Intertwined

Downstream GMP Manufacturing Supervisor (Paid re-lo to Baltimore)

Full Time
Raleigh, NC, USA
Description

 *This role is on-site in Baltimore, MD. Strong re-location assistance provided!


The Denzel Group, an award-winning search firm, has been chosen to work with a global Pharmaceutical leader on their quest for a talented Manufacturing Supervisor. In this role, you will oversee a team of Downstream BioProcess Associates, ensuring GMP compliant operations.


Responsibilities

  • Team management, including scheduling, training, staffing, etc.

  • Perform and monitor compliant manufacturing operations.

  • Generate documentation such as Batch Records and SOP’s.

  • Real time, on the floor, Batch Production Record review.

  • Participate in the installation, operation, cleaning and maintenance of bio-pharmaceutical cGMP equipment.

  • Provide (SME) input for continuous improvement and audits.

  • Partner with QA regarding the storage, use and documentation of bulk and finished product.

  • Drive consistency of operations between departments.

Requirements
  • Must have either:

  • Relevant BS degree and 4+ years’ GMP pharma biologics manufacturing experience.

  • Without a relevant BS degree: 7+ years’ GMP pharma biologics manufacturing experience.

  • 1+ years’ team leadership.

  • Experience operating downstream GMP Pharma biologics manufacturing equipment.


To apply please send your application to mschroeder@thedenzelgroup.com


#IND1


QA, quality assurance, GMP, manufacturing, SOP, batch record, lead, supervisor, manager

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