Hybrid Project Manager- GMP/Pharmaceutical Enviornment - Neshanic Station, United States - CBRE

CBRE Neshanic Station, United States

3 weeks ago

Description

CBRE Global Workplace Solutions (GWS) works with clients to make real estate a significant contributor to organizational productivity and performance.

Our account management model is at the heart of our client-centric approach to delivering integrated real estate solutions.

Each client is entrusted with a dedicated leader and is supported by regional and global resources, demonstrating the industry's most robust platform.

CBRE GWS delivers consistent, measurably superior outcomes for our clients at every stage of the lifecycle, and across industries and geographies.

About the role

The purpose of this position is to coordinate individual, multi-discipline real estate project solutions for a pharmaceutical client, with direct accountability for project delivery.

Some of the work may be in regulated areas such as laboratories, environmentally-controlled areas, and production areas and it would be helpful, although not required, that the candidate is familiar with pharmaceutical good manufacturing practices (GMP) including commissioning processes.

The work will include civil, infrastructure, structural, and interior projects in administrative, laboratories, production, and warehouse areas, regulated and non-regulated environments, and plant utility areas.

What youll do

Manage all facets of project management (budget, schedule, procurement, quality & risk) including planning, design, construction, occupancy and closeout.

Demonstrate capability to read, understand and apply standard to documents affecting real estate projects, including but not limited to: agreements/contracts, leases, work letters, project charters, surveys and drawings.

Interact directly with clients to define project requirements.

Prepares scope of work, project delivery resource requirements, cost estimate & budget, work plan schedule, quality control, and risk identification.

Identify project delivery resources from pre-qualified lists or through individual project qualification process; conducts standard request for proposals; completes bid analysis; recommends resources to clients.

Implement communication plan for meetings and written reports/meeting minutes to keep client and project resources advised.
Implement project documentation governance aligned with company and Client requirements. Ensure project data integrity and documentation is accurate, timely and coordinated.
Supervise progress of each project against goals, objectives, approved budgets, approved timelines. Reports status and variances. Ensure objectives, budget and schedule are met.
Implement change management routines to assess change requests, make recommendations, secure client approvals, and issue change orders.

Demonstrate ability to identify project risks, develop risk mitigation and contingency plans, and implement action plans to reduce or eliminate project risks.

What youll need

Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
Preferred Bachelor's degree. No less than four years of related experience or training.
PMP (US and/or Canada) and LEED AP preferred.
Excellent written and verbal communication skills. Strong interpersonal and problem solving skills.
Requires knowledge of financial terms and principles.
Ability to comprehend, analyze, and interpret documents. Ability to troubleshoot problems involving several options in situations.
Ability to read and understand architectural drawings. Knowledge in MS Project, leases, contracts, and construction practices.
Decisions made with detailed understanding of procedures, company policies, and business practices to achieve general results and deadlines.
Why CBRE?

We value a culture of respect, integrity, service and excellence crafts our approach to every opportunity We are guided by the needs of the cities we inhabit, the communities we build, and the world we thrive in.

Competitive pay and benefits including Medical, Dental, Vision, PTO, 401k, and more that start 1st of the month. Internal advancement available after 6 month mark.
FORTUNE Most Admired Company #1

in real estate for third consecutive year;

Ten

years in a row on the list.
Forbes

Named one of the

best large employers

in America and one of the

World's Best Employers

#J-18808-Ljbffr

Technical employee for finished goods

1 week ago

Apex Dynamics Zarephath, United States

At Bayer, we are visionaries and determined to overcome the greatest challenges of our planet and contribute to a world where access to enough food and adequate medical care are no longer unattainable goals. We do this with energy, curiosity, and pure dedication, constantly learn ...
Document Specialist II

3 days ago

KYYBA Branchburg Township, United States

Job Description · Job DescriptionJob Title: Document Coordinator II · Pay Range: $20-$22/hr · Contract: 6-month W2 contract (potential to extend) · Work Location: Branchburg, NJ 08876 · Work Schedule: 6:30am-8pm (Mondays to Friday, OT as needed - Depends on business needs) · Docu ...
Senior Quality Engineer

2 weeks ago

GForce Life Sciences Raritan, United States

Senior Quality Engineer, Medical Devices · Our client has engaged GForce to identify a Senior Quality Engineer with in-depth understanding of medical device quality system requirements, with specific experience in applying the following: Medical Device product risk management, Me ...
Junior & Senior Consultant- MES PAS-X MBR

1 week ago

Capgemini Engineering Raritan, United States

Position Overview: · We have 2 open roles. 1 for Junior Consultant (0-3 years), For Junior role we will also consider College Graduate who can be trained on the job. and 1 for Senior Consultant (3-8 Years) · As a MES PAS-X MBR Modeler you will play a critical role in the design, ...
Associate Director-Quality Assurance

1 week ago

Clinical Dynamix Raritan, United States

Associate Director-Quality Assurance (QA-CMC); Hybrid (There is an opportunity for the position to be bumped up to a Director level (depending on experience) and salary adjusted accordingly) · Company is seeking a highly experienced, motivated, and innovative quality leader with ...
Biology laboratory technician

