Specialist I - Quality Assurance Systems, Deviations/CAPAs Position Summary: Work Schedule: M-F 8am-5pm 100% on-site Working for Catalent Biologics is an opportunity to join an entrepreneurial team. Catalent Biologics is making significant investments in people and capabilities.
Deviation Writer Summary INCOG BioPharma Services is seeking an experienced and detail-oriented Deviation Writer to join our team. This role is crucial for translating a variety of complex technical events into clear, accurate, and robust investigations. The Deviation Writer
INCOG BioPharma Services is seeking an experienced and detail-oriented Deviation Writer to join our team. This role is crucial for translating a variety of complex technical events into clear, accurate, and robust investigations. The Deviation Writer will work
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice 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
Overview Join a critical role at the intersection of quality, compliance, and operations. As a Deviation Investigation Specialist, youll lead root cause investigations, develop clear and compliant technical documentation, and partner with cross-functional teams to drive continuous
About Site Catalent’s Greendale, Indiana site is a key part of the company’s Wellness business, serving as one of North America’s primary gummy development and manufacturing centers. The site specializes in the formulation and production of
Description Verista’s 500 experts team up with the world’s most recognizable brands in the life science industry to solve their business needs. The nature of our business is to empower growth and innovation within the scientific
Work ScheduleStandard (Mon-Fri) Environmental ConditionsCleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc. allowed, Office Job Description When you’re part of the team at Thermo Fisher Scientific, you’ll do important work,
Company Overview: Process Alliance is a leading engineering consultancy firm dedicated to delivering innovative solutions in engineering, automation, manufacturing services, and medical devices. With a commitment to being a better model of problem solving, we have
Deviation Supervisor 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:
Sr Associate Manufacturing Deviation Owner Environmental & Contamination Control Join Amgens Mission of Serving Patients At Amgen, if you feel like youre part of something bigger, its because you are. Our shared missionto serve patients living with
QA Compliance Specialist 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
Deviation Management Engineer Location: 770 Sumneytown Pike, West Point PA Rate: $41/Hr Qualifications: Education Minimum Requirements: B.S. degree in Engineering or Sciences. Required Experience and Skills: Minimum one (1) year post-bachelors degree experience in a GMP (good
Deviations Specialist The Deviations Specialist supports the Badger Mission and Principles as a member of the Quality Unit. They are responsible day-to-day administration and coordination of the deviation management workflow within the QMS, under QA Supervisor direction. They also
Specialist I - Quality Assurance Systems, Deviations/CAPAs Position Summary: Work Schedule: M-F 8am-5pm 100% on-site Working for Catalent Biologics is an opportunity to join an entrepreneurial team. Catalent Biologics is making significant investments in people and capabilities.
Deviation Specialist A leading pharmaceutical organization is seeking a Deviation Specialist to support its quality and compliance operations within a high-volume sterile manufacturing facility. This role focuses on conducting thorough investigations, driving root cause analysis, and contributing to
Deviation Investigation Level 3 (Day Shift) This position is based in our Portsmouth, NH office. This is a 1st-S shift position operating on a 12-hour rotating schedule (7:00 AM 7:00 PM). The schedule follows a rotating pattern
Deviations/Capa Manager Quality Systems IV Integrated Resources, Inc., is led by a seasoned team with combined decades in the industry. We deliver strategic workforce solutions that help you manage your talent and business more efficiently and effectively.
Deviation Management Pay Rate: $41.50/HR on W2 Location of work: 770 Sumneytown Pike, West Point, PA 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,
MS&T Specialist Deviations Investigator Our client, a Pharmaceuticals company, is looking for a MS&T Specialist Deviations Investigator for their Davie, FL location. Responsibilities: Lead and/or co-author cGMP investigations for OSD manufacturing and complex operations (deviations/nonconformances/atypical events), ensuring clear problem