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Senior Engineer, Process Engineering. Job in Solothurn, Switzerland in Biogen. Nelest.com
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Senior Engineer, Process Engineering

col-narrow-left   

Job ID:

23173

Location:

Solothurn 

Job function:

Engineering
col-narrow-right   

Posted:

03.11.2016

Employment Type:

Full time

Industry:

Healthcare / Pharma
col-wide   

Title:

Senior Engineer, Process Engineering

Job Description:

JOB PURPOSE:

This role will be functionally responsible for process engineering work packages in discrete process areas of the LSM (Large Scale Manufacturing) project, specific to cell culture, purification, or process utilities.
Specific responsibilities include assistance with the development of design and specification of new process systems and equipment, equipment and installation procurement, process construction oversight, factory and site acceptance testing, and commissioning, including cost, schedule, and scope definition within a framework of safety, quality, governance, and good engineering practices.
This position will drive the commissioning planning, document generation, and hands on field commissioning and validation of the respective process area, including training on new manufacturing associates that will be utilized for the commissioning efforts.

MAIN ACCOUNTABILITIES:

1. Execute process engineering activities to ensure effective scope development from design through detailed engineering, construction, testing, commissioning, and validation.
2. Lead the definition of user requirements in conjunction with the project stakeholders.
3. Generate process P&IDs (Piping & Instrumentation Diagram), specify and procure new equipment and systems, and manage change control for process systems throughout the Project.
4. Review, approve, and provide oversight for submittals, system piping layouts, general arrangements, and isometric drawings.
5. Coordinate with all other project stakeholders to ensure overall coordination of the job, including resources, execution strategies
6. Provide construction support oversight and lead commissioning within assigned focus areas, including equipment inspections, factory acceptance testing (FAT), site acceptance testing (SAT), and field verification and revision of equipment and system drawings to as-built status.
7. Ensure effective execution of equipment and system mechanical completion walk-downs, safety walk-downs, system energization plans, lock-out tag-out, development of commissioning plans and execution of commissioning, review and approval of Equipment Installation Manuals, lead the turnover of systems for subsequent validation activities, and provide technical support through validation activities
8. Implement internal policies, procedures, and specifications
9. Interface with stakeholders on the Project to ensure the design, execution, and delivery are in accordance with Global Engineering, Quality, Environmental, and Safety procedures.
10. Prepare status updates that will be reported in project governance meetings and communications to senior company management on project progress, including cost, schedule, safety, quality etc.
11. Development of skills and behaviors that align with the overall project goals, company expectations of potential future opportunities, and personal desire towards career expectations.
12. Attend industry conferences, seminars, and training events to remain abreast of new technology and engineering / construction trends in the biotech and pharmaceutical industries

Job Requirements:

Qualifications- A minimum of 10 years related experience and/or training, or an equivalent combination of education and experience - Demonstrated capability to provide engineering technical support for all cell culture, purification, and pharmaceutical processing equipment and plant utilities. - Must possess good communication and relationship skills - Have been involved in engineering, construction, commissioning, and validation in a pharmaceutical / biotech-manufacturing environment - Be able to travel up to 20%. For the first year, the travel requirements may approach 50%. - Languages: English fluent, fluent in German and/or French and/or Italian preferred Education- Bachelor's Degree in relevant field such as Chemical Engineering, Mechanical Engineering, Bio-Engineering About BiogenBiogen (NASDAQ: BIIB) is a biotechnology leader that discovers, develops and delivers innovative therapies to improve the lives of patients with neurodegenerative diseases, hematologic conditions and autoimmune diseases. Patients worldwide benefit every day from our medicines for multiple sclerosis (MS) and hemophilia.

Founded in 1978, Biogen is one of the world's oldest biotechnology companies. Our development pipeline is focused on areas of high unmet medical need, as we pursue new therapies for patients suffering from diseases with few or no treatment options. These include programs for secondary progressive MS, Alzheimer's Disease, spinal muscular atrophy, lupus and amyotrophic lateral sclerosis (ALS), amongst others.

With approximately 7,500 people worldwide, Biogen is truly a global organization. We are headquartered in Cambridge, Massachusetts, which is home to our research operations. Our international operations are based in Zug, Switzerland and we have world-class manufacturing facilities in North Carolina and Denmark. We offer therapies globally through direct affiliate presence in 30 countries and a network of distribution partners in over 50 additional countries.

All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability or protected veteran status.

Please be advised that all legitimate correspondence from a Biogen employee will come from '@biogen.com' or '@biogenidec.com' email accounts.

