Qc Salary at Ipl Macro BETA

Job Description Job Description Summary: VPE Thermal is seeking a qualified QC Inspector to become a part of our growing team! This individual has the responsibility and authority to perform assigned tasks. Tests and inspects products at various stages of production process and compiles and evaluates statistical data to determine and maintain quality and reliability of products by performing the following duties. Essential Duties and Responsibilities: Interprets engineering drawings, schematic diagrams, or formulas and confers with management or engineering staff to determine quality and reliability standards. Selects products for tests at specified stages in production process, and tests products for variety of qualities such as dimensions, performance, and mechanical, electrical, or chemical characteristics.Records test data, applying statistical quality control procedures. Evaluates data and writes reports to validate or indicate deviations from existing standards. Perform inspectio

Job Description Job Description QC Analyst (Pharmaceutical) Location: Novato, CA. Assignment:12 months (Potential to extend) Pay Rate: $28/hr. On Behalf of our client a leading pharmaceutical company developing therapeutics for patients dealing with life threatening rare genetic diseases. We are seeking for a QC Analyst to join their QC Process team. The ideal candidate will perform microbiological and analytical testing to ensure compliance with cGMP guidelines, facilitate sample processing, and contribute to maintaining inspection readiness in a laboratory environment. This role involves cross-functional collaboration, proactive problem-solving, and opportunities to contribute to method validation and optimization. Key Responsibilities: · Manage the timely receipt, accessioning, and batch assignment of incoming samples across all assay types, adhering to best practices. · Execute microbiological and analytical methods for in-process testing under cGMP guidelines, ensuring timely repo

Job Description Job Description ABCO LABORATORIES QC Technician Summary: ABCO Laboratories is a contract manufacture business that works with customers to make and develop a variety of food seasonings, spices and dietary supplements. Duties for the QC Technician include: Testing incoming raw materials as well as in process and finished products, with a emphasis on food and spice materials. Maintaining accurate record of analysis to company standards, Competently using a variety of bench instruments such as FTIR (Thermo), Refractive Index, pH meters, and UV-Vis spectroscopy, Preparing and submitting samples for in house and 3rd party laboratory testing, Performing data review and release of raw materials and finished goods (electronic and physical), Preparing and placing appropriate identification tags (released, hold, rejected, etc.) on in-process and finished products, Preparing, file and retrieving QC retention samples for in-process and finished product comparison, Maintaining QC re

Job Description Job Description ABCO LABORATORIES QC Technician Summary: ABCO Laboratories is a contract manufacture business that works with customers to make and develop a variety of food seasonings, spices and dietary supplements. Duties for the QC Technician include: Testing incoming raw materials as well as in process and finished products, with a emphasis on food and spice materials. Maintaining accurate record of analysis to company standards, Competently using a variety of bench instruments such as FTIR (Thermo), Refractive Index, pH meters, and UV-Vis spectroscopy, Preparing and submitting samples for in house and 3rd party laboratory testing, Performing data review and release of raw materials and finished goods (electronic and physical), Preparing and placing appropriate identification tags (released, hold, rejected, etc.) on in-process and finished products, Preparing, file and retrieving QC retention samples for in-process and finished product comparison, Maintaining QC re

Job Description Job Description Onsite: Novato Duties: Timely facilitation of incoming sample receipt and accessioning flow, decipher batch assignments across all assay types in accordance with agreed upon best practices. Execute microbiological and/or analytical methods to facilitate in-process testing under applicable cGMP guidelines, as well as contribute to the prompt reporting of results to meet the required timetables of internal customers. Perform environmental monitoring sampling and testing of facilities, equipment, and utilities. Evaluate completed assay validity, calculate and summarize results, analyze data per expected or specification ranges. Assist with the compilation and verification of trend analysis reports. Perform and collaborate with co-workers to appropriately share general housekeeping activity assignments and ensure laboratory maintenance systems are adequate for creating a consistent state of inspection readiness. Assist with monitoring and the control of labo

Immediate opportunity for four (4) Microbiologists to test commercial and clinical samples for release! In this exciting role, you will learn microbiology assays and have an opportunity to gain exposure to validation of methods. As a Microbiologist in Quality Control, you will directly contribute to safety data for in-process and final container of pharmaceutical products. Apply today and join a team committed to excellence in pharmaceutical manufacturing! Schedule/Shift: 1st shift, Mon.-Fri., Tues.-Sat., and Wed. Position Type: 1 year contract Position Overview: Quality Control Microbiology – Perform microbiology (sterility, LAL (Endotoxin), bioburden, identification, virology) assay and validation activities supporting GMP, Clinical, development product release. This position is to support project related QC Assay testing/validation. Essential Duties and Responsibilities: Capable of conducting microbiological method validation including bioburden, sterility, LAL (endotoxin), and viro

Job Description At IPS, we apply our knowledge, skills, and passion to making a difference in the lives of people, solving complex challenges. We are looking for a dedicated QA/QC Specialist to join our talented Mission Critical Data Center team. Position Responsibilities Inspection and Auditing: Conduct routine inspections and audits of data center facilities, including electrical systems, HVAC, security, and other critical infrastructure components to ensure compliance with standards and procedures. Quality Control: Monitor the quality of data center construction and maintenance work to identify and address any deviations from the prescribed standards, specifications, and best practices. Documentation: Maintain accurate records of inspections, test results, and discrepancies, and prepare comprehensive reports for management and regulatory purposes. Regulatory Compliance: Stay informed about relevant industry regulations and standards and ensure that the data center follows all legal

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We're looking for people who are determined to make life better for people around the world. Company Overview: At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our 39,000 employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our