דרושים Supply Chain Lead M/f/d ב-Msd ב-גרמניה
MSD Associate Specialist Validierung & Qualifizierung m/w/d Germany, North Rhine-Westphalia, Cologne
Job Description
Responsibilities
- Work with local and remote team members to upgrade and standardize DeltaV systems.
- Develop strategies to optimize and ensure the quality and stability of process automation systems through future expansion, replacement, or upgrade.
- Develop standards, processes, templates and tools for DeltaV DCS and other Process Control systems for upgrading and patching the operating system and application software, enterprise monitoring, and identify vulnerabilities and non-standard elements.
- Monitor DeltaV and other automation systems and respond to alerts.
- Keep current with global technical standards for DeltaV DCS and other Process Control systems.
- Work alongside corporate security professionals to understand and assess compliance with security standards.
- Provide support in the installation and configuration of a diverse range of interfaces to ensure seamless integration and efficient operation within the system.
- Troubleshoot and provide technical guidance and support in the installation and configuration of DeltaV DCS databases to ensure optimal functionality and performance.
- Contribute well-structured, tailored and practical technical information to a knowledge management system.
Qualifications
- Good understanding of process control systems architecture and control system administration.
- Skilled with Emerson DeltaV system standards, Knowledge Base Articles, Best Practices, Cybersecurity and Guardian support capabilities.
- Significant experience with project execution in technical SME role for DeltaV System upgrade.
- Experience at working with common Automation interface protocols (OPC, MODBUS, PROFIBUS).
- Familiar with DeltaV Live, DeltaV hardware components including Charms I/O.
- Effective interpersonal and communication skills, both verbal and written.
- Excellent organizational skills to work independently on multiple projects.
- Ability to prepare Technical Implementation Standards, Standard Operating Procedures (SOP) and cGMP documents.
- Experience with GMP Quality Systems.
- Familiar with IT systems; specifically, integration of Automation systems with IT systems.
- Networking experience; working knowledge of Enterprise Networking and local control networks.
- Aveeva PI, Dynatrace, Qualys, Ansible or other monitoring platforms.
- Familiarity with Agile project development practices, Jira, Confluence.
Current Contingent Workers apply
*A job posting is effective until 11:59:59PM on the dayBEFOREthe listed job posting end date. Please ensure you apply to a job posting no later than the dayBEFOREthe job posting end date.
משרות נוספות שיכולות לעניין אותך
MSD Biologielaborant m/w/d der Parasitologie Germany, Rhineland-Palatinate
Job Description
Für unseren Forschungs- und Entwicklungsstandort in Schwabenheim suchen wir ab sofort unbefristet und in Vollzeit eine(n) Biologielaborant/in oder Versuchstierpfleger/in (m/w/d) im Bereich Parasitologie.
Deine Aufgaben
Verantwortliche Organisation, Durchführung, Betreuung und Optimierung der Parasiten Stammhaltungen (in vivo und in vitro)
Unterstützung bei der Vorbereitung und Durchführung der Testungen von Substanzen auf Wirksamkeit gegen Parasiten (in vitro und in vivo)
Sicherstellen der allgemeinen Laborroutinen/Labororganisation
Computertätigkeiten (Dateneingaben, allgemeine Dokumentation)
Dokumentation gemäß GxP- und patentrechtlicher Vorgaben
Qualifikation
Biologielaborant/in (Berufsanfänger) oder Versuchstierpfleger/in (Berufserfahrung erwünscht)
Qualifikation nach FELASA-B-Richtlinien wünschenswert
Gute Kenntnisse in MS Office Anwendungen (Word, Excel, Outlook, Teams)
Bereitschaft zum Umgang mit elektronischen, software-gestützten Gerätschaften und elektronisch basierten Laborbüchern
Strukturierte und eigenverantwortliche Arbeitsweise
Teamfähigkeit
Sehr gute Deutsch- und gute Englischkenntnisse
Benefits
Bezahlung nach Tarif, Langzeitkonto, Betriebsrente und Bonuszahlung
Abwechslungsreiche Aufgabengebiete (Forschungsschwerpunkte, Tierarten, Projekte, Schnittstellen)
Flexible Arbeitszeiten
Einbringen von eigenen Ideen in die Prozessgestaltung
Mitarbeit bei der Entwicklung von Tierarzneimitteln
Einblicke in die Arbeitsweise eines großen Unternehmens
Zahlreiche Fort- und Weiterbildungsmöglichkeiten
Kleiner Standort in wunderschöner Lage mit familiärer Atmosphäre
Eigene Kantine
Gesundheitsunterstützung (Massagen, Gesundheitstag, Ressources for Living)
Company Bike, Corporate Benefits, (E-) Parkplät
Current Employees apply
Current Contingent Workers apply
Search Firm Representatives Please Read Carefully
Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.
