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
Job Application
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