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Associate Director - Engineering - Process; Oligonucleotides

Job in Houston, Harris County, Texas, 77246, USA
Listing for: BioSpace
Full Time position
Listed on 2026-07-10
Job specializations:
  • Engineering
    Operations Management, Process Engineer, Quality Engineering
Salary/Wage Range or Industry Benchmark: 123000 - 180400 USD Yearly USD 123000.00 180400.00 YEAR
Job Description & How to Apply Below
Position: Associate Director - Engineering - Process (Oligonucleotides)

Role Overview

Associate Director Process Engineering – Oligonucleotides provides leadership and direction to process engineers to ensure engineering deliverables are resourced and qualified to support the Oligonucleotides production and business agenda.

Lilly is constructing an advanced manufacturing facility for production of API molecules located in Houston, TX. This facility is intended to provide APIs for current and future products, including new modalities. The successful candidate will help build the organization, the facility, and the culture to enable a successful startup into GMP manufacturing operations.

Responsibilities Pre-Startup and Startup Phase
  • Attract, hire, and onboard a significant number of top talents to the Oligonucleotides Process Engineering team, establishing the right attitude, curiosity, and learning agility to deliver on the site mission.
  • Build the organization with the necessary capability, capacity, and culture to operate this facility to the highest standards of safety, quality, and operational excellence.
  • Develop and implement the business systems and processes needed to run the site, leveraging existing Lilly knowledge and incorporating external experience.
  • Establish lean practices and a continuous improvement mindset throughout operations and the direct supporting organizations.
  • Support the project team to deliver the facility, providing feedback and support on design decisions, commissioning & qualification strategies, etc.
  • Collaborate with project team to ensure the right decisions are made to meet project deliverables and longer‑term strategic goals for the site.
  • Organize and implement strategy for creating standard engineering operating procedures (SOPs) for startup and post‑startup phases.
  • Plan and manage business operational expenses, capital, and headcount targets.
Post‑Startup
  • Responsible for supervising and coaching process engineering staff for their respective area, including completing performance reviews and development planning.
  • Provide oversight of process engineering staffing including recruitment, resource planning, and succession planning.
  • Provide process engineering work coordination and input to key functional groups and partners.
  • In coordination with engineering function, set and reinforce standards for engineering work product and utilization of first principles.
  • Partner within Engineering and across functional disciplines to influence and implement technical agenda, site business plan objectives, and GMP Quality Plan objectives.
  • Identify, track, and report key indicators of functional performance.
  • Have oversight of engineering‑related technical issues and improvement initiatives.
  • Review and approve engineering‑related deviations and change controls.
  • Review and approve engineering standard operating procedures (SOPs).
  • Participate appropriately in site planning processes (capital and resource), representing the interests of the team but with a view to the overall site picture.
  • Ensure technical review and approval for documents, including investigations, change controls, validations, annual product reviews, manufacturing tickets, procedures, process flow documents, technical studies, etc.
  • Network across similar technologies to share best practices, rationale, and control strategies to ensure harmonization and alignment between sites.
Basic Qualifications
  • Bachelor of Science degree required in Chemical Engineering or another engineering discipline with extensive API or chemical manufacturing experience.
  • 3+ years of experience and proven capabilities within Oligonucleotides or similar synthetic protein GMP manufacturing environment.
  • 3+ years of experience in manufacturing leadership.
Additional Skills & Preferences
  • Experience in operations including a Process Safety Management (PSM) program.
  • Must possess knowledge and understanding of cGMPs and how they apply to operations.
  • Strong ability to form effective relationships at all levels and across functions; work closely with the Site Engineering Group to ensure alignment with corporate and Manufacturing & Quality objectives.
  • Experience developing and managing extremely talented, engaged, and high performing teams with a…
Position Requirements
10+ Years work experience
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