Principal Engineer - Permanent Job

Where Mining Finds Its People

This job has expired. Click here to see new and active jobs like this one.

Jobs on CareerMine expire for many reasons. Either the employer has requested the advanced expiration of the job (as the vacancy has been filled or cancelled), or the job ad has expired after its normal running-time of 60 days within the CareerMine system. While there is the possibility that the vacancy may still be active, it is most likely that it has been filled or cancelled; otherwise it would be on CareerMine still.

Unfortunately this job has expired. Either the employer has requested the advanced expiration of the job (as the vacancy has been filled or cancelled), or the job advert has expired after its normal running-time of 60 days within the CareerMine system. Please click here to continue your job search.

Start New Search

CareerMine Job Id: 652720 Job Summary
Title:	Principal Engineer - Permanent Job	Employer Job Id:	-------
Location:	Plainsboro, NJ	Posted Date:	December 21, 2011
Employer:	Subscriber - Log In to see Company Name	Closing Date:	February 19, 2012

Principal Engineer - Permanent Job

Job Overview:

Our client is a newly formed biopharmaceutical company focusing on biologics discovery and proof-of-concept development services for the biopharmaceutical industry. At this time, our client is actively looking for a Scientist to join their Principal Engineer Development. This position will directly report to the Head of Process Development and Clinical Manufacturing.

Job Responsibilities:

Participate in recruiting highly talented staff.
Represent process engineering as the subject matter expert focusing on delivering scientifically rigorous solutions to meet project needs for process development and clinical manufacturing.
Develop process simulations that enable process fit experiments earlier in process development
Develop PAT and engineering systems required to support the development functions.
Collaborate with other functions to deliver an efficient low cost solution to customers.
Publish scientific work and present work in leading international conferences.
Support development of Quality by Design principles to process development
Support cGMP operations through investigations, continuous improvement, and risk-based approaches
Play a lead role in the design and start-up of facility and process equipment. Partner with vendors to deliver state of the art technologies specifically around liquid handling systems.
Develop efficient and innovative solutions to enable multi-host development and cGMP facility design and operation.
Interface with maintenance and validation contractors to keep cGMP facility in constant state of compliance.
Develop the site automation strategy maximizing paperless systems.
Follow full GMP guidance and fulfill all Quality Assurance requirements as required.
Operate safely and according to company environmental requirements.
Support business development activities as required.
Support solutions for innovation and collaboration.
Develop customer relationships with peers.
Head of Process Development and Clinical Manufacturing may assign other responsibilities as required.

Job Qualifications:

PhD/MS in Chemical Engineering
Minimum 6+ years of experience with demonstrated ability to lead tech transfer of biologics processes and scale-up rapidly for clinical manufacturing.
Excellent leadership skill in developing models, plans, technologies and collaborating in team environment.
Experience with single-use technology is a must.

Start New Search

Job Seekers

Employers

You are in the Job Seekers section

Inspirational Thought

"Its up to each of us to turn on our own light."

- Katherine Hepburn

Job Tools

Jobs From Same Employer

Director of Industry Marketing -Mill Products/Mining Industries
Newtown Square, PA | USA