Expected Outcomes: A fully or partially automated setup capable of testing and qualifying FAUs according to defined optical and mechanical specifications.A software tool for measurement automation and data processing.A technical report including setup design, validation results, and recommendations for further optimization. Keywords: Fiber array units, optical testing, automation, alignment, mechanical qualification, photonic packaging, precision metrology.
. • Three to five years related manufacturing experience is preferred • Ability to read and interpret documents such as safety rules, customer drawings, operating and maintenance instructions, and procedure manuals. Ability to write routine reports and correspondence. Ability to speak effectively to all levels of management and employees. • Be able to calculate figures and amounts such as proportions, percentages, measurements, area, circumference, and volume
. • Three to five years related manufacturing experience is preferred • Ability to read and interpret documents such as safety rules, customer drawings, operating and maintenance instructions, and procedure manuals. Ability to write routine reports and correspondence. Ability to speak effectively to all levels of management and employees. • Be able to calculate figures and amounts such as proportions, percentages, measurements, area, circumference, and volume
. • Three to five years related manufacturing experience is preferred • Ability to read and interpret documents such as safety rules, customer drawings, operating and maintenance instructions, and procedure manuals. Ability to write routine reports and correspondence. Ability to speak effectively to all levels of management and employees. • Be able to calculate figures and amounts such as proportions, percentages, measurements, area, circumference, and volume
. • Three to five years related manufacturing experience is preferred • Ability to read and interpret documents such as safety rules, customer drawings, operating and maintenance instructions, and procedure manuals. Ability to write routine reports and correspondence. Ability to speak effectively to all levels of management and employees. • Be able to calculate figures and amounts such as proportions, percentages, measurements, area, circumference, and volume
Selbstständige Planung, Durchführung, Auswertung und Dokumentation von Integrationstests im BSL-1 Labor in unterschiedlichsten ProjektphasenAbstimmung der Integrationstests mit internen Schnittstellen und regelmässige Kommunikation an relevante Stakeholder über den Fortschritt der IntegrationstestsVerantwortlich für den Fortschritt der Systems Testing Aktivitäten innerhalb des Projektes gemäss der definierten ArbeitspaketeSie erstellen die erforderlichen technischen Dokumentationen in englischer SpracheSelbständiges Auswerten, Interpretieren und Präsentieren der Testergebnisse nach Regulatorischen und Projektspezifischen AnforderungenIdentifikation, Minimierung, Verfolgen und Reporten von Risiken und Issues nach Prozess und / oder ProjektdefinitionenReview von Produktanforderungen/Requirements hinsichtlich Testbarkeit und die Erstellung von Testfällen für die Verifikation dieser AnforderungenHinterfragen bestehender Laborprozesse, Identifikation von Optimierungsbedarf aus technischer und naturwissenschaftlicher Sicht und anschließende selbstständige Umsetzung Bachelor/Master Abschluss oder Ausbildung mit fundierter ErfahrungErste Test Erfahrung, idealerweise im Medical Device UmfeldSichere Programmierkenntnisse: entwickeln von internen Test-Frameworks und Analyse-Tools weiter mit Unterstützung von Git als Versionierung ToolPython Expertise (z.
Selbstständige Planung, Durchführung, Auswertung und Dokumentation von Integrationstests im BSL-1 Labor in unterschiedlichsten Projektphasen Abstimmung der Integrationstests mit internen Schnittstellen und regelmässige Kommunikation an relevante Stakeholder über den Fortschritt der Integrationstests Verantwortlich für den Fortschritt der Systems Testing Aktivitäten innerhalb des Projektes gemäss der definierten Arbeitspakete Sie erstellen die erforderlichen technischen Dokumentationen in englischer Sprache Selbständiges Auswerten, Interpretieren und Präsentieren der Testergebnisse nach Regulatorischen und Projektspezifischen Anforderungen Identifikation, Minimierung, Verfolgen und Reporten von Risiken und Issues nach Prozess und / oder Projektdefinitionen Review von Produktanforderungen/Requirements hinsichtlich Testbarkeit und die Erstellung von Testfällen für die Verifikation dieser Anforderungen Hinterfragen bestehender Laborprozesse, Identifikation von Optimierungsbedarf aus technischer und naturwissenschaftlicher Sicht und anschließende selbstständige Umsetzung Bachelor/Master Abschluss oder Ausbildung mit fundierter Erfahrung Erste Test Erfahrung, idealerweise im Medical Device Umfeld Sichere Programmierkenntnisse: entwickeln von internen Test-Frameworks und Analyse-Tools weiter mit Unterstützung von Git als Versionierung Tool Python Expertise (z.
