Project Manager (onsite / NOT remote). UPM Pharmaceuticals is an independent, highly experienced and award winning contract development and manufacturing organization (CDMO) located in Bristol, Tennessee. UPM Pharmaceutical’s mission is to advance Client formulation development efforts to the fullest extent possible with the ultimate goal of commercialization, all while adhering to strict standards of quality, timeliness, scientific fundamentals,...
Pharmaceutical Manufacturing Operator II, III. UPM Pharmaceuticals is an independent, highly experienced and award winning contract development and manufacturing organization (CDMO) located in Bristol, Tennessee. UPM Pharmaceutical’s mission is to advance Client formulation development efforts to the fullest extent possible with the ultimate goal of commercialization, all while adhering to strict standards of quality, timeliness, scientific funda...
Maintenance Technician II, III. UPM Pharmaceuticals is an independent, highly experienced, and award-winning contract development and manufacturing organization (CDMO) located in Bristol, Tennessee. UPM Pharmaceutical’s mission is to advance Client formulation development efforts to the fullest extent possible with the ultimate goal of commercialization, all while adhering to strict standards of quality, timeliness, scientific fundamentals, and a...
Operations Equipment Specialist - 2nd Shift. UPM Pharmaceuticals is an independent, highly experienced, and award-winning contract development and manufacturing organization (CDMO) located in Bristol, Tennessee. UPM Pharmaceutical’s mission is to advance Client formulation development efforts to the fullest extent possible with the ultimate goal of commercialization, all while adhering to strict standards of quality, timeliness, scientific fundam...
Direct involvement with all new equipment installations and integrations for Manufacturing and Packaging. Perform technological upgrades of Manufacturing and Packaging equipment. Work with Maintenance to trouble shoot equipment related issues. Represent Operations with manufactures / vendors for new equipment purchases, existing equipment upgrades, and repair of legacy equipment. Qualified candidates must be legally authorized to be employed in t...
Qualified candidates must be legally authorized to be employed in the United States. UPM does not anticipate providing sponsorship for employment visa status (e.g., H-1B or TN status) for this employment position. Essential Duties and Responsibilities. Responsible for technology transfer of solid dose products into Bristol site commercial manufacturing, site transfer of existing commercial products, and scale-up and process development for new fo...
First and Second Shift. Position with training in statistical sampling and inspection of incoming materials, packaged products and processes for conformance to approved written specifications, SOP's, cGMPs, and FDA regulations. Requires physical testing training. Is able to perform sampling and inspection with minimal supervision. Essential Duties and Responsibilites. Performs sampling of raw materials for laboratory Quality Control testing, stab...
Create, maintain, and revise, forms, standard operating procedures, batch records, and material specifications to improve efficiencies while enhancing company GMP compliance. Author and collaborate with authors/initiators of Manufacturing/Packaging/Laboratory Notice of Events (NOEs) and Investigations and subsequently identify appropriate Corrective and Preventative Actions (CAPAs). Qualified candidates must be legally authorized to be employed i...
Under management of quality assurance leadership, performs activities ensuring quality assurance, cGMP, regulatory agency, and internal SOP compliance support for pharmaceutical projects. Essential Duties and Responsibilites. Gather data for input into the quality metrics program. Gather data and documentation to complete product risk assessments for elemental impurities and nitrosamine impurities. Assist in the vendor qualification program. Gath...
Ensures that manufacturing and packaging operations conform to established standards and specifications. Participates in batch record review and evaluation, evaluation of product trends, daily monitoring of manufacturing operations, and audits as assigned. Essential Duties and Responsibilites. Becomes proficient in the manufacturing operations and quality procedures for the area (s) to facilitate compliance to regulations. Assists and supports th...
Under minimum supervision of the Manager, QC Information Systems, the QC Information Systems Specialist provides technical support for the QC Laboratory computerized systems and related processes. Ensures programs and processes are in place that align with the current regulatory requirements and guidance to mitigate laboratory data risk. Identifies opportunities for and coordinates with QC Management for continuous improvements in efficiency, tra...
Plans, writes, implements and reviews Computer Systems Validation protocols in a GMP environment. Ensure that all GxP computer-based systems are operating as intended and meet regulatory requirements. Assist with data integrity assessments, solutions and maintenance. Essential Duties and Responsibilites. Write, review, and execute computer validation documentation (Validation Plan, IQ, OQ, PQ, RTM, summary reports). Perform Gap Analysis of SOPs a...
