919 PROJECT ENGINEER DENMARK
Fecha Publicación:
02/03/2022 0:00:00
Población:
DENMARK
Oferta:
919
Número de Vacantes:
1
Horario:
Descripción:
Our client a leading Pharmaceutical Company is currently searching for a Project Engineer for their company in Danmark area, they are specialised within the Pharma industry. The Project Engineer will be managing a broad spectrum of projects. You will be tasked with execution of projects, scheduling, design review, and organising project charters.



Responsibilities:

• Plan and coordinate project start-up in conjunction with Project Managers, Operation • Managers, and Superintendents
• Maintain contract drawing, shop drawing and submittal controls
• Verify accuracy and completeness of submittal against contract drawings and specifications
• Distribute copies of design drawings and documents to project management team and subcontractors
• Maintain logs for drawings, submittals, change estimates, and requests for information on • Viewpoint
• Assist in project schedule maintenance
• Assist in material expediting
• Attend project meetings; prepare and distribute minutes according to standard format and follow-up on action items
• Prepare and maintain LEED reporting and/or documentation requirements of the LEED • Action Plan (if applicable)
• Maintain and/or assist in documentation of quality assurance and quality control activities.
• Walk project site on daily basis to observe construction sequencing and means and methods used.
• Assist Project Manager in project close-out
• Coordinates and resolves engineering or construction problems with superintendents.
• Reviews design drawings, related vendor drawings and installation instructions and studies interference problems.
• Maintains records of costs and quantity information, evaluates data and prepares applicable reports as requested by project management utilizing established, standardized automation tools.
• Assists with cost estimates and reviews project design and engineering bills of materials to ensure their completeness.
• Assists with field change notices/requests, extra work orders and back charge notices
• Assists in coordination of vendor material deliveries, storage of materials, expediting and engineering reports related to the schedule
• Researches and resolves drawing interpretation problems, applicable codes, conflicts, interference, and errors
• Represent Company at all times with professionalism and a commitment to quality
• Ensure compliance with OSHA regulations to include health, safety, and welfare as appropriate
• Regular and reliable attendance at work
• Other duties as assigned by Company Management


Essential Skills:

• Assists the Project Manager, manage all aspects of a project(s) including the safety, quality, organization, planning, scheduling, subcontractor scheduling, and day-to-day issues, in a manner that results in completion of a project on time, on budget, and a quality that meets or exceeds the customer's expectations.
• Strong knowledge of GMP and regulatory requirements.
• Applied advanced and diverse engineering principles to the design and implementations of major systems, modifications.
• An individual with excellent social, time, and leadership skills
• English fluency , Danish would be an advantage
• Strong problem solver and creative thinker.
• Teamplayer.
• Pro-active thinking.
• Attention to detail
• High level of motivation and strong desire to learn
• Organizational skills and effective time management to succeed in a fast-paced environment.
• Ability to multi-task and meet or beat deadlines
• Ability to interact successfully with all levels of an organization
• Effective communication skills


Job experience:

• Minimum 5-7years + of PE experience.
• Bachelors in Engineering or Science or similar.
• Experience commissioning and qualifying bio-pharmaceutical facilities, systems, and equipment, with project management experience highly preferred.
• Experience with developing user requirements, design specifications, process/product risk assessments, validation requirements, development of testing protocols and test plans, and overall experience with the validation lifecycle is required.
• Experience with CIP/SIP, and aseptic manufacturing is desired.
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VÉRINGER INGENIERÍA AVANZADA
Paseo de Menéndez Pelayo Nº 22
39006 - SANTANDER (CANTABRIA)
942 07 78 41






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