Bachem
Bachem
Bachem is a Swiss-based pharmaceutical and healthcare company developing and manufacturing peptides, oligonucleotides, biochemicals, and active pharmaceutical ingredients. Since 1971, it has supported pharmaceutical and biotechnology organizations across research, clinical development, and commercial production through custom synthesis and specialized manufacturing capabilities. Bachem operates internationally, with teams and sites across Europe, the United States, and Asia.

Senior Engineering Manager - Pharmaceutical Manufacturing, Torrance

Lead engineering operations for Bachem Americas’ pharmaceutical manufacturing facilities, overseeing process design, automation, project delivery, and facility expansion. Support operational excellence across peptide and oligonucleotide production.

Description

  • Lead Bachem Americas’ engineering team.
  • Coordinate the design, development, project planning, and continuous improvement of process workflows and material-flow systems.
  • Provide strategic direction and oversight for technical operations.
  • Optimize personnel, equipment, materials, and facility resources.
  • Create engineering schedules and project timelines.
  • Track project progress, resolve issues, and support on-time delivery.
  • Lead initiatives for manufacturing process design, system enhancement, production improvement, and testing procedure development.
  • Work with management, production, and marketing to evaluate engineering feasibility and cost-effectiveness.
  • Assess technology trends, workforce needs, and market conditions to guide project planning and investment decisions.
  • Implement technologies and automation solutions within manufacturing processes.
  • Improve waste reduction, throughput, and product quality.
  • Develop and implement policies and procedures aligned with industry standards and quality systems.
  • Prepare and oversee the engineering department budget.
  • Forecast operating costs, track spending, and contribute to financial planning.
  • Maintain compliance with company policies, safety requirements, regulatory standards, and strategic objectives.

Requirements

  • Master’s degree in a relevant engineering field plus 8 years of pharmaceutical industry experience, or bachelor’s degree in a relevant engineering field plus 10 years of pharmaceutical industry experience.
  • At least 12 years of engineering and project management experience.
  • At least 5 years of management experience.
  • Experience with HVAC systems, cleanroom design, freeze-drying, downstream bioprocessing, mixing, filtration, process automation, and quality controls.
  • Demonstrated success designing, planning, and managing manufacturing and pilot plant facility expansions.
  • Experience managing projects from initial design and planning through implementation and validation.
  • Strong knowledge of FDA regulations, cGMP guidelines, and 21 CFR Parts 11, 210, 211, and 820.
  • Ability to manage the Torrance engineering team and coordinate with the Vista site engineering team.
  • Excellent written and verbal communication skills.
  • Proactive, solutions-oriented communication style.
  • Ability to work independently and manage time effectively.
  • Advanced computer skills, including proficiency with planning and design software.
  • Ability to collaborate effectively across functions.
  • Strong organizational skills and the ability to manage multiple priorities in a fast-paced, deadline-driven environment.

Benefits

  • Annual performance bonus
  • Medical, dental, and vision coverage
  • 401(k) plan with employer contribution
  • Paid vacation, personal, and sick days

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