Job Details. Essential Duties & Responsibilities. Provides analytical support to the Project Management Office under minimal supervision. Proactively participates in processes and makes recommendations for system refinements within the Project Management Office. Support Planning Sessions as documentation lead and/or workstream lead. Performance Management. Participates in the evaluation and feasibility process for potential projects. Provides cle...
Job Details. Main Duties. Work with Supplier functions to develop PFMEA, Control plans and statistical plans (Cpk s). Ensures that project and/or process control documentation is compliant with requirements and/or contract. Experience advancing Zero Defect culture utilizing advanced Quality tools such as statistical analysis, PFMEA, 8D corrective action. Create/Maintain PFMEA, Control plans documentation using enterprise platform to ensure compli...
MUST HAVES. 5 years of experience in construction safety management. Lead/Supervisory experience. Experience with monthly site audits (LOTO, CSE, Safe Work Permits). Pharmaceutical or Healthcare experience. OSHA certified. PLUSSES. Experience in the construction field supporting existing building or renovation projects. We are looking for a Safety Coordinator to support one of our large pharmaceutical clients in Andover, MA. This person will lead...
Minimum of 7 years of Project Management experience leading large life science construction projects (preferably cell & gene therapy/single use technologies). Experience managing workload/assignments, resource planning, scheduling (preferably MS Project, Primavera or Smartsheet), and reporting on C&Q scope progress to leadership. Excellent communications skills with the ability to foster relationships with the vendors and the internal stakeholder...
Review all IT CSV project and system deliverables including but not limited to. o Planso Requirementso Specificationso Test Protocols, Scripts and associated execution deliverables (such as test incident reports, etc.)o Summary Reportso Change Controls. Review system operational and administration procedures to ensure they are adequate. Document any findings of non-compliance. Assist with strategy regarding remediation activities. Assist with rev...
Experience in. cleaning validation in the biologics or vaccine industry. to include the following. o Experience in. authoring, reviewing, executing and approving validation documents. o Interface with Quality organization and the ability to defend rationale in validation documents.o Ability to d. evelop cleaning cycle. and l. ead the investigation or trouble shooting. o Ability to review and analyze data. Cleaning Validation experience. o. Accept...
We have a position Matlab Developer. Matlab based model testing / HIL testing / Integration testing. Knowledge in code generation using Embedded, C/C. Job Type: Contract. Pay: $45.00 per hour. Experience level. 7 years. Schedule. 8 hour shift. Day shift. Experience. Matlab: 7 years (Required). HIL testing: 7 years (Required). Integration testing: 7 years (Required). Embedded, C/C : 7 years (Required). Work Location: In person
8 to 10 years in Machining Operations.• Medical device machining preferred, or small / precision machining experience will be relevant, that the heavy industry context.• Experience in NC programming for Swiss Lathes and Multi-Axis Machining Center is key skill expected.• Troubleshooting and Code Corrections experience needed.• Process Improvements in NC programming.• Fixturing skills will be added advantage.• Must have strong knowledge in measure...
Test Method Development and Execution experience related to assays. Familiarity with. method verification protocols. SOP and worksheet, execution of protocols, and methods reports. Experience with. Bio burden, Endotoxin, Growth Promotion, Identification, Identity – HPLC, ID-Osmolality, Material Appearance, Osmolality, Solubility, Sterility. . Experience in. validating assays. . Job Type: Contract. Pay: $45.00 per hour. Benefits. 401(k). Dental in...
This role is highlighting a more user-oriented approach to lab systems technology, they are seeking an individual with experience in GMP and CSV, particularly in QC or manufacturing labs. The role involves day-to-day testing, run the testing associated with CSV, and coordinating with multiple teams to ensure seamless system operations on-site. Troubleshooting will be a key responsibility. The Consultant will provide support for new installations,...
You must needed to help support a high volume of complaints coming in, The role will be focused on hands-on Complaints Investigation and Medical Device Reporting (MDR), the consultant will need to retrieve the returned device from the facility warehouse and then reverse engineer the product to determine root cause of the complaint. The consultant will need to complete this work in a Complaints Lab (aseptic environment, requires gowning) and also ...
Knowledge on systems Engineering and Designing experience with MCCB and ACB. Strong mechanical and/or electro-mechanical skills to support on-going engineering efforts in our circuit breaker business. Ideally, we would have someone with circuit breaker knowledge. Qualification. Bachelors’ degree in electrical or Electronics engineering. At least 10 years of experience working in a new product development environment and good experience with circu...
