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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