Employee Status:
RegularRelocation:
VISA Sponsorship:
Travel Requirements:
Flexible Work Arrangements:
Not ApplicableShift:
Valid Driving License:
Hazardous Material(s):
Job Posting End Date:
05/15/2025*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.
Requisition ID: R335339
MSD Senior Scientist m/f/d Preclinical Development Animal Health Germany, Rhineland-Palatinate
Job Description
To support our Drug Safety & Metabolism Team in Schwabenheim (near Mainz), we are looking for you as of now, full time and initially for a fixed term of 2 years, as a
Your Responsibilities and Tasks:
- Scientifically support Research and Development with regard to new and existing products
- Compile and evaluate pharmacological and toxicological profiles of chemical substances by literature search and testing
- Plan, conduct and evaluate inhouse studies according to GLP guidelines, e.g., toxicity, pharmacokinetics, metabolism, and residue depletion, as well as monitor equivalent outsourced studies
- Compile expert reports, other scientific texts, and presentations in English for authorities
- Maintain and extend contact to contract research organizations, external experts and universities
- Act as preclinical representative in international multidisciplinary project teams
Your Qualifications
- Veterinary Medicine degree, including PhD or comparable
- Experience in Research and Development, ideally in the international veterinary pharmaceutical industry
- Experience in managing animal studies, ideally according to GLP
- Profound knowledge in pharmacology, metabolism and toxicology
- Experience in pharmacokinetic and metabolic evaluation of active substances
- Precise, analytical and creative work approach to problem solving
- Fluent written and spoken German and English language proficiency
Our Benefits:
- Flex Time (37.5 hours/week)
- Attractive compensation package (13 monthly salaries plus cash and stock target bonus)
- Company pension plan
- Vacation allowance (1.200€ annually)
- 30 days annual leave
- Hybrid working model
- Employee benefits
- Company bike / bicycle leasing
Current Contingent Workers apply
*A job posting is effective until 11:59:59PM on the dayBEFOREthe listed job posting end date. Please ensure you apply to a job posting no later than the dayBEFOREthe job posting end date.
MSD Biologielaborant/ Biologietechniker m/w/d - Automatisierungs... Germany, Rhineland-Palatinate
Job Description
Für unseren Forschungs- und Entwicklungsstandort in Schwabenheim suchen wir ab sofort unbefristet und in Vollzeit eine(n) Biologielaborant/in / Biologietechniker (m/w/d)- Automatisierungsverfahren.
Aufgaben:
Eigenverantwortliche Organisation und Durchführung von in vitro Testungen zur Evaluierung der antiparasitischen Wirkung von Testsubstanzen, sowie anschließender Dokumentation und Interpretation der Versuchsergebnisse
Etablierung, Validierung und Optimierung neuartiger insbesondere automatisierter parasitologischer in vitro Modelle für das Wirkstoff-Screening
Auswertung und Dokumentation der experimentellen Ergebnisse mittels geeigneter Programme sowie Eingabe und Konsistenzprüfung in Datenbanken
Unterstützung bestehender Parasiten Stammhaltungen (in vitro und in vivo) und Wirkstofftestungen am Tier
Dokumentation gemäß GxP- und patentrechtlicher Vorgaben
Sicherstellen der allgemeinen Laborroutinen/Labororganisation
Qualifikation:
Biologielaborant/in oder Biologisch-Technische/r Assistent/in (BTA) (m/w/d) oder vergleichbare Ausbildung mit mindestens 3 Jahren Berufserfahrung im automatisierten GxP-Umfeld
Sicherer Umgang mit elektronischen, software-gestützten Geräten und elektronischen Datenerfassungssystemen
Erfahrungen in der Implementierung und Validierung automatisierter in vitro Tests sowie in der Zellkultur
Strukturierte und eigenverantwortliche Arbeitsweise, Organisationsfähigkeit und Flexibilität in der Planung, Durchführung und Koordination von Teamarbeiten
Teamfähigkeit und Leidenschaft für manuelle und automatisierte Laborarbeit
Fundierte PC-Anwenderkenntnisse in MS Office (Word, Excel, PowerPoint, Outlook, Teams)
Qualifikation nach FELASA-B-Richtlinien wünschenswert
Sehr gute Deutsch- und gute Englischkenntnisse in Wort und Schrift
Benefits:
Bezahlung nach Tarif, Langzeitkonto, Betriebsrente und Bonuszahlung
Abwechslungsreiche Aufgabengebiete (Forschungsschwerpunkte, Tierarten, Projekte, Schnittstellen)
Flexible Arbeitszeiten
Einbringen von eigenen Ideen in die Prozessgestaltung
Mitarbeit bei der Entwicklung von Tierarzneimitteln
Einblicke in die Arbeitsweise eines großen Unternehmens
Zahlreiche Fort- und Weiterbildungsmöglichkeiten
Kleiner Standort in wunderschöner Lage mit familiärer Atmosphäre
Eigene Kantine
Gesundheitsunterstützung (Massagen, Gesundheitstag, Ressources for Living)
Company Bike, Corporate Benefits, (E-) Parkplätze
Current Employees apply
Current Contingent Workers apply
Search Firm Representatives Please Read Carefully
Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.
