Operations Associate - Parenteral Manufacturing

Society for Conservation Biology; Concord (NC); On-site; USD 64,000 - 141,000; Full time

Job summary

A leading company in the healthcare sector is seeking an Operations Associate to support the commissioning of a new parenteral manufacturing facility. The role involves ensuring compliance with regulatory standards, leading training programs, and managing daily operations. Ideal candidates will have a strong STEM background and experience in manufacturing or operations. Competitive salary and benefits are offered.

Benefits

Competitive salary

Bonus potential

Comprehensive health plans

Qualifications

• At least 2 years of experience in manufacturing or operations.
• Understanding of regulatory requirements (FDA, EMEA, OSHA, etc.).

Responsibilities

• Lead safety initiatives and encourage a safety-first culture.
• Conduct deviation investigations and participate in regulatory inspections.
• Ensure operational consistency and lead readiness activities.

Skills

Communication

Technical Aptitude

Education

Bachelor's degree in a STEM or related field

Job description

Operations Associate - Parenteral Manufacturing

Employer: Eli Lilly and Company

Location: North Concord, North Carolina, US

Salary: Competitive

Closing date: May 11, 2025

Sector: Consultancy/Private Sector

Field: Conservation science

Discipline: Administration/Operations

Salary Type: Salary

Employment Type: Full time

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees work to discover and bring medicines to those in need, improve disease understanding and management, and give back to communities through philanthropy and volunteerism. We prioritize putting people first and striving for excellence.

Position Description

We are seeking a dedicated Operations Associate to support the commissioning, qualification, and validation of our new parenteral manufacturing facility in Concord, NC. The role involves supporting operations readiness, leading training programs, and ensuring compliance with regulatory standards. The successful candidate will be involved in hiring, training, and daily performance management once the facility is operational, collaborating across departments to meet key metrics and uphold safety and quality standards.

Key Responsibilities

• Lead safety initiatives and encourage a safety-first culture.
• Conduct deviation investigations and participate in regulatory inspections.
• Ensure operational consistency and lead readiness activities.
• Support continuous improvement and operational excellence initiatives.
• Build a diverse and capable team, supporting site leadership.

Minimum Requirements

• Bachelor's degree in a STEM or related field.
• At least 2 years of experience in manufacturing or operations.
• Understanding of regulatory requirements (FDA, EMEA, OSHA, etc.).
• Strong communication skills and technical aptitude.

Work Environment & Travel

• Ability to work in cleanroom environments and wear necessary safety gear.
• Ability to work standard hours with overtime as needed.
• Willingness to travel domestically and internationally up to 20% of the time.

Preferred Attributes

• Experience supporting pharmaceutical or similar manufacturing environments.
• Knowledge of automation, aseptic processes, and quality systems.

Lilly is committed to diversity and equal opportunity. We support individuals with disabilities and provide accommodations during the application process. Our benefits include competitive salary, bonus potential, comprehensive health plans, and employee resource groups. Actual compensation will depend on qualifications and location, with an anticipated range of $64,500 - $140,800.