1+ months

Sr. Associate Master Data Management

Amgen
Juncos, Puerto Rico 00777
  • Job Code
    117317441
Amgen

Job ID: R-89925
Location: Juncos, PR, US 00777

The Sr. Associate Master Data Management is responsible for the accurate creation, maintenance and integrity of basic and complex Master Data including Material Master, Bills of Materials, Recipes, Resources and Production Versions.

Responsibilities include:

  • Ensure quality of own work and quality of others impacting SAP
  • Verify accurate set-up of information in the system and maintain accurate information in the material master files
  • Monitor and get resolution of Master Data error metrics
  • Provide input to update policy and procedures
  • Support or manage process improvement initiative, as needed
  • Test SAP functionality, support ERP releases, as needed
  • Provide data entry for all required data fields per SOPs, guidelines, work instructions
  • Extract, compile and interpret data relevant for periodic metrics and reporting needs
  • Leads master data business processes
  • Upholds global master data governance process, partnering with BPOs (Business Process Owners) as necessary
  • Provide business process mentorship/training to internal clients and acts as a technical resource related to own niche area
  • Apply analytical skills to evaluate and interpret complex situations/problems using multiple sources of information
  • Participate in BPO's global forum
  • Monitor functional area data quality reports and identify revisions to data quality reports, to proactively prevent, identify, monitor, and accurate master data errors


Basic Qualifications:

  • Master's Degree


Or

  • Bachelor's Degree with 2 years of relevant experience


Preferred Qualifications:

  • Supply chain data management experience
  • Familiarity with SAP system
  • Proficient in English, both in oral and written communication
  • Good knowledge of Word, Excel and ability to work easily with new software
  • Working knowledge of regulatory and pharmaceutical processes
  • Proven project management, cross functional facilitation, communication and presentation skills
  • Team player, self-starter, persistent, considerate, persuasive, organized, independent worker who tackles ownership in driving tasks/projects to completion
  • Readily adapts to and manages change
  • Able to balance multiple responsibilities and priorities simultaneously under constrained timelines
  • Analytical skills in data management, interpretation and reporting
  • Ability to establish relationships with key stakeholders across multiple disciplines, both onsite and virtually
  • Experience in a pharmaceutical/GMP environment
  • Experience in a Supply Chain environment
  • Ability to meet strict timelines
  • Ability to work in an intense and changing environment
  • Able to follow through on tasks and meet deadlines


Our culture is what makes Amgen a special place to work. We have a powerful shared purpose around our mission - to serve patients. We respect one another, recognize contributions, and have embedded collaboration, trust, empowerment and inclusion in all that we do.

We equip all our staff members to live well-rounded, healthy lives. Most recently, Amgen added benefits for transgender employees and continues to pride itself on industry-leading, family-friendly offerings for families of all compositions.

Amgen focuses on areas of high unmet medical need and uses its expertise to strive for solutions that improve health outcomes and dramatically improve people's lives. A biotechnology pioneer since 1980, Amgen has grown to be one of the world's leading independent biotechnology companies, has reached millions of patients around the world and is developing a pipeline of medicines with breakaway potential.

Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.

We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.

Join Us

If you're seeking a career where you can truly make a difference in the lives of others, a career where you can work at the absolute forefront of biotechnology with the top minds in the field, you'll find it at Amgen.

Amgen, a biotechnology pioneer, discovers, develops and delivers innovative human therapeutics. Our medicines have helped millions of patients in the fight against cancer, kidney disease, rheumatoid arthritis and other serious illnesses.

As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other but compete intensely to win. Together, we live the Amgen values as we continue advancing science to serve patients.

Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.

