Production Operator Biocon Biologics Limited - 3.7 Cranbury, NJ Job Details Full-time $20 - $28 an hour Benefits Health insurance Dental insurance 401(k) Paid time off Vision insurance 401(k) matching Life insurance Referral program Retirement plan Qualifications English GMP Manufacturing standard operating procedures Manufacturing facility experience Batch records Standard operating procedures (SOPs)

Full Job Description Job Title:

Production Operator Category:

Non-Exempt Department/Group:

Production /

Operations Supervisor:

Associate Director Location:

1

Duncan Drive, Cranbury Job Description Job Purpose:

Responsible for the execution of all aspects of solid-dosage manufacturing which includes, but is not limited to, the dispensing, granulation, sifting, milling, drying, encapsulation, coating, compression, and cleaning related activities. Must be able to interact daily with all site support personnel as required. Must be able to complete all required batch record documentation in a thorough, accurate, and legible manner in English. Must be capable of reading and understanding all documented Standard Operating Procedures in English plus demonstrate competency through action and written evaluation. Essential Duties and Responsibilities include the following. Other duties may be assigned. 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. Participate in all Quality Investigations as required. 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 SOPs and good housekeeping practices. Must use required PPE during cGMP activities as specified in the Batch Records and Safety Data Sheets.

SUPERVISORY RESPONSIBILITIES

This job position has no supervisory responsibilities for all hourly (non-exempts) employees.

EDUCATION AND/OR EXPERIENCE

High School Diploma or GED Equivalent (2-5 years related experience in cGMP production operation activities) Bachelor's degree in Physical Sciences or Pharmaceutical life science related field of study (0-2 years related experience in cGMP production operation activities) To perform this job successfully, an individual should have: Familiarity with working in a regulated pharmaceutical solid dosage facility. Ability to read and write documents written in English. Excellent written communications skills. Demonstrated effective verbal communication and interpersonal skills. Familiarity with various cGMP solid dosage Pharmaceutical manufacturing equipment. Able to setup, operate, clean, and troubleshoot the solid dosage Pharmaceutical manufacturing equipment being used. Able to work with minimal supervision. Able to stand on feet throughout an eight-hour work day. Able to lift up to 30 lbs (14 Kgs) without assistance. Maintain personal hygiene habits consistent with working in a cGMP environment. Be capable of wearing all required PPE; including partial and full facepieces based on OSHA guidelines.

Pay:

$20.00 - $28.00 per hour

Benefits:

401(k) 401(k) matching Dental insurance Health insurance Life insurance Paid time off Referral program Retirement plan Vision insurance Application Question(s): Are you open to work in second shift How many years of production operations experience do you have? Are you familiar with solid-dosage manufacturing ?

Experience:

GMP:

2 years (Required) pharmaceutical: 1 year (Preferred) Shift availability: Day Shift (Required) Night Shift (Preferred)

Work Location:

In person