Production and Industrial - Material Handler II

Job Title

Shift: Monday - Wednesday Days - 6:00am - 6:30pm Location: Cincinnati, OH - 2110 East Galbraith Road

As part of the Thermo Fisher Scientific team, you'll client meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world's toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer. Join our Pharma Services team and be a part of a leading contract development and manufacturing organization (CDMO) offering end-to-end services for drug development, clinical trial logistics, and commercial manufacturing! Biotech and biopharma companies trust us for our speed, flexibility, and quality across every phase of drug development. Our Drug Product team supports customers in the formulation, production, and packaging of high-quality drug products! Our dedicated colleagues offer a wide range of services, including formulation development, process optimization, scale-up, fill-finish services, packaging, and labeling. Their efforts ensure the efficient production of various drug products, such as sterile injectables and oral dosage forms. Location/Division Specific Information: The Cincinnati, OH site is a Center of Excellence for specialized oral solid dose manufacturing and drug development within the Pharma Services Group.

What Will You Do?

• Prepares manufacturing areas and equipment for the production of pharmaceutical products
• Safely operates various types of computer-controlled equipment used in dispensing, granulation, compression, or coating
• Disassembles, cleans, and re-assembles equipment using basic hand tools
• Assists with troubleshooting of equipment and process issues
• Maintains accurate, neat, error free records such as batch records and logbooks
• Accurately follows production documents, standard operating procedures (SOP's), and current good manufacturing practices (cGMPs)
• Monitors operations for deviations, quality risk, or mechanical problems and elevates issues as needed
• Identifies safety, quality, and efficiency improvements and actively participates in learning organization development
• Maintains a neat work area and follows department safety rules
• Performs duties in other work areas as required

How Will You Get Here?

• Previous experience as a material handler in a GMP environment is preferred
• High school diploma or equivalent required
• Applicants with the experience/exposure of working in a cleanroom environment are highly sought after
• Ability to complete GMP documentation neatly, correctly, and legibly
• Experience in pharmaceutical production preferred
• Mechanical aptitude and ability to disassemble and reassemble various types of equipment
• Basic reading comprehension and math skills necessary to follow complex technical instructions and complete BPR calculations
• Effective communication skills and ability to work both individually and as part of a team
• Prior computer operation and experience in APACS, is desirable
• Ability to manipulate/handle drums weighing up to 110 kg and lift containers weighing up to 40 kg
• Ability to hand-scoop 5 lbs. intermittently throughout the workday
• Job requires wearing personal protective equipment to include white zone gowning requirements and various styles of respirators (1/2 face, 3-M hood, full face, and dust mask)
• Ability to utilize a stand-up forklift and walkie stacker

EEO: "Mindlance is an Equal Opportunity Employer and does not discriminate in employment on the basis of Minority/Gender/Disability/Religion/LGBTQI/Age/Veterans."