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KBI Biopharma jobs

Job Summary: Responsible for review and approval of Deviations and CAPAs in support of GMP manufacturing operations. Support timely review of events for classification, initiation in EtQ and closure. Support external client review and resolution of comments

KBI Biopharma  26 days ago
KBI Biopharma jobs

Job Summary: Responsible for review and approval of Deviations and CAPAs in support of GMP manufacturing operations and other functional groups as required (e.g. Facilities Engineering, IT, Supply Chain, etc.). Support timely review of events for classification,

KBI Biopharma  9 days ago
INCOG BioPharma jobs

Job Description INCOG BioPharma Services is seeking an experienced and detail-oriented Deviation Writer to join our Manufacturing Engineering team. This role is crucial for translating a variety of complex technical events into clear, accurate, and robust investigations.

INCOG BioPharma  8 days ago
Pella Corporation jobs

Overview: The purpose of a Field Deviation Coordinator is to review deviated items that come back from the field and determine a resolution. Then, effectively communicate, document and rescheduled install date with our customers. Field Deviation Coordinator’s purpose

Pella Corporation  5 days ago

WHO? INCOG BioPharma Services is seeking an experienced and detail-oriented Deviation Writer to join our Manufacturing Engineering team. This role is crucial for translating a variety of complex technical events into clear, accurate, and robust investigations. The

Lead Candidate  25 days ago
Aequor jobs

MS&T Specialist – Deviations Investigator Location: Davie, FL Shift: Monday - Friday 8:00am - 5:00pm Duration: 6 months Temp to Perm: Possibility based on workers performance and openings Core Essential skill sets required: 1. This role will

Aequor  21 days ago

WHO? INCOG BioPharma Services is seeking an experienced and detail-oriented Deviation Writer to join our Manufacturing Engineering team. This role is crucial for translating a variety of complex technical events into clear, accurate, and robust investigations. The

Lead Candidate  1 day ago
JMD Technologies Inc. jobs

Title: Sr. Staff MTO – Deviations, CAPA & Manufacturing Investigations Location: Boston, MA (Seaport – 100% Onsite) Employment Type: Contract (12+ Months) Status: Accepting Candidates About the role Join a Manufacturing Technical Operations (MTO) team supporting Cell

JMD Technologies Inc.  2 days ago

Responsibilities Investigate and author reports on a range of deviating conditions or nonconforming events across multiple technical departments in collaboration with subject matter experts. Gather, analyze, and interpret information to provide evidence supporting investigation conclusions and

Harba Solutions Inc.  1 day ago
Eli Lilly and Company jobs

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

Eli Lilly And Company  29 days ago
Eli Lilly and Company jobs

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

Eli Lilly And Company  29 days ago
Marmon Holdings jobs

Sonnax Transmission Company As a part of the global industrial organization Marmon Holdings—which is backed by Berkshire Hathaway—you’ll be doing things that matter, leading at every level, and winning a better way. We’re committed to making

Marmon Holdings  29 days ago
Controlled Contamination Services jobs

Job DetailsJob Location: Boston, MA 02215Position Type: Full TimeEducation Level: High SchoolSalary Range: $19.00 - $20.00 HourlyJob Shift: AnyControlled Contamination Services has been a national provider of facility solutions, technical and decontamination services, since 1993. Our

Controlled Contamination Services  29 days ago
Capstone Logistics jobs

Cincinnati, OH $650 - $800+/weekly 2nd Shift - 7pm Start Time Vendor Compliance Auditor JOB SUMMARY: This role is responsible for auditing the quality of incoming loads, ensuring compliance with established standards, and identifying any deviations. SUPERVISORY

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Capstone Logistics  29 days ago
Cushman & Wakefield jobs

Job TitleSenior Project Controls Planner, Project & Development Services Job Description SummaryThis senior level role will act as the face of the company responsible for the client relationship with regards to planning. Will make an immediate

Cushman & Wakefield  29 days ago
Novartis jobs

Job Description SummaryLocation: East Hanover, United States Novartis will not sponsor visas for this position. Novartis is unable to offer relocation support for this role: please only apply if this location is accessible for you. This

Novartis  29 days ago
Eli Lilly and Company jobs

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

Eli Lilly And Company  29 days ago
Sanofi jobs

Job Title: Automation Engineer Location: Swiftwater, PA About the Job Join a global network that powers how Sanofi delivers — seamlessly, purposefully, and at scale. In Manufacturing & Supply, you’ll help reimagine how life-changing treatments reach

Sanofi  29 days ago
Fortrea jobs

As one of the largest Clinical Research Organizations in the world, we have four Early Phase Clinical Research Units in the UK and US. We are currently seeking a Sr. Clinical Operations Manager, to interact directly

Fortrea  29 days ago
Vertex jobs

Job Description Job Summary: Vertex is seeking an experienced Associate Director, Quality Control to provide strategic and operational leadership for commercial Cell and Gene Therapy (CGT) programs supported through external manufacturing and testing partners. This role

Vertex  29 days ago

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