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Simtra BioPharma Solutions

Sterile injectable drug manufacturing

Quality Client Services Manager

Regulatory & Quality (Life Sciences)Posted on Nov 12
Full-timeBloomington, IN, USANo salary listedIn-person

About the Job

Requirements

  • A bachelor's degree is required; a science-related field is preferred.
  • A minimum of five years of pharmaceutical experience and one to two years of supervisory experience are required.
  • Knowledge of quality operating procedures and quality and regulatory requirements pertinent to pharmaceutical, biological, and biochemical quality is required.
  • Project management and customer service experience are required.
  • Computer proficiency in Microsoft Word, Excel, and Outlook, and the ability to use enterprise software such as JDE, BPLM, Pilgrim, or Trackwise, are required.
  • The role may require overtime, including nights and weekends.
  • The position requires using hands and fingers to manipulate office equipment, sitting for long periods, and possibly walking or standing for periods.

Responsibilities

  • Manage Quality Client Representatives.
  • Manage client project quality updates and reviews with all levels of management.
  • Make accurate and timely quality decisions regarding client projects, questions, and quality requests.
  • Escalate quality issues to the impacted departmental Quality Manager and/or Quality Director as necessary for corrective action implementation.
  • May oversee quality systems such as CAPA or NCR.
  • Partner with Quality leadership to sign off on applicable documentation, including validations, protocols, non-conformances, CAPA, and annual product reviews.
  • Review and approve exception reports as needed to meet client delivery dates and expectations.
  • Represent Quality in required Project Client Meetings.
  • Track, trend, compile, and report client quality metrics as necessary.
  • Negotiate and provide guidance in the approval process of Quality Agreements.
  • Lead continuous improvement activities to maximize business results.

About the Company

Simtra BioPharma Solutions

Sterile injectable drug manufacturing

Simtra BioPharma Solutions is a contract development and manufacturing organization specializing in sterile injectable medicines. It supports pharmaceutical and biotechnology companies with formulation, process development, clinical and commercial manufacturing, filling, packaging and related technical services. Facilities and teams operate under regulated quality systems suited to complex parenteral products. Simtra is a business-to-business manufacturing partner rather than a consumer drug brand, helping sponsors move therapies from development into reliable supply through dedicated production expertise and capacity.

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