Coordinator 3 – Procurement

Immediate need for a talented Coordinator 3 – Procurement. This is a 12+months contract opportunity with long-term potential and is located in Wilson, NC (Onsite). Please review the job description below and contact me ASAP if you are interested.
 
Job ID:24-48320
 
Pay Range: $25 - $32/hour.  Employee benefits include, but are not limited to, health insurance (medical, dental, vision), 401(k) plan, and paid sick leave (depending on work location).
 
Key Responsibilities:

• Ensures equipment usage is coordinated to support schedule development and avoids mutually exclusive activities are avoided.
• Lead and supervise a team of Piping/Mechanical, Electrical and Instrumentation technicians to support commissioning activities.
• Coordinating the interfaces of commissioning execution (Construction Management Contractor, Utilities, Qualification, Automation, Instrumentation, Electrical, etc.)
• Lead daily coordination meetings to fine-tune the commissioning execution with all involved parties.
• Tracking and reporting of commissioning progress.
• Tracking of deficiencies, including planning and executing the remediation actions.
• Ensuring compliance of the commissioning activities with qualification requirements where test results are subject of leveraging.
• Reviewing commissioning test documents prior to client approval.
• Technical SME – provide mentorship for team members in supporting issue resolution and consistency in approach across the team.
• Co-ordinates the management of change.
• Ensuring full compliance with safety procedures and ensuring permits, SPA, RAMS are in place for area commissioning activities.
• Adhere to and monitor the schedule and timeframes milestones within the schedule. Work with CQV scheduler to prepare and communicate 4 week lookahead plans and micro-schedules as required.
• Manage and close out of exceptions during static and dynamic commissioning.

Key Requirements and Technology Experience:

• Key Skills:Procurement, Pharma, Purchasing .
• BSc qualification (Engineering related discipline).
• At least 10 years’ experience in a Drug Substance Biotech manufacturing environment.
• At least 10-15 years C and Q experience and a proven track record within a cGMP regulated environment.
• At least one major Biotech project as a C and Q Lead.
• Planning and organizing skills.
• Excellent interpersonal and influencing skills.
• Excellent written and oral communication skills.
• Experience of Digital C and Q systems.
• Strong knowledge of Commissioning and Qualification Regulations and Standards.
• Ability to work under pressure and meet deadlines.
• Ability to work in a team, coordinate colleagues, contractors and consultants.
• Strong initiative and the ability to proactively identify required tasks.
• An organized approach to working, task prioritization and time management.
• Special Credentials / Certifications Required:
• Must have C and Q start up experience of Large Molecule Downstream processes
• Total working Experience:10+ years C and Q
• Education Required: Bachelor’s degree is required, in Engineering
• Will travel to Ireland up to possibly 3 times in the first 6 months for training, that can be 1-2 weeks long in duration. Travel will be reimbursed/covered.
• Will also need to be able to travel to PA 25% of the time in the first 6 months of the position.

Our client is a leading Healthcare Industry, and we are currently interviewing to fill this and other similar contract positions. If you are interested in this position, please apply online for immediate consideration.
 
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