Coordinator 3 - Procurement
1 week ago
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 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.
Pyramid Consulting, Inc. provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, colour, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.
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