- Aequor (Thousand Oaks, CA)
- …investigations. The Specialist Stability builds and monitors stability studies within quality systems (eg LIMS), owns and handles product quality and ... -4:30 pm (flex) -Monday - Friday **Candidates must have GMP and pharmaceutical experience** What you will do Let's...vital role, you will provide support to the Product Quality (PQ) organization as a subject matter expert of… 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
- Merck & Co. (Rahway, NJ)
- …a high degree of technical and project management responsibility. The Specialist - Process/Facility Engineering position will report to the Director, Engineering ... production, utility systems and associated infrastructure.- Responsibilities of the Specialist - Process/Facility Engineer include the following:The process engineer… more
- Merck & Co. (Durham, NC)
- Job DescriptionWe are seeking a Growth and Improvement minded Associate Specialist Automation Technician who can help drive our Strategic Operating Priorities.- The ... daily production goals are met safely, efficiently, and in accordance with GMP standards.- They will be responsible for problem resolution, administration and… more
- Merck & Co. (Durham, NC)
- …and pulling; ability to lift up to 50 pounds. Position Description: Specialist , Quality Operations Environmental Monitoring Specific to Environmental and Utility ... Job DescriptionOur Quality Assurance group ensures every single material inside...SME, writing and closing QN and QSAT CAPAs, with GMP experience.Shift: Available for shift work, 4 - 10hr… more
- Catalent (Manassas, VA)
- POSITION SUMMARYThe Quality Assurance Specialist I is responsible for inspection and verification of the products and production processes along all the ... years of experience in regulated environment is required. Knowledge of GMP and Quality systems; Ability to read and follow documents (Standard Operating… 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
- Merck & Co. (Rahway, NJ)
- …job that provides both technical and project management responsibility. The Associate Specialist - Engineering Auto Eng position will report to the Director, ... process control systems to improve production efficiency and product quality .Collaborate with cross-functional teams, including operations, maintenance, and … more
- Novo Nordisk Inc. (West Lebanon, IN)
- …documentation and records to certify compliance with in-house specifications/standards and GMP for all NNUSBPI products. This position has QA signature authority ... Performs walk-through audits of NNUSBPI Manufacturing facilities Releases product based on Quality Assurance record review and approval by Manager, Quality … more
- Merck & Co. (Durham, NC)
- …make our products. We work in the manufacturing plants with a "Safety First, Quality Always" mindset striving for continuous improvement. We work in the local plant ... connected to our global manufacturing network to ensure the highest quality of raw materials, intermediates and finished products. POSITION OVERVIEW The successful… more
- Merck & Co. (Durham, NC)
- …make our products. We work in the manufacturing plants with a "Safety First, Quality Always" mindset striving for continuous improvement. We work in the local plant ... connected to our global manufacturing network to ensure the highest quality of raw materials, intermediates and finished products. The Maurice R. Hilleman Center for… 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 ... documentation and records to certify compliance with in-house specifications/standards and GMP for all NNUSBPI products. This position has QA signature authority… more
- BioAgilytix (Durham, NC)
- …therapeutics to the patients who need them.The Senior Laboratory Automation Specialist will be primarily responsible for leading the programming and implementation ... partners to procure automation equipment and services, ensuring cost-effectiveness and quality .Responsible for assessing the needs of the Operations staff for… more
- Merck & Co. (Rahway, NJ)
- …(small molecule, macrocyclic peptides, bioconjugates) Drug Substance development and GMP clinical manufacturing plant currently planned in Rahway, New Jersey. ... compliance representatives, and other team members to ensure the quality and safe delivery of clinical supplies, the scientific...in addition to support of current capital projects the Specialist may provide direct support to other areas such… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …part of the Technical Operation team and will be responsible to provide specialist knowledge and expertise of cell and gene therapy processes and/or process ... qualification, vendor evaluation, and enterprise system interface engineering support for GMP manufacturing of engineered autologous T cell therapy products. Work… more
- BioAgilytix (Boston, MA)
- …of a traditional lab analyst, peer reviewer, and new system implementation specialist . Tasks will encompass running assays, reviewing data, and devising and ... according to GxP guidelines)Essential Responsibilities: Data Review & DocumentationPerform Quality Control (QC) technical and scientific and compliance review of… more
- System One (Devens, MA)
- Job Title: GMP Biologics Field QA Specialist Location: Devens, MA Hours/Schedule: 5AM - 5PM, 12 hour shift Type: Contract Join the global biopharmaceutical ... Quality , and compliance environments. Prefer to also have knowledge of GMP Manufacturing operations and processes. + Directs quality initiatives that… more
- Novo Nordisk (Clayton, NC)
- …+ Minimum of three (3) years progressively responsible experience in material management &/or GMP quality , required + Experience in one or more of the following ... At Novo Nordisk, we are helping to improve the quality of life for millions of people worldwide. For...regulated industry + API & raw materials + Regulations GMP &/or ISO + Pharmaceutical or other FDA regulated… more
- MD Anderson Cancer Center (Houston, TX)
- …(ESPs), and More than minimally manipulated manufacturing procedure within the GMP facility following standard policies and procedures which include but not ... one (maximum of two for certain procedures) Cell Therapy Specialist who is responsible for the entire process on...CLIA. Document deviations and events, notify supervisor, technical and quality management personnel in timely manner and assist in… more
- Mayo Clinic (Jacksonville, FL)
- …able to independently schedule workday activities with minimal direction. ASQ certification in quality and/or GMP principles (eg, quality process analyst, ... the resources you need to succeed. **Responsibilities** The Sr. Quality Analyst, FDA Regulated Manufacturing will be part of...four, consisting of the site QA manager, one QA specialist and two senior QA specialists. + Is responsible… more
