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Monday, 25 July 2011
Sunday, 24 July 2011
Project Engineer - Stellenausschreibung
A profile of SartoriusThe Sartorius Group is an internationally leading laboratory and process technology provider covering the segments of biotechnology and mechatronics. In 2010, the technology group earned sales revenue of 659.3 million euros. Founded in 1870, the Goettingen-based company currently employs more than 4.500 persons. The major areas of activity in its biotechnology segment focus on fermentation, filtration, purification, fluid management and laboratory applications. In the mechatronics segment, the company primarily manufactures equipment and systems featuring weighing, measurement and automation technology for laboratory and industrial applications. Key Sartorius customers are from the pharmaceutical, chemical and food and beverage industries and from numerous research and educational institutes of the public sector. Sartorius has its own production facilities in Europe, Asia and America as well as sales subsidiaries and local commercial agencies in more than 110 countries.
What you can look forward to accomplishing
Major function of your position: Project management and engineering responsibilities for assigned bioprocess system projects, including scope definition, vendor management, development of P&ID’s and Major component lists and budget and delivery schedule maintenance. Perform other duties as assigned.
- Engineering specification review and interpretation for customized bioprocess equipment. Major function of your position: Project management and engineering responsibilities for assigned bioprocess system projects, including scope definition, vendor management, development of P&ID’s and Major component lists and budget and delivery schedule maintenance. Perform other duties as assigned.
- Manage inter-company projects for systems fabricated at German manufacturing location.
- Develop P&ID, Major Component List and Vessel Specifications.
- Perform design calculations related to equipment sizing.
- Coordinate project activities between manufacturing and automation partner companies.
- Primary customer interface for all project requirements and activities.
- Manage the on-time and on-budget completion of assigned projects and customer
Preparation of Change Orders for definition of project scope changes.
- Manage project billing plans and profitability to maximize cash flow and control project costs
- Generate FAT test protocols and acceptance criteria based on standardized templates.
- Support FAT/SAT testing for custom equipment
- Field service support
- Preparation and compilation of documentation to support development of turnover package.
- Sales support for proposal development including contract review.
- Some international travel required.
- Travel less than 15%
Skills and experience that you need to bring to our company
Bachelor’s degree from a four year college in an engineering discipline. Chemical, Bioprocess or Mechanical preferred.
- Minimum of 2-5 years project management/engineering experience in the biopharmaceutical industry.
- Experience with upstream and downstream bioprocessing equipment and processes, i.e. cell culture, fermentation and filtration systems.
- Experience specifying instrumentation and process control components in a biopharmaceutical environment, i.e. sensors, valves, pumps, etc.
- Knowledge of pharmaceutical industry standards (cGMP, ASME-BPE, etc.)
Other Skills
- Ability to work proficiently with MS Office products, Microsoft Project, Visio etc.
- Ability to work with AutoCAD, AutoDesk Inventor and AutoDesk Vault Manufacturing.
- Familiarity with SAP or other MRP systems.
- Must be detail oriented with exceptional communication and interpersonal skills.
- Ability to work well in a multi-disciplinary, International team environment.
Keine Details erfasst
Kontakt
Sartorius America
Patricia Sileo
5 Orville Drive Bohemia
11716 New York
T: +1.631.254.4249 ext. 8310
F: +1.631.254.4264 patricia.sileo@sartorius.com
Patricia Sileo
5 Orville Drive Bohemia
11716 New York
T: +1.631.254.4249 ext. 8310
F: +1.631.254.4264 patricia.sileo@sartorius.com
Job Posted at : https://recruitingapp-609.umantis.com/Vacancies/2007/Description/2/Default?Redirect=true&
Engineer
Title: Engineer
Job ID: 953984
Start Date: 07/22/2011
Job ID: 953984
Start Date: 07/22/2011
Location:United States-Massachusetts-Andover
Org Marketing Statement | |||
Pfizer Inc: Working together for a healthier world Founded in 1849, Pfizer is the world's premier biopharmaceutical company taking new approaches to better health. We discover, develop, manufacture and deliver quality, safe and effective prescription medicines to treat and help prevent disease for both people and animals. We also partner with healthcare providers, governments and local communities around the world to expand access to our medicines and to provide better quality health care and health system support. At Pfizer, colleagues in more than 90 countries work every day to help people stay happier and healthier longer and to reduce the human and economic burden of disease worldwide. | |||
Role Description | |||
Provide engineering technical support related to the maintenance, installation, startup/commissioning, testing, and qualification of process and automated equipment and systems within a biopharmaceutical manufacturing facility. | |||
Responsibilities | |||
Candidate will be responsible for the design, troubleshooting and qualification of biopharmaceutical manufacturing equipment and control systems. Work includes development of startup documents, commissioning plans, User Requirement Specification (URS), Functional Requirement Specification (FRS), Configuration Specification (CS), validation/qualification documents, execution of commissioning and qualification and assisting maintenance. The position may require equipment maintenance history review, investigation and audit support, process/component improvement project support, and reliability engineering support. | |||
Qualifications | |||
Candidate must have a BS/MS in chemical or mechanical engineering or relevant discipline. Candidate must have a minimum of 5 years of experience working in a biopharmaceutical or pharmaceutical manufacturing facility. Candidate must have a working knowledge of cGMP systems and practices. Candidate must be able to work across functional areas such as operations, maintenance, quality and regulatory. Good communication skills, verbal and written, are required. Must be willing to be on call or work off-shift as needed. Working knowledge with the following systems and applications is preferred: Allen-Bradley PLC Control Logix Visual Basic GE iFix and iHistorian Oracle database or SQL DH+ Control Net AutoCAD Visio MS Office Products | |||
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