PI117317441

<b>Amgen</b><br/><br/><b>Job ID: </b>R-89925<br/><b>Location: </b>Juncos, PR, US 00777<br/><br/>The Sr. Associate Master Data Management is responsible for the accurate creation, maintenance and integrity of basic and complex Master Data including Material Master, Bills of Materials, Recipes, Resources and Production Versions.<br><br><b><b>Responsibilities include:</b></b><br><br><ul><li>Ensure quality of own work and quality of others impacting SAP</li><li>Verify accurate set-up of information in the system and maintain accurate information in the material master files</li><li>Monitor and get resolution of Master Data error metrics</li><li>Provide input to update policy and procedures</li><li>Support or manage process improvement initiative, as needed</li><li>Test SAP functionality, support ERP releases, as needed</li><li>Provide data entry for all required data fields per SOPs, guidelines, work instructions</li><li>Extract, compile and interpret data relevant for periodic metrics and reporting needs</li><li>Leads master data business processes</li><li>Upholds global master data governance process, partnering with BPOs (Business Process Owners) as necessary</li><li>Provide business process mentorship/training to internal clients and acts as a technical resource related to own niche area</li><li>Apply analytical skills to evaluate and interpret complex situations/problems using multiple sources of information</li><li>Participate in BPO's global forum</li><li>Monitor functional area data quality reports and identify revisions to data quality reports, to proactively prevent, identify, monitor, and accurate master data errors</li></ul><br><br><b><b>Basic Qualifications:</b></b><br><br><ul><li>Master's Degree</li></ul><br><br><b>Or</b><br><br><ul><li>Bachelor's Degree with 2 years of relevant experience</li></ul><br><br><b><b>Preferred Qualifications:</b></b><br><br><ul><li>Supply chain data management experience</li><li>Familiarity with SAP system</li><li>Proficient in English, both in oral and written communication</li><li>Good knowledge of Word, Excel and ability to work easily with new software</li><li>Working knowledge of regulatory and pharmaceutical processes</li><li>Proven project management, cross functional facilitation, communication and presentation skills</li><li>Team player, self-starter, persistent, considerate, persuasive, organized, independent worker who tackles ownership in driving tasks/projects to completion</li><li>Readily adapts to and manages change</li><li>Able to balance multiple responsibilities and priorities simultaneously under constrained timelines</li><li>Analytical skills in data management, interpretation and reporting</li><li>Ability to establish relationships with key stakeholders across multiple disciplines, both onsite and virtually</li><li>Experience in a pharmaceutical/GMP environment</li><li>Experience in a Supply Chain environment</li><li>Ability to meet strict timelines</li><li>Ability to work in an intense and changing environment</li><li>Able to follow through on tasks and meet deadlines</li></ul><br><br>Our culture is what makes Amgen a special place to work. We have a powerful shared purpose around our mission - to serve patients. We respect one another, recognize contributions, and have embedded collaboration, trust, empowerment and inclusion in all that we do.<br><br>We equip all our staff members to live well-rounded, healthy lives. Most recently, Amgen added benefits for transgender employees and continues to pride itself on industry-leading, family-friendly offerings for families of all compositions.<br><br>Amgen focuses on areas of high unmet medical need and uses its expertise to strive for solutions that improve health outcomes and dramatically improve people's lives. A biotechnology pioneer since 1980, Amgen has grown to be one of the world's leading independent biotechnology companies, has reached millions of patients around the world and is developing a pipeline of medicines with breakaway potential.<br><br>Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.<br><br>We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.<br><br>Join Us <br> <br> If you're seeking a career where you can truly make a difference in the lives of others, a career where you can work at the absolute forefront of biotechnology with the top minds in the field, you'll find it at Amgen. <br> <br> Amgen, a biotechnology pioneer, discovers, develops and delivers innovative human therapeutics. Our medicines have helped millions of patients in the fight against cancer, kidney disease, rheumatoid arthritis and other serious illnesses. <br> <br> As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other but compete intensely to win. Together, we live the Amgen values as we continue advancing science to serve patients. <br> <br> Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.<br/><br/> <img src="https://analytics.click2apply.net/v/eo2zRdiNQ6jasjxYhdXDl"> <p>PI117317441</p>

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Posted: 2020-01-22 Expires: 2020-02-22

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Sr. Associate Master Data Management

Amgen
Juncos, Puerto Rico 00777

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