41 - 60 of 341 Jobs

Media Prep Lab Services Associate Technician

Software Guidance & Assistance

South San Francisco, California, USA

Contract

Software Guidance & Assistance, Inc., (SGA), is searching for a Media Prep Lab Services Associate Technician for a CONTRACT assignment with one of our premier Pharmaceutical Services clients in South San Francisco, CA. Responsibilities: Support the Lab Services department by working effectively within the group to meet department goals, objectives, and tasks to achieve desired results. Responsible for completing assigned tasks, which include cleaning, sterilizing, and prepping labware. Have

Process Engineer II, Manufacturing Engineering

Thermo Fisher Scientific

Plainville, Massachusetts, USA

Full-time

Work Schedule Standard (Mon-Fri) 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.), Will work with hazardotoxic materials Job Description Process Engineer II will support the clinical and commercial drug manufact

CQV Engineers Needed - Spring House, PA_Onsite job

Stellent IT LLC

Spring House, Pennsylvania, USA

Third Party, Contract

Hiring for - TITLE - CQV Engineers - Spring House, PA_Onsite job They are going to need 25-30 CQV Engineers to assist on this project. Initial 6 12-month project. The areas of focus will be on Cell Therapy and Temperature mapping Need - LINEKDIN match with updated resume, no FAKE people Multiple CQV Engineers needed to support a project in Spring House, PA. The scope includes thermal mapping and qualification of various GMP equipment, with a strong focus on controlled temperature units and lab

Engineering Manager - Food Production

Jobot

Gilroy, California, USA

Full-time

Relocation and Sign on Bonus! This Jobot Job is hosted by: Ray Bahl Are you a fit? Easy Apply now by clicking the "Apply Now" button and sending us your resume. Salary: $150,000 - $185,000 per year A bit about us: We are a global sustainable food ingredients company with more than 60 manufacturing sites in the USA. We offer a servant-leader culture focused on mentoring and continuous improvement. Please apply. Why join us? Profit Sharing Excellent bonus plan Amazing health benefits 401K M

IT infrastructure CSV Consultant

Katalyst Healthcares and Lifesciences

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

VAC-Warehouse Associate

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

Reliability Engineer

Cushman & Wakefield

Boston, Massachusetts, USA

Full-time

Job Title Reliability Engineer Job Description Summary As a key member of the Reliability Engineering team, the lead Reliability Engineering will provide strategic and hands-on support for GxP Facility Operations and Engineering across Vertex GxP sites. This role will drive the implementation of maintenance and reliability best practices, focusing on maximizing equipment and system performance while ensuring compliance with GxP and Good Engineering Practices (GEP). The ideal candidate will lead

Industrial Automation Engineer

CA-One Tech Cloud Inc.

Lithia Springs, Georgia, USA

Contract

Required Skills and Experience: Bachelor s degree in Electrical Engineering, Automation, Mechatronics, or related field.5+ years of experience in industrial automation and control systems.Strong hands-on experience with PLC programming (e.g., Siemens, Allen-Bradley, Schneider).Familiarity with SCADA systems, OPC UA/DA, MQTT, and industrial communication protocols.Experience with IIoT platforms and edge computing devicesDeep expertise with Ignition by Inductive AutomationExperience working in GMP

Line Mechanic L2 - 3rd Shift

CONAGRA

Council Bluffs, Iowa, USA

Full-time

Job DescriptionShift: 10:00 PM-8:00 AM Hourly Rate: $25.47 an hour Job Summary: The Line Mechanic position reports to the Maintenance Team Lead and is responsible for a variety of responsibilities including troubleshooting, line repairs, parts replacement, completing work orders, participation in PM's, cleaning and lubricating equipment according to pre-set standards, performing teardowns and set-up of equipment. Observing all safety regulations and ensuring GMP and quality standards are met to

Plant Process Engineer IM

Alpla Inc.

