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Supports and assists in the manufacture of pharmaceutical products according to Standard Operating Procedures (SOPs), current Good Manufacturing Practices (cGMPs) and batch record specifications. Performs the day to day activities of the production process including but not limited to weighing, blending, filling, encapsulation and/or granulation products, etc. Assists in set up, change over and te
Posted Today
Tris Pharma, Inc
- Monmouth Junction, NJ
Tris Pharma, Inc. (www.trispharma.com) is a rapidly growing, technology driven pharmaceutical company engaged in branded and generic product development. Over the past three years Tris' employee base has grown over 250%. Located in Monmouth Junction, New Jersey, Tris has an immediate opening for a 1st shift Manufacturing Washroom Technician to support our manufacturing operations and departments.
Posted Today
Maintains all assigned Quality related documentation while ensuring adherence to, and compliance with, established company quality policies, practices, SOPs and cGMPs Assists in tracking quality system related documentation including, but not limited to batch records, SOPs, analytical test methods, product specifications, annual product reviews (APRs), Change Control Requests (CCRs), SOP/Form Chan
Posted 4 days ago
Tris Pharma, Inc
- Monmouth Junction, NJ
Clean up and remove garbage from various locations throughout the company, including current Good Manufacturing Practices (cGMP) areas Sweep and clean floors as required and maintain other areas as needed in a neat and orderly fashion Keep production, lab, cafeteria and office areas clean at all times Empty plastic bags from trash receptacles, tie and transport May be required to ensure adequate s
Posted 6 days ago
Performs internal and external audits per approved procedures and regulatory requirements; Ensures compliance to all compendial, internal and client specific requirements (i.e. Standard Operating Procedures (SOPs), Quality Agreements, General and Informational Chapters in multiple compendia as applicable) Assists in maintaining the Supplier Qualification Program for existing and new suppliers Work
Posted 11 days ago
Manager/Sr Manager, Pharma Commercial Insights and Analytics Founded in 2000, Tris Pharma, Inc. (www.trispharma.com) is a technology driven, specialty pharmaceutical company. With our intense focus on application of physical chemistry in the biological systems, coupled with the requirements of manufacturing and market demands, we have grown our employee base over 250% in the past three years. Spe
Posted 20 days ago
Pharma Supply Chain Master Scheduler Tris Pharma, Inc. (www.trispharma.com) is a rapidly growing, technology driven pharmaceutical company engaged in branded and generic product development. Located in Monmouth Junction NJ, Tris has an immediate opening for a Master Scheduler The Master Scheduler is responsible for planning, scheduling, coordinating, and monitoring products through the complete pr
Posted 21 days ago
HVAC Facilities Mechanic Tris Pharma, Inc. (www.trispharma.com) is a rapidly growing, technology driven pharmaceutical company engaged in branded and generic product development. Over the past three years Tris' employee base has grown over 250%. Located in Monmouth Junction, New Jersey, Tris has an immediate opening for a 1st shift HVAC Facilities Mechanic to support our manufacturing operations a
Posted 26 days ago
Develops and implements submission strategies based on regulatory requirements in target global (ex US) territories Conducts a GAP assessments of current applications and identifies areas that may require revised or additional documentation Leads the planning, writing and review of all regulatory submissions being submitted to foreign Health Authorities Independently prepares and submits meeting r
Posted 26 days ago
Tris Pharma, Inc
- Monmouth Junction, NJ
Leads group responsible for all aspects of validation activities, including determining and enforcing the approach and rationale for Validation that comply with cGMPs, SOPs, industry standards and FDA requirements Responsible for reviewing and conducting investigations into process deviations, generating investigation reports and implementing necessary Corrective and Preventative Actions (CAPA) L
Posted 27 days ago
?Perform testing of raw materials, in process, finished product and/or stability samples including dissolution, assay, content/blend uniformity, particle size distribution, and other tests according to the analytical methods, USP, procedures in a regulated laboratory environment. ?Analyze and interpret test results. ?Analyze samples using appropriate instrumentation such as HPLC, UV, IR, Karl Fish
Posted 1 month ago
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