, Permanent
Position: BAS Engineer - Siemens
PharmEng Technology is a leading provider of engineering and consulting services to the pharmaceutical industry. We are seeking a highly skilled and experienced BAS Engineer to join our team in Columbus, OH.
The BAS Engineer will be responsible for designing, installing, and maintaining building automation systems (BAS) for our clients in the pharmaceutical industry. This includes working with Siemens products and systems to ensure that our clients' facilities are running efficiently and in compliance with industry standards.
Key Responsibilities:
- Design and implement BAS solutions for pharmaceutical facilities, utilizing Siemens Teamcenter.
- Conduct site surveys and gather requirements for new projects
- Develop technical specifications and documentation for BAS projects
- Install and configure BAS equipment and systems
- Troubleshoot and resolve technical issues with existing BAS systems
- Conduct testing and commissioning of BAS systems
- Provide training and support to clients on the use and maintenance of BAS systems
- Stay up-to-date with industry trends and advancements in BAS technology
- Collaborate with cross-functional teams to ensure successful project delivery
Qualifications:
- Bachelor's degree in Electrical Engineering, Mechanical Engineering, or a related field
- Minimum of 3 years of experience in designing, installing, and maintaining BAS systems, preferably in the pharmaceutical industry
- Proficiency in Siemens products and systems, including Desigo CC and Apogee
- Strong understanding of building automation protocols, such as BACnet and Modbus
- Experience with programming and troubleshooting PLCs and DDC controllers
- Knowledge of FDA regulations and GMP guidelines for pharmaceutical facilities
- Excellent communication and interpersonal skills
- Ability to work independently and in a team environment
- Willingness to travel to client sites as needed
If you are a highly motivated and skilled BAS Engineer with experience in the pharmaceutical industry, we encourage you to apply for this exciting opportunity. We offer a competitive salary, comprehensive benefits, and opportunities for career growth within our dynamic and fast-paced organization.
PharmEng Technology is an equal opportunity employer and values diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.
PharmEng Technology, now part of Efor Group, leader in Compliance Engineering, is a leading provider of technical services and solutions to the pharmaceutical, biotechnology, and healthcare industries. With over 25 years of experience, we specialize in Commissioning, Qualification, and Validation (CQV) services for facilities, utilities, equipment, and processes.
As part of Efor’s global network of 3,000 experts across 12 countries, we are better equipped than ever to deliver innovative and comprehensive solutions tailored to the unique needs of clients worldwide. This integration strengthens our ability to combine global expertise with local proximity, positioning PharmEng as a strategic partner for the industry’s most prominent players.
Our team of highly skilled professionals brings a wealth of industry expertise and knowledge to every project, ensuring that our clients receive the highest quality services and solutions. We pride ourselves on our ability to provide flexible, innovative, and cost-effective solutions that meet our clients' unique challenges.
At PharmEng Technology by Efor, we are committed to delivering excellence in everything we do. We work closely with our clients to understand their goals and objectives, developing customized solutions that deliver measurable results. Our focus on quality, safety, and compliance ensures that our clients can trust us to meet their most critical needs.
Specialties: PharmEng Technology specializes in the planning, design, construction, and validation of Health Care, Laboratory, API Pharmaceutical, and Biotechnology facilities and equipment, including computer systems. We provide professional services that meet both regulatory and business demands, following current Good Manufacturing Practices (cGMP), Good Engineering Practices (GEP), and Good Laboratory Practices (GLP).
