C&q Coordinator

Proclinical is seeking a highly motivated and detail-oriented individual to join our clients team as a C&Q Coordinator.

This a 6 Month contract with the possibility of an extension.

**Responsibilities**:

- The CQ Execution Coordinator is responsible for supporting the planning, execution and supervision of the Commissioning and Qualification field activities. To support meeting the agreed objectives regarding schedule and functionality according to URS, GMP, Safety and Environmental objectives including all relevant site local and global procedures. To support the implementation of the clients CORP-35 strategy and Kneat platform.
- Reporting to the Project CQV Manager.
- Coordinating the planning and scheduling of commissioning and qualification activities with the construction interface, with the Building/ Building Services interface, and with other disciplines (Automation, Electrical, Instrumentation, User operation and Site engineering, etc.)
- Facilitate coordination execution meetings, providing an update on issues, risks and ‘showstoppers’

Support HSE matters in:

- Implementation of HSE Plan and PTW procedures
- Awareness training & implementation of LOTOTO and Safe Work Method
- Statements/Risk Assessments
- Housekeeping
- Audits with support from HSE manager

Support overall field coordination of Commissioning & Qualification activities:

- With CQV Manager and Workstream CQV Leads
- Schedule, Priorities and Execution Matters
- With CQ Qualification Lead - Lifecycle and Test documentation readiness
- With Project Quality - Quality matters, Incidents, ECN
- With Automation - Field Automation issues / readiness
- With Construction - for Mechanical Completions
- With Technical Package Leads - System Readiness, trouble shooting
- Support look-ahead schedule
- Support measurement of ‘Actual’ progress
- Schedule forecasting
- Support coordinating the commissioning field team including commissioning and qualification engineers, AEI experts, user and site engineers, document controllers and external vendors and contractors
- Support troubleshooting and resolution of commissioning related issues in a timely manner with CQ area leads
- Support the investigation, implementation & closure of deficiencies and deviation
- Support schedule remediation activities
- Reviewing the commissioning test reports and ensuring their completeness post execution
- Ensuring the fulfilment of the pre-requisites prior to starting commissioning execution (Mechanical Completion, availability of tools, utilities, spares, document pre-requisites, etc.)
- Ensuring sufficient safety training for all involved persons
- Performing daily coordination meetings to fine-tune the commissioning execution with all involved parties
- Support document preparation including templates and execution scope according to CORP-35 & Kneat implementation

**Experience**:

- Strong knowledge and experience of Process Commissioning and Qualification.
- Management: Compliance with schedule at a system and area level with the planned resource levels.
- Safety: No lost time accident
- Quality: well executed testing with minimum rework and re-execution.
- Quality: all incidents resolved to Client satisfaction.
- Experience in leading Commissioning and Qualification activities.
- Languages: German preferential. English - fluent in speaking and writing.
- Experience: Minimum 10 yrs.
- Proven experience, expert knowledge in ASTMe2500
- Kneat Power User
- Broad knowledge of engineering disciplines, commissioning, compliance, qualification and quality aspects of biopharma or pharmaceutical manufacturing

**Job Types**: 100%, Temporary / Staffing
Contract length: 6 months

**Salary**: CHF100.00 - CHF120.00 per hour

**Benefits**:

- Company pension

Schedule:

- 8 Hour Shift
- Monday to Friday
- Overtime

Supplemental pay types:

- Overtime pay

Ability to commute/relocate:

- 3930 Visp, VS: Reliably commute or planning to relocate before starting work (preferred)

Work Location: One location

Expected Start Date: 01/06/2023