- American Honda Motor Co Inc (Marysville, OH)
- …want you to join our team to Bring the Future!Job PurposeThe Contract Sr. Specialist is responsible for reviewing contract requests of medium and high complexity as ... compliant with company policies, risk and governance requirements. Contract Sr. Specialist is responsible to review, analyse, redline, assess risk(s) and negotiate… more
- Merck & Co. (Rahway, NJ)
- …job that provides both technical and project management responsibility. The Specialist - Manufacturing Automation position will report to the Director, Engineering, ... production, utility systems and associated infrastructure.- Responsibilities of the Specialist - Manufacturing Automation include the following:The automation engineer… more
- Novo Nordisk Inc. (West Lebanon, IN)
- …will reviews manufacturing and support documentation and records to certify compliance with in-house specifications/standards and GMP for all NNUSBPI products. This ... and reporting/trending Reviews manufacturing and support records to certify compliance with specifications and procedures Works closely with Manufacturing and… more
- Merck & Co. (Durham, NC)
- Job DescriptionThe Specialist is a member of the Focus Factory Automation team responsible for the assigned process control systems in support of manufacturing ... of process control, data collection techniques, and troubleshooting in compliance with SDLC, GMP, safety, and environmental regulations.- Actively support,… more
- Merck & Co. (North Wales, PA)
- …company's diverse development portfolio comprising over 200 clinical trials in compliance with global and local regulations. The Regional organization is comprised ... and pipeline products to produce safe, effective, innovative medicine.As a GSA Specialist you will work closely with experienced GSA team to:Review Clinical Outcome… more
- Merck & Co. (Philadelphia, PA)
- …training and a comprehensive benefits package.- Position Overview:The eSSC Associate Specialist is responsible for activities pertaining to assigned services in ... accordance with departmental guidelines, and in compliance with company Standard Operating Procedures (SOPs) and industry guidelines.Primary activities include, but… more
- Novo Nordisk Inc. (Durham, NC)
- …& QA presence & process confirmation on shop floor. Relationships Manager, Quality Assurance. Essential Functions Ensures site compliance with Regulations, ISO ... life-changing careers, and the opportunity to help improve the quality of life for millions of people around the...and help us make what matters. The Position Performs quality review & approval of Batch Production Records (BPRs),… more
- Novo Nordisk Inc. (Durham, NC)
- …our employees to embark on life-changing careers, and the opportunity to help improve the quality of life for millions of people around the world. In NC, we operate ... with IT, metrology & other key stakeholders to ensure the right quality , cost & timely completion of all deliverables. Relationships Manager. Essential Functions… more
- Aequor (San Diego, CA)
- …and execution of certain post-marketing commitments and ensuring compliance with global regulatory requirements.Position Summary / ObjectiveAppropriately perform ... and contribute to specified PV sections. Ensure pharmacovigilance regulatory compliance with oversight, as needed.Position ResponsibilitiesParticipate in related PV… more
- Novo Nordisk Inc. (West Lebanon, IN)
- …functional understanding of cGMPs, established manufacturing practices and procedures, and compliance with Quality regulations and guidelines Ability to ... and execution of process and equipment improvement programs, reviews completed quality records, generates quality deviation responses, drive investigations and… more
- Merck & Co. (Rahway, NJ)
- …The Small Molecule Analytical Research and Development group has an opening for a Specialist based in Rahway, NJ. Join us and experience our culture first-hand - one ... dedicated colleagues while developing and expanding your career. --In your role as Specialist , you will be part of a team that provides in-process analytical support… more
- Novo Nordisk Inc. (West Lebanon, IN)
- …functional understanding of cGMPs, established manufacturing practices and procedures, and compliance with Quality regulations and guidelines Ability to ... write up Deviations events utilizing Root Cause Analysis Utilize the quality system to implement changes associated with technical operations, engineering, and/or… more
- Merck & Co. (Rahway, NJ)
- …this is the opportunity for you! We are seeking a Growth and Improvement minded Quality & Compliance 3D Technologies Senior Scientist that can help drive our ... and enable innovation. This role will provide support for our Quality & Compliance for cGMP components strategy.Key Responsibilities:Work Independently and as a… more
- Merck & Co. (Durham, NC)
- …issues to improve manufacturing performance, and maintaining the automation systems in compliance with cGMPs. The Manufacturing Automation Sr. Specialist must ... quality , IT, and engineering groups. - The Senior Specialist for Manufacturing Automation is responsible for providing automation technical support… more
- Merck & Co. (Rahway, NJ)
- …job that provides both technical and project management responsibility. The Specialist - Manufacturing Automation position will report to the Director, Engineering, ... production, utility systems and associated infrastructure.- Responsibilities of the Specialist - Manufacturing Automation include the following:Site Operations (GWES)… more
- Catalent (Manassas, VA)
- …all non-conformance to support continuous improvement efforts; Document all areas of non- compliance with the Quality System and ensure corrective action is ... update records and documentation.Comply with SQF, Food Safety Plan (HACCP), and Food Quality Plan (FQP) standards; Responsible for ensuring compliance with FDA… more
- Catalent (Manassas, VA)
- …with complex formulations to help create engaging new products consumers will love.The Quality Assurance Specialist I - Quarantine is responsible for auditing ... Quality Plan (FQP) standards and responsible for ensuring compliance to FDA and cGMP standards for Quality... compliance to FDA and cGMP standards for Quality Control, including continuous training; Responsible for ensuring Dietary… more
- Novo Nordisk Inc. (West Lebanon, IN)
- …together to contribute to a better tomorrow for our patients. Ethics and quality are held in the highest regard, and a patient-focused mindset guides everything ... reviews of manufacturing and support documentation and records to certify compliance with in-house specifications/standards and GMP for all NNUSBPI products. This… more
- Exela Pharma Sciences, LLC (Lenoir, NC)
- … Specialist II - Engineering/Validation is responsible for cGMP compliance ensuring all FDA regulations, internal procedures/specifications, and other regulatory ... communicating with the Engineering and Validation departments. Job Responsibilities Perform Quality review/approval of URS, FAT, SAT, IQ,OQ,PQ protocols and summary… more
- Novo Nordisk Inc. (Durham, NC)
- …our employees to embark on life-changing careers, and the opportunity to help improve the quality of life for millions of people around the world. In NC, we operate ... & participates in systematic problems solving Understand & execute GMP & compliance protocols for instrument validation Executes work according to schedule &… more
