We are seeking an experienced and technically proficient Senior Supervisor – CIP Valve Systems and Routing to lead the planning, installation, integration, and validation of Clean-in-Place (CIP) valve systems across high-purity processing facilities. This role is critical in ensuring hygienic design compliance, operational reliability, and seamless execution of automated CIP systems for industries such as pharmaceuticals, biotechnology, food & beverage, and dairy.
The senior supervisor will provide field leadership, ensure adherence to engineering specifications, and manage cross-functional coordination to meet safety, quality, and project deadlines.
Leadership of CIP Valve System Installations
Compliance with GMP, Sanitary, and Hygienic Design Standards
Advanced Coordination Across Engineering, Automation, and QA/QC
Documentation, Validation Support, and Quality Control
Mentorship, Training, and Field Team Management
Lead end-to-end supervision of sanitary valve installations (e.g., mix-proof, divert, diaphragm, and butterfly valves) and associated CIP piping networks.
Oversee valve manifold installations, routing strategies, and process integration for automated CIP loops.
Resolve field challenges related to routing, clash detection, or valve positioning while maintaining hygienic integrity.
Enforce adherence to ASME BPE, 3-A, EHEDG, and FDA guidelines throughout the installation process.
Ensure valve assemblies meet slope, drainability, dead leg elimination, and cleanability requirements.
Interface with QA/QC and validation teams to ensure design and construction meet GMP expectations.
Collaborate with design engineers, controls/automation teams, and commissioning groups to ensure full system functionality.
Review valve configuration logic, air header design, actuation strategies, and CIP sequencing.
Lead system walkdowns, punch list development, and resolution tracking during project closeout.
Ensure detailed and accurate tracking of valve tags, installation logs, torque specs, and weld certifications.
Support the development of validation documentation (IQ/OQ protocols, redlines, FAT/SAT coordination).
Oversee leak testing (hydrostatic/pneumatic) and visual inspections in preparation for qualification.
Supervise and mentor mid-level supervisors, junior technicians, and contractors.
Conduct technical training sessions on CIP valve technologies, hygienic installation best practices, and documentation protocols.
Monitor site safety compliance and enforce clean construction principles in controlled environments.
Bachelor’s degree or diploma in Mechanical Engineering, Process Engineering, or related technical field.
7+ years of experience in sanitary system installation, with a focus on CIP systems, valves, and hygienic routing.
Proven leadership in executing clean utility or process piping projects in GMP-regulated environments.
Familiarity with CIP skid design, control valve logic, and process automation
Proficiency in reading and interpreting P&IDs, isometrics, and valve data sheets
OSHA 30 or equivalent safety certification
Knowledge of validation processes and cleanroom installation protocols
Experience with installation and testing of automated valve blocks (e.g., Burkert, GEA, Alfa Laval, etc.)
Expert knowledge of sanitary valve systems and CIP process architecture
Strong leadership and field execution abilities
Effective communication with cross-functional teams
High attention to quality, compliance, and system integrity
Proactive problem-solving and risk mitigation on-site