×
Register Here to Apply for Jobs or Post Jobs. X

Quality Manager - Analytical

Job in Carlsbad, San Diego County, California, 92002, USA
Listing for: Allen Spolden
Full Time position
Listed on 2026-01-11
Job specializations:
  • Healthcare
    Data Scientist
  • Quality Assurance - QA/QC
    Data Analyst
Job Description & How to Apply Below

Carlsbad, United States | Posted on 05/02/2024

  • Industry Nonprofit Charitable Organizations
  • Work Experience 5+ years
  • City Carlsbad
  • State/Province California
  • Country United States
Job Description

The Quality Control Manager is responsible for developing and maintaining Quality QC systems for the Analytical department. Achieves organizational objectives through the coordinated achievements of subordinate staff. Establishes departmental goals and objectives and functions with autonomy. Manages the accountability and stewardship of human, financial, and often physical resources in compliance with departmental and organizational goals and objectives. Ensures subordinate supervisors and professionals adhere to defined internal controls.

Manages systems and procedures to protect departmental assets. Demonstrated experience in leadership and a history of developing a culture of teamwork, collaboration, and ability to advance group goals to meet company objectives.

Job Responsibilities

1. Achieves organizational objectives through the coordinated achievements of subordinate staff. Establishes departmental goals and objectives and functions with autonomy. Manages the accountability and stewardship of human, financial, and often physical resources in compliance with departmental and organizational goals and objectives.

2.
• Ensures subordinate supervisors and professionals adhere to defined internal controls. Manages systems and procedures to protect departmental assets. Responsible for developing a culture of teamwork, collaboration, and ability to advance group goals to meet company objectives.

3.
• Responsible for optimization and operation of the quality control laboratory in a biopharmaceutical manufacturing setting, including all related infrastructure, documentation, equipment validation and analyst training. Develops, implements, and maintains quality control systems in accordance with cGMP requirements. Manages all aspects of Quality Control, in support of and in full compliance with established cGMP and company requirements.

4.
• Develop staff to improve individual and departmental performance. Department oversight of manufacturing support testing for multiple projects and related stability studies.

5.
• Oversight of assay verification, qualification, validation, and tech transfer activities. Verification of maintenance, calibration, and qualification of laboratory equipment. Assist in troubleshooting equipment malfunctions, assay system suitability failures, assay deviations, CAPAs, and out of specifications investigations. Coordinate instrument preventive maintenance and validation activities.

6.
• Author and review Quality Control Standard Operating Procedures (SOPs), Assay Qualification Reports, and Stability Protocols

Qualifications:

  • Experience in the development and establishment of operations of QC laboratories in a GMP regulated environment.
  • In-depth experience related to method development, optimization, validation, and tech transfers.
  • Demonstrated ability to manage a team and work independently on projects, and review project data and provide summary analysis reports based upon the data.
  • Ability to provide support for regulatory and client audits, as well as interact with clients.
  • A profound understanding of analytical instrument principals and application of advance instrumentation analysis for pharmaceutical and biologic products which could include HPLC (MWD, DAD, ELSD, RID detection), UV/Vis Spectroscopy, qPCR, Capillary Electrophoresis, MS, Genetic Analyzer, Place Readers, Gel Imagers, etc.
  • Familiarity with analytical testing procedures: AGE, qPCR/dPCR, HPLC (IEX, RP, SEC), Sequencing, Plate Based Assays (BCA, Kanamycin).
  • Strong knowledge of pharmacopeia (USP/EP) and regulatory requirements for the industry (ICH, GDP, cGMP and quality systems including OOS investigations, deviations and CAPAs).
  • Sets stretch goals and links them to strategic outcomes and business deliverables.
  • Strong leadership and motivational capabilities.
  • Exercises sound judgment within defined procedures and policies to determine appropriate action.
  • Strong scientific, analytical, and problem-solving skills as well as sound…
To View & Apply for jobs on this site that accept applications from your location or country, tap the button below to make a Search.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
 
 
 
Search for further Jobs Here:
(Try combinations for better Results! Or enter less keywords for broader Results)
Location
Increase/decrease your Search Radius (miles)

Job Posting Language
Employment Category
Education (minimum level)
Filters
Education Level
Experience Level (years)
Posted in last:
Salary