Raw Material Coordinator

Crynodeb

Job Description - Raw Materials Coordinator

Rate: £15 per hour
Location: Slough
Contract Length: 6 months

Role Purpose & Scope (why this job exists):

Work effectively within the QC Raw Materials team, maintaining required timelines with general guidance and support.
Execute tasks to a high standard and adapt to change within a GMP custom manufacturing environment.
Support team members to ensure high-quality standards are upheld across the department.
Coordinate daily activities within the Raw Materials team.
Ensure Raw Material scheduling is completed, maintained, and on track.
Scan assay forms and manage archiving.

Key Responsibilities:

Support the Sampling and Testing team and report results according to relevant GMP procedures when required.
Use SAP daily to review raw materials.
Lead materials planning meetings and participate in operations meetings if required.
Complete Raw Materials Specification packs for raw materials release.
Release Raw Materials and take ownership of processing RMS for release, ensuring accuracy and compliance.
Follow all safety requirements related to assigned tasks.
Identify, assess, and implement improvements in GMP compliance, safety, and efficiency.
Manage archiving of assay forms and RMS documentation.
Prepare and send RMS release packs to other sites or customers, and support internal audits with required documentation.
Provide vendor certifications on request.
Support the monthly retain audit process.
Manage change effectively and escalate delays to QC management.
Manage own schedule under general direction from the Group Leader/Scheduler and deliver work within required timelines.

Required Skills and Competencies:

Ability to use SAP and LIMS.
Adaptability and willingness to undertake varied tasks to support departmental efficiency.
Proactive, with the ability to anticipate problems and generate solutions.
Ability to maintain a high standard of work.
Strong data review skills with the ability to ensure high standards across the team.
Able to work independently and within a team environment.
Professional handling of confidential information.
Ability to deliver work and projects to agreed timelines while maintaining quality.
Demonstrates loyalty, commitment, and ability to support and train junior staff.

Qualifications

Education Preferred: BSc - Pharmaceutical Sciences or Chemistry

Work Experience:

GMP laboratory environment within the pharmaceutical industry - Entry Level (0-4 years)
SAP experience - Entry Level (0-4 years)

Guidant, Carbon60, Lorien & SRG - The Impellam Group Portfolio are acting as an Employment Business in relation to this vacancy.