Senior QC Analyst

工作内容

SENIOR QC ANALYST – SOUTHPORT

Company overview

The client is a pharmaceutical company based in Southport and is recruiting for a Senior QC Analyst in a permanent position. The site is responsible for the manufacture of oral and topical products (tablets, capsules, creams, gels).

Vacancy overview

The client is looking for a Senior QC Analyst principally to provide support to the QC Manager and facilitate the testing and release of finished products. The Senior Analyst will be responsible for 4 direct reports in their own team.

Main responsibilities

· Supervise/lead of a team of analysts in the Quality Control ensuring compliance with principles of Good Manufacturing Practice (GMP) and Good Laboratory Practice (GLP).

· Review of Batch Manufacturing Documents and analytical test results to facilitate the release for filling.

· Review and approval of product labels for use by the Production Department.

· To perform testing of manufactured product samples for release, stability studies and validation using various analytical techniques, mainly HPLC and GC.

· Assigning duties to analysts’ dependant on production release requirements ensuring the laboratory operations are performed in an organised and efficient manner to prevent any delays in material/product release.

· Reviewing completed analytical testing results.

· Preparation and review of Standard Operating Procedures, Raw Material Documents, Analytical Test Reports, Validation Protocols and Reports.

· Ensuring laboratory housekeeping is maintained to appropriate standards.

· Provide technical support and troubleshooting and equipment and analytical methods.

Requirements

· Management skills and experience of managing a team of analysts.

· Experience of testing of raw materials to British Pharmacopoeia and finished products to registered specifications.

· Excellent communication skills, both verbal and written, with a passion for accuracy and attention to detail.

· Strong analytical thinking and problem solving/troubleshooting.

· Good computer literacy.

· Analytical experience, preferably including IR and NIR spectroscopy, High Performance Liquid Chromatography (HPLC), Gas Chromatography.

· The role owner will have proven Quality Control/Analytical experience within a pharmaceutical manufacturing environment. It is anticipated that the person will have a minimum of five years practical experience of testing of pharmaceutical products to registered specifications.

· A Degree in Chemical Sciences is a requirement although consideration would be given to an applicant with relevant practical experience.

Interested candidates should apply to Alex Prew, Scientific Recruiter at LiCa Scientific.

T: 0161 443 4173

M: 07391 984252

E: admin@licasci.com

Job Types: Full-time, Permanent

Salary: £25,000.00-£30,000.00 per year

Benefits:

• Company pension

Schedule:

• Monday to Friday

Ability to commute/relocate:

• Southport: reliably commute or plan to relocate before starting work (required)

Experience:

• Quality control: 3 years (preferred)
• HPLC/GC: 3 years (preferred)
• Batch documentation review: 3 years (preferred)
• Line management: 2 years (preferred)

Work Location: In person

Reference ID: AP0808