Operations Technician
Rahway, ,
Information Technology
Direct Hire,
$30 - $30
On-site
Other/Non Classified
Rahway, ,
$30 - $30
Direct Hire,
Other/Non Classified
On-site
Information Technology
Job details
Kelly Science and Clinical FSP is currently seeking a Operations Technician I for a long-term engagement in Rahway, NJ with one of our Global Pharmaceutical clients. This person will join our Kelly FSP (Functional Service Provider) division, a managed solution provider and business unit of Kelly Services, Inc. This role is full-time and is offering full benefit options. As a Kelly FSP employee you may be eligible for Medical, Dental, Vision, 401K and a variety of other benefits to choose from. You may also be eligible for paid time off, including holiday, vacation, and sick/personal time.
Job Summary: The Operations Technician I is an entry-level position responsible for executing technical tasks and supporting operational activities. This role requires strong organizational skills and attention to detail. This role is responsible for performing all activities associated with timely packaging, labeling, warehousing, and distribution of bulk and finished good clinical materials. Also responsible for Compliance and Quality-related aspects of Global Clinical Supply Operations, including metrics capture, inventory management and ordering, Standard Operating Procedure (SOP) authoring, and supporting investigations and internal inspections.
Key Responsibilities:
• Maintain cGMP and safety training to site requirements.
• Follow cGMP, Standard operating procedures and safety requirements in all activities.
• Operation in cold vaults, walk in CTUs, and stand up CTUs.
• Execute assigned technical tasks and follow up on their completion.
• Collaborate with team members to ensure operational efficiency.
• Maintain accurate documentation related to technical activities.
• Performs Packaging, Warehousing, and Distribution activities according to GMPs and appropriate safety requirements to meet exacting standards defined by the FDA and EU or other international regulatory agencies:
• Primary and secondary packaging of drug products, and secondary packaging of biologics and vaccines.
• Distribution activities, such as order processing, drug picking/packing/shipping.
• Performs all tasks related to clinical label printing production.
• Warehousing activities, such as bulk and component inventory movement and accuracy.
• Manage the ordering and inventory levels for consumables.
• Supports Quality oversight to the Operations area through the following:
o Authoring or revising SOP’s.
o Supporting batch record reconciliation / review activities.
o Supporting investigations with a focus on true root cause, and creation of appropriate corrective and preventative actions (CAPAs).
o Participate as subject matter expert during internal or external audit from Quality group, safety bodies or regulatory agencies.
• Supports creative problem solving, provides detailed analysis of issues and anticipates technical problems and obstacles. May liaise with other functions in Global Clinical Supply (GCS) or other partner groups.
• Undertake specific projects within the group on as needed basis.
• Ability to repetitively lift, carry, push and pull up to 50 lbs. required for Packaging and Warehouse roles.
• Training on forklift and pallet jack use.
• Demonstrate competency and in-depth knowledge of all processes, methods and procedures related to GMP environment and area-specific tasks. Qualifications:
• Bachelor’s degree preferred; candidates with relevant experience may be considered.
• 0-3 years of experience in a related field; candidates without a degree should have 3+ years of relevant experience.
• Experience using/wearing respiratory equipment
• Understanding of Good Manufacturing Practice (GMP) principles.
• Knowledge of quality and safety requirements for pharmaceutical packaging / handling.
• SAP experience is highly desired.
General Skills:
• Strong organizational and detail-oriented skills.
• Equipment operation and repair skills.
• Problem-solving and troubleshooting abilities.
• Ability to quickly learn new systems required.
• Demonstrate competency and in-depth knowledge of all processes, methods and procedures related to GMP environment and area-specific tasks.
I want more jobs like this in my inbox.
About Kelly
Work changes everything. And at Kelly, we’re obsessed with where it can take you. To us, it’s about more than simply accepting your next job opportunity. It’s the fuel that powers every next step of your life. It’s the ripple effect that changes and improves everything for your family, your community, and the world. Which is why, here at Kelly, we are dedicated to providing you with limitless opportunities to enrich your life—just ask the 300,000 people we employ each year.Kelly is committed to providing equal employment opportunities to all qualified employees and applicants regardless of race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, age, marital status, pregnancy, genetic information, or any other legally protected status, and we take affirmative action to recruit, employ, and advance qualified individuals with disabilities and protected veterans in the workforce. Requests for accommodation related to our application process can be directed to the Kelly Human Resource Knowledge Center. Kelly complies with the requirements of California’s state and local Fair Chance laws. A conviction does not automatically bar individuals from employment. Kelly participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S.
Kelly may use AI-powered tools during the recruitment and hiring process. For full details, including how Kelly uses AI, your rights, and how to request a reasonable accommodation, visit the Recruitment Artificial Intelligence Notice.