Job Description: You will have knowledge of process equipment and systems and manufacturing operations with the primary responsibility to execute process and equipment operation activities during manufacturing operations. Due to your exper...
Responsibilities: Provide clinical data management leadership within the study team to align on and drive data collection requirements for one or more complex clinical development projects. Efficiently plan, coordinate, and deliver compl...
Responsibilities: Lead end-to-end SAP MES projects, ensuring seamless integration with SAP S/4HANA & ECC. Manage stakeholders, vendors, budgets, and project timelines effectively. Drive process improvements and continuous innovation in ...
Responsibilities Create Electrical Block diagrams (AutoCAD). Create Bills of Materials. Create Digital I/O Maps. Create cable kits and. Develop electrical solutions for new product options. Collaborate with Mechanical Engineers on mo...
Responsibilities: Manage day-to-day support of ATO Drug substance operations. Represent plant automation team in Area WCTs. Lead a team of Automation engineers responsible to support and deliver on complex capital construction projects ...
Job summary: Seeking a Facilities Validation Specialist who will be responsible for working across two state-of-the-art medical device facilities. They will have a long-term contract position with significant project ownership an opportun...
Job Description: Seeking a talented and driven individual to join our Quality Assurance Computer System Validation (CSV) team, for the launch of a new building at Rahway NJ site. The candidate will play a pivotal part in ensuring the com...
Roles & Responsibilities: PLC programming is required. 10+ years of Experience. Expertise in Rockwell Controls. Cognex/Keyence Vision System. Experience in SCARA robots. Expertise in conducting Validation Protocols IQ/OQ/PQ for Pharm...
Job Description: The position of the R&D Technician requires individuals to work with Study Directors, associate Toxicologists, Clinical Veterinarians and Study Pathologists in conducting non-clinical laboratory studies as directed by the...
Responsibilities: Author and review of GxP documents (e.g.- SOPs, Protocols, Technical Reports, Trend reports etc. related to QC microbiological and Environmental Monitoring activities). Support site qualification/validation/commissionin...
Roles & Responsibilities: High school diploma or equivalent. 1 to 2 years' experience. Develops skills in basic tasks, techniques and procedures within one skill area / process / method. Applies basic knowledge and skills to complete r...
Responsibilities: Perform routine tests of finished product and stability samples including dissolution, assays, chromatographic purity and content uniformity. Operates analytical instruments such as High-Pressure Liquid Chromatography (...
Responsibilities: Prepare commissioning, qualification, and validation documents for equipment, utilities, and systems. Verify that systems and equipment operate according to design specifications and regulatory requirements. Prepare an...
Responsibilities: As a Regulatory Affairs Coordinator, you will be part of the compliance department supporting various teams. Investigate, maintain, and manage regulatory product certification claims data, databases, and documentation s...
Job description: client is seeking a highly motivated, enthusiastic scientist to assist in formulating novel clinical candidate molecules as a member of our Drug Product team. The Drug Product group at AbbVie works with Development project...
Job Summary The Validation Engineer is responsible for executing equipment and system validation activities within a regulated biopharmaceutical environment. This role involves implementing validation protocols, documenting results, and e...
Roles & Responsibilities: Minimum of Seven (7) years of relevant experience, preferably in a manufacturing environment. Bachelor's degree in engineering is preferred. Strong knowledge of PIMS (Process Information Management Systems) pre...
Job Description: We are seeking a highly skilled and motivated Senior Website Data Analyst who excels in analyzing website data, providing optimization recommendations, identifying opportunities for improvement, understanding business goa...
Job Description: Our client is looking for someone to assist with LabX methods for QC lab data management activities. The client just installed Lab X and recently went live; they need someone to go back into LabX to modify existing method...
Roles & Responsibilities: Minimum of Six (6) years performing lifecycle computer-related systems validation in the biological manufacturing (GMP) industries. Computer Science bachelor's degree preferred. The equivalent combination of ed...