Production Support Technician I (FC)

at  Thermo Fisher Scientific

JOB DESCRIPTION

At Thermo Fisher Scientific Inc., we offer a unique opportunity for you to join our team as a Production Support Technician I (FC). As a valued member of our hard-working and driven team, you will have the chance to make a meaningful contribution to the world. With our commitment to exploration and discovery, combined with our world-class resources and investment in R&D, you will be part of an ambitious organization that is at the forefront of innovation.

REQUIREMENTS:

To succeed in this role, you should have the following qualifications:

• High school diploma/GED is minimally required, while an Associate’s degree is preferred.
• 0-1 years of experience, preferably in a clean room and/or GMP environment.
• Ability to work independently on routine tasks and seek support for resolving complex issues.
• Knowledge of cGMP practices is seen as a plus.
• Proficiency in MS Office, strong prioritization skills, and attention to detail.
• Motivated by achieving desired results, prioritizing safety, and possessing effective English communication skills.

Join us at Thermo Fisher Scientific Inc. and be part of a world-class organization that values collaboration, inclusion, and personal growth. Apply today at http://jobs.thermofisher.com.

Thermo Fisher Scientific Inc. is an equal opportunity employer and is committed to providing reasonable accommodations for individuals with disabilities during the job application process. If you require assistance, please contact us at 1-855-471-2255* to discuss your specific needs.

• This telephone line is reserved solely for job seekers with disabilities requiring accessibility assistance or an accommodation in the job application process. Messages left for other purposes will not receive a response.

RESPONSIBILITIES:

As a Production Support Technician I (FC), your key responsibilities will include:

• Daily cleaning of operations areas, ensuring adherence to established standard operating procedures and compliance with cGMP documentation practices.
• Execution of routine cleaning tasks in manufacturing and support areas, with a focus on flawless execution.
• Prioritization of tasks and documentation of all activities to meet cGMP requirements.
• Completion of preventative maintenance and work notification tasks independently and on time.
• Drafting, reviewing, and revising vital documents such as SOPs and logbooks.
• Maintaining up-to-date training assignments and participating in required activities such as safety inspections and improvement projects.
• Collaborating with the team through shift exchanges, meetings, and lean activities.

To succeed in this role, you should have the following qualifications:

• High school diploma/GED is minimally required, while an Associate’s degree is preferred.
• 0-1 years of experience, preferably in a clean room and/or GMP environment.
• Ability to work independently on routine tasks and seek support for resolving complex issues.
• Knowledge of cGMP practices is seen as a plus.
• Proficiency in MS Office, strong prioritization skills, and attention to detail.
• Motivated by achieving desired results, prioritizing safety, and possessing effective English communication skills