Kansas City, Missouri, USA

Full-time

ALPLA is a global family-owned, privately held company that makes innovative, customized, recycled packaging for top companies such as P&G, Unilever, L'Oreal, Pepsi, and more. ALPLA values their employees, work-life balance, personal growth, compensation and sustainability. What Can You Expect From ALPLA Health and Wellness Care Program- Benefits Child Care Benefits Dependent Care Cost Savings Program Recognition programs; Promotional opportunities 401K Retirement Plan and excellent Matching Pla

Pharmaceutical Manufacturing Technician C shift

Merck Group

Verona, Wisconsin, USA

Full-time

Work Location: Verona, Wisconsin Shift: Yes Department: LS-SC-POWMA6 Verona Manufacturing 6 Hiring Manager: Cory Noltemeyer This information is for internals only. Please do not share outside of the organization. Your Role Employee is responsible to adhere to the GMP requirements defined within 21 CFR parts 210 &211, 820, ICH Q7, Safety standards set under ISO 14001 & 45001. This position primarily involves the safe and efficient manufacturing of active pharmaceutical ingredients (API's) acco

Staff Engineer, Advanced Operations

Stryker

Orlando, Florida, USA

Full-time

Work Flexibility: Hybrid Stryker is one of the world's leading medical technology companies and is dedicated to helping healthcare professionals perform their jobs more efficiently while enhancing patient care. Stryker is looking to hire Staff Engineer, Advanced Operations in Orlando, Florida to support new product introductions at Stryker Medical - Acute Care. Stryker Medical offers a diverse array of innovative medical technologies, including reconstructive, medical, surgical, neurotechnology

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

Lead Engineer, Quality Validation

Katalyst Healthcares and Lifesciences

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

Automation Engineer

Katalyst Healthcares and Lifesciences

Framingham, Massachusetts, USA

Full-time

Roles & Responsibilities: Lead design, configuration, and commissioning of DeltaV and Client-X automation systems for GMP-critical manufacturing equipment and process controls. Support change controls, deviations, and CAPAs involving DeltaV and Client-X logic, batch strategies, and alarm configuration in collaboration with QA and Validation. Develop and modify control modules, phases, and equipment modules within DeltaV in alignment with S88 batch architecture standards. Provide hands-on trouble

Technical Training Program Specialist

B. BRAUN MEDICAL (US) INC

Irvine, California, USA

Full-time

B. Braun Medical, Inc. Company: B. BRAUN MEDICAL (US) INC Job Posting Location: Irvine, California, United States Functional Area: Human Resources Working Model: Onsite Days of Work: Thursday, Wednesday, Tuesday, Friday, Monday Shift: 5X8 Relocation Available: No Requisition ID: 4306 B. Braun Medical Inc., a leader in infusion therapy and pain management, develops, manufactures, and markets innovative medical products and services to the healthcare industry. Other key product areas include nut

Validation Support Engineer

Katalyst Healthcares and Lifesciences

Boston, Massachusetts, USA

Full-time

Job Description: We are seeking an experienced Validation Support Engineer to lead validation activities for Beckhoff Twin CAT PLC-controlled systems in a 24/7 GMP-regulated manufacturing environment. The role focuses on ensuring compliance with FDA regulations (21 CFR Part 11, 210, 211, 820), GAMP5 methodologies, and internal quality standards. Responsibilities: Develop/update Validation Plans (VP) and Master Validation Plans (MVP). Lead GxP risk assessments for system changes. Author and

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

MES Engineer

Sanofi U.S.

Swiftwater, Pennsylvania, USA

Full-time

Job Title: MES Engineer Location: Swiftwater, PA About the Job We deliver 4.3 billion healthcare solutions to people every year, thanks to the flawless planning and meticulous eye for detail of our Manufacturing & Supply teams. With your talent and ambition, we can do even more to protect people from infectious diseases and bring hope to patients and their families. Sanofi is an innovative global healthcare company with one purpose: to pursue scientific miracles to improve lives. Our team str

Validation Engineer

Katalyst Healthcares and Lifesciences

Norwood, Massachusetts, USA

Full-time

Job Description: The purpose of the Validation Engineer (contract position) is to complete assignments in support of Quality and Engineering for equipment qualification, new product development, process validation and test method validation. The successful candidate will assume responsibility for drafting qualification protocols, qualification reports and engineering study reports, along with data analysis and an intermediate level of experience in the use of statistics. This position will also