Analytical Scientist
- East
- Contract
- Life Sciences
This is a fantastic opportunity to be part of a fast-paced, €400 million project; with lots of opportunities to work with and learn about cutting-edge technologies, in addition to developing your own skills.
This is a truly exciting project, which when complete will contribute to the manufacturing of a life changing treatment.
Responsibilities:
- Execution of analytical method validations and transfers and write technical protocols and report
- Execution of analytical testing of drug substance release, stability and characterization for biologics under GMP/GDP
- Support equipment maintenance, calibration and qualification work
- Preparation of analytical methods, SOPs and other documents as required
- Other analytical activities in consultation with the Supervisor
- Works in accordance with applicable internal company regulations: safety, health and environmental protection.
- Train new analysts
- Experience with analytical testing with Ultrahigh Pressure Liquid Chromatography (UPLC)/High Performance Liquid Chromatography (HPLC), Capillary Electrophoresis, or other large molecule characterization technique
- Strong oral and written communication skills
- Ability to work in a team environment with cross-functional interactions is essential
- GMP working experience
- Perform supporting activities for general lab operations, training, new product introduction, method verifications and method transfers.
- Execution and review of analytical method validations and transfers (among different sites, and between the company and CROs)
- Execution and review of analytical testing of drug substance release, stability, method qualification, incoming goods, ID testing, and characterisation for biologics under GMP/GDP.
- Cross-train Scientists within the department for new and existing technologies.
- Ability to organise and establish testing schedules and adhere to deadlines.
- Support equipment maintenance, calibration and qualification work
- Perform periodic review of instrument systems
- Generate instrument data in support of SDLC Validation.
- Initiate, review, and support deviations, CAPAs, and, risk assessments, and change records as required.
- Preparation of analytical methods, SOPs and other documents as required
If this role interests you, apply today!
#LI-TE1
I have always received a highly professional & personable service from the team at Quanta. They listen carefully to the specific requirements of available roles and work tirelessly to supply a pool of potential candidates and make the hiring and contract renewal process an easy activity to manage.
Global Pharmaceutical firm
Once again can I via you recognise the superb support I was given before, during and after this short contract. The support, was as usual professional and every friendly.
QA Specialist
We have worked together with Quanta for seven years now and have always received a professional service. Quanta’s speciality certainly lies within their technical sourcing abilities and they have met our demanding requirements time and time again. Coupled with this are the integrity of Quanta’s people and their ability to deliver.
Global Pharmaceutical firm
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