Deviation Writer - Fishers

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. · ...

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

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

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, ...

Technical Writer – Remote Contract (13 Weeks) · We are seeking a Technical Writer to support documentation and compliance initiatives within a pharmaceutical environment. This is a fully remote 13-week contract. · Key responsibilities: · Draft, review, and maintain SOPs, Supplier ...

Job summary · A QC Microbiology Data Reviewer and Writer for a leading pharmaceutical company. · Responsibilities:Perform independent review of microbiology data for completeness. · ...

Leading pharmaceutical company looking for an experienced QC Microbiology Data Reviewer with 4 years of experience in GMP Microbiology laboratory data review and writing. Responsibilities include reviewing QC microbiology data for completeness and accuracy. · ...

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 ...

Job summary · QC Microbiology Data Reviewer and Writer for a leading pharmaceutical company. · ResponsibilitiesPerform independent review of QC microbiology data. · Verify raw data calculations instrument outputs electronic records. · ...

The Technical Writer/Document Control serves in a key role providing project support to the distribution operations across different functional areas (Operations, Quality,& Compliance) by facilitating, authoring documents,reviewing trackand following up on deviation responses and ...

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 ...

We are seeking an experienced Technical Writer to support documentation within a regulated Life Sciences environment. · Bachelor's degree in Life Sciences, Engineering or related field · 4–6 years of Technical Writing experience in a regulated industry · ...

We are seeking a Senior Microbiologist to perform independent and thorough review of QC microbiology data for completeness, accuracy, and cGMP compliance. · ...

The Technical Writer/Document Control serves in a key role providing project support to the distribution operations across different functional areas (Operations, Quality,& Compliance) by facilitating, · authoring documents, · writing and following up on deviations for intracompa ...

We are seeking a QC Microbiology Data Reviewer to perform independent and thorough review of QC microbiology data for completeness, accuracy, and cGMP compliance. · ...

The Technical Writer - Manufacturing is responsible for performing site Non-Conformance Report (NCR), Significant SNCRs investigations, authoring CAPAs, standard operating procedures (SOPs), Clinical Batch Records, and miscellaneous technical transfer documentation as needed. · ...