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Commissioning & Qualification (C&Q) Project Engineer | Indianapolis, IN |OnsiteJob Title - Commissioning & Qualification (C&Q) Project Engineer | Indianapolis, IN |Onsite

Stellent IT LLCCompany Name - Stellent IT LLC

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Indianapolis, Indiana, USA

Full-time, Contract, Third Party

Title: Commissioning & Qualification (C&Q) Project Engineer Location: Indianapolis, IN |Onsite Duration: 12+ months Role Overview: We are seeking a detail-oriented and proactive C&Q Project Engineer to support commissioning and qualification activities for equipment and systems in an API manufacturing facility. This role is ideal for candidates with technical expertise in facility, utilities, and API manufacturing process systems who excel in documentation, data analysis, and cross-functional

Senior Validation EngineerJob Title - Senior Validation Engineer

Katalyst Healthcares and LifesciencesCompany Name - Katalyst Healthcares and Lifesciences

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Lexington, Massachusetts, USA

Full-time

Responsibilities: Shire Human Genetic Therapies Inc. is seeking a Senior Validation Engineer with the following duties: Write Validation documents per Food Drug Administration (FDA)/Company guidelines; draft Specification documents and Validation Plans (VPs) for pharmaceutical manufacturing and laboratory equipment; Write and execute qualification protocols for new equipment and decommissioning protocols for old equipment. Execute approved protocols per company Good Documentation Practices (cG

Process Development Engineer - Early Phase Peptide/OligonucleotideJob Title - Process Development Engineer - Early Phase Peptide/Oligonucleotide

Eli Lilly and CompanyCompany Name - Eli Lilly and Company

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Indianapolis, Indiana, USA

Full-time

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

Technical Operations Training & Support SpecialistJob Title - Technical Operations Training & Support Specialist

Thermo Fisher ScientificCompany Name - Thermo Fisher Scientific

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Remote or Greenville, North Carolina, USA

Full-time

Work Schedule Flex Shifts 40 hrs/wk Environmental Conditions Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc allowed, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.) Job Description Position Summary: Join Thermo Fisher Scientific Inc. as a Technical training and support engineer and have th

QA CTO Label SpecialistJob Title - QA CTO Label Specialist

TSR Consulting Services, Inc.Company Name - TSR Consulting Services, Inc.

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Summit, New Jersey, USA

Contract

Our client, a leading pharmaceutical company, is hiring a QA CTO Label Specialist on a contract basis Job ID #: 82786 Work Location: Summit, NJ/ONSITE Summary: This is a 100% onsite position. This position is scheduled for Sun-Wed (6:30 am -4:30 pm). PURPOSE AND SCOPE OF POSITION: The Label Control Specialist at the S-12 Cell Therapy manufacturing facility is responsible for supporting site Label Control activities at S-12 in accordance with client policies, standards, procedures and Global c

CQV Engineer (Onsite) Location:San Angelo, TexasJob Title - CQV Engineer (Onsite) Location:San Angelo, Texas

Stellent IT LLCCompany Name - Stellent IT LLC

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San Angelo, Texas, USA

Third Party, Contract

CQV Engineer (Onsite) Location:San Angelo, Texas Job Description :- You will be responsible for: Commissioning Documentation Preparation and execution of Commissioning Protocols Authoring and review of Commissioning Reports Qualification Activities SLIA/VAF Validation Master Plan + Final Report IQ Protocols and IQ Reports Execution of Commissioning and IQ Protocols Coordination with construction, automation, and engineering teams during system turnover and commissioning Review of design docume

Senior Network Engineer -?DWDM in Seattle,WAJob Title - Senior Network Engineer -?DWDM in Seattle,WA

