Immediate need for a talented Commissioning/Qualification Specialist / Specific Commissioning and Validation support. This is a 12 Months Contract opportunity with long-term potential and is located in Warren, NJ (Onsite). Please review the job description below and contact me ASAP if you are interested.
Job ID: (phone number removed)
Pay Range: $55- $61/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:
Commissioning and Qualification:
Administer change control activities and corrective and preventive actions.
Review, approve, and execute test protocols, validation deliverables, and plans as needed.
Author, review, and approve SOPs, work practices, and other procedural documents.
Provide input and guidance for change strategy, risk assessment, testing and compliance gaps.
Serve as an SME for change controls, investigations, CAPAs, and audits, as applicable.
Promotes and provides excellent customer service and support:
Regularly reviews, prioritizes, and promptly responds to customer equipment qualification and support requests.
Provides technical support and guidance on equipment commissioning and qualification. Interfaces with customers to ensure all expectations are met.
Maintains a positive relationship with all the members of the Equipment Commissioning & Qualification department and site customers while promoting a positive team environment.
Communication and Management of Timelines:
Ensures timely completion of equipment commissioning and qualification projects, individually and/or with support of contracted personnel.
Develops an effective mechanism for communicating the current status of all manufacturing and laboratory equipment to affected stakeholders.
Continually seeks opportunities to increase internal client satisfaction and deepen client relationships.
Regulatory Responsibilities:
Ensures manufacturing and laboratory facilities and utilities are maintained in compliance with GMP and other Client standards and regulations.
Acts as equipment commissioning and qualification SME in internal and regulatory audits.
Key Requirements and Technology Experience:
Advanced knowledge of cGMP pertaining pharmaceutical facilities, utilities, and equipment.
Advanced knowledge of pharmaceutical manufacturing and utilities that support cell therapy clinical manufacturing.
CRITICAL FOR THE JOB - Advanced knowledge of commissioning and qualification of clean manufacturing facilities, material pass-throughs, AHUs, compressed gas systems, liquid nitrogen supply systems, autoclaves, isolators, filling and capping equipment, and airflow visualization studies.
Understanding of scheduling and execution fundamentals.
Strong written and verbal communication skills.
Excellent interpersonal skills with experience dealing with a diverse workforce.
Strong multi tasking ability in conjunction with proven organizational skills. Ability to organize assigned tasks in a fast-paced environment and concurrently monitor tasks and assignments with others that may impact timely completion. Ability to effectively manage multiple tasks and activities simultaneously.
High proficiency in Microsoft Office Suite – Word, Excel, PowerPoint and Outlook. Innate ability to learn new software, such as corporate intranet and enterprise business.
Working knowledge of scheduling software and systems, and inventory management systems.
Ability to create and analyze meaningful metrics.
Competencies:
Professional Knowledge
Problem Solving
Team Player / Building Relationships
Multi tasking
Customer Focus
Action and detail oriented
Active Listening
Decisive
CRITICAL FOR THE JOB - BS in Engineering required. Must be able to read and understand construction and mechanical drawings and P&IDs.
Minimum of 7 years of experience in FDA-regulated industry.
Minimum of 3 years of experience executing projects of low to medium complexity.
Strong background and experience in laboratory and manufacturing operations.
Knowledge of cGMP in the pharmaceutical industry.
CRITICAL FOR THE JOB - Thorough knowledge and hands-on experience in commissioning and qualification of common utilities, such as DI water, compressed gases, process air, liquid nitrogen supply systems, AHUs, and autoclaves.
CRITICAL FOR THE JOB - Thorough knowledge of and hands-on experience with operation and qualification of cell therapy manufacturing equipment, including isolators, vial fillers, and vial cappers.
CRITICAL FOR THE JOB - Knowledge and hands-on experience with airflow visualization (smoke studies).
Strong computer skills, knowledge of calibration management and environmental monitoring systems preferred.
Strong problem-solving skills, strong verbal and written communication skills, and the ability to work independently.
Experience interacting with regulatory agents, external and/or internal auditors in a compliance audit environment with direct interaction including face to face interaction and response to audit questions.
Strong interpersonal and communication skills, a team player willing to work in an environment where individual initiative, accountability to the team, and professional maturity are required.
Our client is a leading Pharmaceutical 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.
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, color, 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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