Deviation writer jobs in United States

We're hiring a deviation writer to join a pharmaceutical manufacturing team in Indianapolis, Indiana. This full-time, on-site role is ideal for an early-career scientist or engineer with 1–2 years of experience in GMP manufacturing or quality support. · ...

We are seeking an experienced and detail-oriented Deviation Writer to join our Manufacturing Engineering team. · The Deviation Writer will work closely with the Manufacturing, Production Engineering, Manufacturing Sciences and Technology, Supply Chain, Quality, · and other cross- ...

We're hiring a deviation writer to join a pharmaceutical manufacturing team in Indianapolis. · ...

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 Deviation Writer w ...

Experienced and detail-oriented Deviation Writer sought for Manufacturing Engineering team. Translates complex technical events into clear investigations. · ...

· 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. Th ...

INCOG BioPharma Services seeks an experienced Deviation Writer to join their Manufacturing Engineering team. · Translate complex technical events into clear investigations. · ...

The deviation/investigation writer level 1 will work on deviations of moderate scope where all deviation will be reviewed through the manager. · The positions primary function will be to investigate deviations from all departments, this will include assessing the product impact, ...

Our client, a leading organization in the healthcare manufacturing industry, is seeking a Deviation NCR Writer to join their team. · ...

The Client is seeking a detail-oriented and technically proficient Deviation Investigator to support deviation investigations and technical report writing. · Conduct thorough investigations into deviations, identifying root causes and contributing factorsWrite clear, concise, and ...

We are seeking a detail oriented and technically adept Deviation Investigator to bolster our deviation investigations and technical report writing efforts. · ...

The purpose of this role is to have responsibility for the initiation, investigation and completion of Minor and low/medium severity Major process deviations unassisted, · and the supervised completion of high severity Major and Critical process deviations with the aim at identif ...

Initiate investigation and completion of minor and low/medium severity major process deviations. Identify root cause, determine product quality impact, and implement corrective actions to prevent recurrence. · ...

This is an on-site position located in Pearland, TX. · Technical writing for the educated but uninformed reader, translating difficult and complex scientific events into a brief and cohesive report as a finished product. · Gathering Data from various sources across the site, lead ...

Lilly is actively growing its manufacturing footprint globally to meet the needs of patients and deliver on our exciting future. As a result, Lilly is looking for experienced quality assurance associates to support our growth in Lilly Kenosha County (LKC). This is an outstanding ...

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 p ...

Join Thermo Fisher Scientific as a Quality Specialist II and contribute to global healthcare and scientific advancement. · ...

Join Thermo Fisher Scientific as a Quality Specialist II and contribute to global healthcare and scientific advancement. · Ensure compliance with GMP standards, FDA regulations, and international quality requirements while supporting manufacturing operations across multiple produ ...

This role ensures compliance with GMP standards and supports manufacturing operations across multiple product lines., · Manage Major deviation investigations. · ,Present investigations to regulatory inspectors. · ,, ...

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 ...