Biologist I

Bill: $46.60
Pay: $33-31
Spread:196.6-294.9
Duration: 6 months (with potential extensions)


Number of Positions Needed
1
Length of Initial Contract
6 months (with potential extensions)
Location/Site
Client Bioresearch Center, Worcester, MA
Type of role:
100% Remote | 100% Onsite | Onsite Hybrid (# of days onsite required)
100 % Onsite
Cost Center:
0000636519
Reason for Request
Support of increasing number of late-stage pipeline activities
Daily Work Schedule Expectations
8 hrs/day, 5 days a week, weekend work as necessary
Budget Approval Obtained (Yes/No)
Yes
Top 3 – 5 Skills Needed for each role
1. Ability to work well both independently and in teams
2. Strong written and oral communication skills
3. Demonstrated problem-solving skills and capability to overcome complex issues
4. Must have a "results-oriented” work ethic and a positive "can-do” attitude with a strong sense of urgency and self-motivated desire to achieve
5. Ability to utilize Microsoft Excel and Word to perform tasks
Travel Required: Y/N
N
Number of Interviews (recommend to minimize)
2 for each contractor
Matthew Billups/Wen Chung Lim/Sean McDermott
Matthew Noel/Scott Fredricksen
Job description:
We are seeking a highly motivated Biologist I/II to join the Manufacturing Science and Technology (MSAT) department at Client Bioresearch Center based in Worcester, MA.
As part of the PDS&T Biologics organization, MSAT leads the process technology transfer, optimization, validation, implementation, and continuous process improvement for late-stage and commercial manufacturing of therapeutic proteins. We also provide technical support for manufacturing, GMP compliance, and regulatory filing.
Our mission is to support manufacturing and drive and implement improvement of processes and technologies for commercial products to deliver quality, compliance, financial and innovation goals for the benefit of our customers.
Key Responsibilities Include:
Providing technical support to late clinical stage and commercial biologics manufacturing processes
Supporting lab scale studies relevant to late clinical stage and commercial biologics manufacturing processes
Support the writing and data review of official documentation relevant to late clinical stage and commercial biologics manufacturing processes
Data monitoring and trending for continuous process verification
Applying GMP and GLP principles to all aspects of work and documentation
Qualifications
Education and Experience:
BS/MS degree in a scientific or engineering discipline with 0-2 years related industry experience Knowledge, Skills and Abilities:
Knowledge of applicable regulatory authority, compendia and ICH guidelines
Ability to understand and independently apply GMPs and /or GLPs to everyday work with regard to documentation and instrument use
Ability to utilize Microsoft Excel and Word to perform tasks
Good written and oral communication skills
Time management and project management skills
Problem solving and troubleshooting abilities
Ability to work in a collaborative work environment with a team
Strong organization skills with high attention to detail
Aseptic handling experience desirable
Coding experience or advanced excel capabilities desirable

Bussiness Unit:

OPST - Operations Product Development Science & Technology (OPST)

Cost Allocation:

1007|CC|PDST GloMfg-ABC(R&D) (636519)