QC Technical Writer (Contract)

Location: Salt Lake City, UT - Remote Role Job Summary We are seeking a contract QC Technical Writer to support method transfer and readiness activities for QC Chemistry and QC Microbiology. This role will focus on authoring and revising technical documents to support analytical method transfers, qualification activities, and overall QC operational readiness. Duties and Responsibilities Author and revise method transfer protocols, qualification protocols, and associated reports Support drafting and revision of analytical methods for QC Chemistry and QC Microbiology Develop and update Standard Operating Procedures (SOPs) to support QC readiness and compliance Collaborate with QC scientists and SMEs to gather technical input and ensure accuracy of documentation Ensure all documentation aligns with GMP requirements and internal quality standards Support document lifecycle activities, including review, formatting, and version control Assist in preparing documentation packages to support method transfer and validation readiness Requirements and Qualifications Bachelor's degree in chemistry, Biology, Microbiology, or a related scientific discipline 5+ years of experience in a GMP-regulated environment (biotech or pharmaceutical preferred) Demonstrated experience in technical writing for QC, analytical methods, and microbiology Familiarity with method transfer, qualification, and/or validation documentation Strong understanding of GMP documentation practices and data integrity principles Excellent written and verbal communication skills Preferred Qualifications Experience supporting QC method transfers or assay qualification activities Background in analytical techniques (e.g., HPLC, CE-SDS, ELISA, potency assays) and/or microbiological testing (e.g., endotoxin, bioburden) Experience with document management systems (e.g., MasterControl) Ability to work cross-functionally in a fast-paced environment Desired Skills and Experience Technical writing, QC documentation, method transfer protocols, qualification protocols, analytical method authoring, SOP development, GMP compliance, GMP documentation practices, data integrity, QC Chemistry, QC Microbiology, microbiology documentation, analytical methods, validation documentation, document lifecycle management, document review, formatting and version control, documentation packages, method transfer support, assay qualification, cross-functional collaboration, SME collaboration, scientific documentation, HPLC, CE-SDS, ELISA, potency assays, endotoxin testing, bioburden testing, document management systems, MasterControl, regulatory compliance, quality standards, communication skills Bayside Solutions, Inc. is not able to sponsor any candidates at this time. Additionally, candidates for this position must qualify as Inc.'s candidate. Bayside Solutions, Inc. may collect your personal information during the position application process. Please reference Bayside Solutions, Inc.'s CCPA Privacy Policy at www.baysidesolutions.com. #J-18808-Ljbffr