Senior Consultant, Cqv

Job Description:

At IPS, we are global leaders in developing innovative solutions for the consulting, architecture, engineering, project controls, procurement, construction management, and CQV of technically complex facilities, primarily in the life sciences industry.
We are looking for a dedicated Senior Consultant, CQV to join our team at our office located in Burlington, Massachusetts. In this role, you will perform cGMP compliance-based services (commissioning, qualification, validation, consulting, etc.)
as developed and defined in project agreements with IPS clients.
You will also follow IPS and client standards and requirements, overall good industry practices for C/Q/V services, and regulatory requirements.
Additionally, you will perform site auditing, quality reviews, and C/Q/V services as required to meet project requirements.

What You'll Do
Demonstrated/recognized areas of expertise by industry (Sterile, OSD, Biotech, Medical Device, etc.
), by equipment/systems (critical utilities, manufacturing equipment, packaging equipment, etc.
), or by validation activity (commissioning and qualification, process, cleaning, CSV, methods, etc.).
Provide working knowledge in the delivery of technical projects in these areas.
Provide consulting-based services in areas of expertise.
Support, train, and provide guidance to validation specialists/engineers in the delivery of C/Q/V services and areas of expertise.
Perform cGMP audits of clients facilities and quality systems.
Write or provide input to C/Q/V documents following established standards and templates, including but not limited to the following: C/Q/V Master Plans Commissioning Forms C/Q/V Protocols and Summary Reports Standard Operating Procedures Risk Assessments Specifications (URS/FRS/DDS) FATS/SATs Perform field/site activities including, but not limited to, the following: Attend and witness FATs and SATs as a representative of IPS clients.
Execution of commissioning forms and witnessing vendor start-up and testing.
Execution of C/Q/V protocols.
Walkdown and verification of system drawings (P&IDs, as-builts, etc.)
Compile data and prepare reports for completed C/Q/V activities including ETOPs, protocol data packages, etc.
Assist in non-conformance and out-of-specification investigation and resolution of problems and issues encountered during field execution activities.
Audit project deliverables to ensure compliance with established standards.
Review the work of the assigned project team.
Be self-sufficient and effectively work with limited supervision.
Read, understand, and utilize IPS Best Practices and SOPs for the delivery of client services.
Perform work to meet IPS budget requirements, meet personal billability goals, and quality standards.
Provide consistent, complete, and timely feedback and reports to IPS project leaders, project managers, or management of project status and issues Assist the project leader and/or project manager with project management activities, (schedule, attend/lead meetings, maintenance of budgets/deliverables, etc.).
Assume PL/PM responsibilities as requested and required to meet project requirements.
Act as an IPS representative for developing new company-wide business opportunities and continue to support repeat business.
Develop client relationships and act as IPS liaison (point of contact) on project/client sites.
Maintain professional conduct and deliver services in a professional and acceptable fashion.
Assist in recruiting new staff members and promoting IPS to potential hires.
Make recommendations to IPS for possible project and procedural improvements.
Stay current (training, reading, professional organization involvement) with industry trends and current C/Q/V methodologies.
Present at industry/trade organization seminars.
Other duties as assigned Qualifications & Requirements: Bachelors degree in Engineering or a related discipline or an equivalent technical degree.
15+ years of experience in Pharmaceutical, Biotech, Medical Device Design, Construction, Commissioning, Validation, or QA.
Experience in writing and execution of Master Plans, PFC, FC, IQ, OQ, and PQ forms and protocols for GMP Utilities, Equipment, Systems, and Software.
Experience with Cleaning, Process, Computer System, Methods, and other validation activities and processes.
General exposure and experience in the discipline of GMP/Validation with a knowledge and understanding of pharmaceutical Design/Build/Commission/Validate processes and how they relate to regulatory requirements and cGMP regulations within the E.U.
and U.S. FDA, and international Standards and guidance (ASTM, ICH, ISPE, etc.).
Experience with Risk-Based Approach to Commissioning and Qualification.
Context and Safety
This position will have up to 100% travel to the site, or as required by the assigned project.
You may be assigned to the client site for an extended period.
Overnight travel or staying in the city of the Clients location is possible depending on the assignment.
Travel will be per the IPS Travel Policy, client-specific travel policy, or project-specific travel plan.
You may visit active construction sites and will be required to take site safety training and adhere to site safety rules.
This position is a safety-sensitive position.
The employee is designated for field work and attends activities at client sites where they work in construction, process, packaging, manufacturing, research, or other "non-administrative" areas.


About Us:
IPS, a Berkshire Hathaway Company, is a global leader in developing innovative business solutions for the biotechnology and pharmaceutical industries.
Through operational expertise and industry-leading knowledge, skill, and passion, IPS provides consultancy services, architecture, engineering, project controls, construction management, and compliance services that allow clients to develop and manufacture life-impacting products.
Its newest acquisition, Linesight, specializes in cost, schedule, risk, program, and project management services in various market sectors, including data centers, life sciences, and high-tech industries.
With the addition of Linesight, IPS has over 3,000 professionals in over 45 offices across 17 countries in the Americas, Europe, Asia Pacific, Southeast Asia, Australia, and the Middle East.


Specialties

Process Architecture, Process Design, Engineering, Construction, Commissioning, Qualification, LEAN Project Delivery, Strategic Master Planning, Energy Conservation Management, Project Controls, Program/Project Management, Operations/Logistics Strategy and Planning, EPCMV and Staffing Services.


All qualified applicants will receive consideration for employment at IPS without regard to race; creed; color; religion; national origin; sex; age; disability; sexual orientation; gender identity or expression; genetic predisposition or carrier status; veteran, marital, or citizenship status; or any other status protected by law.
IPS is proud to be an affirmative action and equal opportunity employer.


Attention Search Firms / Third-Party Recruiters: IPS is not seeking assistance or accepting unsolicited resumes from search firms for employment opportunities with IPS.
Regardless of past practice, all resumes submitted by search firms to any employee at IPS via email, the Internet, or directly to hiring managers at IPS in any form without a valid written search agreement in place for a specific position will be deemed the sole property of IPS, and no fee will be paid in the event a candidate is hired by IPS as a result of the referral or through other means. #LI-MG1