QC Chemistry Group Lead – 2nd Shift
: Job Details :


QC Chemistry Group Lead – 2nd Shift

Ajinomoto Bio-Pharma Services

Job Location : San Diego,CA, USA

Posted on : 2025-07-26T01:23:20Z

Job Description :

Join to apply for the QC Chemistry Group Lead – 2nd Shift role at Ajinomoto Bio-Pharma Services.

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Why work for PCI Pharma Services?

At PCI, we focus on quality, operational excellence, and providing an industry-leading customer experience. Our people are key to our success, and we strive to create an authentic culture of purposeful work where talented individuals can grow their careers. We promote intentional learning, real-life experience, and a fair, competitive rewards program.

Job Details

We are seeking a QC Chemistry Group Lead - 2nd Shift. The role ensures the integrity of the laboratory infrastructure, oversees routine and non-routine analysis of proteins, peptides, small and large molecules, and ADCs, and supports development of procedures and initiatives to meet departmental goals.

Responsibilities

  • Lead or collaborate on method establishment for compendial assays and other chemistry methods.
  • Perform routine analysis and testing for various assays such as pH, osmolality, particulate matter, ELISA, CE-SDS, SDS-PAGE, viscosity, and moisture content.
  • Provide scientific direction and technical problem solving to team members and stakeholders.
  • Interact with clients and follow up on inquiries.
  • Review data, reports, deviations, OOS investigations, and test results; provide conclusions and future directions.
  • Write investigations for deviations and out-of-specification reports.
  • Maintain laboratory instrumentation.
  • Ensure reliable attendance and professional behavior.
  • Align actions with PCI's cultural values and department goals.
  • Leadership Responsibilities

  • Promote PCI's culture and empower employees.
  • Create a motivating environment.
  • Set performance standards and provide feedback.
  • Manage employee schedules and provide oversight.
  • Requirements

  • Associate's Degree or equivalent required; Bachelor's in Life Sciences preferred.
  • At least 4 years of relevant quality control experience.
  • At least 1 year of leadership experience.
  • Knowledge of GMP regulations, troubleshooting, and data entry.
  • Strong communication and attention to detail.
  • Ability to work independently or as part of a team.
  • Proficiency in Microsoft Office; experience with electronic Quality Systems preferred.
  • The hourly rate ranges from $34.66 to $46.28 USD, plus 2nd shift pay differential and potential bonuses. Final offers depend on experience, credentials, location, and expertise.

    Join us to help bridge life-changing therapies to patients. Let's discuss your future with PCI.

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