Operator I

at  Thermo Fisher Scientific

OPERATOR I

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.

EDUCATION

• High school diploma or equivalent minimally required.

EXPERIENCE

• 1 year of regulated manufacturing experience, preferably Pharmaceutical experience

KNOWLEDGE, SKILLS, ABILITIES

• Good written and oral communication skills
• Good documentation practices
• Ability to use a computer
• Ability and desire to learn
• Ability to stand for long periods of time
• Ability to work with cross-functional teams comprised of diverse individuals.
• Ability to manipulate (lift, carry, move) weights of 25-50 pounds; occasionally pushing and pulling 50-100+ pounds.
• Full range of motion in upper and lower extremities.
  Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue exceeding $25 billion. Our Mission is to enable our customers to make the world healthier, cleaner and safer. Whether our customers are accelerating life sciences research, solving sophisticated analytical challenges, improving patient diagnostics and therapies or growing productivity in their laboratories, we are here to support them. Our distributed team of more than 75,000 colleagues delivers an outstanding combination of innovative technologies, purchasing convenience and pharmaceutical services through our industry-leading brands, including Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services and Patheon. For more information, please visit www.thermofisher.com.
  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.

• Ensure pharmaceutical products are manufactured in accordance to area SOPs and current cGMP.
• Verify and document production activities in batch records, logbooks and controlled forms.
• Operate vial trayloader
• Filter integrity testing
• Clean pre and post use change parts and prep for sterilization.
• Component/commodity prep.
• General material handling
• Maintain/clean classified and non-classified areas. This includes but is not limited to the aseptic core.
• In-process product inspection
• Participate in the On the Job (OJT) training program, area safety and Lean Manufacturing initiatives.
• Perform other activities as the need arises.