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SAP ATP/GATP Consultant

Trinity Technology Solutions LLC

•

Austin, Texas, USA

Third Party, Contract

Job Description: We are seeking an experienced ATP/GATP SAP Func-Techno Lead to join our team. The ideal candidate will have a strong background in SAP, particularly with Order Management, ATP, and GATP modules, and will be responsible for both functional and technical tasks. Key Responsibilities: Analyse and resolve Production support incidents.Provide solutions and work on enhancements in SAP functional areas.Perform ABAP coding and Fiori changes.Spend 50% of time on functional work and 50% on
Easy Apply
Posted 5 days ago

Biologics Process Engineer

Sunrise Systems, Inc.

•

Wilson, North Carolina, USA

Contract

Job Title: Biologics Process Engineer Job ID:25-07694 Location: Wilson, NC 27893 Duration: 09 Months On W2 Contract Hiring manager Notes: Candidate will need to be in commutable distance to Wilson, NCRole will initially be remote until the Wilson, NC building opens then they will be required to be onsiteMust have a Bachelor's degreeAt least 2 years of experienceExperience in Biologics, Manufacturing, or EngineeringLess focus on "large capital construction systems"Must have Delta Vee system knowl
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Posted 32 days ago | Updated 1 day ago

Analytical Validation Engineer

Zachary Piper Solutions, LLC

•

Hopewell Township, New Jersey, USA

Full-time

Piper Companies is looking for an Analytical Validation Engineer to support commissioning and decommissioning activities for a major pharmaceutical company in the Titusville, NJ area. Responsibilities for the Analytical Validation Engineer include: Experience in Pharmaceutical Laboratory Operations Must be familiar and have experience with laboratory instrument selection, installation (IQ/OQ) and qualification (PQ) Experience supporting laboratory investigations from beginning to end, includ
Posted 3 days ago | Updated 2 hours ago

Validation Engineer

Zachary Piper Solutions, LLC

•

Lynwood, California, USA

Full-time

Piper Companies is currently seeking an experienced Validation Engineer tosupport a highly reputable Pharmaceutical company in Lynwood, California. Responsibilities for the Validation Engineer Oversee validation activities, including risk analysis, packaging, cleaning, and equipment qualification for new and updated processes.Develop, review, and execute validation protocols, reports, and documentation while ensuring compliance with GMP standards.Coordinate validation efforts across shifts, pr
Posted 3 days ago | Updated 2 hours ago

Research Associate II (Virology)

Zachary Piper Solutions, LLC

•

Frederick, Maryland, USA

Full-time

Piper Health and Sciences is seeking a Research Associate II to support a well-known research organization specializing in infectious disease research in the Frederick, MD area. The Research Associate II will be responsible for performing TCID50 and plaque assays. Responsibilities of the Research Associate II include: Design, generate, and characterize recombinant proteins Perform mammalian cell culture, transient transfections, protein expressions, protein purifications, and micro pipetting in
Posted 3 days ago | Updated 2 hours ago

Equipment Commissioning Systems Administrator

Stellent IT LLC

•

New York, New York, USA

Third Party, Contract

Job Title: Equipment Commissioning Systems Administrator Please see attached. No candidates with Visas will be accepted for this role. W2 referrals or 1099 candidates that are USor Citizens are accepted. Thank you Overview: Our Client's equipment is being moved into a GMP sense so there are new requirements and need to get them up to compliance Location: New York Fully onsite. Bill Rate/Budget: 80-$90/hr max Start Date: Early June start date Duration: 12 months with 2 potential extensions
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Posted 4 days ago | Updated 17 hours ago

Validation Engineer

Katalyst Healthcares and Lifesciences

•

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
Posted 5 days ago | Updated 4 hours ago

Validation Engineer

Katalyst Healthcares and Lifesciences

•

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-functional
Posted 5 days ago | Updated 4 hours ago

Validation Engineering

Katalyst Healthcares and Lifesciences

•

Marlborough, Massachusetts, USA

Full-time

Responsibilities: TCU Mapping Protocols: Conduct and document temperature mapping activities to ensure that Temperature Control Units (TCUs) comply with regulatory and operational standards. Protocol Support: Assist in the development and execution of validation protocols, ensuring alignment with both internal and regulatory requirements. Data Collection & Analysis: Support the collection and initial analysis of TCU mapping data to aid in validation reporting and quality control. Collaboration
Posted 5 days ago | Updated 4 hours ago

