Senior Quality Systems Engineer
$45 - $50 per hourCollabera
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Days Left: 27 days, 3 hours left Apply Job Summary:
The Senior Quality Systems Engineer will support quality management systems within a pharmaceutical manufacturing environment, with emphasis on GMP compliance, Change Control, quality documentation, validation, and continuous improvement . This position will oversee quality system activities, review and approve controlled documentation, support audits and inspections, and collaborate across manufacturing and technical functions. Key Responsibilities:
- Support and maintain Quality Management Systems and site Quality and Compliance programs.
- Lead Change Control activities from initiation through implementation, review, and approval.
- Provide records management and Change Control expertise supporting compliant site activities.
- Review and approve SOPs, protocols, risk assessments, and other quality records.
- Maintain quality systems in compliance with current Good Manufacturing Practices and applicable regulatory requirements.
- Support process and cleaning validation, computer system validation, and equipment, facility, and utility qualification activities.
- Support Annual Product Review, quality metrics, data trending, and continuous improvement initiatives.
- Participate in internal, partner, and regulatory inspections and audits as required.
- Support site quality projects, corporate standard assessments, and cross-functional quality initiatives.
- Collaborate with Operations, Manufacturing Science and Technology, Research and Development, Supply Chain, and Quality Control teams.
- Analyze complex quality issues and apply independent judgment and problem-solving to determine appropriate actions.
- Bachelor's degree, preferably in a scientific discipline such as Biology, Chemistry, or a closely related field, or equivalent education and experience.
- Minimum five years of relevant Quality Systems and GMP/Compliance experience within a pharmaceutical manufacturing environment.
- Strong experience with Change Control and quality documentation management .
- Experience reviewing and approving SOPs, protocols, risk assessments, and quality records.
- Quality Assurance experience within pharmaceutical production.
- Strong knowledge of current Good Manufacturing Practices and pharmaceutical quality systems.
- Strong technical writing, documentation, and cross-functional communication skills.
- Ability to work independently, exercise sound judgment, and make higher-level quality decisions.
- Proficiency with MS Office and electronic quality/document management systems.
- Seven or more years of progressive pharmaceutical industry experience.
- Direct experience with pharmaceutical manufacturing and various dosage forms.
- Experience supporting Health Authority inspections.
- Experience with TrackWise, Veeva, Learning Management Systems, Electronic Document Management Systems, and Enterprise Resource Planning systems .
- Project management and advanced presentation skills.
- Experience with quality metrics, data trending, and continuous improvement.
- Quality Systems
- GMP Compliance
- Change Control
- Quality Assurance
- Pharmaceutical Manufacturing
- Technical Writing
- SOP Review
- Risk Assessments
- Quality Documentation
- TrackWise
- Veeva
- Validation
- Recruiter
- Phone
- Gagandeep Singh
- View email address on click.appcast.io
- View phone number on click.appcast.io
Vacancy posted 2 days ago
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