QC Analyst

Allscreens Nationwide Ltd; Stone Cross; On-site; GBP 26,000 - 32,000; Full time

Benefits offered by this job

31 days annual leave

Auto enrolled pension

Healthcare

Death in Service

Private Medical insurance including_de

Job summary

Allscreens Nationwide Ltd in Sandwich area is seeking a Quality Control Analyst for a full-time permanent role. The position is 37.5 hours per week, 8:30am to 5pm with an hour lunch, and a salary of £29,000 per annum plus benefits.

You will support production and QA in GMP-compliant testing, performing physical analytical testing, following protocols, and recording results. A relevant BSc and 2+ years in a similar role, with HPLC experience, are required.

Qualifications

• BSc in Chemistry or related field required.
• Experience in QC testing of APIs, including HPLC and GC.
• 2+ years in a similar role.
• GMP laboratory experience.

Responsibilities

• Perform analytical testing to support QA and production.
• Follow internal methodologies and GMP requirements.
• Accurately record results in data packs.
• Execute testing protocols and maintain laboratory housekeeping.
• Ensure all laboratory equipment is fit for use.

Skills

HPLC experience

Attention to detail

Analytical testing

Education

Bachelor's degree in Chemistry

Tools

GC

Job description

We are working with an established pharmaceutical company who are looking to employ a Quality Control Analyst, permanently in the Sandwich area.

This is an exciting full-time permanent position, 37.5 hours per week, 8.30am to 5pm, with an hour's lunch. Competitive salary of £29,000 per annum, plus a host of benefits, to include:

• 31 days annual leave, inclusive of Bank Holidays.
• Auto enrolled pension scheme
• Healthcare, Death in Service, Private Medical insurance including dependants
• Free parking
• Great working environment

You must be committed and have HPLC experience. Support the production and QA Departments in ensuring all aspects of the manufacture of products are performed in a controlled manner, meeting commitments to international regulatory bodies, as well as Good Manufacturing Practice. Ensure manufactured products are compliant and fit for purpose by performing physical and analytical testing and report accurate results. Duties to include:

• Being responsible for physical analytical testing.
• Follow internal methodologies.
• Adherence to GMP requirements.
• Accurately record microbiological results within data packages, as received.
• Execution of protocols.
• Ensure laboratory housekeeping standards are maintained and documented accurately.
• Ensure all equipment is suitable for use.

Requirements

• A relevant BSc degree, e.g. Chemistry, Analytical Chemistry, Pharmaceutical Sciences, Forensics, or equivalent.
• Experienced in QC testing of API, including HPLC and GC.
• 2+ years' experience in a similar position.
• Previous GMP laboratory experience.
• Good attention to detail, able to prioritise workload, positive and flexible approach.

We are committed to fostering a diverse and inclusive environment in line with the Equality Act 2010. All qualified applicants will be considered regardless of age, disability, gender reassignment, marriage or civil partnership, pregnancy or maternity, race, religion or belief, sex, or sexual orientation.