Sr. Formulation Technician - Control Room & Lyophilization(12hr Days or Nights, 2-2-3 rotation)

Thermo Fisher Scientific • NC

111d

About The Position

Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue exceeding $30 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 complex analytical challenges, improving patient diagnostics and therapies or increasing productivity in their laboratories, we are here to support them. Our distributed team of more than 80,000 colleagues delivers an unrivaled 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. The Drug Product Division - North America (DPD-NA) is one of the five divisions that make up the Pharma Services Group. We are made up of approximately 4400 colleagues across six sites who specialize in taking sterile injectable and oral solid dose drug products from development to commercialization. Night and day full time shifts available. Shift hours are 6pm-6am or 6am-6pm on a 2-2-3 rotating schedule.

Requirements

• High School Diploma or equivalent required.
• Associate’s with 1+ year manufacturing experience preferred.
• Bachelor’s preferred with no manufacturing experience.
• Mechanical and/or similar experience preferred.
• 2 years of Steriles pharmaceutical or manufacturing experience preferred.
• Excels in a team environment.
• Basic math skills.
• Attention to detail while maintaining a quality product.
• Ability to perform repetitive work duties.
• Ability to follow SOPs.
• Ability to concisely communicate with Production leadership to accept daily assignments and report any relevant production-related information.
• Ability to schedule the team’s activities and drive priorities.
• Strong communication skills.
• Proactive in identifying quality opportunities.
• Flexibility/willingness to adapt to operational needs.

Responsibilities

• 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.
• Complete tasks vital to manufacture drug products in an aseptic filling area, including: Cleaning cGMP Areas, Parts Preparation, Filter Integrity Testing, Operating Parts Washers and Autoclaves, Performing Tray Loading, Operating the Filling Isolator, General Material Handling, Troubleshooting Equipment Alarms.
• Designated Trainer/Certified SME.

Benefits

• Competitive remuneration.
• Annual incentive plan bonus.
• Healthcare.
• Range of employee benefits.
• Outstanding career and development prospects.
• Exciting company culture that stands for integrity, intensity, involvement, and innovation.

What This Job Offers

• Education Level: High school or GED
• Number of Employees: 5,001-10,000 employees