healthcare providers and patients and their families. We recognize the courage it takes for patients and their caregivers to begin their journey of advocacy to find the answers they need. Their courage inspires us to challenge convention, ask bold questions and seek answers for them. Every day, we strive for excellence through our willingness to learn, adapt and our tenacity to overcome barriers, together.</span></span><br><br><b><span style=\"font-size:11pt;\"><span style=\"font-family:Calibri, sans-serif;\">Opportunity Overview</span></span></b><br><span style=\"font-size:11pt;\"><span style=\"font-family:Calibri, sans-serif;\">This role serves as the <b>Responsible Person (RP)</b> for Switzerland under the Swissmedic Wholesale Distribution License (WDL). The RP is fully accountable for product quality and regulatory compliance under Art. 11 ff of the Medicinal Products Licensing Ordinance (MPLO; SR 812.212.1).</span></span></span></span></span><br><br><span style=\"font-size:12pt;\"><span style=\"line-height:normal;\"><span style=\"font-family:Aptos, sans-serif;\"><span style=\"font-size:11pt;\"><span style=\"font-family:Calibri, sans-serif;\">In addition to Swiss RP duties, the role provides overall support to the global GDP operations, ensuring alignment and consistency across GDP processes, records, electronic systems, and compliance activities.</span></span></span></span></span><br><br><span style=\"font-size:12pt;\"><span style=\"line-height:normal;\"><span style=\"font-family:Aptos, sans-serif;\"><b><span style=\"font-size:11pt;\"><span style=\"font-family:Calibri, sans-serif;\">Responsibilities and Duties</span></span></b></span></span></span><br><span style=\"font-size:12pt;\"><span style=\"line-height:normal;\"><span style=\"font-family:Aptos, sans-serif;\"><b><span style=\"font-size:11pt;\"><span style=\"font-family:Calibri, sans-serif;\">The RP must (aligned with Swissmedic and GDP expectations):</span></span></b></span></span></span><ul><li class=\"MsoListBulletCxSpFirst\"><span style=\"font-size:12pt;\"><span style=\"line-height:normal;\"><span><span style=\"font-family:Aptos, sans-serif;\"><span style=\"font-size:11pt;\"><span style=\"font-family:Calibri, sans-serif;\">Maintain an effective QMS, overseeing authorized activities and ensuring accurate, high-quality records.</span></span></span></span></span></span></li><li class=\"MsoListBulletCxSpMiddle\"><span style=\"font-size:12pt;\"><span style=\"line-height:normal;\"><span><span style=\"font-family:Aptos, sans-serif;\"><span style=\"font-size:11pt;\"><span style=\"font-family:Calibri, sans-serif;\">Ensure non-conforming medicinal products, such as expired goods or those failing to meet specifications, are clearly labelled and not released to the market, and that packaging complies with current Swissmedic approvals.</span></span></span></span></span></span></li><li class=\"MsoListBulletCxSpMiddle\"><span style=\"font-size:12pt;\"><span style=\"line-height:normal;\"><span><span style=\"font-family:Aptos, sans-serif;\"><span style=\"font-size:11pt;\"><span style=\"font-family:Calibri, sans-serif;\">Deciding on the final disposition of returned, rejected, recalled, or falsified products.</span></span></span></span></span></span></li><li class=\"MsoListBulletCxSpMiddle\"><span style=\"font-size:12pt;\"><span style=\"line-height:normal;\"><span><span style=\"font-family:Aptos, sans-serif;\"><span style=\"font-size:11pt;\"><span style=\"font-family:Calibri, sans-serif;\">Effectively manage product quality complaints and temperature excursions.</span></span></span></span></span></span></li><li class=\"MsoListBulletCxSpMiddle\"><span style=\"font-size:12pt;\"><span style=\"line-height:normal;\"><span><span style=\"font-family:Aptos, sans-serif;\"><span style=\"font-size:11pt;\"><span style=\"font-family:Calibri, sans-serif;\">Conduct regular self-inspections according to a set schedule, monitor GDP compliance, and implement corrective actions as needed.</span></span></span></span></span></span></li><li class=\"MsoListBulletCxSpMiddle\"><span style=\"font-size:12pt;\"><span style=\"line-height:normal;\"><span><span style=\"font-family:Aptos, sans-serif;\"><span style=\"font-size:11pt;\"><span style=\"font-family:Calibri, sans-serif;\">Approve test reports for finished medicinal products or returning saleable products.</span></span></span></span></span></span></li><li class=\"MsoListBulletCxSpMiddle\"><span style=\"font-size:12pt;\"><span style=\"line-height:normal;\"><span><span style=\"font-family:Aptos, sans-serif;\"><span style=\"font-size:11pt;\"><span style=\"font-family:Calibri, sans-serif;\">Ensure appropriate samples are taken and kept as retention samples.