81 - 100 of 381 Jobs

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

Manufacturing Engineer-Medical Device

Trelleborg Group

Paso Robles, California, USA

Full-time

Join Our Team at Trelleborg Medical Solutions! Imagine working for one of the world's leading contract medical device manufacturers, nestled just 30 miles from California's stunning Central Coast. At Trelleborg Medical Solutions, we are not just a premier manufacturer of life-saving medical components; we are a forward-thinking company committed to excellence and innovation. Our journey in lean manufacturing has been ongoing for years, and we are on the path to becoming a showcase of excellence

Engineering - Bio Process Associate - 1st Shift , Devens MA

Futran Solutions

Massachusetts, USA

Contract

Job Description: Bio Process Associate 1st Shift--hours are 7AM - 3PM Monday - Friday. Onsite, Devens--Local candidates Only **Note there are 3 openings on this req** Description: The Bioprocess Associate uses current Good Manufacturing Practices (cGMPs) in the execution of commercial manufacturing processes for the manufacture of therapeutic proteins used in medicines that are revolutionizing the treatment of serious disease. Job Responsibilities: Operate production equipment within an assign

Quality Control Supervisor

Zachary Piper Solutions, LLC

Frederick, Maryland, USA

Full-time

Piper Companies is currently looking for an experienced Quality Control Supervisor in Frederick, MD in a hybrid role. Responsibilities for the Quality Control Supervisor include: Participate in and complete analytical testing in support of release and characterization of genetically-engineered cell therapy products, with a focus on cell-based, PCR, flow cytometry, and ELISA assays Maintain team responsible for laboratory inventory of materials and reagents Environmental monitoring Execute p

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

CSV CONSULTANT :: Remote

TESTINGXPERTS, INC. DBA DAMCOSOFT

New Jersey, USA

Third Party, Contract

Mandatory Skills CSV, Compliance and Assurance services, LIFE-SCIENCES (GXP FDA CSV IQ/OQ/PQ), Veeva, Argus, Defect Tracking Tools_JIRA Primary Skill- Computer System Validation, Computed system assurance, GAMP, GxP risk assessments, Change Management Secondary Skill- JIRA Veeva Argus Agile and Waterfall methodology Jo Description: Strong experience in Validating systems and Experienced in CSV activities in GxP related applications like SAP Systems, Product Serialization systems, MES systems P

Scientific - Assistant Scientist

Futran Solutions

Seattle, Washington, USA

Full-time

Job Description: Job Title: Assistant Scientist Location: Seattle, WA*Onsite Schedule: M-F normal business hours Top Skills: Associate Degree in Biology, Chemical Engineering, Bioengineering or relevant scientific discipline with 0-2 years of industry bioprocess experience. Mammalian cell culture and cell banking experience Experience with cell therapy process development or manufacturing Job scope or job description: The Global Manufacturing Sciences team plays a key role in supporting activ

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

Line Controller - 2nd Shift

E. A. Sween Company

Eden Prairie, Minnesota, USA

Full-time

Who We Are Since 1955, we have been on a mission To Passionately Feed Millions Daily with High Quality Food People Enjoy! We are a third-generation family-owned and professionally managed organization with a commitment to strategic growth. We continue to be successful because of talented people, just like you, who choose to join our family and call E.A. Sween home. We pride ourselves on fostering a welcoming, respectful, and rewarding culture where employees are encouraged to bring their whole

Quality Specialist On Floor Support - 2nd Shift

bioMerieux

Hazelwood, Missouri, USA

Full-time

Position Summary & Responsibilities: The Quality Inspection Specialist is responsible for performing physical inspection of card batches on the production floor, supports quality walkthroughs of production areas and changeovers between batches (as applicable). Initial schedule will be Monday through Friday 1st shift (6 am-2:30 pm) with a transition to 2nd shift schedule once training is complete (Monday through Friday 2 pm to 10:30 pm). Utilize AQL sampling guidance to inspect cards, pouches, an

Sr Network Engineer (LAN/WAN), Data Center Network Design, Routing Switching (leaf Spine), Cisco, Arista, Scripting, Automation 12+ Mths Cont

Zen & Art

Alpharetta, Georgia, USA

Contract, Third Party

Job Id: 3384 L4 Duration: 12 Months Location: Alpharetta GA Title: Sr Network Engineer (LAN/WAN), Data Center Network Design, Architecture Models, end to end network solution, Routing Switching (leaf Spine), Cisco, Arista, Scripting, Automation 12+ Mths Cont Description: Hybrid 3 Days a Week Onsite Responsibilities The engineer will be responsible for evaluating, engineering, designing, and troubleshooting enterprise scale Data Centre networks. As part of the Network Engineering team the eng

