- Aequor (Thousand Oaks, CA)
- …this position performs routine laboratory testing and related activities in support of Quality Control operations. The role requires adherence to current Good ... Manufacturing Practices ( cGMP ), safety guidelines, and regulatory requirements while supporting analytical...individual who is eager to grow in a regulated Quality Control laboratory environment. This role is… more
- Aequor (West Greenwich, RI)
- …and Change Control strategy. Supports inspection readiness activities across Quality Control , and site audits and inspections. Monitor and trouble ... independently and deliver right first-time results Focus on data integrity and cGMP practices Experience with analytical laboratory testing with the ability to plan… more
- Cipla (Fall River, MA)
- …outside of Cipla's US Subsidiaries or Affiliates. Job Title : QA Document Control Associate FLSA Classification : Full-Time, Professional Work Location : Fall ... Range : $64,272 - $77,662 PURPOSE The QA Document Control Associate in a pharmaceutical environment is...Part 11, ICH, and ISO. This role supports the Quality Management System (QMS) by maintaining accurate, secure, and… more
- Aequor (West Greenwich, RI)
- …to cGMP and other regulatory requirements. Key Responsibilities: Provide quality oversight for F&E, IQA Warehouse areas (including Incoming Inspections and the ... Position Overview: In this critical role, you will serve as a Plant Quality Assurance (PQA) professional, providing on-the-floor quality oversight for Facilities… more
- Cipla (Fall River, MA)
- …requirements (eg, FDA, ). Maintain and ensure the proper documentation of all quality systems and records. Oversee document control processes, ensuring that SOPs ... Job Title QA QMS Associate Organization Name InvaGen Pharmaceuticals, Inc. Location 927...role and a member of the InvaGen Pharmaceuticals Plant Quality Team. This role ensures compliance with both internal… more
- Merck & Co. (Rahway, NJ)
- Job Description Associate Specialist - MACS Operations Specialist (P1) - - Description- - The Enabling Facilities (EF) group within the Chemical Engineering Research ... The MACS Operations Specialist position will report to the Associate Director, Engineering and will be a member of...compliance representatives, and other team members to ensure the quality and safe delivery of clinical supplies. Once the… more
- Cipla (Central Islip, NY)
- …such as active pharmaceutical ingredients (API), drug products, analytical development, Quality Control (QC), Good Laboratory Practices (GLP)/Good Manufacturing ... are not limited to the following: Scope: The Analytical Quality Assurance (AQA) associate II and III...negotiable. No remote work available. This role works in cGMP laboratory or manufacturing environment, where personal protective equipment… more
- Cipla (Hauppauge, NY)
- …working outside of Cipla's US Subsidiaries or Affiliates. Job Title: QA Associate (IT) Location: Hauppauge, NY (Onsite) Employment Type: Full Time - Salaried/Exempt ... Range: $72,800-$93,600 Work Hours/Shift: 8:30AM - 5:00PM Job Overview: The QA Associate (IT) is responsible for review of batch production records, ensuring that… more
- Merck & Co. (Rahway, NJ)
- …and global medical device and healthcare regulations, including FDA combination products cGMP , Quality System Regulation, FDA Human Factors guidance, ISO 14971, ... DescriptionAssociate Principal Scientist - Device Technical and Engineering Lead ( Associate Director Equivalent) Our company's Device Product & Process Development… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …demonstrated passion for creating new medicines.Experience with Engineering, Operations, Quality Control and Facilities Management.Experience in effectively ... of an immunotherapy in the treatment of multiple myeloma.Legend Biotech is seeking Associate Director, Engineering as part of the Technical Operations team based in… more
- Merck & Co. (Rahway, NJ)
- …DescriptionReporting into the Director, Logistics and Distribution Technology the Associate Director, Logistics and Distribution Technology will be responsible and ... to shape the technical capabilities lead a global, cross-modality technical team.The Associate Director will lead a team of technical experts responsible providing… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …individual will be responsible for performing training activities for Quality Control Microbiology team members who support cGMP Clinical and Commercial Cell ... and skill check and independent performance qualifications for Quality Control Microbiology inside of laboratory and CAR-T cGMP Manufacturing facility.Ensure… more
- Cipla (Fall River, MA)
- …guidance. Provides data to support management evaluation of performance trends. Owns quality records (change control , CAPA's, deviations) and delivers to ... the validation programs and strategies to customers and regulatory auditors. Performs weekly quality reviews of Master Control database by assuring new documents… more
- Cipla (Fall River, MA)
- …the validation programs and strategies to customers and regulatory auditors. Performs weekly quality reviews of Master Control database by assuring new documents ... the company's document and SOP's procedures while ensuring their accuracy, quality , and integrity. This position reports to the Manufacturing/Packaging and partners… more
- Cipla (Fall River, MA)
- …such as active pharmaceutical ingredients (API), drug products, analytical development, Quality Control (QC), Good Laboratory Practices (GLP)/Good Manufacturing ... not limited to the following: Scope : The Analytical Quality Assurance (AQA) associate I position is...negotiable. No remote work available. This role works in cGMP laboratory or manufacturing environment, where personal protective equipment… more
- Cipla (Fall River, MA)
- …experience in a quality assurance in a GMP environment specific Quality Control Laboratory and Manufacturing operations in a pharmaceutical manufacturing ... Job Title : IT-QA Associate FLSA Classification : Full-Time, Exempt Professional Work...vary based on business needs) Reports To : Site Quality Assurance Head Salary Range : $67,000 - $95,000… more
- Merck & Co. (Durham, NC)
- Job DescriptionThe Quality Associate Director/GMP Lead Site Auditor will have leadership responsibility for the site internal audit program, encompassing the ... Internal Auditing, IS Audit, Management Process, Medical Devices, Molecular Microbiology, Quality Auditing, Quality Control Documentation, Quality… more
- Cipla (Central Islip, NY)
- …of Cipla's US Subsidiaries or Affiliates. Job Title: Quality Control (QC) Lab Technician- Sampling Associate FLSA Classification: Full-Time, ... PM (may vary based on business needs) Reports To: Quality Control Director Hourly Rate: $16.64 -...work visas. Working conditions This role works in a cGMP laboratory or manufacturing environment, where personal protective equipment… more
- Merck & Co. (Durham, NC)
- …Healthcare Innovation, Laboratory Processes, Machinery Operation, Manufacturing, Manufacturing Quality Control , Microbiological Cultures, Operations Consulting, ... our patients. We work in the manufacturing plants with a "Safety First, Quality Always" mindset, striving for continuous improvement, and earn our right to produce.… more
- Merck & Co. (Durham, NC)
- …Good Manufacturing Practices (GMP), Laboratory Techniques, Life Science, Manufacturing Quality Control , Master Batch Records, Material Selection, Microbiological ... our patients. We work in the manufacturing plants with a "Safety First, Quality Always" mindset, striving for continuous improvement, and earn our right to produce.… more
