QC Raw Materials Technologist
- England, London
- Contract
- Compliance / Quality Assurance
Our client, a leading partner to pharmaceutical, biotech and nutrition markets, has an exciting opening for a QC Raw Materials Technologist for their new Capex investment project. As a scientific and technology innovator, this is a superb opportunity to onboard as our client continues to make strides towards a healthier world for all.
Essential duties and responsibilities for this role include, but are not limited to, the following:
- Disposition Raw Materials for their intended use
- To assist in quality records (deviations, CAPAs, investigations, change controls), protocols, reports, and SOPs in the department)
- Testing of samples and reporting of all results according to the relevant procedures in accordance with the expectations of GMP.
- Critically assess all results and report any comments or concerns to QC management in a timely manner
- To approve results generated by other team members
- Be aware of and act in accordance with all safety requirements relevant to task being performed
- Continually identify, assess and implement improvements in GMP compliance, safety and efficiency.
- Be in control of own schedule with general direction from Group Leaders and able to achieve work in required time lines
- Be able to manage change effectively and escalate any delays to QC management
- Train and assist more junior members of staff
- Ensure all members of staff are adhering to the high quality of work as expected in a GMP environment.
- BSc Chemistry
- Requires extensive years experience in a GMP Environment
- The incumbent normally receives little instruction on day-to-day work and receives general instructions on new assignments.
- Willing to undertake a range of tasks for the effective running of the department.
- Proactive - Anticipates problems and shows initiative for problem-solving and generating new ideas.
- Multiple chemical / Biochemical techniques and methods.
- Reporting of data, Quality records. etc
- Ability to deliver work / projects to agreed time lines whilst maintaining a high standard of quality.
- Ability to review data and ensure high standards are being adhered to by other members of staff. Ability to work well alone and within a team. Willing to work with others to achieve the common goal.
- Actively promotes the department. Able to deal with confidential information in an appropriate and sensitive
#LI-CB1
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
I have always received a highly professional & personable service from the team at QCS Staffing. 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
We have worked together with QCS Staffing for seven years now and have always received a professional service. QCS Staffing'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 QCS Staffing's people and their ability to deliver.
Global Pharmaceutical firm
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