Benefits A dynamic role with significant responsibilities and diverse tasks Attractive employment conditions, including a variable salary, 25 vacation days, and 13 ADV days Expense allowance to support work-related costs Pension scheme in accordance with the CAO Technical Installation Company Modern equipment: laptop and mobile phone provided Opportunity to purchase VINCI Energies shares at a discounted rate through the CASTOR savings program Responsibilities Maintain, inspect, and repair electrical components at offshore and onshore substations Test installations and devices according to NEN standards Prepare and follow up on offshore operations Document activities and report defects in wind farms Analyze faults and recommend solutions Create technical work instructions, risk assessments, and maintenance plans Qualifications Technical vocational training in electrical engineering Experience in maintenance and testing of electrical installations Understanding of energy distribution systems (substations / switchgear) Safety-conscious team player, willing to work offshore and in shifts Proficient in Dutch and English, with a valid Class B driver’s license One Group, Many Opportunities As part of VINCI Energies, we benefit from a global network. 102,000 employees generate revenue of more than €20 billion.
Your responsibilities will include: Performing site selection, initiation, monitoring and close-out visits.Supporting the development of a subject recruitment plan.Evaluating the quality and integrity of site practices in accordance with regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution.Collaborating with experts at study sites and with client representatives.Depending on client model there might be remote-monitoring, involvement in study start-up processes, specialization on therapeutic area (pharmaceutical product or medical devices).Mentoring of less experienced team members, support as subject matter expert for specific topics or additional tasks might be included.
. • Completes labor sheets, routers, log sheets, process forms and similar reports and forms. • Performs basic maintenance on production machinery and equipment. • Follows established process specifications and procedures. • Complies with all company policies and procedures. • Maintains housekeeping practices per departmental 5S program. • Meets utilization targets and standard times. • Accurately enters Database/SAP transactions in the computer. • Maintains daily records, including labor sheets and routers. • Responsible for observing and following all Environmental, Health and Safety rules and procedures.
Your responsibilities will include: Performing site selection, initiation, monitoring and close-out visits.Supporting the development of a subject recruitment plan.Evaluating the quality and integrity of site practices in accordance with regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution.Collaborating with experts at study sites and with client representatives.Depending on client model there might be remote-monitoring, involvement in study start-up processes, specialization on therapeutic area (pharmaceutical product or medical devices).
Identify non-conformities, recommend product and process changes, and initiate Fracas fault reports (FRNs). Chair and write up safety reviews. Support UL, CSA and Semi S2 inspections. Conduct EMC emission measurements and support EMC immunity testing.
Prepares concise, accurate, professional and timely Equipment Acceptance Reports, Service Work Reports, Expense Reports and other support documentation for customer visits; communicates with KHS internal staff to report on service activities; completes and submits reports within 3 weeks after the end of a job.
Prepares concise, accurate, professional and timely Equipment Acceptance Reports, Service Work Reports, Expense Reports and other support documentation for customer visits; communicates with KHS internal staff to report on service activities; completes and submits reports within 3 weeks after the end of a job.
What We’re Looking For: Legal Qualification: 1st and 2nd German State Exam; licensed to practice law in Germany.Experience: Minimum 8 years in employment law, including 3+ years in-house.Expertise: Strong knowledge of German law; experience with Swiss, UK, or French employment law is a plus.Skills: Excellent negotiation, drafting, and stakeholder management skills.Industry Background: Pharma, biotech, or medical device experience preferred. Reporting Relationships: The role reports to the Executive Director, Assistant General Counsel, Global Employment Law Why Join Us? Competitive salary and comprehensive benefits package.Flexible hybrid working model.Leadership development programs and career growth opportunities.Wellness perks: 2 additional paid wellness days, mindfulness sessionsCareer development and training opportunitiesFind Diversity, Equality, and Inclusion at all sites and with every colleague.
To learn more please visit http://www.convatecgroup.com The Global Health Economics & Outcome Research Manager (HEOR) will be part of our Market Access and Reimbursement Centre of Excellence (COE) and report into the Director, Global Health Economics and Outcomes Research. This will be a pivotal role in supporting our Convatec Market Access capabilities our business strategy within the evolving global market access and reimbursement landscape.