Qc Salary at Ms Companies BETA

About the job QC Lab Method Scripter QC Lab Method Scripter needs 2+ years experience QC Lab Method Scripter requires: Bachelor's degree in a scientific field, computer science, or related area. Strong analytical and problem-solving skills. Proficiency in Microsoft Word. Ability to read and write formulas in Microsoft Excel Experience with computer scripting or programming in any language is desirable. Prior experience in a GMP laboratory environment is highly desirable. Basic understanding of XML and its applications in data structuring is beneficial. Prior experience with analytical instrumentation highly preferred Must understand basic window file/folder structure architecture Must translate requirements in Analytical Methods to scripted code for semi-automated execution by laboratory personnel QC Lab Method Scripter duties: We are seeking a detail-oriented and technically skilled individual to join our team as a Quality Control Laboratory Method Scripter. Develop and write scripts

**IMMEDIATE OPENING** QA/QC Lab Tech Opportunity ?Interested in this role? Reach out directly to apply TODAY to Grace Williams at grawilliams@actalentservices .com (grawilliams@actalentservices.com) Job Description As a QA/QC Lab Technician, will perform functions to complete all fingerprint and sales sample analysis according to EPA, RCRA and waste analysis plan approved methods in the laboratory. Performing comprehensive laboratory analysis and testing to ensure compliance with Environmental Protection Agency (EPA), Resource Conservation and Recovery Act (RCRA), and the company's Waste Analysis Plan. Operates instrumentation independently, calculates, runs, prepares and analyze samples. Interpret data and reports analytical data findings while monitoring lab instrumentation, and maintaining proper logs and documentation. Works with Plant Manager, CSR's, and TSR's to ensure proper testing of product code analysis is completed. Hard Skills + Laboratory analysis + Operating ICP-OES, GCs

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. Actual compensation will depend on a candidate's education, experience, skills, and geographic location. The anticipated wage for this position is $63,000 - $140,800 Organization Overview At Lilly, we serve an extraordinary purpose. We make a difference for people around the globe by discovering, developing and delivering medicines that help them live longer, healthier, more active lives. Not only do we deliver breakthrough medications, but you a

Responsibilities: Lead and manage a team while fostering strong client relationships. Work as part of a survey team to meet project deadlines, fulfill client requests (both internal and external), and ensure production standards are met. Oversee and coordinate external survey subcontractors. Apply QA/QC processes to ensure the quality of final survey deliverables. Develop fee structures, draft, and review project proposals. Ensure all activities comply with company safety protocols. Maintain regular communication with team members and project managers to keep projects on track and meet client expectations. Qualifications: Licensed Professional Land Surveyor (Indiana registration required). 5–10 years of surveying experience. Interest in acquiring licensure in additional states. Ability to solve complex problems effectively. Valid driver’s license and clean driving record. Committed to maintaining a safe work environment.

Your vision is ambitious. Just like ours. Our people are our success. As one of us, you will contribute to engineering excellence for the high-tech markets of the future, including semiconductors, batteries, pharmaceuticals, biotechnology, and data centers. At Exyte, you will be part of a global community of challenge seekers who are ambitious and passionate about innovation. Together, we will build on our company's long history and keep on leading the way to a better world. Discover your exciting role The Senior QA/QC Inspector located in Indianapolis, IN is responsible for inspections of installed or partially installed process piping systems and monitors the handling of materials in compliance with the site / project quality assurance program. Explore your tasks and responsibilities Conducts and coordinates all activities required to successfully provide quality assurance for an individual project Attends coordination meetings with clients and project kick off meetings Coordinates w

**What Quality Control contributes to Cardinal Health** Quality develops and implements quality policies, procedures, and processes to ensure products and services comply with regulatory standards and specifications. Quality Control is responsible for the analysis or inspection of materials, components, products or processes for compliance with specifications and standards. **Primary Responsibilities** + Reports to Supervisor, Quality Control (Chemistry) + Ensures timely and thorough review of Drug Substance, In-Process and Drug Product sample testing + Reviews method verification, validation and/or transfer protocols + Performs investigations, deviations, change controls and CAPAs, as necessary. + Review stability testing in alignment with stability protocol(s) at the prescribed cadence. + Demonstrates detail-oriented attention in all facets of responsibilities. + Demonstrates knowledge of testing methods, product usage, and applicable regulations and standards. + Aligns work prioriti

**IMMEDIATE OPENING** QA/QC Lab Tech Opportunity ?Interested in this role? Reach out directly to apply TODAY to Grace Williams at grawilliams@actalentservices .com (grawilliams@actalentservices.com) Job Description As a QA/QC Lab Technician, will perform functions to complete all fingerprint and sales sample analysis according to EPA, RCRA and waste analysis plan approved methods in the laboratory. Performing comprehensive laboratory analysis and testing to ensure compliance with Environmental Protection Agency (EPA), Resource Conservation and Recovery Act (RCRA), and the company's Waste Analysis Plan. Operates instrumentation independently, calculates, runs, prepares and analyze samples. Interpret data and reports analytical data findings while monitoring lab instrumentation, and maintaining proper logs and documentation. Works with Plant Manager, CSR's, and TSR's to ensure proper testing of product code analysis is completed. Hard Skills + Laboratory analysis + Operating ICP-OES, GCs

We are seeking a Senior Analyst, QC for a state-of-the-art facility for commercial-scale, sterile manufacturing of therapeutic radiopharmaceuticals. The primary focus of this role is QC testing for same-day batch release, ensuring high standards for quality, efficiency, and reliability. Key Responsibilities: Setup Phase: Complete training in SOPs, radiation/industrial safety, and QC methods. Assist with equipment installation, qualification (IQ/OQ/PQ), and tech transfer. Draft/review SOPs, validation protocols, and related documents. Implement and validate QC methods for production readiness. Production Phase: Primary Focus: Perform QC testing for batch release within hours of production. Maintain compliance with cGMP, SOPs, and regulatory requirements (FDA, NRC, OSHA, EPA). Ensure instruments are calibrated and raw materials are suitable for use. Conduct QC testing: Chemistry (raw materials, APIs, finished products), Microbial testing (sterility, endotoxin, environmental monitoring).