Senior Materials Management Compliance Specialist

Company: Takeda Pharmaceutical
Location: Medford
Posted on: May 10, 2022

Job Description:

By clicking the "Apply" button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda's and . I further attest that all information I submit in my employment application is true to the best of my knowledge.Job DescriptionAbout the role:Join Takeda as a Senior Materials Management (MM) Compliance Specialist where you will lead the investigations, own CAPAs, Change Controls, RMNCMR deviations, and level 2 deviations. You will manage the closure within established timelines, work with QA and management to escalate quality systems. You will be a MM SME for projects to support the MA Biologics Operations. You will also support the MM Compliance Manager in our audits and work to improve the compliance of the MM department. As part of the Compliance team, you will report to Supply Chain Compliance Manager.How you will contribute:

• You will influence the organizational control of Quality systems
• You will own MM deviations, CAPAs, and Change Controls
• You will lead cross-functional investigation teams to identify root cause, evaluate technical impact, and provide recommendations to management on batch disposition
• You will provide subject matter expert input for MMMinimum Requirements/Qualifications:
  • Bachelor's in Science or a related discipline, Master's degree preferred
  • You will have 5 years related industry experience in the manufacturing and development of biologics, pharmaceuticals or devices
  • You have previous technical writing experience and overseeing manufacturing deviations/investigations
  • You have experience managing multiple commodity areas and tasks
  • You have ERP experience in Inventory Warehouse Management / Materials Management /Procurement modules and New Product introduction and plant startups
  • You will manage work and decisions in a high matrix organizational environment
  • You will manage collaboration and cross-functionally for process improvement programs
  • You have experience in manufacturing procedures, shop/work orders, working in a GMP regulated environment, Biotechnology, Medical Device, Pharmaceutical or other Medical-related fields
  • You have demonstrated project management skills, certifications preferred: CQA, APICS, or PMPWhat Takeda can offer you:
    • Comprehensive Healthcare: Medical, Dental, and Vision
    • Financial Planning & Stability: 401(k) with company match and Annual Retirement Contribution Plan
    • Health & Wellness programs including onsite flu shots and health screenings
    • Generous time off for vacation and the option to purchase additional vacation days
    • Community Outreach Programs and company match of charitable contributions
    • Family Planning Support
    • Flexible Work Paths
    • Tuition reimbursementMore about us:At Takeda, we are transforming patient care through the development of novel specialty pharmaceuticals and best in class patient support programs. Takeda is a patient-focused company that will inspire and empower you to grow through life-changing work.Certified as a Global Top Employer, Takeda offers stimulating careers, encourages innovation, and strives for excellence in everything we do. We foster an inclusive, collaborative workplace, in which our teams are united by an unwavering commitment to deliver Better Health and a Brighter Future to people around the world.In accordance with the CO Equal Pay Act, Colorado Applicants Are Not Permitted to Apply. #GMSGQ #ZR1 #LI-MA1EEO StatementTakeda is proud in its commitment to creating a diverse workforce and providing equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, gender expression, parental status, national origin, age, disability, citizenship status, genetic information or characteristics, marital status, status as a Vietnam era veteran, special disabled veteran, or other protected veteran in accordance with applicable federal, state and local laws, and any other characteristic protected by law.LocationsUSA - MA - North Reading - BIO OPSWorker TypeEmployeeWorker Sub-TypeRegularTime TypeFull time

Keywords: Takeda Pharmaceutical, Medford , Senior Materials Management Compliance Specialist, Executive , Medford, Massachusetts