Quality Associate
2 months ago
At Origin, we design, manufacture and distribute primary packaging for the healthcare industry. This year marks our 60th anniversary and in that time, we have grown to be a respected partner to our customers based across the world. As we continue to grow, we are looking for a Quality Associate to join us.
The role will effectively manage key quality processes and programmes, internal operational and customer issues and queries that arise on a day-to-day basis including conducting investigations, troubleshooting and process and procedure improvements as well as conducting routine quality control and quality assurance scheduled tasks and internal quality audits.
The Quality Associate’s key accountabilities and responsibilities include:
- Creating, maintaining and revising SOPs & WIs and providing (or arranging) training at all levels
- Co-ordinating documentation, creating and issuing of COAs and batch release data where applicable
- Supporting audit and site monitoring programmes
- Monitoring suppliers’ performance
- Managing QC inbox
- Maintaining calibrated equipment
- Recording, investigating and concluding Non-Conformance issues (including Complaints, SCARs and NCRs) ensuring remedial actions are followed through
- Creating product specific files, Product Technical Files and any associated product control and manufacturing documentation
- Contributing to site HACCP, Risk Assessments and Change Control
- Providing support and guidance in microbiological best practice with respect to cleanroom and manufacturing activities
- Participating in problem solving and continuous improvement including lean related thinking from a quality perspective
We are looking for someone with these attributes:
- Experience in GMP
- Experience in Quality Systems
- Experience of controlling change within GMP
- Experience of Internal and/or External Auditing
- Excellent organisational and planning skills
- Effective oral and written communication skills (English) and data manipulation and reporting (Maths/Excel)
- Proactive problem solving skills and drive for continuous improvement
- Resilient
- Positive can-do attitude
- Methodical approach and attention to detail
- Experience of Pharmaceutical Deviation Investigations (desirable)
- Work in high pressure high throughput laboratories and/ or production QC (desirable)
- Minimum of 4 year previous Technical and Quality experience (desirable)
- Experience of risk management, HACCP planning and/ or microbiological environment controls and monitoring (desirable)
- A salary of up to £30,000
- 20 days holiday plus bank holidays
- Personal CPD budget
- Pension with company contribution
**Job Types**: Full-time, Permanent
**Salary**: Up to £30,000.00 per year
**Benefits**:
- Company pension
- On-site parking
- Sick pay
Schedule:
- Monday to Friday
Ability to commute/relocate:
- North Ferriby: reliably commute or plan to relocate before starting work (required)
**Education**:
- A-Level or equivalent (preferred)
Work Location: In person
Reference ID: Origin-Qual-Assoc
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