Quality Assurance Intern Salary at Amazon Robotics Llc BETA

Job Description Job Description Sr. Manager, Drug Product Site Planning Location: Cambridge, MA 5 Month Assignment to Start in April 2025 Payrate: $85/hr Hybrid Schedule 8/8:30 to 5/5:30 Weekly Pay and Benefits! Our leading Pharmaceutical client is seeking a highly motivated and experienced Sr. Manager, Drug Product Site Planning to join their supply chain team. This role will be responsible for managing and optimizing production planning across their external drug product manufacturing network. The Sr. Manager will ensure that external manufacturing operations align with demand forecasts, regulatory requirements, and company objectives. Additionally, this role will support financial responsibilities, including inventory reconciliation and cost management activities. The ideal candidate will have a strong background in pharmaceutical or biotech manufacturing, with extensive experience managing external manufacturing relationships, complex production schedules, and cross-functional coll

Company: American Surgical Company Job Title: Regulatory Affairs and Quality Assurance Associate Location: Salem, MA Summary: Regulatory Affairs and Quality Assurance Associate is responsible for identifying, evaluating, and ensuring compliance with all applicable laws, regulations, and standards. The Regulatory Affairs and Quality Assurance Associate shall also conduct reviews of all and all future target markets to ensure knowledge and fulfillment of establishment registration, device licensing, surveillance, adverse event and corrective action reporting, translation, product standards, and all other requirements necessary to support import, sales, distribution, and support in all chosen distribution markets. Essential Duties and Responsibilities: Remain aware of new or updated regulations, laws, standards and other official enactments that may apply to the company. Provide detailed analysis, official recommendations, and gap analyses for new or revised standards and regulations. Man

Company Overview: Our client is a small entrepreneurial manufacturing company located in Peabody, MA. There are three different divisions that primarily supply automated Semiconductor OEM's. The Precision Fabrication Group has the engineering expertise and the machining capabilities to make challenging components and assemblies. The Specialized Welding Group supports stainless steel gas lines and panels as well as vacuum process chambers. The System Manufacturing Group is a contract manufacturer that builds and tests complete systems for our customers. Job Summary: The Production Manager will be responsible for leading the production teams across three divisions to ensure the efficient, cost-effective, and timely manufacturing of a wide range of products in a high-mix, low-volume environment. The ideal candidate will have a deep understanding of contract manufacturing operations and possess the ability to adapt to varying customer requirements and changing production demands. This role

The field of gene therapy is growing rapidly and Genezen is here to meet the exacting needs of our clients. We provide process development, produce GMP viral vectors, and provide cell transduction for gene and cell therapy clinical trials and are proud to be a part of the process that leads to new cures. WORKING AT GENEZEN Many people have worked in environments where you feel like just another nameless part of an enormous machine. Genezen is different. We want our employees to be innovative, collaborative problem solvers who are dedicated to meeting the challenges of working at a fast-growing company. We are dedicated to empowering our employees to be their best and making Genezen a rewarding place to work. Every employee contributes to the success of the company and you can be part of that team. JOB SUMMARY The QC Scientist - Critical Reagents is responsible for overseeing all reference standards and other critical reagents in line with internal SOPs and ICH guidelines. This individu

The field of gene therapy is growing rapidly and Genezen is here to meet the exacting needs of our clients. We provide process development, produce GMP viral vectors, and provide cell transduction for gene and cell therapy clinical trials and are proud to be a part of the process that leads to new cures. WORKING AT GENEZEN Many people have worked in environments where you feel like just another nameless part of an enormous machine. Genezen is different. We want our employees to be innovative, collaborative problem solvers who are dedicated to meeting the challenges of working at a fast-growing company. We are dedicated to empowering our employees to be their best and making Genezen a rewarding place to work. Every employee contributes to the success of the company and you can be part of that team. JOB SUMMARY The Quality Assurance Specialist II supports the day-to-day quality operations via oversight of all elements of the Quality Management System (QMS), including but not limited to d

**Quality Assurance Specialist II Night** **Position Summary:** Catalent is a global, high-growth, public company and a leading partner for the pharmaceutical industry in the development and manufacturing of new treatments for patients worldwide. Your talents, ideas, and passion are essential to our mission: to help people live better, healthier lives. The Boston-area facility is Catalents global Center of Excellence for spray dry dispersion and Dry Powder Inhaler (DPI) capsule manufacture and packaging. The site features inhaled powder spray drying, as well as multiple commercial-scale lines for capsule filling and blister packaging. On-site spray dryers include best-in-class GEA Niro SD1, SD4 and SD7, the latter being the largest CGMP unit of its kind for DPI in North America. Catalent Pharma Solutions is hiring a Quality Assurance Specialist II - Operations who is responsible for supporting operations in a GMP Manufacturing Facility. This individual provides oversight of production

Company Overview: Our client is a small entrepreneurial manufacturing company located in Peabody, MA. There are three different divisions that primarily supply automated Semiconductor OEM’s. The Precision Fabrication Group has the engineering expertise and the machining capabilities to make challenging components and assemblies. The Specialized Welding Group supports stainless steel gas lines and panels as well as vacuum process chambers. The System Manufacturing Group is a contract manufacturer that builds and tests complete systems for our customers. Job Summary: The Production Manager will be responsible for leading the production teams across three divisions to ensure the efficient, cost-effective, and timely manufacturing of a wide range of products in a high-mix, low-volume environment. The ideal candidate will have a deep understanding of contract manufacturing operations and possess the ability to adapt to varying customer requirements and changing production demands. This role

Convergent Therapeutics is seeking a Manager of Quality Operations to support critical CMC activities for our growing clinical-stage radiopharmaceutical product. This person will be responsible for overseeing the build and deployment of internal quality assurance systems in support of CMC as well as providing quality oversight of all external manufacturing operations for drug substance and drug product. As a start-up organization, we value team members eager to make an impact and grow with us professionally. We are seeking an individual who enjoys multi-tasking and has the willingness and flexibility to assume additional responsibilities as assigned. Responsibilities: Review and approve specifications affecting product quality and oversee the development of batch records and validation protocols. Oversee the quality operations for drug substance, drug product, packaging/labeling, and third-party logistics vendors. Interacts with manufacturing, clinical, operations, or other functional