Production Operator - Solid Dosage (Pharma) 46003

Cephas Consultancy Services Private Limited; Cranbury Township (NJ); On-site; USD 40,000 - 60,000; Full time

Job summary

Cephas Consultancy Services Private Limited in Cranbury, New Jersey, United States, is seeking a Production Operator for solid-dosage pharmaceutical manufacturing. The role covers dispensing, granulation, sifting, milling, drying, encapsulation, coating, compression, and related documentation in English.

Ideal candidates will have 2–15 years of experience in regulated pharmaceutical production, familiarity with cGMP equipment, and the ability to work with minimal supervision while adhering to

Qualifications

• Familiarity with working in a regulated pharmaceutical solid dosage facility.
• Reading and writing documents in English.
• Familiarity with cGMP solid dosage manufacturing equipment.
• Ability to work with minimal supervision.
• Ability to stand for an 8-hour shift.
• Ability to lift up to 30 lbs (14 kg).
• Maintain hygiene in a cGMP environment.
• Capable of wearing PPE per OSHA guidelines.

Responsibilities

• Assist Production Management with scheduled and requested activities.
• Ensure manufacturing activities are completed on time.
• Set up, operate, and clean cGMP equipment used in production.
• Participate in Quality Investigations as required.
• Follow SOPs, Batch Records and Safety Procedures.
• Maintain clean cGMP area and good housekeeping.
• Wear required PPE during cGMP activities.

Skills

Regulated pharmaceutical environment

Reading & writing English

cGMP equipment familiarity

Self-supervision

Eight-hour stamina

Lifting up to 14 kg

Personal hygiene in cGMP

PPE usage

Education

High School Diploma or GED

Bachelor’s in Physical Sciences or pharmaceutical life science

Job description

Production Operator - Solid Dosage (Pharma) 46003

Cephas Consultancy Services Private Limited Cranbury, New Jersey, United States

About this position

Positions:2 Full Time
Experience
2 - 15 Years

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 SOP’s and good housekeeping practices.
• Must use required PPE during cGMP activities as specified in the Batch Records and Safety Data Sheets.

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.
• 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 Ibs (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.

Education :

High School Diploma or GED Equivalent.

Bachelor’s degree in Physical Sciences or Pharmaceutical life science related field of study.