What are the responsibilities and job description for the Mechanical Engineer position at The O'Connor Group?
We're looking for a Mechanical Engineer for our client, ZETA!
About ZETA
ZETA is a privately owned global supplier of turnkey projects and is specialized in designing, engineering, development, manufacture, automation and maintenance of customized process solutions for liquid aseptic applications in the biopharma and biotechnology industry.
ZETA is perceived in the marketplace as a solution and process systems provider. ZETA aspires to be considered for all major capital projects globally. ZETA is a single-source expert for engineering, automation, plant design and construction and is a best-in-class partner for customized system solutions.
Continuous innovation and a right-first-time approach ensure the highest quality products and services for our customers. This is how we secure sustainable corporate development and maintain our competitiveness and profitability.
Responsibilities
Responsible for allocated work packages.
Preparation of PFDs and P&IDs, from basic to detailed engineering, installation plans and installation concepts.
Maintenance of the design data of the purchased components in the engineering software tools (equipment, fittings, measuring instruments etc.).
3D modelling of customer-specific systems in the pharmaceutical sector.
Creation of component specifications and creation of real devices in the engineering software tools.
Creation of component lists for fittings, measuring instruments and equipment.
Preparation of production drawings and piping isometrics.
Maintains effective communication with project team members (Process Engineering, Production and EI&C) and with the customer.
Responsibility for activities to ensure that construction, installation, and operational testing conform to functional specifications, recognized codes, standards and customer requirements.
Internal coordination for projects and technical support for project management.
Compliance with the budget targets within the framework of the projects.
Contribution to the further development and implementation of standards of the department
Support of the sales and service departments in project development and customer communication.
Project management for internal projects.
Support for customers’ Commissioning Qualification and Validation (CQV) teams.
Support and monitoring of our clients and/or suppliers during execution phase.
Requirements
A degree in Engineering, Bio processing or Life Sciences or completed accredited training in mechanical engineering or bio-pharmaceutical plant construction.
Preferred experience in the bio processing or bio-pharmaceutical manufacturing industry.
Comprehensive IT knowledge of and skills in MS-Office (especially Excel) and ERP systems experience.
Extensive CAD experience (2D/3D) in COMOS, AVEVA-E3D, Cadison, AutoCAD or similar
Preferred knowledge of GAMP5, electrical engineering, process engineering and quality management processes employed in the pharmaceutical sector.
Preferred knowledge of GMP & GEP procedures and project management.
Excellent communication skills (written and spoken) in English (German would be very beneficial)
A keen sense of responsibility, self-motivation, team spirit, flexibility, accuracy, quality awareness, target orientation and cooperation.
Excellent spatial imagination and awareness.
Professional experience in design or plant planning desirable
Ability to work autonomously and as part of a cross-functional team
Self-assured and comfortable working in customer-facing situations.
Comfortable with frequent, and sometimes prolonged, domestic and international travel.
Benefits
Competitive salary
Attractive benefits package (vacation, healthcare, 401(k)).
Dynamic and varied work within an international interdisciplinary project team.
Extensive travel (domestic and foreign).
Focused training and education.
Open-minded, egalitarian, innovative and respectful working culture.
Development opportunities in a fast-growing, up-and-coming company
Flat hierarchy (matrix environment) with short decision-making process
TOCGRP is proud to provide equal-opportunity employment to all employees and applicants, without regard to race, creed, color, religion, national origin, citizenship, ancestry, age, veteran status, disability, pregnancy, marital status, genetic information, or any other categories protected by federal, state, or local law.
About ZETA
ZETA is a privately owned global supplier of turnkey projects and is specialized in designing, engineering, development, manufacture, automation and maintenance of customized process solutions for liquid aseptic applications in the biopharma and biotechnology industry.
ZETA is perceived in the marketplace as a solution and process systems provider. ZETA aspires to be considered for all major capital projects globally. ZETA is a single-source expert for engineering, automation, plant design and construction and is a best-in-class partner for customized system solutions.
Continuous innovation and a right-first-time approach ensure the highest quality products and services for our customers. This is how we secure sustainable corporate development and maintain our competitiveness and profitability.
Responsibilities
Responsible for allocated work packages.
Preparation of PFDs and P&IDs, from basic to detailed engineering, installation plans and installation concepts.
Maintenance of the design data of the purchased components in the engineering software tools (equipment, fittings, measuring instruments etc.).
3D modelling of customer-specific systems in the pharmaceutical sector.
Creation of component specifications and creation of real devices in the engineering software tools.
Creation of component lists for fittings, measuring instruments and equipment.
Preparation of production drawings and piping isometrics.
Maintains effective communication with project team members (Process Engineering, Production and EI&C) and with the customer.
Responsibility for activities to ensure that construction, installation, and operational testing conform to functional specifications, recognized codes, standards and customer requirements.
Internal coordination for projects and technical support for project management.
Compliance with the budget targets within the framework of the projects.
Contribution to the further development and implementation of standards of the department
Support of the sales and service departments in project development and customer communication.
Project management for internal projects.
Support for customers’ Commissioning Qualification and Validation (CQV) teams.
Support and monitoring of our clients and/or suppliers during execution phase.
Requirements
A degree in Engineering, Bio processing or Life Sciences or completed accredited training in mechanical engineering or bio-pharmaceutical plant construction.
Preferred experience in the bio processing or bio-pharmaceutical manufacturing industry.
Comprehensive IT knowledge of and skills in MS-Office (especially Excel) and ERP systems experience.
Extensive CAD experience (2D/3D) in COMOS, AVEVA-E3D, Cadison, AutoCAD or similar
Preferred knowledge of GAMP5, electrical engineering, process engineering and quality management processes employed in the pharmaceutical sector.
Preferred knowledge of GMP & GEP procedures and project management.
Excellent communication skills (written and spoken) in English (German would be very beneficial)
A keen sense of responsibility, self-motivation, team spirit, flexibility, accuracy, quality awareness, target orientation and cooperation.
Excellent spatial imagination and awareness.
Professional experience in design or plant planning desirable
Ability to work autonomously and as part of a cross-functional team
Self-assured and comfortable working in customer-facing situations.
Comfortable with frequent, and sometimes prolonged, domestic and international travel.
Benefits
Competitive salary
Attractive benefits package (vacation, healthcare, 401(k)).
Dynamic and varied work within an international interdisciplinary project team.
Extensive travel (domestic and foreign).
Focused training and education.
Open-minded, egalitarian, innovative and respectful working culture.
Development opportunities in a fast-growing, up-and-coming company
Flat hierarchy (matrix environment) with short decision-making process
TOCGRP is proud to provide equal-opportunity employment to all employees and applicants, without regard to race, creed, color, religion, national origin, citizenship, ancestry, age, veteran status, disability, pregnancy, marital status, genetic information, or any other categories protected by federal, state, or local law.
