Director of Operations, GmbH

Bereich: Laborleitung

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Basic Function and Scope of the Position
  • The Director of Operations is responsible for all aspects of the day-to-day operations of the laboratory and ensuring that the testing performed under the implemented quality management system.
  • Implement the directives and task assigned by senior management.
Impact
Successful performance of a Director of Operations is paramount to providing high quality clinical testing to our clients and growth of the company.

Job Responsibilities
  • Ensures that all necessary resources are available to the clinical testing personnel.
  • Ensure a safe and efficient working environment.
  • Ensure that testing personnel are meeting performance expectations.
  • Participate in all quality and safety meetings.
  • Participates in NCMRs, MRB, and CAPAs.
  • Work with project managers and department heads during project launches to ensure smooth transition from Development through product launch. 
  • Participates in Development Projects. Organize, write and maintain standard documentation and compile project specific reports.
  • Prepare and monitor budget.
  • Monitor all expenses associated with LabPMM.
  • Maintain intramural relationships with important persons in the field of molecular diagnostics.
  • Meet with clients and physician users.
  • Generate and evaluate marketing materials.
  • Organize trade show/conference booths and marketing material.
  • Cultivate new clients.
  • Design and implement work efficiency improvements.
  • Research and evaluate new clinical assays.
  • Human resource management including: employee evaluations, tracking employee productivity, hiring and termination, employee scheduling.
  • Coordinate with the officers of LabPMM to ensure adequate resources are available for high quality clinical testing.
Education and Experience
Required:
  • MSc in Biological sciences with a preference for a PhD.
  • A minimum of 5 years managing a molecular laboratory.
  • Ability to consistently meet critical deadlines.
  • Ability to manage multiple projects and changing priorities.
Desired:
  • M.S. in biological sciences
  • MBA
  • Experience with ISO 15189 and NY state clinical laboratory regulations.
  • Previous experience with CAP and other accrediting agency regulations and inspections.
Supervisory Experience
A minimum of 5 years of supervisory experience.

Physical Requirements and Work Environment
  • Occasional lifting of up to 20 kg.
  • Administrative tasks will be required.
  • Some activities will take place at a desk and on a computer.

How to apply:
SPECIFY THE POSITION AND APPLY AS FOLLOWS:
- Submit your resume and cover letter to hr@invivoscribe.com.
- Be sure to reference Job Code: MBDO in the subject line of either your email or cover letter to be considered for this position.
- No phone calls or walk-ins inquiring about this position.

Kontaktdaten


Kontakt für Bewerbungen
SPECIFY THE POSITION AND APPLY AS FOLLOWS:
- Submit your resume and cover letter to hr@invivoscribe.com.
- Be sure to reference Job Code: MBDO in the subject line of either your email or cover letter to be considered for this position.
- No phone calls or walk-ins inquiring about this position.

Details der Stellenanzeige


Arbeitszeit
Vollzeit
Vertragslaufzeit
Festanstellung
Stellentyp
Geschäftsführung & Vorstand
Berufserfahrung
Berufserfahrung vorausgesetzt
Region
Deutschland (Bayern)
Arbeitsort
82152 Martinsried
Fachgebiet
Biotechnologie
JETZT BEWERBEN

Über Invivoscribe Technologies

Invivoscribe Technologies, Inc. , is a privately-held corporation dedicated to improving the quality of healthcare worldwide by providing high quality, reliable, cutting-edge tools for molecular research, molecular diagnostics, and personalized molecular medicine. Invivoscribe provides a comprehensive selection of PCR-based gene rearrangement, chromosome translocation, and gene mutation...

Mehr über die Invivoscribe Technologies

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