Deviations - 221+ job offers

Actalent

Job Title: Quality Systems Specialist - CAPAs and Deviations Job Description The Quality Systems Specialist plays a crucial role in supporting cGMP quality system activities within a biopharmaceutical manufacturing environment. The position involves executing and maintaining quality processes such a

Purpose And Scope Of Position: This position will work independently and with the team in supporting QA oversight of CTLs for CTO Vector External Manufacturing operations. external from our CTLs. This role is accountable for oversight of routine Quality responsibilities related to outsourced testing

Advancing medicine to save lives. Together. Thanks to many decades of experience and our passion for what we do, we make an essential contribution to the global availability of biopharmaceuticals, especially for patients with rare and serious diseases. Rentschler Biopharma SE is a leading contract d

Legend Biotech is a global biotechnology company dedicated to treating, and one day curing, life-threatening diseases. Headquartered in Somerset, New Jersey, we are developing advanced cell therapies across a diverse array of technology platforms, including autologous and allogenic chimeric antigen

Kindeva Drug Delivery

$198,500 - $262,850 /year

Our Work Matters At Kindeva we make products that save lives, ensuring better health and well-being for patients around the world. The Impact You Will Make The Sr Director / Site Head of Quality is responsible for leading all Quality Assurance (QA) and Quality Control (QC) functions at the Northridg

Location: Newark, CA | Shift: Day Shift | Reports to: Quality Engineering Manager What a day looks like You start your day by powering up the AXI/5DX system and confirming the correct program is loaded. As boards arrive from the line, you guide each one through the automated X-ray process, ensuring

Lonza

QA Product Manager Location: Tampa, Florida – Onsite The QA Product Manager based at our Tampa, Florida and plays a critical role in ensuring customer products meet the highest quality and compliance standards. As a dedicated quality advocate and subject matter expert, you will partner closely with

Your Role: The QC Specialist is responsible for ensuring the compliant execution, oversight, and continuous improvement of Quality Control activities supporting Cell and Gene Therapy (CGT) products under cGMP conditions. This role provides subject matter expertise in analytical testing, quality even

NorthStar Medical Radioisotopes

Overview Join the best radiopharmaceutical company in the world! If you’re looking to make an impact while building a meaningful career in a specialized, fast-growing field, NorthStar Medical Radioisotopes is the place to do it. NorthStar Medical Radioisotopes is a growing, commercial-stage company

Evotec

$141,120 - $193,200 /year

Job Title: Director, Raw Materials Quality Location: Site Based, Redmond, WA with some travel to Seattle Site. Shifts: Monday to Friday, Days. About Us: this is who we are At Just Evotec Biologic, we believe that curiosity is the spark that drives innovation and success. As a forward-thinking team,

Cyprotex

$141,120 - $193,200 /year

Job Title: Director, Raw Materials Quality Location: Site Based, Redmond, WA with some travel to Seattle Site. Shifts: Monday to Friday, Days. About Us: this is who we are At Just Evotec Biologic, we believe that curiosity is the spark that drives innovation and success. As a forward-thinking team,

The Position Welcome to Holly Springs, North Carolina— home to Roche/Genentech's largest-ever investment: a $2B greenfield start-up where next-generation technology, high-performing teams and Operational Excellence converge to create the global standard for high-volume, highly-efficient Drug Product

FORMULATED Solutions LLC

PRIMARY PURPOSE: THE QUALITY PRODUCT MANAGER IS RESPONSIBLE FOR ENSURING THAT THE PRODUCTS MANUFACTURED IN THE FACILITY CONSISTENTLY MEET QUALITY, SAFETY, AND REGULATORY STANDARDS ACROSS THEIR ENTIRE LIFECYCLE. THIS ROLE INTEGRATES QUALITY OVERSIGHT WITH PRODUCT STRATEGY BY DIRECTLY PARTNERING WITH

Summary The Quality Assurance (QA) Specialist III – Deviations/CAPAs/Complaints , will be responsible for the review and approval of Deviations/CAPAs/Complaints. The QA Compliance Specialist III – Deviations/CAPAs/Complaints, will handle all associated responsibilities in compliance with Fujifilm qu

## Position Overview Summary : The Quality Assurance (QA) Specialist III – Deviations/CAPAs/Complaints, will be responsible for the review and approval of Deviations/CAPAs/Complaints. The QA Compliance Specialist III – Deviations/CAPAs/Complaints, will handle all associated responsibilities in compl

About the Company Client’s Manufacturing Division (MMD) is dedicated to providing high-quality pharmaceutical and biotech solutions. Our mission is to innovate and excel in the manufacturing process while fostering a culture of collaboration and continuous improvement. About the Role The role involv

Elanco

At Elanco (NYSE: ELAN) – it all starts with animals! As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets. At Elanco, we are driven by our vision of Food and Companionship Enriching Life and our

Northrop Grumman

$139,100 - $208,700 /year

RELOCATION ASSISTANCE: Relocation assistance may be available CLEARANCE REQUIRED FOR START: Yes CLEARANCE TYPE: Secret TRAVEL: Yes, 25% of the Time Description At Northrop Grumman, our employees have incredible opportunities to work on revolutionary systems that impact people's lives around the worl

Bristol Myers Squibb

$82,236 - $99,650 /year

At RayzeBio, every day is an opportunity to ignite meaningful change. As a wholly-owned subsidiary of Bristol Myers Squibb, RayzeBio blends the nimble, pioneering spirit of an emergent biotech with the global expertise and resources of a leading innovator in oncology. Our mission is to develop trans

FUJIFILM Biotechnologies

The Quality Assurance (QA) Specialist III – Deviations/CAPAs/Complaints will be responsible for reviewing and approving Deviations, CAPAs, and Complaints, ensuring compliance with Fujifilm quality policies and site SOPs. The specialist will handle all associated responsibilities, assist with trackin