Deviation - 267+ job offers

Job Title: Deviation Investigator Job Description The Deviation Investigator is responsible for identifying, documenting, investigating, and resolving deviations from standard procedures, protocols, and regulatory requirements within a pharmaceutical environment. This role ensures that all deviation

United States, Portsmouth (New Hampshire) Deviation Investigator Level 2 Location: This position is based in our Portsmouth, NH office. The typical work schedule is Monday through Friday, 8:00 AM–5:00 PM EST. What You Will Get Below you will find a comprehensive summary of the benefits package we of

ThermoFisher Scientific

Work Schedule Standard (Mon-Fri) Environmental Conditions Adherence to all Good Manufacturing Practices (GMP) Safety Standards, 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

Work Schedule Standard (Mon-Fri) Environmental Conditions 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 As part of the Thermo Fisher

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

BrainChild Bio

$120,000 - $135,000 /year

BrainChild Bio is seeking to hire a Senior Process Engineer to add to our growing team. This role will provide critical support to technology transfer, process development and manufacturing activities of BrainChild programs including but not limited to helping driving technology transfers to externa

INCOG BioPharma Services

Operations Batch Review Specialist The Operations Batch Review Specialist is responsible for reviewing batch documentation post execution to ensure that all work completed was carried out in accordance with regulatory requirements, Good Manufacturing Practices (cGMP) and Standard Operating Procedure

Work Schedule Standard (Mon-Fri) Environmental Conditions 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.) As part of the Thermo Fisher Scientific team

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

Aptask Global Workforce (AGW) is seeking a Deviation Management Specialist - I (Assistant) for an Onsite position with a leading Pharmaceutical Company located in West Point, PA. This is a 12 month contract opportunity. This role provides daily technical support to cGMP manufacturing operations. The

United States, Portsmouth (New Hampshire) Deviation Investigation Level 2 – (Night Shift) Location: This position is based in our Portsmouth, NH office. This is a 3rd shift position operating on a 12-hour rotating schedule (7:00 PM – 7:00 AM). The schedule follows a rotating pattern of Monday–Tuesda

United States, Portsmouth (New Hampshire) Deviation Investigation Level 3 – (Night Shift) Location: This position is based in our Portsmouth, NH office. This is a 3rd shift position operating on a 12-hour rotating schedule (7:00 PM – 7:00 AM). The schedule follows a rotating pattern of Monday–Tuesda

Flexible & Integrated Technical Services, LLC

For Manufacturing Services in the Quality Systems a rea. WHAT MAKES YOU A FIT: The Technical Part: Bachelor's Degree with five (5) years of experience as a Scientist within the pharmaceutical or regulated industry. Bilingual (English & Spanish). Project Management skills. Shift: Administrative a

Integrated Resources, Inc ( IRI )

Qualifications: B.S./M.S. degree in appropriate engineering/scientific field Minimum of 0-3 years post-Bachelors degree experience in a cGMP environment (e.g. Production, Development, Process Engineering, Technical Services or related field) in pharmaceutical/ biotech industry Previous experience in

Job Title: Deviation Management Specialist Location: West Point PA Duration: 12+ Months Qualifications: •B.S./M.S. degree in appropriate engineering/scientific field •Mini mum of 0-3 years post-Bachelors degree experience in a cGMP environment (e.g. Production, Development, Process Engineering, Tech

Job Title: Deviation Investigator Duration: 6 Months Location: Devens, MA: 50% onsite required Work Schedule: Mon- Fri(normal business hours) Major Duties and Responsibilities: Conduct and manage the resolution of deviations, root cause investigations, impact assessments, and CAPAs. Liaise with mult

Job Title: Deviation Management Specialist Location: West Point PA Duration: 12+ Months Qualifications: •B.S./M.S. degree in appropriate engineering/scientific field •Mini mum of 0-3 years post-Bachelors degree experience in a cGMP environment (e.g. Production, Development, Process Engineering, Tech

SOKOL GxP Services

SOKOL GxP Services is seeking a junior-level Associate Scientist to support deviation investigations and CAPA activities within a regulated biopharmaceutical environment. This role focuses on root cause analysis, investigation execution, and technical report writing , with cross-functional collabora

Integrated Resources, Inc ( IRI )

Duration: 6 months+ Must Haves: Required Bachelor’s degree in chemical/biochemical engineering, biological sciences, or a related discipline with 2–4 years of relevant experience (or equivalent). Prior experience leading cGMP investigations using formal Root Cause Analysis tools required. Conduct an

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