Deviation Management Specialist Position Available In Durham, North Carolina

Tallo's Job Summary: The Deviation Management Specialist position in Durham, NC, at a top pharmaceutical company involves leading quality control and manufacturing deviation investigations, conducting interviews, and authoring GMP documentation. Qualifications include 1+ years of pharmaceutical manufacturing experience and proficiency in technical writing. Compensation is based on experience with comprehensive benefits offered.

Company:
Piper Companies
Salary:
JobFull-timeOnsite

Job Description

Deviation Management Specialist 4.4 4.4 out of 5 stars Durham, NC Piper Companies is currently seeking a Deviation Management Specialist based in Durham, NC for work at a leading pharmaceutical company. The Deviation Management Specialist will play an integral role in conducting manufacturing/QC deviation investigations, authoring investigations as well as resolutions Responsibilities of the

Deviation Management Specialist:

Lead Quality Control and manufacturing operation deviation investigations Conduct interviews with QC and manufacturing personnel working alongside quality assurance (QA) Author/revise GMP documentation in support of commercial release of vaccine products Write, review, and revise other GMP documentation such as SOPs, batch records and work instructions Qualifications of the

Deviation Management Specialist:

1+ years of experince within pharmaceutical manufacturing 2+ years of deviation investigation experince 1+ years of technical writing experince Proficient in Microsoft Office Suite Familiarity with FDA and GMP compliance regulations Compensation for the

Deviation Management Specialist:

Compensation is commensurate with experience Comprehensive Benefits package: Medical, Dental, Vision, 401

K, PTO Keywords:

GMP, Pharmaceutical, Quality Control, QC, Deviations Investigation, Deviation Management, Quality Assurance, Commercial, FDA, CAPAs, Risk Management, RMPs, Change Controls, Biotechnology, Technical Writer, SOPs, Standard Operating Procedures, Writing, Reviewing, Revising, Authoring, #

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