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Supplier Management Engineer (REMOTE)

Thermo Fisher Scientific

•

North Carolina, USA

Full-time

Work Schedule Standard (Mon-Fri) Environmental Conditions Able to lift 40 lbs. without assistance, Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Loud Noises (Equipment/Machinery), Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Warehouse Job Description As part of the Thermo Fisher Scientific team, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues
Posted 1 day ago | Updated 4 hours ago

Data Integrity Manager

Thermo Fisher Scientific

•

Greenville, North Carolina, USA

Full-time

Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description Job Summary: The Data Integrity Manager will be responsible for ensuring flawless data management and compliance across our Greenville site. This outstanding opportunity allows you to lead a multidisciplinary team, ensuring the highest standards of data integrity in both cultural and technical aspects. You will be instrumental in implementing and maintaining compliance with 21CFR Part 11 and Annex 11 regulations
Posted 37 days ago | Updated 4 hours ago

Associate Serialization Process Engineer

Thermo Fisher Scientific

•

Allentown, Pennsylvania, 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.) Job Description Join Thermo Fisher Scientific to contribute to meaningful projects like curing cancer and ensuring food safety.
Posted 21 days ago | Updated 4 hours ago

Associate Process Engineer

Thermo Fisher Scientific

•

Allentown, Pennsylvania, 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.) Job Description Join Thermo Fisher Scientific to contribute to meaningful projects like curing cancer and ensuring food safety.
Posted 22 days ago | Updated 4 hours ago

HVAC Engineer Lilly Medicine Foundry

Lilly

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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
Posted 19 days ago | Updated 7 hours ago

Site Compliance Quality Head

Software Guidance & Assistance

•

Billerica, Massachusetts, USA

Full-time

Software Guidance & Assistance, Inc., (SGA), is searching for a Site Compliance Quality Head for a FULL-TIME assignment with one of our premier Pharmaceutical Services clients in Billerica, MA. Responsibilities: Implement and manage the records in electronic Quality Systems, such as QMS, EDMS, and LMS, etc. providing procedures and training for employees to effectively use the electronic Quality Systems Supervise the QA Documentation department in the creation, issuance, maintenance, archivi
Posted 7 days ago | Updated 1 hour ago

Quality Control Manager

Zachary Piper Solutions, LLC

•

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
Posted 48 days ago | Updated 29 days ago

MES Automation Support Engineer

Stellent IT LLC

•

Raleigh, North Carolina, USA

Third Party, Contract

Job Title:- MES Automation Support Engineer Job Location:- Holy Springs NC (Onsite) Long Term Contract Position Overview: We are seeking a MES Automation Support Engineer to support the development and deployment of a DeltaV MES (Syncade) platform, enabling fully digital manufacturing with integrated ERP, MES, and DCS systems at a cutting-edge CDMO site. This role will involve collaborating closely with cross-functional teams to drive paperless operations and enforce validated workflows. Ke
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Posted 2 days ago | Updated 5 hours ago

Global IT Compliance Sr Specialist

Thermo Fisher Scientific

•

Pennsylvania, USA

Full-time

Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description As part of the Thermo Fisher Scientific team, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing so
Posted 3 days ago | Updated 4 hours ago

QA Clinical Supplies Specialist

Zachary Piper Solutions, LLC

•

Lansdale, Pennsylvania, USA

Full-time

Piper Companies is seeking a QA Clinical Supplies Specialist to join a major pharmaceutical manufacturing company located in Lansdale, PA. This is a Hybrid role. The QA Clinical Supplies Specialist will ensure the quality, compliance and integrity of clinical trial supplies. Responsibilities of the QA Clinical Supplies Specialist include: Ensure clinical supply materials meet company policies and regulatory standards. Lead projects aimed at improving process performance, including yiel
Posted 60+ days ago | Updated 29 days ago

Engineer (R3-R4)

Eli Lilly and Company

•

Durham, North Carolina, 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 31 days ago | Updated 4 hours ago

Sr. Engineer - Oligonucleotide (R2-R4)

Eli Lilly and Company

•

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
Posted 31 days ago | Updated 4 hours ago

Sr. Principal Engineer - QA

Eli Lilly and Company

•

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
Posted 5 days ago | Updated 4 hours ago

Software Quality Engineer

Katalyst Healthcares and Lifesciences

•

Irving, Texas, USA

Full-time

Responsibilities: Review and Approval of software lifecycle (SLC) Deliverables for Regulated applications; Risk Classifications, Requirements, Config/Design Specs, IQ, OQ, PQ, Trace Matrix, Summary Reports etc. Collaborate with the cross-functional teams to build compliance capabilities to assure the quality of the deliverables and ensure the business needs are met. Review of CAPAs, Change Controls and Defects for GxP applications. Working with Global teams and providing audit support. Work
Posted 60+ days ago | Updated 4 hours ago

Senior Engineer, Quality

Novo Nordisk Inc

•

Bloomington, Indiana, USA

Full-time

About the Department At Novo Nordisk, we want to make a difference. For more than 100 years, we have led the way in diabetes care. Being part of Novo Nordisk allows our employees to embark on life-changing careers, and the opportunity to help improve the quality of life for millions of people around the world. Our Bloomington, Indiana site is a state-of-the-art facility where we have an integrated model from process and formulation to clinical and commercial biomanufacturing and drug product f
Posted 25 days ago | Updated 4 hours ago

Quality Coordinator (Plasma Quality Release) - Evening Shift

Biolife Plasma Services

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Social Circle, Georgia, USA

Full-time

By clicking the "Apply" button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda's and . I further attest that all information I submit in my employment application is true to the best of my knowledge. Job Description Job Description This role is responsible for reviewing documentation associated with plasma receipt and dispositioning, as well as release of acceptable plasm
Posted 2 days ago | Updated 1 hour ago

Quality Coordinator (Plasma Quality Release)

Biolife Plasma Services

•

Social Circle, Georgia, USA

Full-time

By clicking the "Apply" button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda's and . I further attest that all information I submit in my employment application is true to the best of my knowledge. Job Description Job Description This role is responsible for reviewing documentation associated with plasma receipt and dispositioning, as well as release of acceptable plasm
Posted 2 days ago | Updated 22 hours ago

Senior CQV Engineer

Johnson & Johnson

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Remote or Athens, Georgia, 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
Posted 60+ days ago | Updated 4 hours ago

Sr Director - Engineering

Eli Lilly and Company

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Pleasant Prairie, Wisconsin, 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 60+ days ago | Updated 4 hours ago

Senior Engineer, Quality (M-F Day Shift)

Novo Nordisk Inc

•

Bloomington, Indiana, USA

Full-time

About the Department At Novo Nordisk, we want to make a difference. For more than 100 years, we have led the way in diabetes care. Being part of Novo Nordisk allows our employees to embark on life-changing careers, and the opportunity to help improve the quality of life for millions of people around the world. Our Bloomington, Indiana site is a state-of-the-art facility where we have an integrated model from process and formulation to clinical and commercial biomanufacturing and drug product f
Posted 56 days ago | Updated 4 hours ago