Manufacturing Associate- Packaging And Serialzation at RK PHARMA INC

Pearl River, New York, United States -

Full Time

Start Date

Immediate

Expiry Date

20 Sep, 26

Salary

95000.0

Posted On

22 Jun, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Packaging Operations, Serialization, GMP Compliance, Labeling, Cartoning, Aggregation, Data Reconciliation, Line Clearance, Batch Record Documentation, Track-and-Trace Systems, Quality Control, SOP Adherence

Industry

Pharmaceutical Manufacturing

Description

Description Who We Are RK Pharma is a pharmaceutical organization focused on developing and manufacturing high-quality, affordable drug products through disciplined execution and strong internal collaboration. We operate in regulated environments where consistency, documentation, and careful work matter every day. We value people who take pride in doing work the right way, follow processes thoughtfully, and contribute to reliable outcomes across teams. About the Role The Pharmaceutical Manufacturing Associate – Packaging & Serialization supports packaging line operations and serialization activities within a GMP environment. This role is responsible for ensuring that products are packaged, labeled, and serialized accurately and in compliance with regulatory and company requirements. This position is best suited for someone with hands-on packaging experience who understands the importance of detail, traceability, and process discipline. Success in this role comes from consistency, accuracy, and the ability to follow structured processes while maintaining awareness of product quality and compliance. Key Responsibilities Operate and support packaging line activities, including labeling, cartoning, and product handling Execute serialization processes, including aggregation, data entry, and system reconciliation Ensure serialized product data integrity in accordance with company procedures and regulatory requirements Perform line clearance, setup, and changeover activities as required Complete batch records, logs, and documentation accurately and in real time Monitor packaging operations to identify and escalate issues or deviations Support inspection readiness, audits, and compliance activities Follow SOPs, GMP requirements, and safety procedures consistently Collaborate with Quality, Manufacturing, and Engineering teams as needed Maintain a clean, organized, and compliant work environment What We’re Looking For Required High school diploma or associate’s degree (or equivalent experience) 3–5 years of experience in pharmaceutical manufacturing or packaging operations Experience working in a GMP-regulated environment Hands-on experience with packaging operations such as labeling, cartoning, or inspection Experience supporting serialization or track-and-trace systems Strong attention to detail and documentation accuracy Ability to follow structured procedures and work consistently Good communication and teamwork skills Preferred Experience with serialization systems (e.g., aggregation, data reconciliation) Familiarity with packaging equipment and automated lines Experience preparing for audits or supporting inspections Understanding of cGMP requirements in packaging environments How We Work At RK Pharma, quality comes before speed. Procedures are followed for a reason, and attention to detail is expected. Team members are encouraged to ask questions, escalate concerns early, and contribute to a reliable, well-run operation. People who succeed here are steady, detail-oriented, and take pride in work that others can depend on. What We Offer Competitive compensation aligned with experience and local market A stable, quality-focused work environment Clear expectations and structured training Opportunities to build expertise in packaging and serialization Equal Opportunity Employer RK Pharma is an equal opportunity employer committed to fair, consistent, and respectful hiring practices.

Responsibilities

Operate packaging lines and execute serialization processes including aggregation and data entry. Ensure all products are labeled and packaged in strict compliance with GMP and regulatory requirements.