Senior Quality Systems Specialist (12 month role)
Senior Quality Systems Specialist (12 month role)
Posted on :
23-08-2025
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1 Vacancy
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Job Description
Title: Senior Quality Systems Specialist
Job Purpose:
This position will support the execution of the Sites Quality Management System Processes and deliver Quality System projects. This person will drive the flawless and compliant execution of the assigned processes to meet customer and business needs while ensuring the processes are in compliance with regulatory requirements. This role will involve liaising with the Franchise/Sector teams on driving improvement and streamlining of the assigned processes.
List main areas of responsibility:
Drives compliant execution of the following for their assigned processes and projects
Manages specified quality system processes.
Works directly with various customers of the quality system processes to ensure compliance to site/sector/enterprise /franchise/regulatory requirements
Work directly with the various owners/teams to ensure investigations/actions are implemented and accurately documented in a timely manner
Compiles contextualizes evaluates and presents Quality Systems data and metrics for all metric review meetings. Utilizes quality tools to track trend and communicate quality performance metrics in presentations/reports/dashboards.
Understand and uses data key metrics and statistical methods quality tools or computer based solutions to improve processes
Responsible for identifying and communicating the need for process improvement opportunities to responsible management.
Identifies personnel that require training on the relevant processes and rolls out training as required.
Proactively examines/reviews systems and processes to identify/assess areas for review improvement change or elimination and with specific focus in simplifying and standardizing processes. Lead and drive improvements as required
Establishes linkages to other key quality systems/programs like Design Controls Technology Transfer Production & Process Controls External Manufacturing Calibration Preventive Maintenance etc.
Support the assigned processes during internal and external audits.
Systems SME for Internal and External Audits
Conducts internal audits to ensure compliance to regulatory and customer requirements.
Responds to and drive/ participates in investigations and corrective action implementation for identified quality issues including internal/external audits actions
Represents the processes and systems as required at cross-site meetings.
Assists in creating a culture of quality awareness and communicating the quality management system GMP and associated documents and procedures to all staff.
In addition to the above duties the Senior Quality Systems Specialist role also encompasses responsibility of supporting the Quality Systems Manager in the planning and directing of overall Quality System activities.
Provides continuous support and mentoring to Quality Systems Specialists and Department members.
Education and Experience Required for Role
Essential:
At a minimum a Diploma in a Quality Science or Engineering discipline and 3 or more years of related experience
Additional Essential Requirements for a Senior Quality System Specialist:
At a minimum a Diploma in a Quality Science or Engineering discipline and 5 or more years of related experience
Desirable :
Experienced SME for FDA and other regulatory authority audits.
Proven leadership skills
Successful Completion of Global Projects
Proficiency in applicable GMP/QSR regulations and in- depth knowledge of Quality Systems
Ability to prioritize and manage the workload and as required be able to manage shifting priorities based on critical deadlines so that business needs are always met.
Demonstrate excellent communication skills (verbal and written) with all levels within the organization clients and regulatory auditors
Must show innovative development techniques and strategic thinking abilities
Demonstrated success in managing multiple projects
Ability to develop and give presentations on technical and regulatory topics.
Ability to work on own initiative and a high level of attention to detail
Ability to train/mentor associates
Ability to effectively deal with a variety of conflicting issues and diplomatically solve those issues.
Ability to read analyze and interpret complex technical documents and manuals
Ability to define problems collects data establish facts and draw valid conclusions.
Note:
Responsibilities and accountabilities will vary for all positions and the scope of individual roles may not be limited to the contents of this position description. QUMAS procedures will define responsibilities from time to time and each manager is responsible for complying with these processes which supplant any responsibility outlined within. As such adherence to company procedures is also a responsibility of any roles encompassed within this Job Description.
INDHP
Required Experience:
Senior IC
Employment Type
Full Time
Key Skills
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