</span></span></span></span></span></span></li><li class=\"MsoListBulletCxSpMiddle\"><span style=\"font-size:12pt;\"><span style=\"line-height:normal;\"><span><span style=\"font-family:Aptos, sans-serif;\"><span style=\"font-size:11pt;\"><span style=\"font-family:Calibri, sans-serif;\">Complete all mock or actual recalls accurately and within the specified time frame.</span></span></span></span></span></span></li><li class=\"MsoListBulletCxSpMiddle\"><span style=\"font-size:12pt;\"><span style=\"line-height:normal;\"><span><span style=\"font-family:Aptos, sans-serif;\"><span style=\"font-size:11pt;\"><span style=\"font-family:Calibri, sans-serif;\">Supplying medicinal products in Switzerland only to customers authorised to distribute them under GDP.</span></span></span></span></span></span></li><li class=\"MsoListBulletCxSpMiddle\"><span style=\"font-size:12pt;\"><span style=\"line-height:normal;\"><span><span style=\"font-family:Aptos, sans-serif;\"><span style=\"font-size:11pt;\"><span style=\"font-family:Calibri, sans-serif;\">Ensure suppliers and subcontracted activities are approved and qualified.</span></span></span></span></span></span></li><li class=\"MsoListBulletCxSpMiddle\"><span style=\"font-size:12pt;\"><span style=\"line-height:normal;\"><span><span style=\"font-family:Aptos, sans-serif;\"><span style=\"font-size:11pt;\"><span style=\"font-family:Calibri, sans-serif;\">Ensure that initial and continuous training programs are implemented and maintained.</span></span></span></span></span></span></li><li class=\"MsoListBulletCxSpMiddle\"><span style=\"font-size:12pt;\"><span style=\"line-height:normal;\"><span><span style=\"font-family:Aptos, sans-serif;\"><span style=\"font-size:11pt;\"><span style=\"font-family:Calibri, sans-serif;\">Act as contact person for Swissmedic.</span></span></span></span></span></span></li><li class=\"MsoListBulletCxSpMiddle\"><span style=\"font-size:12pt;\"><span style=\"line-height:normal;\"><span><span style=\"font-family:Aptos, sans-serif;\"><span style=\"font-size:11pt;\"><span style=\"font-family:Calibri, sans-serif;\">Ensure Swiss-specific assessment and evaluation of APQRs are conducted in accordance with Swissmedic timelines.</span></span></span></span></span></span></li><li class=\"MsoListBulletCxSpMiddle\"><span style=\"font-size:12pt;\"><span style=\"line-height:normal;\"><span><span style=\"font-family:Aptos, sans-serif;\"><span style=\"font-size:11pt;\"><span style=\"font-family:Calibri, sans-serif;\">Conduct Annual Management Reviews.</span></span></span></span></span></span></li><li class=\"MsoListBulletCxSpMiddle\"><span style=\"font-size:12pt;\"><span style=\"line-height:normal;\"><span><span style=\"font-family:Aptos, sans-serif;\"><span style=\"font-size:11pt;\"><span style=\"font-family:Calibri, sans-serif;\">Manage deviations and changes appropriately, and promptly notify Swissmedic of any major change according to Art. 41 of MPLO.</span></span></span></span></span></span></li><li class=\"MsoListBulletCxSpMiddle\"><span style=\"font-size:12pt;\"><span style=\"line-height:normal;\"><span><span style=\"font-family:Aptos, sans-serif;\"><span style=\"font-size:11pt;\"><span style=\"font-family:Calibri, sans-serif;\">Ensure that appropriate Corrective and Preventive Actions (CAPAs) are clearly defined as required and effectively managed throughout their implementation.</span></span></span></span></span></span></li><li class=\"MsoListBulletCxSpMiddle\"><span style=\"font-size:12pt;\"><span style=\"line-height:normal;\"><span><span style=\"font-family:Aptos, sans-serif;\"><span style=\"font-size:11pt;\"><span style=\"font-family:Calibri, sans-serif;\">Ensuring potential risks are thoroughly analyzed and managed effectively.</span></span></span></span></span></span></li></ul><br><span style=\"font-size:12pt;\"><span style=\"line-height:normal;\"><span style=\"font-family:Aptos, sans-serif;\"><b><span style=\"font-size:11pt;\"><span style=\"font-family:Calibri, sans-serif;\">Overall Support for Global GDP Operations</span></span></b></span></span></span><br><span style=\"font-size:12pt;\"><span style=\"line-height:normal;\"><span style=\"font-family:Aptos, sans-serif;\"><b><span style=\"font-size:11pt;\"><span style=\"font-family:Calibri, sans-serif;\">The role will:</span></span></b></span></span></span><ul><li class=\"MsoListBulletCxSpMiddle\"><span style=\"font-size:12pt;\"><span style=\"line-height:normal;\"><span><span style=\"font-family:Aptos, sans-serif;\"><span style=\"font-size:11pt;\"><span style=\"font-family:Calibri, sans-serif;\">Support global GDP operations by reviewing documents, preparing batch disposition and returns paperwork, and coordinating approval processes within Veeva.