Senior QA Auditor

Altasciences; Columbia Township (MO); Hybrid; USD 90,000 - 120,000; Full time

Benefits offered by this job

Telework when applicable

Job summary

Altasciences is seeking a Senior QA Auditor to perform independent audits of study-related activities to ensure GLP compliance and accurate reporting per SOPs and regulations. You will mentor junior staff and communicate findings to management.

The role requires a scientific degree and 2–3 years of GLP auditing experience, with professional certifications encouraged. Hybrid work in Columbia, MO, and a strong quality focus are essential.

Qualifications

• Bachelor degree in a scientific discipline or equivalent experience.
• 2–3 years related technical experience with GLP auditing.
• Professional certification such as RQAP-GLP or ASQ-CQA recommended.

Responsibilities

• Audit nonclinical and laboratory studies, reports, and related documents for regulatory compliance.
• Lead audits on studies and projects and mentor junior staff.
• Identify process improvements based on findings and ensure SOPs are current.

Skills

Auditing

GLP Compliance

Regulatory Knowledge

Documentation Control

Education

Bachelor's degree in science

Tools

Microsoft Office Suite

Job description

## Senior QA AuditorPostuler: Hybride: Columbia, Missouri: Temps plein: Publié il y a 3 jour(s): R103059**About The Role** The Senior QA Auditor is responsible for carrying out systematic and independent examination (i.e., audit) of multiple study related activities and documents, to determine whether the evaluated study related activities were conducted, and the data were recorded, analyzed, and accurately reported according to the protocol, standard operating procedures (SOPs), GLP (21 CFR Part 58 and Part 11) and the applicable regulatory requirements. The Senior QA Auditor is responsible for reporting any findings to the Study Director or Responsible Person and Testing Facility Management. The Senior QA Auditor is responsible for building and maintaining effective working relationships throughout the organization and is responsible for mentoring/coaching lower-level staff.**What You'll Do Here*** Audits phases of nonclinical and laboratory studies, reports, and performs related duties (e.g., issues audits and QA statements) to ensure regulatory compliance.* Audits all disciplines (examples of disciplines include Method Validations, Non- Clinical GLP Studies).* Performs in-life audits, process audits, vendor qualifications, equipment and software validation audits.* Performs facility audits to ensure that the facility is in compliance with regulations.* Acts as lead auditor on studies and projects.* Maintains computerized files to support audit activities.* Supports project planning and implementation.* Provides risk-based compliance opinions and guidance.* Writes and issues inspection reports. Works with internal clients to ensure that inspection findings are clearly communicated and understood. Evaluates inspection finding responses to ensure they are written to address the findings appropriately.* Ensures through phase and data inspections that the SOPs, which are involved in the conduct of a study, are current and practiced.* Identifies and communicates opportunities for process improvements based on audit and inspection observations. Participates in and guides process improvement activities in both small intradepartmental groups as well as complex and possible multi-departmental interactions.* Maintains necessary documentation of QA records and study files.* Notifies management of observed quality and compliance trends in the areas inspected.* Autonomously performs SOP QA review, client hosting, regulatory agency hosting and external test site/clinical site/bioanalytical laboratory qualifications.* Under supervision of a mentor/coach, performs the following tasks: interpretation of FDA, regulations; project management; regulatory guidance review; quality issue investigations; and QA data collection, trending and analysis.* Recommends modifications in procedures to fit special needs or problems and involves manager when assistance in process improvement/resolution is necessary.* Interprets and can train on GLP and associated regulatory documents to facilitate auditing and process improvement recommendations.* Carries out appropriate self-development efforts as directed.* Assists with regulatory training of staff.**What You'll Need to Succeed*** Bachelor degree or higher in a scientific discipline, or equivalent combination of education and experience.* 2 - 3 years related technical experience and/or training. A minimum of two years auditing in a GLP-regulated environment.* Professional certification such as RQAP-GLP (Registered Quality Assurance Professional-GLP) or ASQ-CQA (American Society of Quality– Certified Quality Auditor) or other certification is recommended.* Proficient with Microsoft Office Suite* Training needs for this position include on-the-job training in performing audits and inspections, and independent reading of professional articles, journals and internal SOPs. Attendance at training seminars, regional and national meetings in Quality Assurance, regulatory affairs and validation, along with continual GLP training.**Work Authorization & Sponsorship**Applicants must be legally authorized to work in the United States. Altasciences is unable to provide sponsorship, sponsorship transfers, or visa maintenance for this position. All applicants must possess valid work authorization that does not require employer sponsorship now or in the future.**What We Offer**Altasciences offers a wide variety of benefits to help our employees live healthy and fulfilling lives both at and outside of work.**Altasciences’ Benefits Package Includes:*** Health/Dental/Vision Insurance Plans* 401(k)/RRSP with Employer Match* Paid Vacation and Holidays* Paid Sick and Bereavement Leave* Employee Assistance & Telehealth Programs* Telework when applicable.**Altasciences’ Incentive Programs Include:*** Training & Development Programs* Employee Referral Bonus Program#LI-ES1