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Our client is looking for a project manager with IT regulatory experience in the biotech industry. The position is located in cambridge, MA. Project Manager – Regulatory IT Job Summary: The INSIGHT Project Manager is responsible for the planning and execution of business process improvement and regulatory information management project. The INSIGHT Project Manager will work with business process owners, information technology staff, and subject matter experts to lead business process ...

- Production Associate - The Manufacturing Associate 2 in the Manufacturing department operates ancillary equipment and operates process equipment downstream activities. Follows and maintains good manufacturing practices and standard operating procedures to comply with regulatory requirements. Experienced operator who continues to improve and refine knowledge of area/technologies. Receives minimal supervision, expected to make adjustments to day to day operations to ensure the schedule is met. ...

The Manufacturing Associate 2 in the Manufacturing department operates ancillary equipment and operates process equipment downstream activities. Follows and maintains good manufacturing practices and standard operating procedures to comply with regulatory requirements. Experienced operator who continues to improve and refine knowledge of area/technologies. Receives minimal supervision, expected to make adjustments to day to day operations to ensure the schedule is met. Provides guidance to lower ...

 My name is Erica and I represent The Fountain Group.  We are a national staffing firm and are currently seeking someone for a Biomedical R&D Engineer position with a prominent Fortune 500 client of ours.  The position is located in Billerica, MA.  If the position sounds like it may be of interest to you, please respond with an updated resume and acceptable salary range.  I will get in touch with you to further discuss the position.   Job Description: ·         Ability to understand and perform ...

Quality Engineer - Mechanical Engineering - Medical Devices Long-term Contract, Littleton, MA claudia | 646.790.8355 Job Description: Design of Experiments (DOE) and Statistical Process Control (SPC),Develops and implements strategic plans ,Develops plans to evaluate process repeatability and stability ,Develops product and process improvements, Participates in procedure writing and review ,Performs process and equipment validations ,Provides technical support to other engineers ,Reviews product ...

Quality Engineer - Electrical Engineering Medical Devices, Littleton, MA Long-term contract Claudia | 646.790.8355 Job Description: Completes Design History File documentation ,Design of Experiments (DOE) and Statistical Process Control (SPC),Develops and implements strategic plans ,Develops plans to evaluate process repeatability and stability ,Develops product and process improvements,Performs process and equipment validations ,Provides technical support to other engineers ,Reviews product ...

our client in Cambridge, MA is looking for a QC Associate with cGMP experience. This is a long term consulting position. If interested, please apply to this ad Associate I, Product Complaints The primary responsibility of this position is to provide technical and administrative support within client’s Quality organization, specifically for the Technical Product Complaint group. Duties include, but are not limited to, assisting the Technical Product Complaints department in maintaining timely ...