Packaging Operator - Pharam

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

Job summary

An established industry player in pharmaceutical manufacturing is seeking a dedicated Human Resources Business Partner to oversee solid-dosage manufacturing operations. This role involves ensuring compliance with cGMP standards, operating and maintaining packaging equipment, and adhering to safety procedures. The ideal candidate will have a strong background in pharmaceutical production and the ability to work independently in a fast-paced environment. Join a team that values quality and efficiency, and contribute to the success of innovative pharmaceutical solutions.

Qualifications

• 3-10 years of experience in cGMP production/packing operations.
• Ability to read and write documents in English.

Responsibilities

• Assist in scheduled packaging activities efficiently.
• Ensure all packing activities are completed on time.

Skills

cGMP compliance

Solid dosage manufacturing

Equipment operation and troubleshooting

Documentation in English

Personal hygiene in cGMP environment

Education

High School Diploma or GED

Bachelor’s degree in physical sciences

Tools

cGMP equipment

Job description

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Human Resources Business Partner | PGPMHR

Job Purpose

Responsible for the execution of all aspects of solid-dosage manufacturing which includes but is not limited to packout of finished goods bottles. In addition, responsible for all 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 Packaging Management with all scheduled and requested activities in an efficient and smooth operation.
• Ensure all scheduled commercial and non-commercial packing activities are completed on time.
• Become proficient in the setup, operation, and cleaning of all cGMP equipment used during packaging 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 primary and secondary packaging 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 workday.
• 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 and/or Experience:

Education: High School Diploma or GED Equivalent, bachelor’s degree in physical sciences or pharmaceutical life science related field of study.

Years of related experience and/or training

3-10 years related experience in cGMP production/packing operation activities.

Seniority level

• Seniority level

  Associate

Employment type

• Employment type

  Full-time

Job function

• Job function

  Production

• Industries

  Pharmaceutical Manufacturing

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