Manufacturing Execution System (MES) Site Lead

Merck Sharp & Dohme LLC
San Francisco, CA, United States
3 days ago
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Role details

Contract type
Permanent contract
Employment type
Full-time (> 32 hours)
Experience level
Expert
Experience required
5 years minimum
Compensation
$117,000.0 - $184,200.0
Working hours
Regular working hours
Job source

Tech stack

Data Analysis Software Applications Microsoft Office Systems Development Life Cycle Software Engineering Real Time Systems Data Management

Job description

An opportunity has arisen for an MES (Manufacturing Execution System) Site Lead to join our team at the high-tech DeSoto site, within the Digital Records Design Hub. At our company, we aspire to be the premier research-intensive biopharmaceutical company. We’re at the forefront of research to deliver innovative health solutions that advance the prevention and treatment of diseases in people and animals. Join us to use the power of leading-edge science to save and improve lives around the world., * Active participation in the Tier process and proactively resolving technical issues before they impact the business priorities.

  • Responsible and accountable for supporting MES related components of the process including on-floor support of manufacturing activities.
  • Active participation in the Tier process and proactively resolving technical issues before they impact the business priorities.
  • Developing and implementing optimal methodologies for the management of MES Systems Version 3.4 and future Versions, in compliance with company policies, quality regulations and industry norms.
  • Managing vendor performance and contracts
  • Supporting investigations by finding resolutions to MES problems
  • Supporting, maintaining, and developing MES recipes and capabilities
  • Collaborating with other technical functions to provide robust recipes and functionality that deliver reliable and sustainable performance.
  • Preparing and performing Update/Change Process and ensure they are raised and closed on time in compliance with required quality standards.
  • Providing expertise and technical knowledge to technical functions on MES
  • Performing MES administration and maintenance and ensure automation systems remain in a validated state.
  • Identify opportunities for continuous improvement.
  • Developing and update SOP’s and conduct MES training.
  • Ensuring all documents must comply with SDLC (System Development Life Cycle) requirements.
  • Represent De Soto MES team within our Company global & corporate teams

Requirements

Required

  • Bachelor of Science (BS) degree in a technical field (engineering or science) or equivalent.
  • Minimum of five (5) years’ experience in Manufacturing Execution System (MES)
  • Ability to manage multiple priorities and know when to escalate for resolution.
  • Proven ability to work cross-functionally, delivering technical solutions to MES issues.
  • Strong problem-solving and troubleshooting skills.
  • Knowledge of regulatory/code requirements to USDA, European and International Codes, Standards and Practices.
  • Proficiency in Microsoft Office and job-related computer applications.
  • Report, standards, policy writing skills.

Preferred

  • Experience in the application of Lean Six Sigma Methodology.
  • Pharmaceutical and Biotechnology manufacturing process experience.
  • Extensive knowledge of equipment and process validation.
  • Effective communication and interpersonal skills to interface effectively with all levels of colleagues in a team environment, and with external customers.
  • Customer-focused.
  • Self-motivated with a flexible approach.
  • Effective time management and multi-tasking skills.
  • Excellent attention to detail.
  • Strong data analysis capability.
  • Training skills.
  • Demonstrable analytical and systematic problem-solving skills.
  • Leadership qualities include focus on customers and patients, collaboration, acting with candor and courage, making rapid, disciplined decisions, driving results, building talent, and demonstrating ethics and integrity., Audit Management, Audit Management, Automation, Automation Systems, Business Process Improvements, Communication, Corporate Ethics, Customer-Focused, Data Analysis Tools, Data Management, Decision Making, Ethical Standards, Multitasking, Proactive Behavior, Problem Identification, Problem Management, Public Policy Writing, Quality Management, Real-Time Programming, Regulatory Compliance, Software Development Life Cycle (SDLC), Standards Compliance, Task Management, Team Communication, Vendor Management {+ 1 more}

Benefits & conditions

We are proud to be a company that embraces the value of bringing together, talented, and committed people with diverse experiences, perspectives, skills and backgrounds. The fastest way to breakthrough innovation is when people with diverse ideas, broad experiences, backgrounds, and skills come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another’s thinking and approach problems collectively.

Learn more about your rights, including under California, Colorado and other US State Acts (https://www.msdprivacy.com/us/en/CCPA-notice/)

The salary range for this role is

$117,000.00 - $184,200.00

About the company

Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.

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