Company Info
Biogen

Cambridge, MA, United States

Phone: +1 781-464-3260, +1 781-464-3260
Web Site: www.biogene.com

Company Profile

Company Info


Biogen
Cambridge, MA, United States
Phone: +1 781-464-3260, +1 781-464-3260
Web Site: www.biogene.com

Senior Engineer, Process Engineering

col-narrow-left   

Job ID:

23173

Location:

Solothurn 

Job function:

Engineering
col-narrow-right   

Posted:

03.11.2016

Employment Type:

Full time

Industry:

Healthcare / Pharma
col-wide   

Title:

Senior Engineer, Process Engineering

Job Description:

JOB PURPOSE:

This role will be functionally responsible for process engineering work packages in discrete process areas of the LSM (Large Scale Manufacturing) project, specific to cell culture, purification, or process utilities.
Specific responsibilities include assistance with the development of design and specification of new process systems and equipment, equipment and installation procurement, process construction oversight, factory and site acceptance testing, and commissioning, including cost, schedule, and scope definition within a framework of safety, quality, governance, and good engineering practices.
This position will drive the commissioning planning, document generation, and hands on field commissioning and validation of the respective process area, including training on new manufacturing associates that will be utilized for the commissioning efforts.

MAIN ACCOUNTABILITIES:

1. Execute process engineering activities to ensure effective scope development from design through detailed engineering, construction, testing, commissioning, and validation.
2. Lead the definition of user requirements in conjunction with the project stakeholders.
3. Generate process P&IDs (Piping & Instrumentation Diagram), specify and procure new equipment and systems, and manage change control for process systems throughout the Project.
4. Review, approve, and provide oversight for submittals, system piping layouts, general arrangements, and isometric drawings.
5. Coordinate with all other project stakeholders to ensure overall coordination of the job, including resources, execution strategies
6. Provide construction support oversight and lead commissioning within assigned focus areas, including equipment inspections, factory acceptance testing (FAT), site acceptance testing (SAT), and field verification and revision of equipment and system drawings to as-built status.
7. Ensure effective execution of equipment and system mechanical completion walk-downs, safety walk-downs, system energization plans, lock-out tag-out, development of commissioning plans and execution of commissioning, review and approval of Equipment Installation Manuals, lead the turnover of systems for subsequent validation activities, and provide technical support through validation activities
8. Implement internal policies, procedures, and specifications
9. Interface with stakeholders on the Project to ensure the design, execution, and delivery are in accordance with Global Engineering, Quality, Environmental, and Safety procedures.
10. Prepare status updates that will be reported in project governance meetings and communications to senior company management on project progress, including cost, schedule, safety, quality etc.
11. Development of skills and behaviors that align with the overall project goals, company expectations of potential future opportunities, and personal desire towards career expectations.
12. Attend industry conferences, seminars, and training events to remain abreast of new technology and engineering / construction trends in the biotech and pharmaceutical industries

Job Requirements:

Qualifications- A minimum of 10 years related experience and/or training, or an equivalent combination of education and experience - Demonstrated capability to provide engineering technical support for all cell culture, purification, and pharmaceutical processing equipment and plant utilities. - Must possess good communication and relationship skills - Have been involved in engineering, construction, commissioning, and validation in a pharmaceutical / biotech-manufacturing environment - Be able to travel up to 20%. For the first year, the travel requirements may approach 50%. - Languages: English fluent, fluent in German and/or French and/or Italian preferred Education- Bachelor's Degree in relevant field such as Chemical Engineering, Mechanical Engineering, Bio-Engineering About BiogenBiogen (NASDAQ: BIIB) is a biotechnology leader that discovers, develops and delivers innovative therapies to improve the lives of patients with neurodegenerative diseases, hematologic conditions and autoimmune diseases. Patients worldwide benefit every day from our medicines for multiple sclerosis (MS) and hemophilia.

Founded in 1978, Biogen is one of the world's oldest biotechnology companies. Our development pipeline is focused on areas of high unmet medical need, as we pursue new therapies for patients suffering from diseases with few or no treatment options. These include programs for secondary progressive MS, Alzheimer's Disease, spinal muscular atrophy, lupus and amyotrophic lateral sclerosis (ALS), amongst others.

With approximately 7,500 people worldwide, Biogen is truly a global organization. We are headquartered in Cambridge, Massachusetts, which is home to our research operations. Our international operations are based in Zug, Switzerland and we have world-class manufacturing facilities in North Carolina and Denmark. We offer therapies globally through direct affiliate presence in 30 countries and a network of distribution partners in over 50 additional countries.

All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability or protected veteran status.

Please be advised that all legitimate correspondence from a Biogen employee will come from '@biogen.com' or '@biogenidec.com' email accounts.
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