</span></span></span></span></span></span></li><li class=\"MsoListBulletCxSpMiddle\"><span style=\"font-size:12pt;\"><span style=\"line-height:normal;\"><span><span style=\"font-family:Aptos, sans-serif;\"><span style=\"font-size:11pt;\"><span style=\"font-family:Calibri, sans-serif;\">Manage temperature excursions and distribution events ensuring all incidents are properly recorded and corrective actions are implemented in line with global GDP standards. </span></span></span></span></span></span></li><li class=\"MsoListBulletCxSpMiddle\"><span style=\"font-size:12pt;\"><span style=\"line-height:normal;\"><span><span style=\"font-family:Aptos, sans-serif;\"><span style=\"font-size:11pt;\"><span style=\"font-family:Calibri, sans-serif;\">Support GDP audits and self‑inspections, including management of records within Veeva eQMS.</span></span></span></span></span></span></li><li class=\"MsoListBulletCxSpMiddle\"><span style=\"font-size:12pt;\"><span style=\"line-height:normal;\"><span><span style=\"font-family:Aptos, sans-serif;\"><span style=\"font-size:11pt;\"><span style=\"font-family:Calibri, sans-serif;\">Support maintenance of global GDP procedures, work instructions, forms, and templates to ensure consistent execution across all Rhythm GDP markets.</span></span></span></span></span></span></li><li class=\"MsoListBulletCxSpMiddle\"><span style=\"font-size:12pt;\"><span style=\"line-height:normal;\"><span><span style=\"font-family:Aptos, sans-serif;\"><span style=\"font-size:11pt;\"><span style=\"font-family:Calibri, sans-serif;\">Contribute to global GDP change control, deviation, CAPA, and quality event administration, ensuring consistent documentation and follow‑up across regions.</span></span></span></span></span></span></li><li class=\"MsoListBulletCxSpLast\"><span style=\"font-size:12pt;\"><span style=\"line-height:normal;\"><span><span style=\"font-family:Aptos, sans-serif;\"><span style=\"font-size:11pt;\"><span style=\"font-family:Calibri, sans-serif;\">Coordinate global GDP training activities.</span></span></span></span></span></span></li></ul><br><span style=\"font-size:12pt;\"><span style=\"line-height:normal;\"><span style=\"vertical-align:baseline;\"><span style=\"font-family:Aptos, sans-serif;\"><span style=\"font-size:11pt;\"><span style=\"font-family:Calibri, sans-serif;\"><b>Qualifications and Skills</b></span></span></span></span></span></span><ul><li class=\"MsoListBulletCxSpFirst\"><span style=\"font-size:12pt;\"><span style=\"line-height:normal;\"><span><span style=\"font-family:Aptos, sans-serif;\"><span style=\"font-size:11pt;\"><span style=\"font-family:Calibri, sans-serif;\">Meets requirements to serve as RP under Swissmedic WDL</span></span></span></span></span></span></li><li class=\"MsoListBulletCxSpMiddle\"><span style=\"font-size:12pt;\"><span style=\"line-height:normal;\"><span><span style=\"font-family:Aptos, sans-serif;\"><span style=\"font-size:11pt;\"><span style=\"font-family:Calibri, sans-serif;\">Preferred with 8 +years of relevant industry work experience</span></span></span></span></span></span></li><li class=\"MsoListBulletCxSpMiddle\"><span style=\"font-size:12pt;\"><span style=\"line-height:normal;\"><span><span style=\"font-family:Aptos, sans-serif;\"><span style=\"font-size:11pt;\"><span style=\"font-family:Calibri, sans-serif;\">Broad knowledge of EU GDP </span></span></span></span></span></span></li><li class=\"MsoListBulletCxSpMiddle\"><span style=\"font-size:12pt;\"><span style=\"line-height:normal;\"><span><span style=\"font-family:Aptos, sans-serif;\"><span style=\"font-size:11pt;\"><span style=\"font-family:Calibri, sans-serif;\">Excellent documentation, organizational, and administrative skills</span></span></span></span></span></span></li><li class=\"MsoListBulletCxSpMiddle\"><span style=\"font-size:12pt;\"><span style=\"line-height:normal;\"><span><span style=\"font-family:Aptos, sans-serif;\"><span style=\"font-size:11pt;\"><span style=\"font-family:Calibri, sans-serif;\">Proven experience in managing outsourced GDP activities in a virtual environment</span></span></span></span></span></span></li><li class=\"MsoListBulletCxSpMiddle\"><span style=\"font-size:12pt;\"><span style=\"line-height:normal;\"><span><span style=\"font-family:Aptos, sans-serif;\"><span style=\"font-size:11pt;\"><span style=\"font-family:Calibri, sans-serif;\">In-depth knowledge of the Swiss healthcare system, medical landscape, and current trends in industry</span></span></span></span></span></span></li><li class=\"MsoListBulletCxSpMiddle\"><span