Find Jobs
Find Jobs Near You – Available Work in Your Location
Skip to job details
KB
KBI Biopharma
Senior Engineer, MS&T
Career Insights for Pharmaceutical Manufacturing Process Engineer
See where this job fits in the broader career landscape. Knowing your career path helps you see what's possible from here.
Scorecard
Based on Colorado data
Review key factors to help you decide if this role fits your goals. How is this calculated?
What they do
A Pharmaceutical Manufacturing Process Engineer designs and maintains manufacturing equipment, facilities and processes for a pharmaceutical company. Maintains process controls for the specific sterile processing requirements of pharmaceutical manufacturing.
$111,597 / year median in Colorado
+8% projected growth
Job Description
Senior Engineer, MS&T KBI Biopharma - 2.6 Boulder, CO Job Details Full-time $118,000 - $178,000 a year 9 hours ago Benefits Paid holidays Health insurance Dental insurance Paid time off Vision insurance 401(k) matching Sabbatical Qualifications Customer communication GMP Project management experience in manufacturing Manufacturing facility experience Production validation processes Bachelor's degree Pharmaceutical company experience Leading team collaboration initiatives Bioprocessing Cross-functional communication Pharmaceutical manufacturing facility experience Full Job Description The Manufacturing Science and Technology (MS&T) Senior Engineer is responsible for technology transfer activities (mainly downstream focused), document authoring/review, and manufacturing facility support to ensure client program success. The role requires significant collaboration with all departments Facilities and Engineering, Process Development, Supply Chain, Quality, and Manufacturing teams to ensure projects are executed efficiently. The Senior Engineer should demonstrate proven technical expertise in downstream microbial biologics and have strong knowledge of industry best practices. Key Responsibilities Provides process engineering ownership for a product, including all process transfer and implementation decisions. Subject Matter Expert of all downstream drug substance operations (chromatography, tangential flow filtration, clarification, normal filtration, etc.) Reviews and approves significant technical documents including process descriptions, process qualification protocols and reports, and CPV reports. Ability to generate technical solutions to a wide range of difficult problems through individual effort and leveraging external expertise. Ability to delegate and manage the work product of others. In-depth knowledge of process validation practices and associated regulatory expectations. Requirement for on call or on the manufacturing floor activities to support 24/7 plant operations on a rotating basis. Works with minimal direction toward predetermined long-range goals and objectives. Conceives plans and conducts engineering studies in areas of considerable scope and complexity. Leads efforts of organization within functional boundaries and influences efforts of adjacent organizations. May be expected to directly supervise project resources. Represents KBI as one of the primary technical contacts with clients on projects.