Compañía

NovartisVer más

addressDirecciónCiudad de México
CategoríaTecnologías de la información

Descripción del trabajo

395374BR

Manufacturing Technical MES System Specialist

Mexico

Sourcing Statement

You are applying to be part of the Novartis Talent Pool. We are not currently recruiting for this role but we are building a pipeline for future opportunities. If you would like to be considered for a similar position in future, then please submit your CV.

About the role

This is an Open Role, Available for Immediate Job Selection.
Novartis is unable to offer relocation support for this role. Please only apply if Mexico City is accessible for you. This role will remotely support international manufacturing locations.
The Manufacturing Execution System (MES) Systems Specialist will provide oversight and execution for the automated digitalized business processes, information flow and documentation for the production lifecycle. This role supports the maintenance, functionality, and change updates of the MES system to manufacture biopharmaceutical products for remote United States manufacturing locations.
Key Responsibilities:
  • Fluent English oral and written communicator who is proactive, responsive, and able to work independently with all levels of the organization. Ability to handle multiple conflicting tasks in a fast-paced environment is a must. Very high attention to detail is critical, including strong technical writing and proofreading skills.
  • Skilled in Master Batch Record (MBR) creation and maintenance using MES (Manufacturing Execution Systems).
  • Update Manufacturing SOPs as required. Own and support Change Control tasks, Quality Events, and CAPAs related to MES updates.
  • Support all aspects of the MES system - paperless manufacturing instructions, paperless in process control, enforces process sequencing and electronic go/no go decisions, process validation ranges, formulas to ensure the final yield is within acceptable percentages, interface with SAP System to issue materials to Master Batch Records (MBR) that are acceptable & released.
  • Coordinate the review and revisions of procedures, R&D documentation, and FDA regulations for inclusion in Production instructions and Quality Control manuals.
  • Communicate with broader MES global team to ensure alignment with the Global format and structure.
  • Responsible for ensuring compliance with Federal, State and local regulations and adherence to all company policies and procedures relating to GMP’s, Health, Safety & Environmental.

EEO Statement

We are Equal Opportunity Employers and take pride in maintaining a diverse environment. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status. We are committed to building diverse teams, representative of the patients and communities we serve, and we strive to create an inclusive workplace that cultivates bold innovation through collaboration and empowers our people to unleash their full potential.
Accessibility and Reasonable Accommodations: Individuals in need of a reasonable accommodation due to a medical condition or disability for any part of the application process, or to perform the essential functions of a position, please let us know the nature of your request, your contact information and the job requisition number in your message:
  • Novartis: e-mail us.reasonableaccommodations@novartis.com or call +1 (877)395-2339
  • Sandoz: e-mail reasonable.accommodations@sandoz.com or call: +1-609-422-4098

Role Requirements

Essential Requirements:
  • Bachelor’s degree required.
  • 3 years’ experience in a regulated cGMP environment or other regulatory related industry
  • 1 - 3 years Manufacturing Execution Systems
  • Fluent English speaking and written communication.
  • Strong aseptic manufacturing knowledge background preferred.

Why Novartis: Our purpose is to reimagine medicine to improve and extend people’s lives and our vision is to become the most valued and trusted medicines company in the world. How can we achieve this? With our people. It is our associates that drive us each day to reach our ambitions. Be a part of this mission and join us! Learn more here: People and Culture | Novartis.
You can find everything you need to know about our benefits and rewards in the Novartis Life Handbook. https://www.novartis.com/careers/benefits-rewards
Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Novartis and our career opportunities, join the Novartis Network here: Novartis Talent Pool.

Division

Operations

Business Unit

CELL & GENE THERAPY

Work Location

Ciudad de México

Company/Legal Entity

NOV PHA MEX

Functional Area

Technical Operations

Job Type

Full Time

Employment Type

Regular

Shift Work

No

Early Talent

No
Refer code: 1079103. Novartis - El día anterior - 2024-04-07 19:01

Novartis

Ciudad de México

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