Facilities/Utilities SME

Zachary Piper Solutions, LLC

Bloomington, Indiana, USA

Full-time

Piper Companies is seeking a BioPharma Facilities/Utilities Subject Matter Expert (SME) to join an expansion project team of a new facility build for a CDMO out in Bloomington, IN. The role has an onsite expectation and slated through 2026 and potentially beyond. The SME will provide technical expertise and strategic guidance for all utility systems-both clean and plant-throughout the design, construction, and commissioning of our new GMP manufacturing facility. This role is critical to ensuring

Engineering Tech

bioMerieux

Durham, North Carolina, USA

Full-time

Position Summary & Responsibilities: The normal working hours for this role are anticipated to be Monday - Friday from 8:00am - 5:00pm. The Reliability Engineering Technician is responsible for Reliability and troubleshooting of bioMrieux manufacturing, formulation, filling, and packaging equipment systems within the site quality management system processes. Reliability of Manufacturing, Formulation, Filling, and Packaging EquipmentConduct root cause analysis (RCA) and failure modes and effect

Maintenance Mechanic I (3rd Shift)

Wimmer Solutions

New Brunswick, New Jersey, USA

Full-time

We are seeking a Maintenance Mechanic I to support a pharmaceutical manufacturing facility by maintaining, troubleshooting, and repairing equipment and utilities while ensuring compliance with Good Manufacturing Practices (GMPs), safety standards, and regulatory requirements.Key ResponsibilitiesPerform Preventive Maintenance (PM) and breakdown maintenance consistent with cGMP engineering requirements.Conduct routine maintenance on manufacturing machinery, utilities, and infrastructure.Troublesho

Validation Engineer

ACL Digital

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 equipme

Maintenance Technician - 223 schedule

ABR Employment Services

Clintonville, Wisconsin, USA

Full-time

Are you looking for a great opportunity to join a growing team in Clintonville, Wisconsin? Our client is looking for a Maintenance Technician! Maintenance Technicians - Level 2 and Level 3 Location: Clintonville, WI Shifts Available: Day and Night (2-2-3 rotating schedule) Wage Range: Level 2: $29 to $32 per hourLevel 3: $29 to $33 per hourNight shift premium: Additional $1.00 per hour Compensation and Benefits Competitive wages based on experience and level$1.00 per hour night shift premiumAddi

Maintenance Technician

Ledgent Technology

Irvine, California, USA

Contract

We are seeking a Maintenance Technician to work onsite in Irvine, CA. We have two roles available and involve the following shifts: 5:30AM to 2PM, Sunday to Thursday or Tuesday to Saturday. This job requires some experience with working in a clean room environment. This role is for 18 months and is W2 hourly with Roth Staffing (Ledgent Technologies is a division of Roth Staffing). Summary: The main function of a maintenance technician is to perform work involving the skills of two or more m

Validation Engineer Senior

ACL Digital

Thousand Oaks, California, USA

Full-time

Responsibilities: Plan and track implementation of commissioning & qualification actions/documentation versus project(s) timelines. Work with project teams to develop the commissioning and qualification strategy and document in qualification plans. 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 discrepancie

R&D Technician - Onsite

VIVA USA INC

Valhalla, New York, USA

Contract

Title: R&D Technician - Onsite Mandatory skills: Excel, Word, MS Outlook, setting up benchtop, pilot plant experiments, managing product inventories, product entries, purchase orders, pilot plant trials, product packing, shipping, labeling, GLP, GMP, data entry, documentation, manufacturing sites, ingredient purchasing, Citrus lab, preparation, testing, evaluation of beverage batches, prepare beverage, beverage concentrates, product development, brand maintenance, pilot plant productions, sampl

Construction Project Manager (BioPharma)

Zachary Piper Solutions, LLC

Bloomington, Indiana, USA

Full-time

Piper Companies is seeking a BioPharma Construction Project Manager to manage the construction and communication of a new facility build for a CDMO out in Bloomington, IN. The role has an onsite expectation and slated through 2026 and potentially beyond. The Construction Project Manager will oversee the planning, execution, and delivery of our new facility buildout project in Bloomington, ensuring it is completed on time, within scope, and within budget. This is a high-impact role that requires