style=\"font-size:12pt;\"><span style=\"line-height:normal;\"><span><span style=\"font-family:Aptos, sans-serif;\"><span style=\"font-size:11pt;\"><span style=\"font-family:Calibri, sans-serif;\">Willingness to travel</span></span></span></span></span></span></li></ul><br><span style=\"font-size:12pt;\"><span style=\"line-height:115%;\"><span style=\"font-family:Aptos, sans-serif;\"><i><span style=\"font-size:10pt;\"><span style=\"background:#FFFFFF;\"><span style=\"line-height:115%;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">More about Rhythm</span></span></span></span></span></i></span></span></span><br><span style=\"font-size:12pt;\"><span style=\"line-height:115%;\"><span style=\"font-family:Aptos, sans-serif;\"><i><span style=\"font-size:10pt;\"><span style=\"line-height:115%;\"><span style=\"font-family:Calibri, sans-serif;\">We are a dynamic and growing global team spanning more than a dozen countries. At Rhythm we are dedicated to transforming the lives of patients living with rare neuroendocrine diseases by rapidly advancing care and precision medicines that address the root cause. Our team is passionate about expanding access to reach more patients and developing novel therapies for other rare neuroendocrine diseases, including congenital hyperinsulinism. </span></span></span></i></span></span></span><br><br><span style=\"font-size:12pt;\"><span style=\"line-height:115%;\"><span style=\"font-family:Aptos, sans-serif;\"><i><span style=\"font-size:10pt;\"><span style=\"background:#FFFFFF;\"><span style=\"line-height:115%;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">At Rhythm Our Core Values Are</span></span></span></span></span></i></span></span></span><br><span style=\"font-size:12pt;\"><span style=\"line-height:115%;\"><span style=\"font-family:Aptos, sans-serif;\"><i><span style=\"font-size:10pt;\"><span style=\"background:#FFFFFF;\"><span style=\"line-height:115%;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">•      We are committed to advancing scientific understanding to improve patients’ lives</span></span></span></span></span></i></span></span></span><br><span style=\"font-size:12pt;\"><span style=\"line-height:115%;\"><span style=\"font-family:Aptos, sans-serif;\"><i><span style=\"font-size:10pt;\"><span style=\"background:#FFFFFF;\"><span style=\"line-height:115%;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">•      We are inspired to tackle tough challenges and have the courage to ask bold questions</span></span></span></span></span></i></span></span></span><br><span style=\"font-size:12pt;\"><span style=\"line-height:115%;\"><span style=\"font-family:Aptos, sans-serif;\"><i><span style=\"font-size:10pt;\"><span style=\"background:#FFFFFF;\"><span style=\"line-height:115%;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">•      We are eager to learn and adapt</span></span></span></span></span></i></span></span></span><br><span style=\"font-size:12pt;\"><span style=\"line-height:115%;\"><span style=\"font-family:Aptos, sans-serif;\"><i><span style=\"font-size:10pt;\"><span style=\"background:#FFFFFF;\"><span style=\"line-height:115%;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">•      We believe collaboration and ownership are foundational for our success<br>•      </span></span></span></span></span></i></span></span></span><span style=\"font-size:12pt;\"><span style=\"line-height:115%;\"><span style=\"font-family:Aptos, sans-serif;\"><i><span style=\"font-size:10pt;\"><span style=\"background:#FFFFFF;\"><span style=\"line-height:115%;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">We value the unique contribution each individual brings to furthering our mission</span></span></span></span></span></i></span></span></span><br> ",
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          "addressRegion": "Zurich",
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      "validThrough": "2026-06-09",
      "uniqueJobCode": "job_20260311130848_K924LDF9EVAXQTWD",
      "employmentType": "FULL_TIME",
      "hiringOrganization": {
        "logo": "https://s3.amazonaws.com/resumator/customer_20190426145212_8TPBAQEQKXNCTAQH/logos/20190923141333_Rhythm_Logo.png",
        "name": "Rhythm Pharmaceuticals",
        "@type": "Organization",
        "sameAs": "https://www.rhythmtx.com/careers/careers-at-rhythm/"
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      "experienceRequirements": "Experienced"
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    "id": "vItXDErLMo",
    "title": "Swiss Responsible Person and GDP Quality Assurance",
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