Manufacturing Technician - 2nd Shift

Tris Pharma Inc•South Brunswick, NJ

17h•$23 - $34•Onsite

About The Position

Tris Pharma, Inc. is a leading privately-owned biopharmaceutical company in the U.S. focused on developing and commercializing innovative medicines. The company has a strong patent portfolio and markets several branded ADHD products, while also licensing products internationally. Tris Pharma has a robust pipeline in neuroscience and other therapeutic categories, utilizing proprietary science and technology. The company values its team members, emphasizing respectful, open, and honest communication to support individual and team success. This role is located in Monmouth Junction, New Jersey, and is for the 2nd shift, Monday to Friday, 2:00 PM – 10:00 PM. The Manufacturing Technician supports and assists in the production of pharmaceutical products in accordance with SOPs, cGMPs, FDA standards, and batch record specifications. This role involves operating, setting up, and maintaining various pharmaceutical production equipment, and accurately documenting all activities to ensure regulatory compliance.

Requirements

High school diploma or equivalent
Minimum 1 year work experience (for Manufacturing Tech I)
Minimum 3 years work experience (for Manufacturing Tech II)
Minimum 5 years work experience (for Sr Manufacturing Tech) – Solid Dosage experience required
Demonstrated ability to read and interpret documents such as safety and environmental policies, operating and maintenance instructions and procedure manuals, etc.
Basic PC skills
Ability to work independently and collaboratively, as required, in a fast paced, matrixed, team environment consisting of internal and external team members
Analytical thinking with problem-solving skills and the ability to adapt to changing priorities and deadlines
Planning, organization and time management skills including the ability to support and prioritize multiple projects
Fluent in English (verbal and written)
Ability to identify and distinguish colors
Ability and willingness to work additional hours as required by business needs
Working knowledge of manufacturing procedures and federal regulations pertaining to manufacturing processes
Working knowledge of good manufacturing systems and familiarity with regulatory and manufacturing SOPs and cGMPs

Nice To Haves

Associates degree or some college coursework

Responsibilities

Supports and assists in the manufacture of pharmaceutical products according to SOPs, cGMPs, FDA standards and batch record specifications
Performs the day to day activities of the production process as assigned, including but not limited to: weighing, blending, filling, compression, coating and/or granulation, etc.
Assists in set up, change over and test runs of equipment for various sized batches and various products, as needed
Collaborates with other production staff and departments
Accurately and consistently completes and documents batch records and other required paperwork
Precisely follows work orders and specifications
Adheres to all plant safety policies and procedures