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Director, Quality

Employer
Molecular Templates, Inc.
Location
Austin, TX
Start date
Feb 15, 2019

View more

Discipline
Quality, Quality Assurance
Required Education
Bachelors Degree
Position Type
Full time

Job Details

Company Description:

 

Molecular Templates (MTEM) is a clinical stage biopharmaceutical company targeting a variety of cancers through development of its innovative proprietary Engineered Toxin Body (ETB) platform. MTEM's first immunotoxin, MT-3724, is in clinical development for non-Hodgkin's lymphoma. Pipeline products for additional oncology targets are being advanced toward clinical development. For more information, please visit MTEM's website at www.mtem.com.

 

Position Overview:

 

Molecular Templates is seeking an experienced and highly-motivated professional to lead quality efforts, including QA and QC. The Director will oversee the development, implementation and maintenance of quality systems for QA and QC and activities to meet 21 CFR Part 211 compliance.  This position will management for generation and review of documents used in good manufacturing practices and monitor audits of production and quality control areas. This requires excellent technical skills and abilities, analytical and mathematical skills, organizational and time-management skills, interpersonal skills, plus ability to apply attention to detail

 

Job Responsibilities will include:

 

  • Manage the development, implementation and maintenance of quality assurance systems and activities, such as Deviations, Out of Specifications, Out of Tolerances, Change Control, CAPA, Master Validation Plans, and Validation
  • Oversee generation and review of documents used in good manufacturing practices, such as batch record review
  • Monitor audits of production and Quality Control areas, such as batch record review and release, nonconformities, technology transfer, scale-up, validation, training and other GMP activities
  • Lead investigations and resolve potential product quality issues to improve efficiency. 
  • Develop, implement and maintain the activities of quality control systems.
  • Oversee development and implementation of standards, methods and procedures for inspecting, testing and evaluating the precision, accuracy and reliability of company products.   
  • Make recommendations for corrective action necessary to ensure conformity with quality specifications. 
  • Ensure finished products conform to government and Company standards and satisfy good manufacturing practices regulations. 
  • Coordinates interdepartmental activities.
  • Select, develop and evaluate personnel to ensure the efficient operation of the function.
  • Complete additional projects, for example process improvements

 

Qualifications:

 

    • Bachelor's degree from accredited institution in life science, chemistry, pharmaceutical science or related field. Advanced Degree, preferred
    • Minimum of seven (7) years of related professional experience in QA and/or QC
    • Thorough knowledge of cGMP regulations, 21 CFR Part 211, quality systems, and regulatory requirements
  • Excellent problem-solving and analytical skills applied to investigations
  • Excellent project management, time management, and multi-tasking skills
  • Excellent written and verbal communication skills
  • Excellent interpersonal skills
  • Excellent computer skills with knowledge of spreadsheet, word processing and statistical analysis software
  • Ability to manage competing priorities and projects
  • Ability to function independently, exercise good judgement and work in a team-based environment
  • Ability to identify problems and solutions then act to resolve
  • Demonstrated ability to resolve operational and strategic issues
  • Ability to understand instructions and to learn how to maintain equipment
  • Ability to apply attention to detail as applied to data review and compliance
  • High degree of reliability and professionalism

 

Reporting Structure:

 

This position will have supervisory responsibilities for Quality Control and Quality Assurance. This position reports to Sr. Director, Quality.

 

 

Molecular Templates, Inc. is an Equal Opportunity Employer and offers competitive salaries and benefits.



For more information, or to apply now, you must go to the website below. Please DO NOT email your resume to us as we only accept applications through our website.

https://mtem.isolvedhire.com/jobs/54801-19034.html

Company

Molecular Templates, Inc. (MTEM) is a clinical stage biopharmaceutical company focused on the discovery and development of biologic therapeutics for the treatment of cancer and other serious diseases. The company primarily develops a pipeline of therapies through its proprietary biologic engineered toxin body (ETB) drug platform with unique mechanisms of actions which are highly differentiated from antibody drug conjugates (ADCs). MTEM is developing MT-6402, which is in a Phase I clinical trial for PD-1/PD-L1 antibody relapsed/refractory patients; MT-5111, which is in a Phase I clinical trial for the treatment of HER2-positive cancers; and MT-0169, which is in a Phase I clinical trial to treat relapsed/refractory myeloma. Additional preclinical compounds derived from our ETB platform technology are being advanced toward clinical development.  Additional information about MTEM can be obtained at www.mtem.com.  

OWNERSHIP: Public

STOCK SYMBOL: MTEM

STOCK EXCHANGE: NASDAQ

Company info
Website
Phone
512-869-1555
Location
9301 Amberglen Blvd, Ste 100
Austin
TX
78729
US

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