Senior Process Engineer/Project Manager
Position
Summary:
Senior Process Engineer/Project Manager will lead a team of Process Engineers/Project Managers in the design of systems for both small and large Biotechnology companies. Sr. PE/PM will possess strong process knowledge and mechanical design including size equipment, valves and pumps. Sr. PE/PM will also interact with customers on applications to select, develop and size out equipment.
Primary
Responsibilities:
Define technical process (technology selection, sizing, design testing etc.) working with the customer on requested equipment.
Provide technical proposal and costing for the proposed solution.
Own the project execution and guide a multidisciplinary team from inception through project completion (establish the project plan, coordinate project team activities, report progress.
Control project scope, schedule and budget relative to the established baseline.
Elaborate design detail design (including functional specification, define and creation of instrument, valve, apparatuses and fitting lists etc.).
Ensure design comply with current pharmaceutical standards applicable for the project such as ASME BPE, GAMP, cGMP, ISPE guidelines.
Work in accordance to our established quality management system.
Supply all technical documentation in accordance to the specification for the project.
Execute and coordinate all qualification activities included in the project (pre-Factory Acceptance
Testing, Factory Acceptance Testing, and Site Acceptance Testing).
Assist customers in their qualification and validation activities if requested
Travel up to 20% in North America including Puerto Rico
Qualifications:
Define technical process (technology selection, sizing, design testing etc.) working with the customer on requested equipment.
Provide technical proposal and costing for the proposed solution.
Own the project execution and guide a multidisciplinary team from inception through project completion (establish the project plan, coordinate project team activities, report progress.
Control project scope, schedule and budget relative to the established baseline.
Elaborate design detail design (including functional specification, define and creation of instrument, valve, apparatuses and fitting lists etc.).
Ensure design comply with current pharmaceutical standards applicable for the project such as ASME BPE, GAMP, cGMP, ISPE guidelines.
Work in accordance to our established quality management system.
Supply all technical documentation in accordance to the specification for the project.
Execute and coordinate all qualification activities included in the project (pre-Factory Acceptance
Testing, Factory Acceptance Testing, and Site Acceptance Testing).
Assist customers in their qualification and validation activities if requested
Travel up to 20% in North America including Puerto Rico
Preferred
Qualifications:
MSc in Biochemical engineering, Process engineering, Chemical engineering, Mechanical engineering, or equivalent.
The above describes the essential content of and requirements for proficient performance in the position and is not meant to be all-inclusive.
#LIFE
Pall Corporation is an Equal Opportunity Employer who encourages diversity in the workplace. All qualified applicants will receive consideration for employment without regard to gender, race, color, national origin, ancestry, citizenship, religion, age, physical or mental disability, medical condition, sexual orientation, gender identity or gender expression, military or protected veteran status or marital status.
. Apply now!Estimated Salary: $20 to $28 per hour based on qualifications.
Summary:
Senior Process Engineer/Project Manager will lead a team of Process Engineers/Project Managers in the design of systems for both small and large Biotechnology companies. Sr. PE/PM will possess strong process knowledge and mechanical design including size equipment, valves and pumps. Sr. PE/PM will also interact with customers on applications to select, develop and size out equipment.
Primary
Responsibilities:
Define technical process (technology selection, sizing, design testing etc.) working with the customer on requested equipment.
Provide technical proposal and costing for the proposed solution.
Own the project execution and guide a multidisciplinary team from inception through project completion (establish the project plan, coordinate project team activities, report progress.
Control project scope, schedule and budget relative to the established baseline.
Elaborate design detail design (including functional specification, define and creation of instrument, valve, apparatuses and fitting lists etc.).
Ensure design comply with current pharmaceutical standards applicable for the project such as ASME BPE, GAMP, cGMP, ISPE guidelines.
Work in accordance to our established quality management system.
Supply all technical documentation in accordance to the specification for the project.
Execute and coordinate all qualification activities included in the project (pre-Factory Acceptance
Testing, Factory Acceptance Testing, and Site Acceptance Testing).
Assist customers in their qualification and validation activities if requested
Travel up to 20% in North America including Puerto Rico
Qualifications:
Define technical process (technology selection, sizing, design testing etc.) working with the customer on requested equipment.
Provide technical proposal and costing for the proposed solution.
Own the project execution and guide a multidisciplinary team from inception through project completion (establish the project plan, coordinate project team activities, report progress.
Control project scope, schedule and budget relative to the established baseline.
Elaborate design detail design (including functional specification, define and creation of instrument, valve, apparatuses and fitting lists etc.).
Ensure design comply with current pharmaceutical standards applicable for the project such as ASME BPE, GAMP, cGMP, ISPE guidelines.
Work in accordance to our established quality management system.
Supply all technical documentation in accordance to the specification for the project.
Execute and coordinate all qualification activities included in the project (pre-Factory Acceptance
Testing, Factory Acceptance Testing, and Site Acceptance Testing).
Assist customers in their qualification and validation activities if requested
Travel up to 20% in North America including Puerto Rico
Preferred
Qualifications:
MSc in Biochemical engineering, Process engineering, Chemical engineering, Mechanical engineering, or equivalent.
The above describes the essential content of and requirements for proficient performance in the position and is not meant to be all-inclusive.
#LIFE
Pall Corporation is an Equal Opportunity Employer who encourages diversity in the workplace. All qualified applicants will receive consideration for employment without regard to gender, race, color, national origin, ancestry, citizenship, religion, age, physical or mental disability, medical condition, sexual orientation, gender identity or gender expression, military or protected veteran status or marital status.
. Apply now!Estimated Salary: $20 to $28 per hour based on qualifications.
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