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Quality Control Manager

MTBI-diagnostics
Badr City, Cairo
Posted 4 years ago
109Applicants for1 open position
  • 46Viewed
  • 9In Consideration
  • 8Not Selected
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Job Details

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Job Description

  • Review executed QC test records for product release, including the investigation and resolution of deviations.
  • Perform routine QC testing as needed.
  • Serve as a QC subject matter expert on various methods within the company's team and with external partners.
  • Plan, organize and coordinate the activities related to QC Analytical and Stability testing to ensure timely completion of tasks.
  • Write, organize and review QC analytical result tables, protocols and reports.
  • Works in conjunction with other Assay development to qualify, validate and transfer QC analytical methods as applicable.
  • Participate in continuous improvements of quality systems (procedures and systems) to improve organization effectiveness, quality assurance compliance, and regulatory and other requirements.
  • Assist in Quality Metric review processes, assess data for adverse trends, develop solutions and oversee implementation.
  • Authors and Reviews company's regulatory submissions.
  • Works with QC management and project team lead to identify and mitigate risks to meeting QC milestones and goals.
  • Coordinate with the Quality Assurance Department for required review and approval of documents.
  • Responsible for development of direct reports.
  • Responsible for training of QC staff.

Job Requirements

  • 5 to 7 years in (pharmaceutical or biotechnology industry) with at least 3 years in QC management role or equivalent.
  • Solid knowledge and understanding of international regulations and guidance applicable to Quality Control and method validation.
  • Experience in quality control required. A strong background in biology is desired.
  • Experience transferring assays from Assay Development to Quality Control is required.
  • Experience in assay qualification and validation strongly desired. Experience in in vitro diagnostic is prefer.
  • Knowledge of FDA and regulatory requirements pertaining to biotechnology and pharmaceutical industries required. Must have laboratory experience with a variety of analytical techniques including, but not limited to, quantitative lateral flow, ELISA, and cell-based methods.
  • Knowledge of statistical methods applicable to the analysis of data.
  • Proficient in general and non-routine laboratory skills.
  • Experience working with contract testing labs.
  • Excellent interpersonal, communication and organizational skills.
  • Ability to make sound decisions about team activity scheduling, allocation of resources, and priorities.
  • Flexibility in problem solving, providing direction and work hours to meet business objectives.
  • Good oral and written communication skills. MS Office skills; equipment related software.

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