Russell, Tobin & AssociatesCompany Name - Russell, Tobin & Associates

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Seattle, Washington, USA

Contract

Title: Senior Network Engineer - DWDM Location: Seattle,WA (5 days on site) Pay: $75-$85/hr on W2 (DOE) Contract: W2; 9 months contract Daily Schedule: Mon-Fri 9-5 Estimated Start Date: ASAP Client: Fortune 50 CompanyPrimary responsibilities * Design, build and rollout our global DWDM networks; * Drive scaling designs to meet the demand of our customers; * Create processes that help operate and build our optical network; * Work closely with other Networking teams; * Evaluate new products and dr

Controls TechJob Title - Controls Tech

Advantage TechnicalCompany Name - Advantage Technical

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Acton, Massachusetts, USA

Full-time

Job Overview Hands-on role supporting, maintaining, and improving automated manufacturing equipment. Work includes troubleshooting, installations, wiring, documentation, and training. Key Responsibilities Troubleshoot and maintain PLCs, HMIs, vision systems, drives Wire, install, and test automation equipment Perform preventive maintenance and equipment upgrades Create and follow maintenance documentation and SOPs Support production setup and changeovers Train operators and techs Record main

Validation EngineerJob Title - Validation Engineer

Katalyst Healthcares and LifesciencesCompany Name - Katalyst Healthcares and Lifesciences

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Irvine, California, USA

Full-time

Responsibilities: NPD, NPI, Process & product development. Process and Equipment Validation. Process Characterization. good manufacturing practices and documentation. Process Improvement. Requirements: GMP (Good Manufacturing Practices) & ISO (International Organization for Standardization) 13485 and regulatory affairs. Knowledge in Experiment design and SPC. Management of statistical procedures. Strong creative, analytical and problem-solving skills. Comprehension of standard costs and

Process Validation EngineerJob Title - Process Validation Engineer

Katalyst Healthcares and LifesciencesCompany Name - Katalyst Healthcares and Lifesciences

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Albany, Georgia, USA

Full-time

Responsibilities: Spearhead qualification protocols for next-generation manufacturing processes. Drive manufacturing investigations and implement innovative solutions. Design validation strategies for new product launches and technology transfers. Lead comprehensive IQ/OQ/PQ validation activities across multiple projects. Create robust standard operating procedures for manufacturing excellence. Ensure continuous process verification for robust manufacturing operations. Coordinate cross-fu

Sr IT Support Engineering AssociateJob Title - Sr IT Support Engineering Associate

Gilead Sciences, Inc.Company Name - Gilead Sciences, Inc.

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Raleigh, North Carolina, USA

Full-time

At Gilead, we're creating a healthier world for all people. For more than 35 years, we've tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer - working relentlessly to develop therapies that help improve lives and to ensure access to these therapies across the globe. We continue to fight against the world's biggest health challenges, and our mission requires collaboration, determination and a relentless drive to make a difference. Every member of Gilead's team plays a critical ro

Reliability Engineer - Valdosta, GAJob Title - Reliability Engineer - Valdosta, GA

Archer Daniels MidlandCompany Name - Archer Daniels Midland

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Valdosta, Georgia, USA

Full-time

Job Description Reliability Engineer - Valdosta, GA This is a full time, exempt level position. Job Summary: This position will focus on improving plant reliability by analyzing bad actors and equipment issues through failure analysis and zero loss methodology. In addition, they will take a proactive approach to new equipment installations by incorporating reliability into the design as well as supporting the commissioning of new equipment. Essential Job Functions:Perform duties in a safe man

IT infrastructure CSV ConsultantJob Title - IT infrastructure CSV Consultant

Katalyst Healthcares and LifesciencesCompany Name - Katalyst Healthcares and Lifesciences

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Cranbury, New Jersey, USA

Full-time

Responsibilities: We are seeking a Validation & IT Systems Specialist to join our dynamic team. This role combines expertise in validation and computer system validation (CSV) with IT administrative support for regulated systems and applications. IT Infrastructure guy who has worked in the Pharma industry, having 21 CFR part 11 exp. Provide administrative support for IT systems and applications, ensuring smooth operations in a regulated environment. Manage system configurations, troubleshooting

