Associate Director, External Drug Product Manufacturing

Celldex Therapeutics•Hampton, NJ

4d•$153,616 - $199,501•Onsite

About The Position

This position of Associate Director, External Drug Product Manufacturing will oversee on-going and new drug product aseptic filling demands at Contract Manufacturing Organizations (CMO’s) and budget management while adhering to Good Manufacturing Practices, company policies and procedures. This individual shall support the Contract Manufacturing Organization providing oversight of aseptic drug product manufacturing.

Requirements

Bachelor’s or Master’s degree in Engineering or Biological Sciences.
5-8 years’ experience in managing aseptic drug filling operations at CMO’s or in-house.
Experience managing internal resources and external contractors/vendors.
Knowledge of secondary packaging operations.
Interpersonal skills to effectively manage internal and external communications.
Analyze inventory, forecasts and budget spreadsheets.
Project management skills
High level of competence in aseptic Drug Product biopharmaceutical manufacturing of vials and pre-filled syringes.
Knowledge of biopharmaceutical quality standards, validation guidelines and regulatory compliance issues
Strong experience writing and implementing batch records and SOPs in a cGMP environment.
The ability to work with long term planning and development of capital requests.
Strong communication and organizational skills.
Team player with demonstrated ability to prospectively identify issues and to influence key project decisions to achieve positive outcomes.
Proficient in the use of MS Outlook, Word, Excel, Power Point, Project

Nice To Haves

Project Management Certification

Responsibilities

Provide oversight as person-in-plant (PIP) For Drug Product fills at CMOs.
Lead CMO’s by providing forecasts, requesting quotations for drug product manufacturing operations.
Liaise with the clinical teams and commercial teams to create product forecasts.
Investigate and onboard new Drug Product Manufacturing CMO’s.
Review and approve invoices.
Review master and executed batch records.
Review excursions or deviations that may occur during shipment, handling, and storage of drug products. Drive such investigations to resolution in collaboration with Quality, CDMO and clinical sites and define and implement procedures to minimize future occurrences.