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Quality Officer
4 months ago
RECRUITMENTiQ is working in partnership with a leading global contract development and manufacturing organization (CDMO) that provides drug substance, drug product, and analytical services across the entire drug lifecycle.
Over the past 40 years, the business has developed and manufactured APIs and dosage forms for global clients from its North American and European sites. Known for our scientific and manufacturing excellence, as well as our strong customer focus, we offer numerous career opportunities throughout our global network. We strive to improve the quality of life for patients around the world in collaboration with our customers.
Our company is seeking a Quality Officer who will report to a Quality Manager and will play a crucial role in ensuring the Quality Management System (QMS) is operating effectively.
**Requirements**:
- Bachelor's degree in chemistry or a related field (or relevant experience).
- A minimum of 2 years of experience in the pharmaceutical or biotechnology industries working with Good Manufacturing Practices (GMP).
- Knowledge and experience with techniques such as HPLC, GC, FT-IR, UV/Vis, Karl Fischer, Total Particle Counters, and Chromatography data systems are advantageous.
- Experience in validation, release testing and/or stability environment would be desirable as would ISO 9001:2015 QMS knowledge.
- Be well organised and able to plan one’s own work effectively based around business/quality priority needs.
- Possess good problem-solving and effective time management skills.
- Demonstrate ability to think critically and pragmatically and to focus on details of execution.
- Be enthusiastic team player with strong interpersonal skills to communicate with members within the quality and operations departments.
**Key Accountabilities**
- Assist with tracking/administration duties, investigations, change management, CAPAs, and SOPs.
- Ensure all activities were performed as per approved SOPs/methods/protocols and comply with specifications by critically evaluating the reported data and results for accuracy and compliance.
- Assist with internal, external, and regulatory audits.
- Assist and lead the continuous improvement of the quality management system.
- Advise and guide the operations team in QMS requirements.
- Create an effective relationship with Quality team, colleagues, and clients.
- Perform assigned tasks carefully and on schedule.
- Assist the Quality Manager in collating and reporting of quality related key performance indicators.
- Other duties as assigned.
A motivated individual who is continuously seeking to develop and improve as well as share knowledge and best practices within the industry would be ideal for the position.
You will have the opportunity to do challenging work, and be a part of a team that values performance, quality, and innovation.
**Job Types**: Full-time, Permanent
**Benefits**:
- Company pension
Schedule:
- Day shift
- Monday to Friday
Ability to commute/relocate:
- Penicuik: reliably commute or plan to relocate before starting work (preferred)
**Experience**:
- Quality experience & GMP in the pharma or bio/tech: 2 years (required)
Work Location: In person
Application deadline: 28/08/2023
