QC Analyst

ARx Recruitment Services; Wellingborough; On-site; GBP 32,000 - 42,000; Full time

Benefits offered by this job

Morning & Afternoon Shift Allowance £2

Night Shift Allowance £3,500 per annum

Job summary

ARx Recruitment Services is seeking a QC Analyst for a shift-based role in a pharmaceutical quality control laboratory near Wellingborough. The position is full-time (40 hours per week) with shifts Monday to Sunday on a rotational basis.

Morning, afternoon, and night shifts include distinct allowances. You will perform routine and non-routine analyses using HPLC and other analytical techniques, review results, and ensure compliance with GMP, data integrity, and CFR guidelines.

Qualifications

• Bachelor's degree in Chemistry or Pharmaceutical Sciences.
• Hands-on HPLC experience and familiarity with multiple analytical techniques.
• Experience with GMP, data integrity and regulatory compliance.
• Experience with OOS/OOT investigations and CAPA processes.

Responsibilities

• Perform routine and non-routine analytical testing using HPLC and other techniques.
• Test raw materials, finished products, stability, and in-process samples.
• Review and interpret analytical results accurately.
• Ensure lab documentation complies with GMP, data integrity and CFR requirements.
• Support OOS, OOT, deviation investigations and CAPA activities.
• Participate in method validation, verification, and transfer activities.
• Maintain SOPs and calibrations; assist with lab housekeeping and equipment maintenance.
• Collaborate with other site departments.

Skills

HPLC Experience

Analytical & problem-solving

Documentation skills

Independent work & prioritisation

Stability studies & method validation

CDS software experience

Investigation exposure (OOS/OOT)

Education

Degree in Chemistry or Pharmaceutical Sciences

Tools

Chromeleon CDS software

Job description

This is a Shift Based Role | Full Time 40hrs Per Week | Monday to Sunday (5 Days Out of 7 Working on a Rotational Basis)

• Morning Shift - 05:45am - 2:15pm
• Afternoon Shift - 1:45pm - 10:15pm
• Evening Shift - 9:45pm - 06:15am
• Morning & Afternoon Shift Allowance £2,500.00 Per Annum
• Night Shift Allowance £3,500.00 Per Annum

Our Client, Located Near to Wellingborough are Seeking an QC Analyst to join their Pharmaceutical Quality Control Laboratory Team, who are Responsible for Performing Analytical Testing, Conducting Investigations, and Ensuring Regulatory Compliance.

ROLE

• Routine and Non-Routine Analysis, Using HPLC and Other Analytical Techniques
• Testing of Raw Materials, Finished Products, Stability Samples, and In-Process Samples
• Accurately Review and Interpret Analytical Results
• Ensure Laboratory Documentation is Completed in Compliance with GMP and Data Integrity Requirements
• Support OOS, OOT, Deviation, and CAPA Investigations
• Participate in Method Validation, Verification, and Transfer Activities
• Maintain Compliance with SOPs, GMP, ICH Guidelines, and CFR Requirements
• Assist with Laboratory Housekeeping, Calibration, and Equipment Maintenance
• Work Collaboratively with Other Site Departments

REQUIRED

• Degree in Chemistry or Pharmaceutical Sciences
• Minimum 3 to 4 Years' Experience in a Pharmaceutical QC Laboratory
• Hands-on HPLC Experience
• Experience with a Variety of Analytical Techniques e.g. UV, FTIR, and Karl Fischer
• Sound Knowledge and Experience of GMP, Data Integrity, and Regulatory Compliance
• Experience with Chromeleon or Similar CDS Software
• Strong Analytical and Problem-Solving Skills
• Good Documentation Skills
• Ability to Work Independently and Manage Priorities Effectively
• Experience with Stability Studies and Method Validation
• Exposure to Investigations, Including OOS/OOT