181 - 200 of 1,825 Jobs

Sr Manager, IT Business Analysis - SAP BRH Architect

Gilead Sciences, Inc.

Foster City, California, 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

Digital Media & Content Supervisor

Omega Hires

New York, New York, USA

Contract, Third Party

Screening & Gear Management Location :Culver City,CA and New york,NY Running screenings in the Apple TV+ Screening and Review Rooms.Providing onsite support M-F 9AM-6PM.Managing timely responses in the Post Screenings inbox.Scheduling, and coordinating screenings in Apple TV+ Screening and Review rooms.Maintaining screen booker requests, approving and/or denying requests appropriately.Editorial support, assisting with delivery QC issues and needed corrections (approximately 20+ per week).Schedul

Need - SAP ATTP Consultant

ASCII Group LLC

Richardson, Texas, USA

Contract, Third Party

Hi, The following requirement is open with our client. Title : SAP ATTP Consultant Location : Richardson, TX Duration : 12+ Months Relevant Experience (in Yrs.): 8+ Detailed Job Description: ATPGATP SAP Func Techno lead located in the US. If the resource is from the Bay Area, we want them to be available onsite for three days a week otherwise, it will be virtual.The ideal candidate should have over 8 years of experience in SAP, particularly with Order Management, ATP, or GATP modules, SAP vers

Validation Engineer

Zachary Piper Solutions, LLC

Lynwood, California, USA

Full-time

Piper Companies is looking for a Pharmaceutical Validation Engineer to support commissioning and decommissioning activities for a major pharmaceutical company in the Los Angeles County area. Responsibilities for the Validation Engineer include: Experience in Pharmaceutical Laboratory Operations Proficiency with cleaning validation as this is a multi-product production space Must be familiar and have experience with laboratory and manufacturing instrument selection, installation (IQ/OQ) and qua

Senior CQV Engineer

Zachary Piper Solutions, LLC

Raleigh, North Carolina, USA

Full-time

Piper Companies is actively seeking a Senior CQV (Commissioning, Qualification, and Validation) Engineer to join our team. The ideal candidate will have 7-10 years of CQV experience with large-scale process equipment, including upstream, downstream, and CIP (Clean-In-Place) systems. This role is critical to ensuring the successful commissioning and validation of our biopharmaceutical manufacturing processes. This is a Monday - Friday, traditional hours role located in the greater Raleigh, NC are

Validation Engineer

Katalyst Healthcares and Lifesciences

Thousand Oaks, California, USA

Full-time

Responsibilities: Plan and track implementation of commissioning & qualification actions/documentation versus project(s) timelines. Author/evaluate qualification/validation protocols including DQ, IQ, OQ, FT, PQ protocols and final reports for new or modified GMP utilities, facilities, and process equipment. Execute DQ, IQ, OQ, FT, PQ protocols, which involve protocol discrepancies, investigation, and corrective action activities for new or modified GMP utilities, facilities, and process equi

Validation Engineer

Katalyst Healthcares and Lifesciences

Nashville, Tennessee, USA

Full-time

Responsibilities: Ensure all manufacturing equipment (e.g., mixers, conveyors, packaging lines) undergoes: These confirm proper functionality and adherence to operational specifications. Validate manufacturing processes (e.g., blending, cutting, rolling, and packaging) to ensure consistent production of high-quality products. Conduct revalidation of equipment and processes when changes occur, such as: ssess risks related to equipment, processes, and production areas that could impact product qua

Application Programmer V

Mitchell Martin, Inc.

Plano, Texas, USA

Full-time, Contract

Title: Application Programmer VLocation:Southwestern Region (Onsite)Employment Type: ContractCompensation Pay Range:$47.04-$67.20/HrsDescription: * Seeking a mid to senior level developer with expertise in data processing and analysis. * Requires experience in data querying and analysis with a strong background in data warehousing. * Involves working on data gap remediation efforts and specific initiative changes. * Opportunity to contribute to a development project focused on data optimization.

Construction Manager (Life Sciences)

The Ranger Group

Chicago, Illinois, USA

Full-time

The Ranger Group is a leading professional services firm providing solutions to Life Sciences customers. We are seeking a highly experienced Construction Manager to oversee capital expansion (CAPEX) projects for a pharmaceutical client in the Chicago IL Area. The ideal candidate will bring proven expertise in managing complex construction projects in regulated industries, with a strong understanding of FDA requirements and GMP environments. This is a 100% onsite position requiring daily coordin

Commissioning Qualification Validation Engineer

Zachary Piper Solutions, LLC

Durham, North Carolina, USA

Full-time

Piper Companies is currently looking for an experienced Commissioning Qualification Validation Engineer (CQV) in Raritan, New Jersey (NJ) to work for an innovative and growing pharmaceutical manufacturer. Responsibilities for the Commissioning Qualification Validation Engineer (CQV) include: Commissioning: Lead commissioning activities for new laboratory equipment, systems, and facilities, ensuring they are installed and function as intended. Qualification: Develop, execute, and document qualif

