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Manufacturing Supervisor - Biomed Engineer

  • Specialty:

    Engineering
    • City:

      Memphis
    • State:

      TN
    • 38118
  • Assignment Type:

    Direct Hire
  • Job Id:

    59208

Description

The Role:

This position is responsible for on the floor oversight (Person in Plant) of a contract manufacturing organization (CMO) located in the Memphis Tennessee area. The incumbent will partner with internal and external stakeholders to drive production activities for clinical and commercial Cell Therapy (drug substance / drug product) products. Responsibilities include operational support of production activities (batch production, record review, document revisions, training) and quality management systems (deviation investigations, change management, and product disposition) all in accordance with good manufacturing practices (cGMP). Reporting to the Sr. Manager, External Manufacturing, he/she will provide the oversight, support, and results focus to reliably meet and/or exceed the company’s manufacturing goals while maintaining high levels of quality. The incumbent will also be responsible for implementing and maintaining defined operational excellence tools and metrics. This position requires an individual capable of partnering across and outside the organization to manage a complex cell therapy manufacturing process and deliver transformative medicine to patients.

Responsibilities:

Production Oversight

  • This position is in Memphis Tennessee and will have direct in-person oversight (Person in Plant) for cell therapy manufacturing at a CMO located in Memphis Tennessee.
  • Working in a in a cleanroom facility, ensuring adherence to established procedures and compliance to cGMP’s. Will require work during non-standard working hours and/or weekends (during campaigns).
  • Lead after action review meetings (immediately following production runs), documenting outcomes and tracking action items to closure. Working closely with CMO to identify and track to closure all open items/corrective actions.
  • Perform manufacturing review of executed batch records and discrepancy documents. Provide operational SME input into the resolution of non-conformance events.
  • Closely partner with CMO and Quality Assurance group, manage and ensure the timely production, review, and release of product.
  • Through frequent presence on site, establish professional and technical credibility and build sustainable, positive relationships to achieve defined program objectives.
  • Proactively identify, assess, and mitigate quality, operational, and organizational risks; escalate key risks and issues.
  • Provide on-site support during regulatory inspections.
  • Review and/or author technical and project protocols/plans and reports in support of technical studies, stage gate reviews, and global regulatory filings.

 

 

Continuous Improvement / Operational Excellence

  • Partner with technical teams and program management to facilitate technical transfer of processes to new CMOs including development / revision of batch records and procedures, management of change controls, and establishing process and equipment training programs.
  • Monitor CMO goals, individual goals, and key performance indicators in alignment with company goals; maintain and report applicable metrics/milestones.
  • Proactively respond to key performance indicators and drive continuous improvement initiatives that improve contract manufacturer performance (safety, quality, cost).
  • Other duties as assigned.

Qualifications:

Education and Experience

  • Bachelor's degree and 3-5 years of related pharmaceutical/biopharmaceutical work experience.
  • 1-2 years in a supervisory role (ex. Sr. Operator/Lead Operator).
  • Aseptic processing experience is required.
  • Experience in commercial or clinical manufacturing (pharma/biotech) required.
  • Working knowledge of cGMP Quality Systems (change management, discrepancy management, and validation).
  • Preferred experience in cell and/or gene therapy operations and contract manufacturing.

Skills and Ability

  • Frequent in-person onsite at CMO in Memphis, TN.
  • Ability to aseptically gown and navigate cleanroom manufacturing areas.
  • Strong analytical and problem-solving skills, strong attention to details
  • Excellent written and verbal communication skills.
  • Ability to work independently and as part of a team.
  • Demonstrated ability to partner and build trust, cultivating positive working relationships as Person-in-Plant at the CMO(s).
  • Effectively communicate changes and resolve issues with CMOs.
  • Lead and/or participate in cross functional manufacturing projects to ensure company objectives.
  • Minimal. Up to 10% travel, domestic

Quick Apply

  • As an Equal Employment Opportunity Employer, DAVIS has reporting requirements which require us to invite employees to voluntarily self-identify their race/ethnicity. Submission of this information is voluntary and refusal to provided it will not subject you to any adverse treatment. The information obtained will be kept confidential.
  • Accepted file types: pdf, doc, docx, txt, rtf.
  • By applying to this position and providing my contact information, I give The DAVIS Companies permission to provide me with email communications and information.

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