Utilities Qualification(Validation) Engineer

Katalyst Healthcares and Lifesciences

•

Salt Lake City, Utah, USA

Full-time

Job Description: A pharmaceutical/biotech client in Utah is seeking a mid-to-senior level Utilities Qualification Engineer with 5+ years of experience in critical utilities validation and qualification. The candidate will support GMP manufacturing operations by qualifying and documenting systems like AHUs, purified water, compressed air, and legacy cleanroom systems. This is a fully onsite role and requires a self-driven individual with hands-on experience in IQ/OQ/PQ, EDMS tools (Glorya
Posted 5 days ago | Updated 4 hours ago

CQV Engineer

Katalyst Healthcares and Lifesciences

•

Raleigh, North Carolina, USA

Full-time

Roles & Responsibilities: Experience in Commissioning, Qualification, and Validation activities for upstream, downstream and support equipment. CQV support for all Simple Direct Impact Equipment and No Impact Equipment for all Buildings. Work with equipment and area owners from initial design, procurement, qualification (if required) to final Handover. Work with CQV Document Generation Lead in relation to generation and approval of; DQ/Design Reviews/SLIA/Test Matrices/Risk Assessments/QA Vend
Posted 5 days ago | Updated 4 hours ago

Production Planner IV

Sunrise Systems, Inc.

•

Irvine, California, USA

Contract

Job Title: Production Planner IV Job ID: 25-08159 Location: Irvine, CA Duration: 18 Months On W2 Contract Job description Responsible for all or a major portion of processing operations in a plant for 2nd shift operations. Responsible for production operations, maintenance, plant engineering, safety, quality control, scheduling, accounting, and workforce level. Promotes good relations with community, government agencies, and customers. May conduct or participate in labor negotiations and admini
Easy Apply
Posted 5 days ago | Updated 1 day ago

Manufacturing Tech 1, Line 4 - Day Shift (A)

bioMerieux

•

Durham, North Carolina, 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 $10,000 per calendar year Onsite cafeteria with daily food stipend Position Summary & Responsibilities: Normal working hours: 7:00am - 7:30pm working a 2-2-3 rotation schedule. The anticipated hiring range for this role is $19.25 - 20.00/hr with shift differential and an
Posted 7 days ago | Updated 2 hours ago

Engineer - Process Development (R1-R2)

Eli Lilly and Company

•

Boston, Massachusetts, 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
Posted 7 days ago | Updated 4 hours ago

Army Staff Accountant

Intrepid

•

Indianapolis, Indiana, USA

Full-time

Intrepid sets the standard for delivering excellence in the federal marketplace and is known for treating employees like family. We provide our employees with a challenging and supportive work environment, paired with a competitive salary and an industry-leading 401k contribution. We are looking for an Army Staff Accountant to join our team to support the USAFMCOM; Army Accounting and Audit Operations (A3O). The Army Staff Accountant will provide recommendations and services to improve the accur
Posted 19 days ago | Updated 1 hour ago

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
Posted 3 days ago | Updated 2 hours ago

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
Posted 3 days ago | Updated 2 hours ago

SAP ATP/GATP SAP Func-Techno Consultant: Bay Area, CA or Austin, TX

radient.ai

•

Austin, Texas, USA

Contract, Third Party

Hello, This is Swaroop from Radient.AI. I have reached you regarding the job SAP ATP/GATP SAP Func-Techno Consultant. The job description is mention below kindly have a look and let me knows your thoughts. Role: SAP ATP/GATP SAP Func-Techno Consultant Location: Bay Area, CA or Austin, TX Job Description: We are seeking an experienced ATP/GATP SAP Func-Techno Lead to join our team. The ideal candidate will have a strong background in SAP, particularly with Order Management, ATP, and GATP modules,
Easy Apply
Posted 6 days ago

Group Lead

Cargill

•

Albert Lea, Minnesota, USA

Full-time

New, easy-to-apply options are available for this role: chat with our recruiting assistant Ana at careers.cargill.com or text CargillJobs to 60196. Want to build a stronger, more sustainable future and cultivate your career? Join Cargill's global team of 160,000 employees who are committed to safe, responsible and sustainable ways to nourish the world. This position is in Cargill?s protein and salt business, where we provide wholesome, high-quality food products to a wide range of customers, fro
Posted 27 days ago | Updated 21 hours ago

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
Posted 5 days ago | Updated 4 hours ago