Novartis

Pharmaceutical

ManufacturingSpecialist

$365–510k ~AI est. Mexico City, Mexico FULL TIME Remote Friendly
Market Sentiment
HIGH DEMAND

Neural analysis suggests this role is
optimal for Mid+ candidates.

The Brief

“Manufacturing Specialist at Novartis. Skills: Manufacturing execution systems, Electronic batch records, Process improvement. Configure and update MES records. Maintain master batch record interfaces”

What You'll Achieve.

Keep manufacturing operations running smoothly; Enable reliable, compliant, and efficient production; Support product readiness; Support system improvements; Support day-to-day manufacturing success

Industry & Context.

Pharmaceutical
Problems you'll solve

Resolve master batch record issues; System workarounds

Eligibility Requirements

Shift work expected, Cover Saturday and Sundays

What They're Looking For.

Must Have

1-3 years manufacturing execution systems experience, Experience with electronic batch record systems, Experience in regulated manufacturing environments, Practical knowledge of GMP requirements, Experience supporting system interfaces, Ability to collaborate effectively, Fluency in Spanish and English

Nice to Have

PAS-X experience, Emerson experience, Rockwell Automation experience

What You'll Do.

Configure and update MES records

Maintain master batch record interfaces

Communicate master batch record design changes

Provide real-time production support

Perform system testing

Support internal and external audits

Ensure MES records align with requirements

How You'll Work.

Team & Collaboration

Global and local cross-functional stakeholders; Operations, Quality, and Development teams

Communication Scope

Communicate effectively

Full Job Description

**Job Description Summary** #LI-Hybrid Location: Mexico City, Mexico Relocation Support: This role is based in Mexico City, Mexico. Novartis is unable to offer relocation support: please only apply if accessible. In this role, you will play a key part in keeping manufacturing operations running smoothly by shaping how digital batch records and systems support real work on the shop floor. You will work closely with Operations, Quality, and Development teams to design, maintain, and improve electronic manufacturing records that enable reliable, compliant, and efficient production. This is a hands-on role with real visibility, where your work directly supports product readiness, system improvements, and day-to-day manufacturing success. **Job Description** **Key Responsibilities** * Configure and update manufacturing execution system records to reflect site-specific master batch record design changes * Maintain master batch record interfaces with laboratory and enterprise planning systems * Communicate master batch record design changes with global and local cross-functional stakeholders * Provide real-time production support to resolve master batch record issues or system workarounds * Perform system testing with development, quality, and production teams during manufacturing execution system upgrades * Support internal and external audits by providing system data, records, and subject matter expertise * Ensure manufacturing execution system records align with validated equipment and cleaning requirements **Essential Requirements** * One to three years of hands-on experience with manufacturing execution systems such as PAS-X as the primary experience if not, Emerson or Rockwell Automation * Experience working with electronic batch record systems in regulated manufacturing environments, including pharmaceutical or comparable industries * Practical knowledge of current Good Manufacturing Practice requirements and compliance standards * Experience supporting or maintaini

Free ATS check

Applying for this Manufacturing Specialist role?

Most applicants get filtered before a human reads their resume. See if yours makes the cut.

How to Apply on Workday

  • Workday has a multi-step form — save your progress after every section.
  • "Apply With LinkedIn" can fail or lose data; manual entry is more reliable.
  • Watch for the "Submit for Review" final step — hitting "Save" alone does not submit.
  • Job requisition numbers are useful when following up with HR by email.

ANONYMOUS · UNFILTERED

What do employees actually say about Novartis?

Real rants from real employees. Read before you apply.

Read Company Rants →