Process Engineer in Massachusetts

We are seeking an experienced Senior Process Engineer to lead a strategic initiative aimed at improving the design and robustness of our single-use bioreactor platform. The role focuses on optimizing existing single-use assemblies, associated equipment, and enhancing aseptic handling processes to support upstream manufacturing.

Key Responsibilities:

• Lead cross-functional design reviews of single-use bioreactor platforms to identify areas for improvement and standardization.
• Enhance the layout, installation, and usage of single-use assemblies to optimize aseptic handling and reduce operational risks.
• Drive design enhancements in key areas, including:
• Media feed and waste management
• Aseptic connections and disconnections
• Assembly design and sampling processes
• Procedural controls and operator training
• Oversee the qualification and validation of new and existing...

Verista’s 600 experts team up with the world’s most recognizable brands in the life science industry to solve their business needs. The nature of our business is to empower growth and innovation within the scientific community and to help researchers, organizations, and companies solve some of the world’s most pressing healthcare challenges. Verista provides innovative solutions and services that empower informed decision-making and are the result of our significant investment in our people and our capabilities.

Our ability to grow is driven by world-class people who thrive in a team environment and share our mission to enable life sciences clients to improve lives. Our talented and dedicated professionals are committed to making an impact every day.

Company Culture Guidelines & Values:

• We empower and support our colleagues
• We commit to client success at every turn
• We have the courage to do...

We are seeking an experienced Senior Process Engineer to lead a strategic initiative aimed at improving the design and robustness of our single-use bioreactor platform. The role focuses on optimizing existing single-use assemblies, associated equipment, and enhancing aseptic handling processes to support upstream manufacturing.

Key Responsibilities:

• Lead cross-functional design reviews of single-use bioreactor platforms to identify areas for improvement and standardization.
• Enhance the layout, installation, and usage of single-use assemblies to optimize aseptic handling and reduce operational risks.
• Drive design enhancements in key areas, including:
• Media feed and waste management
• Aseptic connections and disconnections
• Assembly design and sampling processes
• Procedural controls and operator training
• Oversee the qualification and validation of new and existing...

Dew Software is seeking a highly motivated and experienced Process Validation Engineer to join our team. As a leading software and technology company, we prioritize excellence and innovation in all aspects of our work. The Process Validation Engineer will play a critical role in ensuring the quality and efficiency of our manufacturing processes. This is an excellent opportunity to work with Fortune 500 clients and contribute to their success and growth.

Responsibilities

• Develop and execute process validation protocols, including IQ, OQ, and PQ.
• Collaborate with cross-functional teams to identify process improvement opportunities.
• Analyze and interpret validation data to ensure compliance with industry standards.
• Identify and implement continuous improvement initiatives to optimize manufacturing processes.
• Conduct risk assessments and develop mitigation strategies.
• Work with external vendors to validate and qualify...

• Setting up and troubleshooting all standard printed circuit board assembly processes.
• Working knowledge of ISO 9001 AS9100 practices and IPC-610-A Workmanship Standards required.
• Support the production schedule to meet customer satisfaction and company revenue goals.
• Constantly monitor processes and operations and draw from training and experience to identify opportunities for improvement.
• Support generation and reporting of process metrics.
• Ability to multi-task with a strong sense of urgency.
• Ability to meet deadlines and to work with a minimum of oversight and direction.
• Analyzing Information, Reporting Research Results and Documentation Skills

Requirements

• Strong Process Development skills and experience are required.
• Experience with setting up and troubleshooting all standard printed circuit board assembly processes.
• Experience with screen-printer...

At Editas Medicine, we are pioneering the possible. Our mission and commitment is to translate the power and potential of the CRISPR/Cas12a and CRISPR/Cas9 genome editing systems into a robust pipeline of medicines for people living with serious diseases around the world.  Our goal is to discover, develop, manufacture, and commercialize transformative, durable, precision genomic medicines for a broad class of diseases.  

Why Choose Editas?

At Editas Medicine, we’re a team of courageous problem solvers, harnessing the power and potential of CRISPR gene editing to transform the future of medicine. Driven by a shared purpose to serve people living with serious diseases, we succeed together through collaboration, mutual respect, and innovation. If you want to be part of a team where your voice is heard and respected, where you can operate at the forefront of gene editing, and push the boundaries of what’s possible in medicine, come join us and...

Summary:

Perform functions to research, develop, document, qualify, and implement production processes for standard and custom packaged semiconductor products. Establish stable manufacturing processes at the prototype phase and release to production. Review, develop, and update statistical process control methods and related documentation, working within the limits of established policies.

Essential Duties & Responsibilities:

• Develops new processes and identifies and implements changes in product flow to support the production ramp-up of RF Systems products through application of lean manufacturing principles.
• Works with others to implement process improvements and to train operators as needed.
• Participates in weekly Technical Review Board (TRB) meetings for the disposition of discrepant material and determination of root cause/corrective action.  Documents customer corrective action requests....

Polymer Process Engineer

Springfield, MA

Description:

This is a great opportunity in a beautiful upscale town outside of Springfield, MA near VT and NH (no tax) with nearby colleges. This 200-person site produces a variety of extruded polymer films for medical devices, electronic devices, passport covers, and for use in the automotive industry. You will provide day-to-day support, lead six sigma efforts, design and install new equipment and implement safety initiatives. This position is open due to the incumbent being promoted and reports to the Production Manager as do three other process engineers. This company has multiple US and overseas sites and is bonus eligible with a great vacation policy.

Requirements

Minimum Requirements:

• B.S. Mechanical or Chemical Engineering
• 2+ years’ experience in films, resins or polymers, extruded products,...