Pharmaceutical Manufacturing Associate

Virtue America; New York (NY); On-site; USD 28,000 - 41,000; Part time

Job summary

Virtue America is seeking a Pharmaceutical Manufacturing Associate to support production activities in a regulated environment. The role focuses on manufacturing operations, equipment setup, documentation, and GMP compliance in a contract setting.

The ideal candidate has 0–2 years of pharmaceutical manufacturing experience, with basic GMP/SOP knowledge and strong attention to detail. Team collaboration and accurate record keeping are essential for success.

Qualifications

• 0–2 years of pharmaceutical manufacturing experience or fresh graduates welcome.
• Basic GMP and SOP knowledge.
• Good documentation, communication, and attention to detail.
• Ability to follow written procedures and work effectively in a team.

Responsibilities

• Assist in manufacturing of tablets, capsules, liquids, and other products.
• Operate and monitor production equipment per SOPs.
• Perform raw material dispensing, weighing, mixing, granulation, and packaging.
• Complete batch manufacturing records and production logs.
• Follow GMP, safety, hygiene, and contamination-prevention procedures.
• Support equipment cleaning, line clearance, and routine checks.
• Report equipment malfunctions, deviations, and quality issues to supervisors.
• Coordinate with QA, QC, and maintenance teams.
• Maintain a clean and organized production environment.

Skills

GMP knowledge

SOP adherence

Documentation skills

Team collaboration

Job description

Job Title: Pharmaceutical Manufacturing Associate

Location: NY

Type: Contract

Experience:0–2 Years

Job Summary

We are seeking a motivated and detail-oriented Pharmaceutical Manufacturing Associate to support pharmaceutical production activities in a regulated manufacturing environment. The ideal candidate will assist with manufacturing operations, equipment preparation, documentation, and compliance with Good Manufacturing Practices (GMP).

Key Responsibilities

• Assist in the manufacturing of tablets, capsules, liquid formulations, and other pharmaceutical products.
• Operate and monitor production equipment according to approved Standard Operating Procedures (SOPs).
• Perform raw material dispensing, weighing, mixing, granulation, and packaging activities as assigned.
• Complete batch manufacturing records, production logs, and equipment cleaning documentation.
• Follow GMP, safety, hygiene, and contamination-prevention procedures.
• Support equipment cleaning, line clearance, and routine production checks.
• Report equipment malfunctions, deviations, and quality issues to supervisors.
• Coordinate with Quality Assurance (QA), Quality Control (QC), and maintenance teams.
• Maintain a clean and organized production environment.

Required Qualifications

• Fresh graduates and candidates with 0–2 years of pharmaceutical manufacturing experience are encouraged to apply.
• Basic understanding of GMP, SOPs, pharmaceutical manufacturing processes, and safety practices.
• Good documentation, communication, and attention-to-detail skills.
• Ability to follow written procedures and work effectively in a team.

Preferred Skills

• Exposure to pharmaceutical production equipment.
• Knowledge of batch records and manufacturing documentation.
• Familiarity with GMP-regulated environments.
• Basic knowledge of pharmaceutical dosage forms and production processes.