Production Operator

YO AI Labs; Cranbury Township (NJ); On-site; USD 40,000 - 65,000; Full time

Job summary

YO AI Labs in Cranbury Township, NJ is seeking a dedicated Production Operator to ensure efficient manufacturing operations. Candidates should have a bachelor’s degree in Physical Sciences or a related field and at least 3 years of relevant experience in a pharmaceutical environment.

Responsibilities include assisting production management, ensuring timely completion of activities, and maintaining compliance with cGMP standards and safety protocols. Strong familiarity with pharmaceutical manufacturing equipment and a commitment to operational excellence are essential.

Qualifications

• Minimum 3 years experience in a Pharma company.
• Familiarity with cGMP solid dosage Pharmaceutical manufacturing equipment.
• Capable of wearing required PPE as per OSHA guidelines.

Responsibilities

• Assist Production Management with scheduled activities.
• Ensure timely completion of manufacturing activities.
• Become proficient in the setup and operation of cGMP equipment.
• Adhere to all Standard Operating Procedures and Safety Procedures.
• Maintain cleanliness of the cGMP area as per SOPs.

Skills

Experience in Pharma

Operation of cGMP equipment

Knowledge of manufacturing processes

Ability to adhere to safety procedures

Education

Bachelor's degree in Physical Sciences or related field

Tools

cGMP production equipment

Job description

Job Description

• Job title: Production Operator
• Experience: 3-18 Years
• Location: Cranbury, New Jersey, USA
• Job Type: Full-time

Must Haves

• Worked in a Pharma company for minimum 3 years.
• Minimum 2-3 years of current relevant experience as a production operator.
• Familiarity with working in a regulated pharmaceutical solid dosage facility.
• Performing tasks like dispensing, granulation, sifting, milling, drying, encapsulation, coating, compression, and cleaning activities.
• Proficiency in setup, operation, and cleaning of all Machines, cGMP production equipment, combined with strict adherence to Standard Operating Procedures (SOPs), Batch Records, safety procedures, and good housekeeping practices, ensuring efficient, compliant, and safe manufacturing operations
• Familiarity with various cGMP solid dosage Pharmaceutical manufacturing equipment.

Qualifications

• Bachelor's degree in Physical Sciences or Pharmaceutical life science related field of study.
• Familiarity with working in a regulated pharmaceutical solid dosage facility.
• Familiarity with various cGMP solid dosage Pharmaceutical manufacturing equipment. Able to setup, operate clean, and troubleshoot the solid dosage Pharmaceutical manufacturing equipment being used.
• Be capable of wearing all required PPE; including partial and full facepieces based on OSHA guidelines.

Key Responsibilities

• Assist Production Management with all scheduled and requested activities in an efficient and smooth operation.
• Ensure all scheduled commercial and non-commercial manufacturing activities are completed on time.
• Become proficient in the setup, operation, and cleaning of all cGMP equipment used during production operations.
• Adhere to all approved Standard Operating Procedures, Batch Records, and Safety Procedures as written when performing all daily activities.
• Ensure the cGMP area is cleaned and maintained following all SOP's and good housekeeping practices.