Packaging and Labeling Technician

Thermo Fisher Scientific•Indianapolis, IN

1d•Onsite

About The Position

As part of Thermo Fisher Scientific, the Packaging and Labeling Technician performs manual and automated manufacturing and packaging work that supports the company’s mission to make the world healthier, cleaner, and safer. The position is located at 1221 W Morris Street, Indianapolis, Indiana, and involves producing and packaging pharmaceutical products in a cGMP environment. Work includes following approved instructions, handling components and drug product, operating qualified packaging equipment, conducting in-process checks, and completing production documentation accurately.

Requirements

High school diploma or equivalent.
At least 1 year of work experience in a manufacturing, operations, production, laboratory setting, or related field.
Ability to read, write, perform basic mathematical calculations, and accurately follow written instructions.
Hand-eye coordination, manual and finger dexterity, attention to detail, and ability to perform repetitive tasks accurately.
Ability to learn new tasks with assistance and coaching, and demonstrate proficiency through training and qualification.
Basic computer skills for production systems and data entry.
Effective teamwork and communication, reliability, and willingness to escalate issues appropriately.
Ability to work in cleanrooms, cold rooms, and controlled environments ranging from -2°C to 8°C, as required.
Ability to stand and walk for extended periods and perform repetitive hand and finger movements.
Ability to lift and/or carry up to 50 pounds as required by the work assignment.
Ability to bend, squat, reach, push, pull, grasp, and perform fine manipulation as required.
Ability to wear required PPE, which may include filtering face masks, N95 masks, half-face masks, protective eyewear, and other site-required PPE.
Must meet applicable visual acuity and color-vision requirements for inspecting pharmaceutical products, components, and labels in a cGMP environment.
Flexibility to work assigned shifts, overtime, weekends, and holidays based on business needs.

Nice To Haves

Experience in a cGMP environment.

Responsibilities

Perform manual and automated assembly, filling, packaging, labeling, and related production activities according to approved instructions and established procedures.
Review and follow batch paperwork, work instructions, drawings, and assembly instructions; seek guidance when requirements are unclear or unfamiliar.
Accurately count, stage, and account for components and drug product before, during, and after assigned work.
Operate qualified stationary and/or handheld packaging equipment and complete required equipment and room cleaning activities.
Perform assigned in-process checks, inspections, and verifications within training and qualification scope; escalate defects, discrepancies, or unusual conditions.
Complete required computer transactions, data entry, and documentation accurately and contemporaneously.
Follow cGMP, SOP, safety, PPE, and quality requirements and support line clearance, staging, and reconciliation activities as directed.
Collaborate with peers, Room Leaders, Group Leaders, Quality, and Supervisors to complete work safely, accurately, and on schedule.