Technical Support Packaging, Senior Specialist Planning & Scheduling (m/f/d)
Bewerben
remote type
Not Applicable
locations
CHE - Schachen - Werthenstein
time type
Vollzeit
posted on
Heute ausgeschrieben
time left to apply
Enddatum: 18. August 2026 (Noch 12 Tage Zeit für Bewerbung)
job requisition id
R403334
Stellenbeschreibung
We are looking for an experienced, quality-focused professional to join our team in Technical Support Packaging. In this role, you will independently manage and support quality-related and technical activities in a GMP-regulated environment, including investigations, documentation, systems support and continuous improvement initiatives. The position requires strong technical judgment, a structured way of working and effective collaboration across functions.
Responsibilities:
- Own and coordinate deviation records, supporting timely investigations and effective CAPA implementation
- Support and monitor change control activities to ensure compliant and efficient implementation of process and system changes
- Create, maintain and improve Standard Operating Procedures (SOPs) and Good Manufacturing Process (GMP) documentation that support robust and inspection-ready operations
- Execute calibration, validation and qualification activities for equipment and systems in accordance with approved standards and procedures
- Investigate technical issues, perform root-cause analyses and help implement sustainable corrective actions
- Perform quality risk assessments to support sound decision-making and maintain a high level of compliance
- Partner with cross-functional stakeholders to support audits, inspections and ongoing readiness activities
- Contribute to improvement projects that enhance compliance, system performance and operational efficiency
- Support Environmental Health & Safety activities, including Management of Change, where applicable
- Ensure accurate, complete and timely technical and quality documentation across assigned responsibilities
Your Profile
- Bachelor’s or Master’s degree in Life Sciences, Engineering, Pharmacy, or a related field preferred
- Several years of experience in a GMP-regulated pharmaceutical, biotechnology, or clinical manufacturing environment
- Hands-on experience in deviation management, change control, CAPA management and SOP/documentation processes
- Practical knowledge of calibration, validation and qualification activities for equipment and systems
- Strong technical problem-solving skills with the ability to work independently and make sound decisions within established procedures
- Solid understanding of GMP requirements and quality risk management principles
- A collaborative mindset and the ability to work effectively across functions and with diverse stakeholders
- Fluent in English, written and spoken; additional language skills are an advantage
- A structured, reliable and detail-oriented working style with a continuous improvement mindset
- Comfortable managing multiple priorities in a fast-paced and regulated environment
- Experience with systems such as SAP, ProCal, eVal, DeltaV, Veeva Vault, MEDS, or eShop Floor is considered an advantage.
THE COMPANY
Our Company is a leading biopharmaceutical company employing over 1,000 people in Switzerland at three sites. The company’s headquarters are in Lucerne. At the site in Zurich, the company operates a global innovation and development hub. In addition, we manufacture medicines for global clinical trials and operate a forensic laboratory in Schachen (Canton Lucerne). We conduct around 40 clinical trials annually in Switzerland. The main therapeutic areas include oncology, infectious diseases, cardiovascular and cardiometabolic diseases. We also have a broad portfolio of vaccines for the prevention of diseases in children, adolescents, and adults and we are one of the leading companies in veterinary medicine. Furthermore, we take our responsibility to the local community seriously and have been involved for many years in initiatives such as the «Trendtage Gesundheit Luzern» and the «Alliance Health Competence».
We are proud to be certified as a “Top Employer Switzerland” and “Top Employer Europe” showing the company’s commitment to our employees and the community around us.
Required Skills:
Aktenführung, Aktenführung, Anbieterauswahl, Anpassungsfähigkeit, Biotechnologie, Biowissenschaften, GMP Compliance, Kalibrierverfahren, Klinische Herstellung, Klinische Studienprotokolle, Klinisches Versorgungsmanagement, Kontinuierliche Verbesserung voranbringen, Logistik-Koordination, Management der klinischen Supply-Chain, Persönliche Initiative, Produktionsplanung, Qualitätsrisikobeurteilung, Sicherheitsmanagement, Sicherheitsprotokolle, Sicherheitsverfahren, Stakeholder-Management, Standard Operating Procedure (SOP) Schreiben, Supply-Chain-Kennzahlen, Technische Probleme, Unabhängig arbeiten {+ 2 more}
Preferred Skills:
Current Employees apply HERE
Current Contingent Workers apply HERE
Personalberatungsvertreter, bitte sorgfältig lesen
Merck & Co., Inc., Rahway, NJ, USA, auch als Merck Sharp & Dohme LLC, Rahway, NJ, USA, bekannt, akzeptiert keine unaufgeforderte Unterstützung von Personalvermittlungsfirmen. Alle Lebensläufe, die von Personalberatungen an einen Mitarbeiter unseres Unternehmens gesendet werden, ohne dass eine gültige schriftliche Vermittlungsvereinbarung für diese Position besteht, gelten als alleiniges Eigentum des Unternehmens. Im Falle der Einstellung eines Bewerbers durch unser Unternehmen in Folge einer Agenturempfehlung wird keine Gebühr entrichtet, sofern keine entsprechende vorherige Vereinbarung besteht. Wenn Vereinbarungen mit der Agentur vorhanden sind, sind die Einführungen positionsspezifisch. Bitte keine Anrufe oder E-Mails.
Mitarbeiter-Status:
Fest angestellt
Umzug:
No relocation
Visa-Sponsoring:
No
Reiseanforderungen:
10%
Flexible Arbeitszeitvereinbarungen:
Not Applicable
Schicht:
Not Indicated
Gültige Fahrerlaubnis:
No
Gefahrstoff(e):
N/A
Job Posting End Date:
08/18/2026
*A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.
