Senior Manager, Quality Salary at Ge Power Conversion BETA

Job Title: Validation Engineer – APS Location: Boston, MA Overview: We are seeking 2-3 local Validation Engineers with 5-8 years of experience to support ongoing validation and APS (Aseptic Process Simulations) activities. Candidates should possess strong knowledge of validation principles, demonstrate autonomy in executing APS protocols, and have experience with CQV (Commissioning, Qualification, and Validation) for maintenance activities rather than new equipment or process startups. Key Responsibilities: APS Protocol Execution: Independently execute Aseptic Process Simulations (APS) to ensure compliance with GMP and regulatory requirements. Revise, update, and maintain APS protocols and associated documentation as necessary. Validation Documentation: Draft, review, and revise validation protocols, test plans, and reports, ensuring alignment with regulatory standards. Maintain meticulous records of validation activities for audits and inspections. CQV for Ongoing Maintenance: Support

Responsibilities: Developed and optimized efficient, cost-effective, and validated manufacturing processes for medical devices, focusing on capital and/or disposable devices, including assembly, lot release testing, sterilization, and packaging. Produce production-level assembly and part drawings for all components and sub-assemblies. Incorporate Design for Manufacturing (DFM), Six Sigma, and LEAN principles into product and process designs to ensure manufacturability, minimize costs, and achieve optimal production efficiency through activities like DFMA reviews and cycle time optimization. Proactively identify and evaluate potential contract manufacturing partners by analysing quality, cost, delivery timelines, and regulatory compliance capabilities to recommend optimal providers. Lead and collaborate with contract manufacturers in selecting and developing the most efficient and reliable manufacturing processes and sites while fostering strong partnerships. ct as the liaison between C

Veeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. As one of the fastest-growing SaaS companies in history, we surpassed $2B in revenue in our last fiscal year with extensive growth potential ahead. At the heart of Veeva are our values: Do the Right Thing, Customer Success, Employee Success, and Speed. We're not just any public company - we made history in 2021 by becoming a public benefit corporation (PBC), legally bound to balancing the interests of customers, employees, society, and investors. As a Work Anywhere company, we support your flexibility to work from home or in the office, so you can thrive in your ideal environment. Join us in transforming the life sciences industry, committed to making a positive impact on its customers, employees, and communities. The Role Veeva is looking for a hands-on Senior QA Manager who has an automation-first mindset to lead our QA team for the Digital

About the Role >>> Senior Director, Quality Assurance As the Senior Director of Quality Assurance, reporting to the Vice President of Regulatory Affairs and Quality Assurance, you will lead all quality activities supporting Olema's pipeline. You will oversee the development, implementation and maintenance of quality assurance systems and activities, and you will lead and build the quality team and function. You will be responsible for managing business relationships with defined stakeholder groups and leaders in the organization for the strategic development and delivery of risk-based quality management and vendor quality oversight. This role is based out of our Cambridge or San Francisco office and will require 15% travel. Your work will primarily encompass: * Contribution to the development of the GxP (GLP, GCP/GMP/GPV) Quality Management Systems, conduct risk assessments, develop and implement risk-mitigations and potential process improvements * Creation and implementation of a GxP

At BBH we value diverse backgrounds, so if your experience looks a little different from what we've outlined and you think you can bring value to the role, we will still welcome your application! What You Can Expect At BBH: If you join BBH you will find a collaborative environment that enables you to step outside your role to add value wherever you can. You will have direct access to clients, information and experts across all business areas around the world. BBH will provide you with opportunities to grow your expertise, take on new challenges, and reinvent yourself-without leaving the firm. We encourage a culture of inclusion that values each employee's unique perspective. We provide a high-quality benefits program emphasizing good health, financial security, and peace of mind. Ultimately we want you to have rewarding work with the flexibility to enjoy personal and family experiences at every career stage. Our BBH Cares program offers volunteer opportunities to give back to your comm

Job Description Job Description Connexion’s mission is to provide "best in class" services to job seekers. We strive to achieve excellence in job placement, staffing, and recruiting services, while treating candidates with the professionalism and respect they deserve. Senior Staff, Manufacturing Technical Operations 3 openings for 3 shifts- “run day times” is the harvest shift when they require 24 hr coverage for production. These occur occasionally and the team is flex. SHIFTS A2: Sun-Wed 12:30pm-11:00pm (run day hrs 3:30pm-2:00am) B1: Wed-Sat 7:00am-5:30pm (run day hrs 5:00am-3:30pm) B2: Wed-Sat 12:30pm-11:00pm (run day hrs 3:30pm-2:00am) Heavy quality-based role supporting manufacturing Most of the work is done behind the scenes but must be willing to gown up and enter the cleanroom to triage issues in real time Experience with investigation tools CAPA, deviations, effectiveness checks, change controls, quality events, risk Nice to have = cell manufacturing & cell and gene therapy F

Salary: $115,772.80 Annually Location : 10 Park Plaza, Boston Job Type: Full-Time Job Number: 24-20663 Department: MBTA - Capital Programs - Capital Support Area: 508-Capital Support Opening Date: 11/21/2024 Closing Date: 12/19/2024 11:59 PM Eastern Licenses / Certifications: A valid Driver's License is required. Union Affiliation: L453 Professional On-Call or 24/7: No; this position is not classified as on-call or 24/7. Safety Sensitive: Yes; this is a Safety Sensitive position. Employees in this role will be subject to periodic physical examinations plus random drug and alcohol testing. Essential Classification (Emergency Staff): No; this position is classified as non-essential (during declared States of Emergency). At the MBTA, we envision a thriving region enabled by a best-in-class transit system. Our mission is to serve the public by providing safe, reliable, and accessible transportation. MBTA's core values are built around safety, service, equity, and sustainability and each em

Job Location Boston Job Description P&G Manufacturing is all about safety, quality, and productivity. It’s where our products are packaged and palleted, ready to be shipped. But this is far beyond traditional warehousing. Typical production lines are an important part of our work here, but our world also includes innovative robotics, automation, zero-touch systems, and even “zero waste to landfill” capabilities. Our team of analysts, engineers, leaders, and managers are responsible for ensuring the irresistible superiority for our 65 iconic, trusted brands throughout P&G's global end-to-end supply chain. From Day 1, you’ll be trusted to dive right in, take the lead, use your initiative, and build billion-dollar brands that help make everyday activities easier and make the world a better place! Our company offers purposeful work that will take your career places you never envisioned, in creative workspaces where innovation thrives and where your technical expertise is recognized and rew