QC Analyst, Level 4 - 18 Month FTC
Norgine B.V., Cefn Hengoed, Caerffili - Caerphilly
QC Analyst, Level 4 - 18 Month FTC
Salary Not Specified
Norgine B.V., Cefn Hengoed, Caerffili - Caerphilly
- Full time
- Temporary
- Onsite working
Posted 2 days ago, 29 Oct | Get your application in today.
Closing date: Closing date not specified
job Ref: c4e687222d8c424b856e4dc5809af720
Full Job Description
We have an exciting opportunity for a QC Analyst Level 4 to join Norgine on an 18 month FTC - contract. The person holding this position will report to the QC Team Leader and be a member of the QC team. Working a shift pattern of mornings and afternoons and 1 weekend in 4, If you want a multi-dimensional 3D career in a leading healthcare organisation, join us. Main Tasks
- Perform the analysis of starting materials, intermediates and finished products in accordance with written procedures.
- Provide accurate records of work carried out.
- Perform all duties in accordance with GCLP (Good Control Laboratory Practice), GMP (Good manufacturing Practice) and safe working practices.
- Propose improvements to analytical methods or working practices and participate in department and company improvement projects
- Perform calibration checks in accordance with written procedures.
- Perform calculation checks on analysis records.
- To carry out tasks as required to suit business needs and department needs and as appropriate to the job role.
- Meet day to day and longer term schedules and performance objectives Complexity The products/materials handled are diverse in their nature and complexity. The job holder must have a wide range of analytical skills ranging from traditional wet chemistry to a working knowledge of modern instrumental techniques. Although the tasks of the job holder are well covered by procedures and policies, a degree of initiative will be required in solving problems arising from analytical methods, particularly those associated with more sophisticated equipment. Analysts receive direction from the Shift Team Leader - QC. Accountability The job holder is responsible for carrying out all work in accordance with written procedures. He/she is responsible for informing the Shift Team Leader - QC of any non conformities discovered and for actively investigating any non-conformities with a view to establishing root cause. He/she is responsible for keeping accurate, legible written records of their work and following GXP's at all times Relationships Required to liaise with Operations, Global Technical, Pharmaceutical Development and Regulatory Affairs Departments on a variety of issues and information exchanges, Our benefits may vary per location. Please liaise with the Norgine TA representative to obtain more information.
- Chromatographic Analysis
- Spectroscopic Analysis
- Oral Solid Dose Testing (including Dissolution, Disintegration, Hardness, etc)
- Pharmaceutical / Healthcare Experience
- Experience with Regulatory Bodies (FDA, MHRA, Etc)
- EXPERT USER - Analysis using Instruments
- Project work
- Writing/Amending SOP's
- Experience with wet chemical techniques
- Analytical trouble shooting
- Use of Pharmacopoeias
- Use of balance and calibration
- Preparation of volumetric solutions and dilutions
- Input into Equipment and Method Validation
- Final data checks and data reporting for QC results
At Norgine, our colleagues Dare themselves to be different and try new things, Drive to achieve their goals and beyond, and Develop themselves and their community. We call it the 3D career at Norgine and it offers you a fully-rounded experience with no limits. Bring everything about yourself that you're proud of, whether that's your passion for making a difference, focus on others' well-being, or intellectual curiosity to unleash in a fast-paced environment and supportive community. In return, get a sense of belonging, a long-term career with ongoing development and upskilling, and a company that cares about people's wellness as much as you do. Because at Norgine, we transform lives with innovative healthcare solutions.
Level 4 - Ideally qualified to degree level in chemistry or a life science. Lesser formal qualifications may be acceptable when coupled with substantial pharmaceutical analytical laboratory experience, in addition to level 3 responsibilities a level 4 analyst is required to have knowledge around analytical and equipment validation and data/report reviews and approval. Skills / Experience