Auftragsdetails

Quality Control SME(NGS Sequencing) - Redwood City, CA (REF11520Y) - propharma group

Datum der Veröffentlichung: Nov 12, 2022
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Auftragsdetails

  • Ort:
    Redwood City, California, United States of America
  • Gesellschaft:
  • Typ:
    Full Time/Permanent
  • Shift:
    First Shift (Day)
  • Karrierelevel:
    Experienced Professional
  • Positionen:
    5
  • Erfahrung:
    7 Year
  • Geschlecht:
    Keine Präferenz
  • Grad:
    Bachelors
  • Vorher bewerben:
    Nov 30, 2023

Job Summary

Company Description

ProPharma Group is an industry leading, single source provider for regulatory compliance, pharmacovigilance, and medical information services across the full development lifecycle for pharmaceutical, biotechnology, and medical device companies. Operating around the world with offices in Australia, Canada, Germany, Japan, the Netherlands, Sweden, United Kingdom, and the United States, ProPharma Group’s fully integrated service offerings will provide clients with a comprehensive suite of global support services that are required to be competitive in today’s dynamic markets. We build successful long-term relationships with clients by providing leading industry knowledge, experience, and proven processes.

Detailed Description

Job Description

We have a client that is based in Redwood City, CA that is looking for a QC SME that can help the QC team with the lab onsite for 3 months. You would need to have bench experience and specific Sanger sequencing experience.

The responsibilities for this role would be the following:

  • transfer a sanger sequencing method for our gRNA from research to QC
  • validate the method, including documentation (Protocol, Report, SOP)
  •  train existing QC staff to perform the method

Qualifications

Qualified candidates must have:

  • QC Sanger Sequencing experience as well as bench experience
  • B.S./B.A. in scientific discipline as a minimum. 
  • A Graduate degree in a scientific discipline is preferred.
  • Minimum 7 years’ quality Control  experience in related industry.
  • Proven record with team leadership, problem solving, project tracking and budgeting, and facilitation of efficient communication between the client and the team. 
  • Demonstrated ability to lead people and get results through others.
  • Quality orientation and high attention to detail.
  • Ability to interact in a professional and positive manner with clients and co-workers. 
  • Strong  GMP documentation, including protocols, reports, SOPs, and method validation, etc.
  • Effective written and oral communication skills; ability to write, type, express or exchange ideas by means of the spoken word; convey information/instructions accurately; receive detailed information through oral or written forms and to translate those instructions into physical execution of tasks.

Additional Information

We celebrate our differences and strive to create a workplace where each person can be their authentic self. We are committed to diversity, equity, and inclusion. Employees are encouraged to unleash their innovative, collaborative, and entrepreneurial spirits. With a holistic approach as an Equal Opportunity Employer, we provide a safe space where all employees feel empowered to succeed.

***ProPharma Group does not accept unsolicited resumes from recruiters/third parties. Please, no phone calls or emails to anyone regarding this posting.***

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Company Overview

Berlin, Berlin, Germany

ProPharma Group is the leading global, independent, single-source provider of regulatory, clinical, and compliance services serving the pharmaceutical, biotechnology, and medical device companies. Our team of experts brings a comprehensive portfolio... Read More

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