MODA ES EBR SME

Bytecubit Technologies

Remote

Contract

Job Title: MODA ES EBR SMELocation: RemoteDuration: 12+ monthsPay Rate: 60/hr-80/hr (depending on experience)Job Description:Seeking an SME of MODA ES EBR Execution Systems to bridge the gap for the sites MODA module.Resource will act as an owner s rep for the master data control and support the integration of the CGMP ES systems and analytical equipment.Will oversee configuration and data capture to provide quality data flow for the site.Will be involved in training of analysts in LIMS MODA, a

Manager of Internal Audit / Seattle

Motion Recruitment Partners, LLC

Seattle, Washington, USA

Full-time

Job Description A major airline company is looking for a Manager of Internal Audit to join their growing team! You'll play a critical role on their SOX Program Compliance team, overseeing the company's financial compliance efforts around Sarbanes Oxley internal controls program. Ideal candidates have experience with SOX, IT controls, and auditing background is a big plus. This role is remote hybrid, 3 days on-site at SEA TAC Airport. Required Skills & Experience 6+ years of experience in publi

Oracle EPM Consultant (Spanish & English speaking)

Paramount Software Solutions, Inc

US

Full-time, Part-time, Contract, Third Party

Job Title: Oracle EPM Consultant Location: 100% Remote Duration: Long Term Note: Should have a Spanish and English-speaking skills Job Description: Mush have experience collaborating with business stakeholders to understand their functional requirements and translate them into technical specifications. Should be good at customer service, with a strong customer focus, excellent problem-solving and analytical skills Must have an experienced EPM consultant with a consistent track record of design

Validation Engineer II

Zachary Piper Solutions, LLC

Lynwood, California, USA

Full-time

Piper Companies is seeking an experienced Validation Engineer II to support a highly reputable Pharmaceutical company in Lynwood, California. Responsibilities: Responsible for risk analysis, packaging validation, cleaning validation, and equipment qualification required for new products, processes, and equipment and any changes to existing products, processes, and equipment. Provide recommendations for product disposition or other actions related to product and equipment performance issue

Senior Manager of Manufacturing

GEA

Fresno, California, USA

Full-time

Responsibilities / Tasks Essential Duties and Responsibilities include the following, other duties may be assigned :Responsible for all manufacturing procedures per GMP and FDA requirements.Follow all batching instructions per individual batch tickets.Must rotate raw material stock on a first-in, first-out basis.Report all tank readings prior to the start of the shift.Check all chemicals before the start of a batch to assure availability of raw materials and packaging items and communicate with

Sr Assembler

bioMerieux

Hazelwood, Missouri, USA

Full-time

Benefits at bioMerieux: Low-cost medical, dental, and vision benefits starting day one 11 paid holidays 160 hours of paid time off Annual bonus 9.5% 401k company contribution with no vesting period Tuition reimbursement up to $10000 per calendar year Onsite cafeteria with daily food stipend Normal working hours are Monday - Friday from 6:00am - 2:30pm Position Summary & Responsibilities: To perform assembly, refurbishment, subassembly and test functions of electrical and mechanical components

Validation Engineer

Katalyst Healthcares and Lifesciences

Richmond, Virginia, USA

Full-time

Responsibilities: Ensure that all manufacturing equipment (e.g., mixers, conveyors, packaging lines) undergoes Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) to confirm that they function correctly and meet operational specifications. Validate manufacturing processes to ensure they are capable of consistently producing products that meet quality standards. This includes processes like blending, cutting, rolling, and packaging. Regularly revali

Validation Engineer

Katalyst Healthcares and Lifesciences

South Carolina, USA

Full-time

Responsibilities: Provide technical input to validation activities. Represent process validation during equipment installations. Support process validation Quality Systems. Identify opportunities for personal and professional development, continuous improvements, and help deploy best practices. Participate in regulatory agency inspections for Process Validation. Serve as one of the main points of contact in communication to customers whose equipment and processes are being validate. Responsible

Process Engineer

Katalyst Healthcares and Lifesciences

Frederick, Maryland, USA

Full-time

Position Overview: The Process Engineer will provide technical support to manufacturing and logistics operations. This includes troubleshooting, modifications, and improvements related to process systems, including clean-in-place, steam-in-place, washing, and sterilizing equipment. The engineer will be comfortable working in various production areas, such as CNC space, ISO classified rooms, and grey spaces. Responsibilities: Technical Support: Troubleshoot and resolve technical issues related

CSV Engineer

Katalyst Healthcares and Lifesciences

Nutley, New Jersey, USA

Full-time

Job Description: Looking for someone who has done Validation.Google Cloud Platform and CSV. Must understand the business of clinical. We are seeking a versatile professional with the ability to review documents meticulously and support the creation of validation deliverables as needed. The ideal candidate will thrive in a challenging environment and possess the skills to effectively communicate the importance of validation processes to stakeholders outside the validation team. Responsibilities: