Science Engineer Salary in Bedford, New Hampshire

Sr. Quality Control Engineer - Danvers, MA Full Time / Direct Hire -- $100,000 to $130,000 Annually **NO C2C or Visa Sponsorship Available at this Time** Job Description: We are currently seeking a Senior Quality Control Engineer with extensive experience to ensure the manufacturing and delivery of our product at the highest standard. As a senior member of the team, you will be responsible for leading quality control efforts, driving process improvements, and maintaining regulatory compliance. Collaborating closely with cross-functional teams, you will play a pivotal role in upholding our commitment to exceptional product quality and operational efficiency. Responsibilities: • Lead and execute comprehensive inspections and testing of raw materials, components, and finished products to uphold stringent quality standards. • Develop and refine quality control processes and procedures to proactively identify and mitigate defects, ensuring consistent product excellence. • Utilize advanced s

12 HOUR SHIFTS - NIGHTS 7PM-7AM NIGHT Shift Rate: $27.00 Description: The Manufacturing Associate is responsible for the manufacturing of therapeutic proteins (API) under cGMP conditions. Associates are expected to execute process recipes, follow written procedures (SOPs), monitor equipment and processes, perform basic laboratory tasks, including pH, conductivity, sampling, and conduct routine sanitization tasks to maintain facility and equipment. They are expected to attain a basic understanding of cGMP compliance while training under close supervision, demonstrating aseptic technique in handling of products and materials. up, operate equipment, and monitor production processes, including clean-in-place (CIP) and steam-in-place (SIP) operations and report production in written and electronic documents in accordance with good manufacturing practice (GMPs) and good documentation procedures (GDPs), review documentation as appropriate. qualification for all assigned tasks and maintain ind

SENIOR PACKAGING DEVELOPMENT SCIENTIST II, Boston areaOur client is a multi-billion-dollar manufacturer of dairy and beverage products, with fifteen manufacturing plants in the US. Founded over 100 years ago, today they are one of the largest and most trusted food and beverage manufacturers in the United States. They are putting together a new team in R&D, and they are seeking a Senior Packaging Development Scientist II.Job SummaryThis person will serve as subject matter expert for area of expertise/segment. They will manage and execute multiple projects simultaneously, performing packaging tasks and providing guidance for team members in a category. They will design and implement challenging packaging projects and resolve complex packaging issues focused on new products, value engineering, customer packaging improvement and/or continuous improvement. They will ensure application of common packaging science/engineering principles and concepts to team projects and leverage relationships

A local EHS consulting firm is seeking a Sr. Environmental Engineer to assist with providing technical direction and accurate completion of projects. This company has a wide variety of clients in several different industries and is seeking well-established consulting professionals to work closely with the senior management to assure the quality of work expected by the clients is within the budget and schedule. The Role: Maintaining Regulatory Compliance programs in compliance with local, state, and federal regulations. Help prepare proposal estimates of time and expense and participates in the presentation to clients. Work closely with clients during all phases of the projects, as well as maintaining a close relationship with the client after the project is completed. Determine major project design decisions in conjunction with the client and the rest of the Project Management team. Traveling upwards of 50-75% within the New England area. Open to hybrid-remote working schedule The Cand

12 HOUR SHIFTS - NIGHTS 7PM-7AM NIGHT Shift Rate: $27.00 Description: The Manufacturing Associate is responsible for the manufacturing of therapeutic proteins (API) under cGMP conditions. Associates are expected to execute process recipes, follow written procedures (SOPs), monitor equipment and processes, perform basic laboratory tasks, including pH, conductivity, sampling, and conduct routine sanitization tasks to maintain facility and equipment. They are expected to attain a basic understanding of cGMP compliance while training under close supervision, demonstrating aseptic technique in handling of products and materials. up, operate equipment, and monitor production processes, including clean-in-place (CIP) and steam-in-place (SIP) operations and report production in written and electronic documents in accordance with good manufacturing practice (GMPs) and good documentation procedures (GDPs), review documentation as appropriate. qualification for all assigned tasks and maintain ind

Job Description: Position Description: Creates, maintains, and communicates multi-year product roadmaps. Owns the product management lifecycle. Influences broader strategic decisions for products. Collaborates with other leaders to set multi-team roadmaps and coordinate and resolve dependencies. Sets, refines, and communicates the squad s strategy and mission in alignment with product area strategies. Primary Responsibilities: Negotiates product changes with internal and external partners and stakeholders. Enables delivery of product value with quality and standards. Defines, reviews and tracks squad objectives and Key Performance Indicators (KPIs). Manages vendor relationships and procurement. Reviews project plans to plan and coordinate project activity. Prepares or reviews operational reports or project progress reports. Sets vision, goals, and direction of team/organization. Plans and leads organization-wide initiatives. Regularly provides guidance, training, and coaching to other