Lead Engineer, Quality ValidationJob Title - Lead Engineer, Quality Validation

Katalyst Healthcares and LifesciencesCompany Name - Katalyst Healthcares and Lifesciences

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Andover, Massachusetts, USA

Full-time

Job Description: The contract Lead Engineer, Quality Validation will be responsible for providing quality and technical support for qualification and validation activities related to laboratory instruments, temperature control units and LFH/BSC units for internal customers. The individual will support and facilitate the review and approval of qualification/validation documentation for all stages of the equipment life cycle qualification process. Responsibilities: Provide quality oversight of Bl

Process Engineering Technician IVJob Title - Process Engineering Technician IV

Johnson & JohnsonCompany Name - Johnson & Johnson

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Jacksonville, Florida, USA

Full-time

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn m

Quality Engineer - Casa Grande Nutrition Plant - ArizonaJob Title - Quality Engineer - Casa Grande Nutrition Plant - Arizona

Abbott LaboratoriesCompany Name - Abbott Laboratories

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Casa Grande, Arizona, USA

Full-time

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues serve people in more than 160 countries. Abbott Nutrition in Casa Grande, AZ is seeking a Quality Engineer. The Quality Engineer is involved in all aspects of the manufacturing operation fro

Embedded Software Engineer RDK-BJob Title - Embedded Software Engineer RDK-B

Global IT FamilyCompany Name - Global IT Family

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Dallas, Texas, USA

Contract

Hi This is the requirement from TCS. Please share resume of your candidate for this below requirement at Job Title- Embedded Software Engineer RDK-B Location- Dallas TX 4 DAY ONSITE TCS Contract position: Specify together with our Marketing team and our customers the features of the products designed for our NAM customers Define technical solutions and implement new functions in the product Ensure the product quality (unit-tests, code reviews, ) Investigate and solve issues reported by the cus

Upstream Manufacturing AssociateJob Title - Upstream Manufacturing Associate

Zachary Piper Solutions, LLCCompany Name - Zachary Piper Solutions, LLC

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Washington, District of Columbia, USA

Full-time

Upstream Manufacturing Associate - Clinical Production Piper Health and Sciences is seeking an Upstream Manufacturing Associate to support clinical production in a cGMP biopharmaceutical environment. This role offers hands-on experience in bioprocessing and cell culture, helping advance therapies into clinical trials. Ideal for candidates looking to grow in biotech manufacturing . Responsibilities for Upstream Manufacturing Associate Include: Operate upstream biomanufacturing equipment: biorea

Quality Control ManagerJob Title - Quality Control Manager

Zachary Piper Solutions, LLCCompany Name - Zachary Piper Solutions, LLC

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Wayne, Pennsylvania, USA

Full-time

Piper Companies is seeking a Quality Control Manager to join a reputable Biologics Quality Control Testing company located in Wayne, Pa. Responsibilities of the Quality Control Manager include: Lead projects, collaborate with clients and teams, and ensure expectations are met Oversee testing, manage deviations, and ensure adherence to global regulations Represent the team in audits, address issues, and implement corrective actions Manage assay development, validation, and ongoing compliance

Validation EngineerJob Title - Validation Engineer

Katalyst Healthcares and LifesciencesCompany Name - Katalyst Healthcares and Lifesciences

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Richmond, Virginia, USA

Full-time

Responsibilities: Develop and implement comprehensive validation plans for packaging lines, labelers, case packers, and low-speed pen assembly. Lead the validation of various systems, including SEA Vision Yudoo and AVI systems, ensuring compliance with industry standards and regulatory requirements. Prepare, execute, and document Installation Qualification (IQ), Operational Qualification (OQ), Performance Qualification (PQ), and Validation Summary Reports (VSR). Collaborate with cross-functi