QC Raw Materials Technologist

Quanta Consultancy Services Ltd; Slough; On-site; GBP 35,000 - 50,000; Full time

Job summary

A leading consultancy in the pharmaceutical industry is seeking a QC Raw Materials Technologist for a 6-month contract in Slough. The role involves overseeing raw material dispositions, ensuring quality compliance, and training junior staff. If you have a BSc in Chemistry and extensive GMP experience, this is a fantastic opportunity to join a fast-paced environment driving innovation in healthcare.

Qualifications

• Requires extensive experience in a GMP environment.
• Ability to deliver projects to agreed timelines while maintaining high standards.
• Proactive and capable of working independently or as part of a team.

Responsibilities

• Disposition raw materials for their intended use.
• Assist in quality records and adhere to GMP expectations.
• Train and assist junior members of staff.

Skills

Quality Control

GMP Compliance

Problem-Solving

Training

Education

BSc Chemistry

Job description

QC Raw Materials Technologist - UK, Slough - 6 Months Contract

Our client, a leading partner to pharmaceutical, biotech and nutrition markets, has an exciting opening for aQC 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.

Desirable experience:

• 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

If this role is of interest to you, please apply now!

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