Director, Technical Services — Pharma Manufacturing & Reliability

Evonik Industries AG; Birmingham (AL); On-site; USD 140,000 - 210,000; Full time

Benefits offered by this job

On-the-job training

Performance-related pay

Professional development

Job summary

Evonik Corporation is seeking a Director of Technical Services in Birmingham, AL to lead Engineering, Facilities, Validation, and Maintenance for our cGMP pharmaceutical manufacturing operations. You will mentor teams, manage asset planning, and drive performance improvements in a regulated environment.

The role requires a strong background in engineering management, cGMP knowledge, and cross-functional collaboration with Operations, Quality, Validation, and Supply Chain.

Qualifications

• Bachelor's degree in Engineering; advanced degree preferred.
• 10+ years engineering, maintenance, or technical operations in regulated manufacturing (pharma/biotech/medical device).
• 5+ years of management experience.
• Strong knowledge of FDA cGMP regulations, validation, and facility utilities.

Responsibilities

• Lead Engineering, Facilities, Validation, and Maintenance organizations supporting cGMP pharmaceutical manufacturing.
• Develop and mentor high-performing engineering and maintenance teams.
• Oversee preventive maintenance, reliability, utilities, and facilities operations to maximize uptime.
• Manage site capital projects, budgets, and long-range asset planning.
• Drive continuous improvement initiatives to increase efficiency and reduce costs.

Skills

Leadership

Engineering Management

Regulatory compliance

cGMP knowledge

Capital projects

Budget management

Cross-functional collaboration

Communication

Education

Bachelor's degree in Engineering

Advanced degree preferred

Job description

Evonik Corporation is seeking a Director of Technical Services in Birmingham, AL to lead Engineering, Facilities, Validation, and Maintenance for our cGMP pharmaceutical manufacturing operations. You will mentor teams, manage asset planning, and drive performance improvements in a regulated environment.

The role requires a strong background in engineering management, cGMP knowledge, and cross-functional collaboration with Operations, Quality, Validation, and Supply Chain.