Project Planner/ Scheduler - PDP - USA
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Project Delivery Partners
San Francisco, CA, US
Summary
Support the EPCmV group in planning and executing large-scale CAPEX projects by providing critical decision-making information. Responsibilities include managing master schedules, performing risk analysis, and coordinating schedule inputs from multiple contractors and vendors.
Job Description
Job Title: Project Planner (Intermediate & Senior)
Sector: Biotechnology / Life Sciences
Location: USA (Remote & On-site)
Job Description:
PDP is hiring Intermediate & Senior Project Planners to support multiple projects both supporting & leading planning teams with relevant clients in the United States.
These individuals shall report to the PDP Project controls manager. The Planners, in conjunction with the relevant planning teams, have a primary objective to support the engineering, procurement, construction and Commissioning (EPCmV) group in the planning, and execution of large-scale CAPEX projects by providing management with critical, decision-making information that ensures projects deliver on time.
The Project Planner function includes advanced planning, scheduling, progress measurement, change management implementation and analysis that may involve a major project or several smaller projects. A thorough understanding is required of policies, methods, and procedures that includes advanced Planning and Scheduling techniques, Risk Analysis, Risk Management, and support of project objectives. The Planner will provide expertise and best practice implementation in the workplace for the region with regard to the planning and scheduling discipline.
Main Responsibilities
- Expertise in project controls and time/schedule management is required preferably within the Pharma/ Biotech or associated sectors.
- Expert experience level using project scheduling tools (MS Project, Primavera P6), Excel, PowerPoint and Pertmaster.
- Ability to coordinate/organize multiple sources of schedule inputs/performance data into a master schedule platform and deliver project/program status reports as required.
- Implement Project Planning/Scheduling strategy, plans and procedures, reflecting both Company and contractor roles, responsibilities and expectations.
- Coordinate the development and implementation of project Work Breakdown Structures (WBS).
- Perform probabilistic analysis on integrated schedules and contractor schedules.
- Conduct the required project schedule analysis, critical path analysis and schedule risk analysis for the project as a whole.
- Analyze deviations from the baseline in the Project Master schedule highlighting bottlenecks / delays and propose corrective actions.
- Prepare the Integrated Planning / Scheduling contribution to the Monthly Project Report and specific reports / presentations.
- Analyze and highlight the overall schedule impact of any variance / change order.
- Prepare resourcing plans for the overall and individual project phases, identifying any excessive peak numbers and making recommendations for peak leveling.
- Ensure that schedule related data from vendors, suppliers, engineering and construction contractors is aligned and integrated to the overall Integrated Master Schedule.
- Ensure the accuracy and completeness of the schedules produced, maintaining independence as a planning engineer when advising on issues requiring judgment.
- Ability to balance multiple projects executed in multiple locations and by multiple contractors.
- Excellent communication and interpersonal skills
- Develops good working relationships with project team
- Other work as needed in support of successful project delivery.
Qualifications
- 5 - 10 years of experience in CAPEX projects with roles in planning/scheduling: preferably in Biotech or Pharmaceutical industries.
- Significant experience in schedule set up, baselining, monitoring and controlling on large scale projects across the all phases of EPCmV.
- Comprehensive understanding of risk and change management.
- Demonstrated problem-solving ability in cross-functional environment.
- Advanced MS Excel.
- Software systems and packages including Primavera P6
- Ability to work within a high-performance, cross-functional organization with extremely tight timelines and aggressive goals.
- Strong interpersonal and communication skills.
- Good Level in English, written and spoken.
PharmEng Technology, now part of Efor Group, leader in Compliance Engineering, is a leading provider of technical services and solutions to the pharmaceutical, biotechnology, and healthcare industries. With over 25 years of experience, we specialize in Commissioning, Qualification, and Validation (CQV) services for facilities, utilities, equipment, and processes.
As part of Efor’s global network of 3,000 experts across 12 countries, we are better equipped than ever to deliver innovative and comprehensive solutions tailored to the unique needs of clients worldwide. This integration strengthens our ability to combine global expertise with local proximity, positioning PharmEng as a strategic partner for the industry’s most prominent players.
Our team of highly skilled professionals brings a wealth of industry expertise and knowledge to every project, ensuring that our clients receive the highest quality services and solutions. We pride ourselves on our ability to provide flexible, innovative, and cost-effective solutions that meet our clients' unique challenges.
At PharmEng Technology by Efor, we are committed to delivering excellence in everything we do. We work closely with our clients to understand their goals and objectives, developing customized solutions that deliver measurable results. Our focus on quality, safety, and compliance ensures that our clients can trust us to meet their most critical needs.
Specialties: PharmEng Technology specializes in the planning, design, construction, and validation of Health Care, Laboratory, API Pharmaceutical, and Biotechnology facilities and equipment, including computer systems. We provide professional services that meet both regulatory and business demands, following current Good Manufacturing Practices (cGMP), Good Engineering Practices (GEP), and Good Laboratory Practices (GLP).
Company size
201-500 employees
Industry
Pharmaceutical Manufacturing
Org type
Privately Held
Headquarters
Toronto, Ontario
PharmEng Technology, now part of Efor Group, leader in Compliance Engineering, is a leading provider of technical services and solutions to the pharmaceutical, biotechnology, and healthcare industries. With over 25 years of experience, we specialize in Commissioning, Qualification, and Validation (CQV) services for facilities, utilities, equipment, and processes.
As part of Efor’s global network of 3,000 experts across 12 countries, we are better equipped than ever to deliver innovative and comprehensive solutions tailored to the unique needs of clients worldwide. This integration strengthens our ability to combine global expertise with local proximity, positioning PharmEng as a strategic partner for the industry’s most prominent players.
Our team of highly skilled professionals brings a wealth of industry expertise and knowledge to every project, ensuring that our clients receive the highest quality services and solutions. We pride ourselves on our ability to provide flexible, innovative, and cost-effective solutions that meet our clients' unique challenges.
At PharmEng Technology by Efor, we are committed to delivering excellence in everything we do. We work closely with our clients to understand their goals and objectives, developing customized solutions that deliver measurable results. Our focus on quality, safety, and compliance ensures that our clients can trust us to meet their most critical needs.
Specialties: PharmEng Technology specializes in the planning, design, construction, and validation of Health Care, Laboratory, API Pharmaceutical, and Biotechnology facilities and equipment, including computer systems. We provide professional services that meet both regulatory and business demands, following current Good Manufacturing Practices (cGMP), Good Engineering Practices (GEP), and Good Laboratory Practices (GLP).
Company size
201-500 employees
Industry
Pharmaceutical Manufacturing
Org type
Privately Held
Headquarters
Toronto, Ontario