QC Microbiology Data Reviewer and Writer - Indianapolis

ECLARO is looking for a QC Microbiology Data Reviewer and Writer to perform independent review of QC microbiology data for completeness, accuracy, cGMP compliance. · ...

This position involves performing independent review of quality control microbiology data for completeness accuracy cGMP compliance verifying raw data calculations instrument outputs electronic records ensuring documentation meets ALCOA+ integrity principles identifying discrepan ...

The Scientific Writer will draft study reports and study summaries to support regulatory submissions for both biotech and crop protection products. · Draft high-quality Product Chemistry study reports and study summaries to support Crop Protection regulatory submissions. Strong s ...

· Technical Writer needs 3+ years technical writing experience · Technical Writer requires: · Technical writing · SOPs · Analyze · Training material · Technical Writer duties: · Develop and Edits standard operating procedures, user tools, training materials, glossary content and ...

· Technical Writer needs 5+ years experience. Pharma, medica device industry · Technical Writer requires: · Technical writing · Documentation · SOPs · Pharma medical device industry · Technical Writer duties: · Develop and edits standard operating procedures, user tools, trainin ...

The Scientific Writer will draft study reports and study summaries to support regulatory submissions for both biotech and crop protection products. · ...

Job Title: Technical Writer · Location: Onsite — Plainfield Distribution Center, Plainfield, Indiana · Reports To: Associate Director – Operations or Associate Director - Senior Operations Associate · Work Schedule: Monday–Friday, 8:00 AM–4:30 PM (5 days/week). Must be flexible t ...

The Scientific Writing Team drafts study reports and study summaries to support regulatory submissions for both biotech and crop protection products. · Draft high-quality Product Chemistry study reports and study summaries to support Crop Protection regulatory submissions. · ...

We are seeking a Medical Technical Writer to support our Quality Management System by developing GxP documentation within Veeva QualityDocs. · Migrate legacy content into approved templates ensuring compliance with regulatory requirements. · ...

Regulatory Specialist-Scientific Writer BS Chemistry/BioChem, Prior experience with scientific writing, GLP experience highly preferred. · ...

· Manufacturing Technical Writer needs 2+ years' tech writing , quality assurance experience · Manufacturing Technical Writer requires: · Bachelors Degree or Work Experience · Experience in Technical Writing · Strong communication and attention to details skills · Ability to wor ...

Apex Systems is seeking an experienced Technical Writer to support the global Laboratory Information Management System (LIMS) migration. · This role focuses on standardizing SOPs across dozens of facilities to create documentation that all sites can follow as Global Standards. · ...

A pharmaceutical manufacturing company is seeking a detail-oriented Technical Writer with expertise in deviations and change control documentation. This onsite role plays a critical part in ensuring regulatory compliance and supporting quality operations through precise, timely, ...

Automotive Service Writer – Indianapolis, IN · Your next career move starts here — anonymously, quickly, and directly with the hiring manager. · Indianapolis shops are busy, customers are lined up, and great Service Writers are in short supply. If you know how to run a service la ...

Perform independent and thorough review of QC microbiology data for completeness accuracy and cGMP compliance Verify raw data calculations instrument outputs electronic records for assays including but not limited to bioburden sterility endotoxin media qualification environmental ...

This position involves reviewing QC microbiology data for completeness, accuracy, and cGMP compliance. · Perform an independent review of QC microbiology data. · ...

The Senior Microbiologist will perform independent review of QC microbiology data for completeness accuracy and cGMP compliance verify raw data calculations instrument outputs electronic records for assays including bioburden sterility endotoxin media qualification and environmen ...

Horner Industrial Group is seeking an experienced estimator/service writer for our industrial Manual Machining Repair Job Shop located in Indianapolis. · ...

About Little Red Door Cancer Agency is a non-profit organization that provides cancer services to medically underserved residents in central Indiana. · The Grant Writer will be responsible for planning, coordinating and executing grant activities including researching and prepari ...

· Technical Writer Deviations & Change Control · Our client, a pharmaceutical manufacturing company, is seeking a detail-oriented Technical Writer with expertise in deviations and change control documentation. This onsite role plays a critical part in ensuring regulatory compli ...