trackwise Jobs

1 - 20 of 189 Jobs

Staff Product Validation EngineerJob Title - Staff Product Validation Engineer

Thermo Fisher ScientificCompany Name - Thermo Fisher Scientific

•

Santa Clara, California, 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, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.) Job Description Join us as we expand our business and quality department, which is passionate about revolutionizing the way things are done in our industry! We are seeking a highly skilled and experie

Data Integrity ManagerJob Title - Data Integrity Manager

Thermo Fisher ScientificCompany Name - 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

Associate Serialization Process EngineerJob Title - Associate Serialization Process Engineer

Thermo Fisher ScientificCompany Name - 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.

Associate Process EngineerJob Title - Associate Process Engineer

Thermo Fisher ScientificCompany Name - Thermo Fisher Scientific

•

Allentown, Pennsylvania, USA

Full-time

HVAC Engineer Lilly Medicine FoundryJob Title - HVAC Engineer Lilly Medicine Foundry

LillyCompany Name - Lilly

•

Lebanon, 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

HVAC Engineer Lilly Medicine FoundryJob Title - HVAC Engineer Lilly Medicine Foundry

LillyCompany Name - Lilly

•

Lebanon, Indiana, USA

Full-time

Quality Control ManagerJob Title - Quality Control Manager

Zachary Piper Solutions, LLCCompany Name - 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

Veeva Change Control Engineer / Quality LeadJob Title - Veeva Change Control Engineer / Quality Lead

Stellent IT LLCCompany Name - Stellent IT LLC

•

Indianapolis, Indiana, USA

Third Party, Contract

Job Title:- Veeva Change Control Engineer / Quality Lead Job Location:- Indianapolis IN (Onsite) Long Term Contract The Change Control implementation team consists of a cross-functional Core Team. We are looking for a resource to serve as the Engineer on the Core Team. The Core Team participates in the design and testing of the Veeva Change Control configuration, serves as a subject matter expert for procedure and training development, executes testing during the system validation, and suppor

Staff Software Quality Engineer, Post MarketJob Title - Staff Software Quality Engineer, Post Market

StrykerCompany Name - Stryker

•

Portage, Michigan, USA

Full-time

Work Flexibility: Hybrid or Onsite Stryker is hiring a Staff Software Quality Engineer, Post Market to support our Medical's Digital Health division and portfolio Software as a Medical Device (SaMD)/Software in a Medical Device (SiMD) to support projects as a quality engineer for post-market activities to drive customer quality. Workplace Flexibility & Location requirements: This is a hybrid role requiring the candidate to be within commuting distance of one of the following locations: San Jos

QC Analyst IIIJob Title - QC Analyst III

Sunrise Systems, Inc.Company Name - Sunrise Systems, Inc.

•

Portsmouth, New Hampshire, USA

Contract

Job Title: QC Analyst Job ID: 25-08265 Location: Portsmouth, NH Duration: 12 months on W2 contract The Quality Control Technical Transfer Analyst 3 will act as a team member of the Quality Control department to support production by contributing to the completion of the technical transfer activites. Also participate in quality testing for customer in-process, final product testing and stability studies when needed. Applies job skills and company's policies and procedures to complete a variety o

Application Architect (W2, Medical Device, Salesforce)Job Title - Application Architect (W2, Medical Device, Salesforce)

TEKsystems c/o Allegis GroupCompany Name - TEKsystems c/o Allegis Group

•

North Chicago, Illinois, USA

Full-time

Description Application Architect. W2, Contract, Remote This person must come from a medical device area/experience 8+ years of experience in enterprise application architecture. Proven experience with validated systems in a regulated industry (medical devices or pharmaceuticals). Strong understanding of system validation lifecycle (SDLC, CSV, 21 CFR Part 11). Experience with enterprise integration patterns and middleware technologies. Excellent communication and stakeholder management skills.

QA Clinical Supplies SpecialistJob Title - QA Clinical Supplies Specialist

Zachary Piper Solutions, LLCCompany Name - 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