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Manufacturing/BioProcessing Associate (cGMP – Pharmaceutical) JD820743

JD820743

DPS is looking for capable Manufacturing Support resources to work with a pharmaceutical client in the Norwood/Canton, MA area. This individual will be expected to support bioprocess unit operations and cGMPs with the ability to operate pilot-scale bioprocessing equipment.

Category:
Miscellaneous Personnel
Location:
Massachusetts
Years of Experience Req.:
2+
Date Posted:
15/07/2020
Days Remaining:
4
Employment Type:
Full-time
Education Level Req.:
Bachelors Preferred

 

Manufacturing/BioProcessing Associate (cGMP – Pharmaceutical)             JD820743

 

Norwood, MA area

 

 

 

Summary:

 

 

 

DPS is looking for capable Manufacturing Support resources to work with a pharmaceutical client in the Norwood/Canton, MA area. This individual will be expected to support bioprocess unit operations and cGMPs with the ability to operate pilot-scale bioprocessing equipment.

 

 

 

Core Responsibilities:

 

·         Operate bioprocessing equipment within fast-paced cGMP environment.

 

·         Support activities include maintaining supplies, preparing solutions, setting up and disassembling processing equipment, cleaning and maintaining equipment, and basic troubleshooting.

 

·         Interact with process development group during the technical transfer of new programs.

 

·         Interact with validation, metrology and facilities groups to ensure equipment is maintained for cGMP use.

 

·         Submit samples for QC and other testing.

 

·         Interact with QA when compliance issues arise.

 

·         Participate in revising/writing SOPs and batch records.

 

·         Establish and follow written procedures for the clear and accurate documentation of equipment operation and process instructions, and of process data.

 

·         Monitor process operations to ensure compliance with specifications.

 

·         Adhere to gowning procedures and maintain a clean general operating area.

 

 

 

Education and Qualifications:

 

·         Bachelor’s degree in Engineering or Sciences is preferred.

 

·         Associates with 2+ years related experience or 4+ years of related GMP experience.

 

·         Proven track record of success in a fast-paced production environment at a biotech/pharmaceutical company.

 

·         Ability to collaborate fluidly with peers, supervisors and cross functional support groups required.

 

·         Strong written and oral communication skills.

 

·         Highly organiz508027.869967ed with effective time management (ensuring completion of work tasks).

 

·         Strong attention to detail.

 

·         Ability to work well cross-functionally with various people and groups.

 

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