Software Tester Salary at Innowrap Technologies BETA

ProStaff Workforce Solutions is seeking a Senior Associate, Quality Assurance for one of the largest pharmaceutical companies in Billerica, MA 01821. Our client is one of the leading pharmaceutical companies in the region and specializes in the production and sale of radiopharmaceuticals and formulation, analytical methods development and production of parenteral drugs. If you believe you are qualified, we would be excited to connect and discuss this opportunity in more detail. Full-time Onsite Direct Hire Job Summary Performs QA review of testing records of raw materials, in-process and finished products, stability samples, and non-routine sample analyses per established procedures and methodology. Area Of Responsibility QC Testing data review of products, raw materials, stability lots Oversee and continuously improve FDA / regulatory compliant Quality System for QC laboratory system Plan, direct and coordinate QC batch record review, logbook review, QC test review, and lot dispositio

**Compliance Specialist** Do you want to be part of an inclusive team that works to develop innovative therapies for patients? Every day, we are driven to develop and deliver innovative and effective new medicines to patients and physicians. If you want to be part of this exciting work, you belong at Astellas! Astellas Pharma Inc. is a pharmaceutical company conducting business in more than 70 countries around the world. We are committed to turning innovative science into medical solutions that bring value and hope to patients and their families. Keeping our focus on addressing unmet medical needs and conducting our business with ethics and integrity enables us to improve the health of people throughout the world. For more information on Astellas, please visit our website at www.astellas.com . **Astellas Institute for Regenerative Medicine (AIRM)** is a wholly owned subsidiary of Astellas Pharma Inc and focused on the development and commercialization of stem cell and regenerative medi

Repligen is an innovative life sciences company focused on developing and commercializing high-value bioprocessing products, technologies, and solutions critical in the production of biologic drugs. We are currently seeking a QA Associate I to join our Quality team in Marlborough, supporting Hollow Fiber and Single Use ATF Manufacturing. The QA Associate I will actively participate in the Repligen ISO 9001 Quality Management System, reviewing production records and releasing product, as well as supporting other QA team members and areas of work, as needed. The successful candidate will have a positive attitude and be able to communicate effectively. This candidate will be responsible for assisting the QA department to revise/create, file, organize, and review production documents. The candidate will work closely with the manufacturing teams to ensure accuracy of production documentation throughout the production process. This position involves completing the QA review of production rec

Summary: The Business Analyst will become a Charles River product expert and help to ensure that our software products effectively aid our end users with their trading and front office workflows. In consultation with our financial industry clients and internal product teams, they will utilize business and technical knowledge to improve product performance and competitive advantages. The Business Analyst will work within a specific module of the product and several instrument types (equity, fixed income, derivatives, FX, etc.), participating in the full software development lifecycle and contributing as a member of a feature-focused product development team They must be familiar with both financial and technical concepts, with a strong ability to deliver against specific requirements in a timely fashion on a project-by-project basis. Responsibilities: Apply detailed knowledge of business requirements and workflows to assist in product development Research and produce business and techni

To offer best-in-class experience to internal and external customers, this accessibility (A11Y) QA consultant will test and guide QAs and developers on A11Y remediation to ensure proper implementation of accessibility WCAG 2.1 AA standards. This consultant will collaborate closely with Tracker project team to ensure A11Y compliance while solving for business needs. Top 5-10 responsibilities of this position? •Collaborate with project team to review and test digital product for accessibility. •Use A11Y automated and manual testing tools for validation in conformance with accessibility standards and guidelines. •Use assistive technologies to perform manual testing of digital properties and content. •Log defects in Jira/confluence project management tool. •Remediate identified defects. •Coach project team in understanding defects at code level and how to remediate them. •Monitor progress and create scorecards to report compliance. •Serve as a bridge between enterprise A11Y and project del

Health Advances is seeking a Business Development (BD) Analyst to support the firm's senior leadership in executing business development processes to build client relationships and support our mission of creating an enduring, positive impact on healthcare globally. The BD Analyst will play a key role as part of the Commercial and Growth team executing workstreams to support the business development process to identify, qualify, and progress leads to opportunities to write compelling business proposals. The BD Analyst will help customize selling materials and proposals, manage lead and opportunity activity in CRM, facilitate the development of new business via proactive outreach, prepare for sales meetings and industry conferences, and collaborate on other internal business development and marketing initiatives. This role requires attention to detail, a sales mindset, analytical thinking, and strong organizational skills. Excellent communication skills and collaborative teamwork are cri

Job Description Job Description Overview The Manager of Quality Assurance Operations will work within the DP / CMC / Alliance QA Operations team and is responsible for providing support to all GMP aspects of drug product (DP) manufacturing, CMC and alliance management. This role will work cooperatively with their counterparts in Quality Operations to provide quality oversight to ensure clinical through commercial lifecycle activities meet cGMP regulatory requirements and guidelines. This position reports to the Director of Quality Assurance. Key Responsibilities Execute quality oversight of external manufacturing of both clinical and commercial drug product through lot disposition Provide QA review and approval of internal and external Deviations, Change Controls, CAPAs. Provide QA support for review and data verification of clinical regulatory filings Engage with alliance partners to assure compliance to their quality systems and practices as related to manufacturing through dispositi

ROBOTICS PYTHON API DEVELOPER Full-time position Lexington, MA Base salary range: $130,000 - 160,000 annually Benefits: Medical, Dental, Vision coverage, 401k, PTO, Paid Holidays, Health Savings Account Primary Job Function: ? Collaborate with a multidisciplinary team to develop innovative software solutions for robotic applications focused on package handling. ? Act as an interface between DevOps and software teams, ensuring seamless integration and deployment of services. ? Enable and optimize robotic systems to deliver critical product features, ensuring efficiency, reliability, and scalability. ? Develop and manage software and integration tools, including process management and environment setup, while facilitating the transition of applications to new platforms. Minimum Skills/Technical Requirements: o 5+ years in software development. o Proven commercial experience in a fast-paced, agile environment. o Ability to work effectively as part of an interdisciplinary team. Proficienci