Sr. Engineering Project Manager
Bachem AG · Vista, CA, US, 92081 · United States · On-site
Pay: USD 126,317 – 173,686 a year
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A brief overview
The Sr. Engineering Project Manager leads the implementation of large‑scale production processes and equipment at Bachem, applying best‑practice project management methodologies to capital projects. This role oversees system start‑up activities and ensures that engineers and operations staff are fully trained to operate and troubleshoot new equipment effectively.
What you will do
Transfer Bachem proprietary manufacturing technology from Bachem Switzerland to Bachem America.
Leverage engineering design principles and large‑scale production technologies used in Bachem Switzerland to guide equipment implementation and ensure alignment with global standards.
Implement and build manufacturing infrastructure to mirror Bachem Switzerland utilizing experience gained in Bachem to maximize capabilities
Lead cross-functional teams (Quality, Production, Facilities, Engineering) within a matrix environment
Oversee CapEx projects for new GMP laboratories and equipment (AHU, dehumidifiers, chillers, etc.), cleanrooms and lyophilizers, as well as controls and automation associated with these activities
Develop and train employees on the utilization of maintenance schedules for new equipment
Support the Engineering Director on capital projects for facility remodeling and expansion
Perform activities associated with the design and qualifications of the new and existing equipment used in a manufacturing plant
Create new process and equipment drawings based on specifications and standards
Act as the lead project manager for the design and construction of new plant expansions and plat-related capital projects
Work with other departments, contractors, and vendors
Perform process development studies for new and existing projects. Write summary reports to support the process development data. Write standard operation procedures, standard test procedures, master batch records and other related GMP documents
Qualifications
Master’s degree in engineering, science, business or related field with 5+ years of relevant work experience
Bachelor’s degree in engineering, science, business or related field with 10+ years of relevant work experience
Associate’s degree in engineering, science, business or related field with 15+ years of relevant work experience
Minimum of 8 years pharm/biotech experience
Work experience in GMP-related capital projects
Knowledge of cGMP, pharmaceutical manufacturing methods and engineering principles
Technical knowledge of processes, equipment, and utilities (batch processing, tank, filtration, lyophilization, purified water systems etc.)
Experience with peptides (preferred)
General lab instrument (GC, FTIR, NMR and KF) knowledge and operation experience (preferred)
PMP certification (preferred)
Strong MS Suite skills, particularly MS Project, Sharepoint, etc.
Excellent written and oral communication skills
Ability to effectively organize, multitask,…