MES Support Engineer at Gilead Sciences

Cork, County Cork, Ireland

Gilead Sciences Logo
Not SpecifiedCompensation
Mid-level (3 to 4 years)Experience Level
Full TimeJob Type
UnknownVisa
Biotechnology, PharmaceuticalsIndustries

Requirements

  • Bachelor’s degree in IT, Computer Science, Engineering, or Pharmaceutical Manufacturing
  • Extensive experience with MES systems, preferably Körber PAS-X
  • Strong understanding of pharmaceutical manufacturing processes and MES lifecycle
  • Experience with SAP-MES integration and Level 2 automation systems
  • Familiarity with ISA-95/S88 standards and MES architecture
  • Experience with system profile creation, reporting tools, and ITIL frameworks (desired)
  • Excellent communication and stakeholder engagement skills (desired)

Responsibilities

  • Monitor MES system performance and resolve issues to minimize production downtime
  • Provide on-site and on-call support for PAS-X MES during manufacturing activities
  • Diagnose and resolve system issues including latency, system configuration, interface failures, user access problems, and security settings
  • Perform root cause analysis for MES-related incidents and implement corrective actions
  • Support integration between MES and ERP systems (e.g., SAP), while maintaining operational readiness across interfaces
  • Participate in validation activities (IQ/OQ/PQ) and ensure compliance with GxP, GAMP, and 21 CFR Part 11 standards
  • Maintain audit trails, logbooks, and documentation for regulatory inspections
  • Participate in system upgrades, patches, and validation activities
  • Deliver user training and maintain SOPs for MES operations
  • Work closely with cross-functional teams during MES workshops and design phases
  • Contribute to change management planning and system upgrade strategies

Skills

MES
Manufacturing Execution Systems
support engineering
troubleshooting
pharmaceutical manufacturing

Gilead Sciences

Develops and commercializes biopharmaceuticals

About Gilead Sciences

Gilead Sciences focuses on discovering, developing, and commercializing medicines for various medical conditions, including HIV/AIDS, liver diseases, cancer, inflammatory and respiratory diseases, and cardiovascular issues. The company conducts extensive research and development to create new therapies, which are then marketed to healthcare providers, hospitals, and pharmacies after receiving regulatory approval. Gilead differentiates itself from competitors through its strong commitment to R&D and strategic partnerships, such as with SAP Ariba, to enhance its operations and product offerings. The company's goal is to improve health equity and access to care globally, working with communities to ensure that its medicines reach those in need.

Foster City, CaliforniaHeadquarters
1987Year Founded
$15,873.6MTotal Funding
IPOCompany Stage
Biotechnology, HealthcareIndustries
10,001+Employees

Benefits

Paid family time off and paid parental time off
Generous 401(k) contribution matching
Comprehensive medical plans that cover both physical and mental healthcare
Global Wellbeing Reimbursement
Time Off
Global Volunteer Day
Giving Together Program
Employee Support Programs
Flexible Work Options

Risks

Increased competition in HIV treatment from ViiV Healthcare's expanding drug portfolio.
Regulatory scrutiny over drug pricing could impact Gilead's U.S. market operations.
Patent expirations, like Truvada's, lead to increased generic competition and revenue loss.

Differentiation

Gilead's lenacapavir is recognized as the 2024 Breakthrough of the Year for HIV care.
Partnerships with LEO Pharma and Tubulis enhance Gilead's focus on inflammatory and cancer therapies.
Gilead's commitment to health equity initiatives like COMPASS and HepConnect sets it apart.

Upsides

Gilead's strategic partnerships expand its reach in inflammatory and oncology drug markets.
Investment in digital health technologies enhances Gilead's R&D and patient engagement.
Focus on sustainability improves Gilead's operational efficiency and corporate reputation.

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