QCL EM Analyst
QCL EM Analyst
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Job Description
The purpose of this job is to perform scientific procedures and produce accurate results within the required time frame under the customer quality system using customer company procedures and while adhering to Eurofins Lancaster Laboratories general policies and standards.
Job Responsibilities
- Performing routine and nonroutine analysis as requested by the Group Leader or customer representative.
- Preparing and approving results for tests in which they have received the appropriate training and are deemed competent.
- Notify immediately to the Group Leader or a customer representative any anomalous or out of specification results.
- Participating in all training required and scheduled by the Group Leader or the customer. Being prepared and on time for that training. Engaging in training processes and ensuring all information received is completely understood.
- Completion of training records and ensuring that all records presented for review and approval are at the appropriate standard.
- Providing training to other team members as instructed by the Group Leader. Ensuring all training delivered is documented appropriately.
- Ensuring at all times that all documentation and laboratory records are up to date and of an appropriate standard.
- Ensuring that all work carried out is approached Right First Time so as to avoid any rework or errors.
- Gain a clear understanding of all related customer supplemental processes such as deviation handling training documentation document and records control.
- Being constantly aware of customers requirements and striving to meet or exceed those requirements keeping in mind the customer process end points.
- Gaining a clear understanding of the customer relationship and service goals. Gaining a clear understanding of the customer process flow in terms of destination and use of data generated and consequences of substandard data.
- Dealing with customer queries and to contact designated personnel with any relevant information or issues relating to test results or the service in general.
- Keeping up to date with any technological or method revisions in their area ensuring their training is complete and adjusting their work as required with approval from the Group Leader.
- Performing second person verification checks as required by the laboratory schedule
- Performing QC samples in accordance with customer procedures.
- Assisting in the processing of laboratory consumables as required labelling acceptance testing.
- Revising SOPs and updating other documentation as required by the Group Leader.
- Providing cover for other members of staff as required and for taking part in the customers weekend rota and/or overtime schedule.
- Ensuring that all documentation is completed on time. Ensuring that it is accurate and legible and conforms to the relevant quality standards.
- Assisting in laboratory investigations as appropriate.
- Adhering to all customer standards in the areas of safety housekeeping and quality notifying management of any discrepancies.
- Ensuring that customers requirements are fully met or exceeded and in so doing will be flexible to work in any area of the business as is required.
- Ensuring that all decisions are handled with customer service in mind.
- Ensuring uniformity reproducibility and reliability in all work practices.
- Keeping the laboratory area clean and tidy in both seen and unseen areas.
- Identifying any opportunities for improvement of quality and service and work with the team to implement continuous improvement.
- Participating in Team Meetings and giving updates to rest of team as necessary.
Qualifications :
- A degree or diploma in microbiology / chemistry or a related subject.
- At least 1 years experience in a pharmaceutical industry GMP laboratory
- Good team player organised accurate have strong documentation skills
- Flexible adaptable to changing priorities
- Passionate about quality and customer service.
- Good communication skills both internally and externally.
Additional Information :
Additional information
This is an opportunity to join Eurofins on a full time permanent basis.
Working a rotating shift pattern as below:
Week 1: 08:00 20:00 11 hour per day) Monday Tuesday Friday Saturday & Sunday.
Week 2: 08:00 20:00 11 hour per day) Wednesday & Thursday.
Benefits of pension contribution medical insurance health insurance and bonus are included in package.
Eurofins Management and Team on client site for support.
Opportunity to get to know fantastic people and be part of a great team.
Eurofins Scientific is an international life sciences company providing a unique range of analytical testing services to clients across multiple industries to make life and our environment safer healthier and more sustainable. From the food you eat to the water you drink to the medicines you rely on Eurofins works with the biggest companies in the world to ensure the products they supply are safe their ingredients are authentic and labelling is accurate. Eurofins believes it is a global leader in food environmental pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics discovery pharmacology forensics CDMO advanced material sciences and in the support of clinical studies.
In over just 30 years Eurofins has grown from one laboratory in Nantes France to over 50000 staff across a network of more than 900 independent companies in over 50 countries and operating more than 800 laboratories. Eurofins offers a portfolio of over 200000 analytical methods to evaluate the safety identity composition authenticity origin traceability and purity of biological substances and products as well as providing innovative clinical diagnostic testing services as one of the leading global emerging players in specialised clinical diagnostics testing.
Remote Work :
No
Employment Type :
Parttime
Employment Type
Part-time
