Entry-Level Pharmaceutical Manufacturing Associate (GMP)

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

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.