Associate Director - Manufacturing Peptide Operations

Eli Lilly and Company

Indianapolis (IN)

On-site

USD 118,500 - 173,800

Full time

14 days+

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Benefits offered by this job

Company bonus
Comprehensive benefits program

Job summary

A global healthcare leader in Indianapolis is seeking an Associate Director for Peptide Operations. This role leads frontline teams to ensure the accurate execution of manufacturing processes, fostering a culture of operational excellence. The ideal candidate has a B.S. in engineering/chemistry/biochemistry and at least 5 years of manufacturing experience, preferably in biosynthetic processes. The position offers competitive compensation, including a salary range of $118,500 - $173,800 and benefits.

Qualifications

  • Minimum 5 years of applicable manufacturing-related experience, preferably in biosynthetic, fermentation, or purification operations.

Responsibilities

  • Lead frontline leaders and teams in achieving accurate execution of manufacturing instructions.
  • Drive operational excellence and ensure compliance with regulations.
  • Manage departmental budget and develop business plans.

Skills

Teamwork
Independence in decision-making
Project management
Effective communication

Education

B.S. in engineering/chemistry/biochemistry

Job description

Associate Director - Manufacturing Peptide Operations

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 around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We put people first and seek individuals determined to make life better for people around the world.

Position Overview

The Associate Director for Peptide Operations provides oversight for the operational resources assigned to the peptide Process Team including Operations Leaders. The chief deliverable of this role is the leadership of frontline leaders and their teams in achieving accurate execution of manufacturing instructions (e.g., batch production records, SOPs) used for the safe manufacture of high-quality medicine. This team operates in a high-demand environment to ramp production to meet supply chain needs. The role serves as the key integrator of the broader cross-functional team to achieve production goals while driving safety, quality, and continuous improvement per the Manufacturing Standards for Operational Excellence. The Associate Director provides leadership, has accountability for all of the Process Team, and ensures appropriate staffing is in place.

Key Objectives / Deliverables

  • Drive application and fidelity to the vital behaviors of execution: Read, Do, Sign
  • Achieve accurate execution via continuous, programmatic reinforcement of the rudiments of operational excellence
  • Ensure adequate staff is available to conduct departmental operations
  • Ensure departmental staff is properly equipped to conduct necessary operations
  • Direct operations leaders to ensure operations are conducted in a manner consistent with regulatory and business drivers
  • Escalate issues to the appropriate management level when necessary; ensure operations are conducted following all HSE and GMP requirements
  • Ensure self and direct reports are in compliance with necessary training and applicable qualifications for the assigned tasks
  • Ensure performance management and development plans are in place for all operations staff
  • Use appropriate balance of recognition and discipline to drive accountability of staff
  • Ensure adequate supply of material is available to the downstream customer
  • Serve as a coach and mentor
  • Develop business plans for the department and manage the departmental budget
  • Work with functional leadership to organize, prioritize, and deliver on initiatives to drive continual improvements

Basic Requirements

  • Minimum B.S. in engineering/chemistry/biochemistry or equivalent work experience
  • Minimum 5 years of applicable manufacturing-related experience, preferably some biosynthetic, fermentation, and/or purification operations experience

Additional Preferences

  • Ability to instill teamwork within the department and demonstrate key interpersonal skills
  • Ability to make decisions independently and to network with others as appropriate
  • Ability to function in a team environment as a leader and as a member of management teams
  • Demonstrated skills in project management and coordination
  • Ability to communicate effectively both verbally and in writing to audiences at all levels of the broader manufacturing organization

Other Information

  • Must complete Learning Plan for Associate Director – Mfg Ops
  • No certifications required
  • Tasks require entering manufacturing areas that require wearing appropriate PPE

Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form for further assistance. Lilly is proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status. Our employee resource groups (ERGs) offer strong support networks for their members and are open to all employees. Learn more about all of our groups. Actual compensation will depend on a candidate’s education, experience, skills, and geographic location. The anticipated wage for this position is $118,500 - $173,800. Full-time employees are eligible for a company bonus and a comprehensive benefits program. Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion.

Note: This description reflects the current scope and responsibilities of the role and may be adjusted as needed.

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