Operator II

Job Description

Job Description

Finding a  Onsite  job that fits your lifestyle isn't always easy. That's where Kelly comes in. We're seeking a Operator II to work at a premier client in Fremont, CA 94538

Pay rate and Shift
Job Duration: 12 Month
Shift: 1st shift 6:00AM to 2:45PM, Monday Through Friday

Position Summary: 
The Operator II position will interact and work closely with production leads and managers within Manufacturing Services department to support production demand and ensure achievement of company goals following the 4i values.

 

 
Key Responsibilities

• Responsible for signatures as review on SOP’s and other work instruction documents.
• Understands and can communicate workflow and technologies used in the production environment.
• Manufacture and/or test complex products following cGMP and completes all vital documentation in accordance with Quality System. Records information such as time and date performed.
• Share standard process.
• Set up and operate production floor equipment including troubleshooting and adjustments under the direction of a Production Operator Lead or Supervisor
• Read and understand work orders to successfully set up materials on-line, verify and count the amounts required as per work order.
• lInspect material and products at each set up of production process.
• Assist the Production Operator Lead in the assignment of jobs as required by their assignment on the production line.
• Close and seal containers, sort bundles or filled containers, label containers, container tags, or products as needed.
• Pack special arrangements or selections of products as needed.
• Make necessary entries in the QAD System related to material use.
• Line Clearance – responsible to reconciliation and disposal of materials related to the job.
• Clean and sanitize work areas, machines and printers as needed or directed.
• Work with Production Lead, Production Operator II’s and Sr Operator as a team to solve Production Floor scheduling, equipment, and logistic issues.
• Support Engineer in process improvement and equipment validation activities.
• Responsible for following ISO/cGMP Quality System Regulations with focus on SOP completion accuracy, product quality, and housekeeping activities.
• Follow all written procedures. Report discrepancies in procedures (SOP's, batch records, etc.) to the Area Supervisor and perform all work activities in a safe manner and wear personal protective equipment as required.
• Participate in Practical Process Improvement (PPI), Lean, and 5-S programs while working with other departments to troubleshoot  processes/procedures to deliver recommended solutions
• Perform other job duties as required by department and/or Management

 
Keys to Success:

• High School Diploma or equivalent required.
• Minimum of 1 year of direct work experience in manufacturing, operations, production, lab setting.
• Preferred:
• Direct experience in a cGMP environment, Good Documentation Practices (GDP), and Good Warehouse Practices.
• Direct machine operation experience.
• Knowledge of Microsoft Word and Excel is required.
• Ability to use electronic management systems such as QAD and Oracle to print all required documents to complete the daily work as indicated in the production schedule.
• Ability to read, write and comprehend English language, both written and verbally.
• Ability to read and interpret as related to documents such as safety rules, operating and maintenance instructions, and procedure manuals. Ability to understand and carry out instructions furnished in written, oral, or diagram form.
• Ability to add, subtract, multiply, and divide in all units of measure, using whole numbers, common fractions, and decimals.
• Ability to handle multiple tasks and react appropriately to changing priorities and impending deadlines.
• Must be highly collaborative in teamwork environment.
• Ability to perform basic math.
• Ability to stand for sustained periods of time

Physical Requirements / Work Environment:

• Able to lift up to 50 lbs. Without assistance.
• May work in cold environments (as low as -20C) and around loud-noise equipment.
• Personal protective equipment (PPE) such as steel-toe shoes, lab coats, gloves, safety glasses, and ear protection required.
• Controlled Substance Handling: This role involves handling, management, and oversight of controlled substances (Schedules I–V) in accordance with DEA, FDA, and organization guidelines. Exposure to Controlled Substances: Proper safety protocols and protective measures must be strictly followed.
• Safety Protocols: Adherence to all safety procedures is mandatory to ensure a safe working environment

What happens next:
Once you apply, you'll proceed to next steps if your skills and experience look like a good fit. But don't worry-even if this position doesn't work
out, you're still in our network. That means all of our recruiters will have access to your profile, expanding your opportunities even more.
Helping you discover what's next in your career is what we're all about, so let's get to work.
Apply to be an  Operator II today!
#P3
#CB

As part of our promise to talent, Kelly supports those who work with us through a variety of benefits, perks, and work-related resources. Kelly offers eligible employees voluntary benefit plans including medical, dental, vision, telemedicine, term life, whole life, accident insurance, critical illness, a legal plan, and short-term disability. As a Kelly employee, you will have access to a retirement savings plan, service bonus and holiday pay plans (earn up to eight paid holidays per benefit year), and a transit spending account. In addition, employees are entitled to earn paid sick leave under the applicable state or local plan. Click here for more information on benefits and perks that may be available to you as a member of the Kelly Talent Community.

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