Senior Process Improvement Specialist

Bachem

. Collect, statistically analyze, and visualize production data to improve process performance, robustness, and efficiency .

Posted 10/24/2026full-timeSan Diego • California • United StatesSenior💰 $94,104 - $129,393 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in statistical analysis and process improvement within manufacturing, particularly in the pharmaceutical industry. Proficient in managing projects, developing data acquisition processes, and ensuring compliance with cGMP guidelines.

Highest-signal resume keywords

Statistical AnalysisProcess ImprovementSAP ExperienceCGMP ComplianceData Visualization

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Statistical AnalysisProcess ImprovementData AcquisitionKey Performance IndicatorsQuality MetricsTrend AnalysisContinuous Process VerificationManufacturing Process AnalysisTroubleshootingProject Management

Soft Skills

Excellent CommunicationOrganizational SkillsDetail-OrientedProactive Problem SolvingIndependent Time Management

Tools & Technologies

SAPHyperionBrioMinitabAdonisPower BIPowerPoint

Industry Keywords

Pharmaceutical ManufacturingCGMP EnvironmentBachem Quality Management SystemManufacturing Process ParametersCross-Functional Collaboration

About the role

Key responsibilities & impact

Collect, statistically analyze, and visualize production data to improve process performance, robustness, and efficiency
Analyze manufacturing processes and recommend process controls or other actions to increase efficiency
Generate key performance indicators and report process performance to department leadership
Develop standard data acquisition processes applicable to all projects
Manage multiple time-sensitive projects and deliver targeted outcomes
Support short- and long-term business objectives and organize departmental process-improvement efforts
Identify, prioritize, and assess the impact of manufacturing process parameters
Train team members to perform data analysis
Identify causes of variability in multi-stage production processes using process maps
Define quality metrics and use trend analysis to identify manufacturing improvement opportunities
Manage and monitor Continuous Process Verification programs
Present findings to stakeholders using PowerPoint, graphs, and charts
Draft and review MBPRs, SOPs, deviations, investigations, and other technical documents
Track CAPAs related to manufacturing to ensure commitments are met on time
Assist managers with scheduling, data entry in planning systems, and production coordination
Report to the production department and coordinate with cross-functional teams and other sites
Serve as a potential SAP key user for production-related activities

Requirements

What you’ll need

Bachelor's degree in life sciences, computer information systems, or related field
4+ years of experience with reporting tools such as Hyperion/Brio or other statistical software systems
4+ years of process improvement or operations experience
SAP experience preferred
Previous manufacturing experience, preferably in the pharmaceutical industry
Experience working in a cGMP environment preferred
Experience with statistical analysis applied to pharmaceutical manufacturing preferred
Knowledge of SAP transactions and troubleshooting
Excellent verbal, written communication, and presentation skills
Excellent organizational skills
Detail-oriented with the ability to troubleshoot and resolve technical and analytical problems
Strong understanding of interdependencies with cross-functional stakeholders and business implications of decisions
Positive and determined attitude with proactive, solution-focused communication
Ability to work independently and manage one's time
Exposure to statistical reporting tools including Minitab, Adonis, and Power BI
Compliance with Bachem Quality Management System and cGMP guidelines

Benefits

Comp & perks

Annual performance bonus
Comprehensive medical, dental, and vision coverage
401(k) plan with employer contribution
Paid vacation, personal, and sick days
Equal opportunity and inclusive workplace