1 week ago

Nebula Ventures Linden, United States

Specialist Quality Control Services (Microbiology) (m/f/d) · We are looking for a Specialist Quality Control Services (Microbiology) (m/f/d) to join our Quality Control department starting in July 2024 on a part-time basis (30 hours/week). · About us: · Dr. Pfleger Arzneimittel G ...
Lab Tech Ops

2 weeks ago

Dawar Consulting Somerville, United States

Job Description · Our client, a world leader in Pharmaceuticals & In vitro diagnostics (IVD), is looking for a "Lab Tech Ops - 1st Shift". for Branchburg, NJ · Job Duration: Long Term Contract(Possibility Of Extension) · Responsibilities: Perform weighing and dispensing of raw ...
MBR Engineer

3 weeks ago

Ztek Consulting Raritan, United States

Job Title: MBR Engineer · Location: Raritan, NJ · Job Description: · Position Overview: As a Senior MES PAS-X MBR Modeler you will play a critical role in the design, implementation, and maintenance of our MBR using Werum PAS-X V2/V3. You will ensure compliance with industry s ...
Analytical Validation Engineer

4 weeks ago

Piper Companies Raritan, United States

Piper Companies · is looking for an · Analytical Validation Engineer · to support commissioning and decommissioning activities for a major pharmaceutical company in the · Raritan, NJ area. · Responsibilities for the · Analytical Validation Engineer · include: · Experience ...
QC Biochemistry Analyst

1 day ago

Planet Pharma Hopewell, United States

6-month initial contract · 3 openings · Perform QC biochemistry laboratory assay validation and transfer activities to support GMP manufacturing, testing and release of material, intermediates and finished products under FDA/EU regulations, applicable International Regulations, c ...
Scientist 3

2 weeks ago

Pioneer Data Systems Raritan, United States

Position Details: · Our client, a world-leading Pharmaceutical Company in Spring House, PA is currently looking for a Bioprocess Manufacturing Associate to join their expanding team. · Job Title: Bioprocess Manufacturing Associate / Cell Therapy, CAR-T · Duration: 6 months contr ...
Scientist 2

2 weeks ago

Pioneer Data Systems Raritan, United States

Position Details: · Our client, a world-leading Pharmaceutical Company in Raritan, NJ is currently looking for a Microbiologist II to join their expanding team. · Job Title: Microbiologist II / Pharma Manufacturing · Duration: 12 months contract, extendable up to 24 months · Loca ...
CSV Specialist

1 day ago

eTeam Raritan, United States

Provide compliance leadership, direction and oversight to project teams in the area of Computer System Validation Responsible for the quality oversight of GxP regulated computerized systems (e.g. manufacturing plant systems, laboratory systems and enterprise applications). Manage ...
Engineer 2

4 weeks ago

Pioneer Data Systems Raritan, United States

Position Details: · Our client, a world-leading Pharmaceutical Company in Raritan, NJ is currently looking for a CMMS Specialist (Maximo preferred) to join their expanding team. · Job Title: CMMS Specialist (Maximo preferred) / Pharma Industry · Duration: 9 months contract, ex ...
Quality Systems Specialist

2 days ago

Kenvue Skillman, United States

Kenvue is currently recruiting for: · Quality Systems Specialist · Who we are · At Kenvue, we realize the extraordinary power of everyday care. Built on over a century of heritage and rooted in science, we're the house of iconic brands - including Neutrogena, Aveeno, Tylenol, L ...
Sr. Director, External Quality

20 hours ago

Kenvue Skillman, United States

Go to the main content section. · Investors · Healthcare Professionals · Media · Careers · Put your passion to work · Come work at the forefront of science - and help the brands you grew up with grow and evolve into the next generation. · Explore Students & Recent Graduates Opp ...
Director, Global Project Management Center of Excellence

5 days ago

J&J Family of Companies Skillman, United States

Director, Global Project Management Center of Excellence & Analytics W · Description · Kenvue is currently recruiting for: · Director, Global Project Management Center of Excellence & Analytics · This position reports to the Sr Director, Global Project & Portfolio Management Offi ...
Associate Director, Operations Compliance and Investigations Management

2 weeks ago

Legend Biotech Corp Raritan, United States

Company Information · Legend Biotech is a global biotechnology company dedicated to treating, and one day curing, life-threatening diseases. Headquartered in Somerset, New Jersey, we are developing advanced cell therapies across a diverse array of technology platforms, including ...
Analyst, Laboratory Quality Control

2 weeks ago

J&J Family of Companies Raritan, United States

Analyst, Laboratory Quality Control (1 of W · Description · Janssen Pharmaceuticals, Inc., a member of Johnson & Johnson's Family of Companies, is recruiting for an Analyst, Laboratory Quality Control - CAR-T in Raritan, NJ · At the Janssen Pharmaceutical Companies of Johnson ...
Associate Director, Operations Compliance and Investigations Management

2 days ago

Legend Biotech US Raritan, United States

Company Information · Legend Biotech is a global biotechnology company dedicated to treating, and one day curing, life-threatening diseases. Headquartered in Somerset, New Jersey, we are developing advanced cell therapies across a diverse array of technology platforms, including ...