Employee Status:
RegularRelocation:
No relocationVISA Sponsorship:
NoTravel Requirements:
No Travel RequiredFlexible Work Arrangements:
Not ApplicableShift:
Not IndicatedValid Driving License:
NoHazardous Material(s):
N/AJob Posting End Date:
05/18/2025*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.
Requisition ID: R340939
MSD Senior Scientist m/f/d Preclinical Development Animal Health Germany, Rhineland-Palatinate
Job Description
To support our Drug Safety & Metabolism Team in Schwabenheim (near Mainz), we are looking for you as of now, full time and initially for a fixed term of 2 years, as a
Your Responsibilities and Tasks:
- Scientifically support Research and Development with regard to new and existing products
- Compile and evaluate pharmacological and toxicological profiles of chemical substances by literature search and testing
- Plan, conduct and evaluate inhouse studies according to GLP guidelines, e.g., toxicity, pharmacokinetics, metabolism, and residue depletion, as well as monitor equivalent outsourced studies
- Compile expert reports, other scientific texts, and presentations in English for authorities
- Maintain and extend contact to contract research organizations, external experts and universities
- Act as preclinical representative in international multidisciplinary project teams
Your Qualifications
- Veterinary Medicine degree, including PhD or comparable
- Experience in Research and Development, ideally in the international veterinary pharmaceutical industry
- Experience in managing animal studies, ideally according to GLP
- Profound knowledge in pharmacology, metabolism and toxicology
- Experience in pharmacokinetic and metabolic evaluation of active substances
- Precise, analytical and creative work approach to problem solving
- Fluent written and spoken German and English language proficiency
Our Benefits:
- Flex Time (37.5 hours/week)
- Attractive compensation package (13 monthly salaries plus cash and stock target bonus)
- Company pension plan
- Vacation allowance (1.200€ annually)
- 30 days annual leave
- Hybrid working model
- Employee benefits
- Company bike / bicycle leasing
Current Contingent Workers apply
*A job posting is effective until 11:59:59PM on the dayBEFOREthe listed job posting end date. Please ensure you apply to a job posting no later than the dayBEFOREthe job posting end date.
Job Description
Responsibilities
- Work with local and remote team members to upgrade and standardize DeltaV systems.
- Develop strategies to optimize and ensure the quality and stability of process automation systems through future expansion, replacement, or upgrade.
- Develop standards, processes, templates and tools for DeltaV DCS and other Process Control systems for upgrading and patching the operating system and application software, enterprise monitoring, and identify vulnerabilities and non-standard elements.
- Monitor DeltaV and other automation systems and respond to alerts.
- Keep current with global technical standards for DeltaV DCS and other Process Control systems.
- Work alongside corporate security professionals to understand and assess compliance with security standards.
- Provide support in the installation and configuration of a diverse range of interfaces to ensure seamless integration and efficient operation within the system.
- Troubleshoot and provide technical guidance and support in the installation and configuration of DeltaV DCS databases to ensure optimal functionality and performance.
- Contribute well-structured, tailored and practical technical information to a knowledge management system.
Qualifications
- Good understanding of process control systems architecture and control system administration.
- Skilled with Emerson DeltaV system standards, Knowledge Base Articles, Best Practices, Cybersecurity and Guardian support capabilities.
- Significant experience with project execution in technical SME role for DeltaV System upgrade.
- Experience at working with common Automation interface protocols (OPC, MODBUS, PROFIBUS).
- Familiar with DeltaV Live, DeltaV hardware components including Charms I/O.
- Effective interpersonal and communication skills, both verbal and written.
- Excellent organizational skills to work independently on multiple projects.
- Ability to prepare Technical Implementation Standards, Standard Operating Procedures (SOP) and cGMP documents.
- Experience with GMP Quality Systems.
- Familiar with IT systems; specifically, integration of Automation systems with IT systems.
- Networking experience; working knowledge of Enterprise Networking and local control networks.
- Aveeva PI, Dynatrace, Qualys, Ansible or other monitoring platforms.
- Familiarity with Agile project development practices, Jira, Confluence.
Current Contingent Workers apply
*A job posting is effective until 11:59:59PM on the dayBEFOREthe listed job posting end date. Please ensure you apply to a job posting no later than the dayBEFOREthe job posting end date.
משרות נוספות שיכולות לעניין אותך
