Hi Everyone,


Please share suitable profiles along with the rate, location and
availability ASAP.



*TITLE:*

Process Engineer

*DEPARTMENT:*

Global Manufacturing & Supply

*LOCATION:*

Devens, MA

*Length:*

6 months



*GENERAL DESCRIPTION:*



The BMS Devens, MA MS&T organization is seeking to fill a Process Engineer
position for an 8+ month contract. The successful candidate will provide
meaningful contributions toward commercial manufacturing support, process
monitoring, technology transfer and process validation activities. The
successful candidate will have a demonstrated background in bioprocessing
(upstream and/or downstream), experience troubleshooting manufacturing
processes and strong technical documentation skills (memos, protocols,
reports).



Responsibilities:

-       Work independently to provide commercial manufacturing technical
support, process monitoring, technology transfer and process validation
activities for downstream processes.

-       Provide process troubleshooting during scale-up and routine
manufacturing. Provide process subject matter expertise and ownership of
assigned deliverables.

-       The successful candidate will work effectively in highly
cross-functional project teams, matrix management environments, as well as
independent working environments to support the site.

-       Perform data analysis and monitoring for process performance and
product quality outputs.

-       The position will interface with Manufacturing, Quality,
Engineering, and internal MS&T departments at multiple sites throughout the
BMS network



*QUALIFICATIONS**:*



-       Strong communication and technical writing skills are required.

-       B.S./M.S. or Ph.D. in Chemical Engineer, Biochemical Engineer,
Biomedical Engineer, Biochemistry or related field (Advanced degree is
preferred)

-       Required: Prior experience (Ph.D: 0 – 2 years; BS/MS: 2 – 6 years)
in process development, process validation or manufacturing support in
bioprocessing (upstream and/or downstream)

-       Preferred: Prior experience scaling up biopharma manufacturing
processes (upstream/downstream), facility fit assessments, process scale-up
from bench/pilot to production, process troubleshooting and optimization,
and process validation. Hands-on experience working with chromatography,
ultrafiltration and depth filtration process acquired through lab, pilot or
production scale experience.

-       Preferred: Experience performing manufacturing investigations for
biologics manufacturing.

-       Preferred: Experience providing start-up support for new biologics
manufacturing processes (Person-In-Plant)

-       Preferred: Experience with statistical methodologies (DOE, SPC,
etc), cGMP regulations, and regulatory requirements is expected.





Thanks & Regards,



*Gole Govardhan **I **Senior Bench Sales Executive*

*W* *(312) 985 -0412  **I* Fax 248.715.6434.

Email: [email protected] *I* www.rsrit.com  Hangouts:
[email protected]

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