QC Analyst

TN United Kingdom; Stone Cross; On-site; GBP 29,000; Full time

Job summary

An established industry player is seeking a Quality Control Analyst for a full-time role in the Sandwich area. This exciting opportunity involves supporting production and QA departments to ensure compliance with regulatory standards and GMP. The successful candidate will perform physical and analytical testing, maintain laboratory standards, and ensure all equipment is properly maintained. With a focus on quality and attention to detail, this position offers a supportive working environment and a range of benefits, including generous annual leave and private medical insurance. Join a team committed to excellence in the pharmaceutical sector.

Benefits

31 days annual leave

Auto-enrolled pension scheme

Healthcare

Private Medical Insurance

Free parking

Great working environment

Qualifications

• BSc degree in relevant field is essential.
• 1-2 years' experience in a similar role is preferred.

Responsibilities

• Support production and QA departments to ensure compliance with regulatory standards.
• Perform physical and analytical testing to ensure product quality.
• Maintain laboratory standards and ensure equipment is suitable.

Skills

MS Office

Attention to detail

Prioritization skills

Experience in QC testing

HPLC

GC

Wet chemistry techniques

Education

BSc in Chemistry

BSc in Analytical Chemistry

BSc in Pharmaceutical Sciences

BSc in Forensics

Job description

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Job Opportunity: Quality Control Analyst

We are working with an established pharmaceutical company seeking to employ a Quality Control Analyst on a permanent basis in the Sandwich area.

This is an exciting full-time position with the following details:

1. Hours: 37.5 hours per week, 8.30am to 5pm, with a one-hour lunch break
2. Salary: £29,000 per annum
3. Benefits include:

• 31 days annual leave, including Bank Holidays
• Auto-enrolled pension scheme
• Healthcare, Death in Service, Private Medical Insurance (including dependents)
• Free parking
• Great working environment

Key Responsibilities:

• Support production and QA departments to ensure manufacturing processes meet regulatory standards and GMP
• Perform physical and analytical testing to ensure product compliance and quality
• Record microbiological results accurately within data packages
• Follow internal methodologies and protocols
• Maintain laboratory housekeeping standards
• Ensure all equipment is suitable and properly maintained

Candidate Requirements:

• BSc degree in Chemistry, Analytical Chemistry, Pharmaceutical Sciences, Forensics, or equivalent
• Proficiency in MS Office and computer literacy
• Experience in QC testing of API, including HPLC and GC; wet chemistry techniques are a plus
• Attention to detail, good prioritization skills, positive and flexible attitude
• 1-2 years' experience in a similar role is preferred but not essential
• GMP experience is desirable

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