Job Description

At Thermo Fisher Scientific, each one of our 100,000 outstanding minds have a unique story to tell. Join us and contribute to our singular mission-enabling our customers to make the world healthier, cleaner and safer!

When you're part of the team at Thermo Fisher Scientific, you'll do important work, like helping customers in finding cures for cancer, protecting the environment or making sure our food is safe. Your work will have real-world impact, and you'll be supported in achieving your career goals!

Position Summary:

BMS/EMS candidate should have the ability to work in a fast paced, multifaceted climate-controlled environment & be able to communicate optimally and professionally. A motivated self-starter with high levels of initiative, Responsible for supporting and maintaining the EMS/BMS system. The primary focus of this position is to provide support as a BMS/EMS specialist to the Facilities team, Space planning, R&D and Lab Groups. To trouble-shoot, investigate root-cause, and provide solutions to sustain environmentally controlled spaces that fall under GMP and cGMP requirements. Also, the candidate must be able to work well in a team-based environment with limited supervision, and be available to work any shift, weekends and holidays as needed.

Key Responsibilities:

• GMP Building/Environmental Management Systems (preferably Siemens Design)
• Commissioning and qualification of BMS/EMS
• Strong in administration and networking of enterprise applications
• Cleanroom certification, TAB, Validation of warehouse/cold storage and equipment
• Respond to excursions and alarms.
• Perform root-cause analysis with the Quality team.
• Works with internal customers to scope, plan, and implement site-wide environmental projects.
• Understands building design, laboratory design, automation infrastructure design, utility design and general site related projects.
• Suggests improvements with Facilities team to improve workflow and support PPI projects and initiatives.
• Works with the direction of the Space Planners and Doc Control in revision controls under GMP practices.

Minimum Requirements/Qualifications:

• Minimum Bachelor of Science degree in Engineering required. Chemical, Bio, or Mechanical Engineering in a Medical Manufacturing Environment. (Class 7 & 8 Cleanrooms, R&D and BS II Labs) preferred
• Minimum of 2+ years in the pharmaceutical manufacturing (or similar) industry required; 4-6+ years preferred.
• Proven knowledge of current Good Manufacturing Practices (cGMP) in active pharmaceutical ingredients and/or finished pharmaceutical manufacturing.
• Knowledge and experience in a regulated environment to ensure regulatory compliance is achieved.
• Must possess a high level of proficiency and technical strength.
• Excellent verbal and written communications skills with Facilities team members.
• Understanding of sub-zero storage controls, designs, and space planning.

Other Job Requirements:

• Implement EHS policies and procedures and ensure a safe and healthy workplace environment
• Define process requirements and establish project design criteria based on engineering analysis and evaluation.
• Work around bio pharmaceuticals, chemicals, plant utilities equipment and at construction sites.
• Proficient with CAD, Microsoft Project, and Microsoft Office applications.
• Formal Project Management training and certification, such as PMP, is a plus.

Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.

We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.