Lead Specialist-Maintenance Standard Room at Eli Lilly and Company

Carolina, Puerto Rico, Puerto Rico

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Not SpecifiedCompensation

Mid-level (3 to 4 years), Senior (5 to 8 years)Experience Level

Full TimeJob Type

UnknownVisa

Pharmaceuticals, HealthcareIndustries

Requirements

Bachelor’s degree in Electronics with a concentration in Instrumentation or Bachelor’s degree in Engineering Technology or Science is preferred; alternatively, an Associate’s degree in Instrumentation or a technical area with five or more years of experience in a related field
Between 3 to 5 years of experience in maintenance of pharmaceutical equipment operations in general, is preferred
Proficiency in Spanish (verbal and written communication) and basic proficiency in English (verbal and written communication)
Ability to read and interpret specifications, drawings, procedures in both English and Spanish
Teamwork oriented
Good interpersonal and customer service skills internally and externally
Ability to communicate effectively with all levels within the company
Strong compliance (safety, environmental and quality) mindset and sound judgement
Ability to handle multiple priorities and work under minimal supervision

Responsibilities

Manage and coordinate tasks related to secondary standards and special tools, including support in the selection of contractors and suppliers, obtaining quotes, documentation, and contract approval
Oversee and coordinate the execution of work orders, maintain control of billing and documentation, and ensure compliance with operational processes for equipment and instrumentation systems
Identify when it is necessary to purchase new standards, obtain quotations, and communicate the needs to supervision to proceed with the purchase
Coordinate and perform preventive and corrective maintenance, inspect and send standards and special tools for calibration, and document diagnostics and solutions in work orders
Generate work orders, document work orders following cGMPs and ALCOA+ principles
Evaluate preventive and corrective certifications
Generate deviations and communicate secondary standard certification failures
Complete investigations of technical events or deviations related to standards on time
When required, participate in the Deviation Review Board for technical investigations
Maintain control and organization of the Secondary Standards and Special Tools Room, verify instrument conditions, and participate in internal and external audits
Look for innovation in order to maintain the compliance of the Secondary Standards
Communicate/train staff for continuous improvement
Participate in and complete assigned training, verify compliance, and apply acquired knowledge in daily work
Join safety, operational excellence, and metrics teams, attend meetings, and contribute to action plan follow-up
Properly dispose of hazardous waste, ensure use of approved containers, label and transport waste, and notify supervision of spills

Skills

cGMP

ALCOA+

Preventive Maintenance

Corrective Maintenance

Calibration

Work Order Management

Deviation Investigation

Supplier Coordination

Contract Approval

Audit Participation

Instrumentation Systems

Eli Lilly and Company

Develops and delivers prescription medicines globally

About Eli Lilly and Company

Eli Lilly and Company is a global pharmaceutical company that focuses on discovering, developing, and delivering medicines to improve health. The company has a long history of scientific achievements, including the creation of insulin, the first life-saving treatment for diabetes. Lilly's operations involve extensive research and development to create new medications and enhance existing ones, ensuring they are safe and effective. Their products are primarily prescription medicines sold to healthcare providers for various medical conditions, including diabetes, cancer, and pain management. What sets Lilly apart from its competitors is its strong commitment to ethical practices and the protection of its products from counterfeiting. The company's goal is to enhance lives through innovative medical solutions while maintaining high standards of quality and ethics.

Indianapolis, IndianaHeadquarters

1876Year Founded

$1,180.1MTotal Funding

IPOCompany Stage

Biotechnology, HealthcareIndustries

10,001+Employees

Risks

Competition from Novo Nordisk's Ozempic may impact tirzepatide's market share.

Potential construction delays in Indiana could affect GLP-1 drug production timelines.

Regulatory challenges may hinder Kisunla's expansion in new Alzheimer's markets.

Differentiation

Eli Lilly's rich history includes the first life-saving insulin treatment.

Lilly's strategic partnerships enhance its position in neurodegenerative disease treatments.

FDA approval of Zepbound opens new therapeutic markets for sleep disorder treatments.

Upsides

Lilly's $9 billion complex in Indiana boosts GLP-1 drug production capacity.

Kisunla's approval in China expands Lilly's Alzheimer's treatment market in Asia.

Collaboration with EVA Pharma enhances Lilly's reputation as socially responsible.

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