Packaging Supervisor

2 weeks ago


Stratford, United Kingdom QMED Clinical Services Full time

**Responsibilities**:
**The responsibilities of a Clinical Packaging Supervisor at QCS include**:

- Ensure that the quality of packaged clinical trial materials are consistent with the Protocol, IMPD and any other sponsor requirements.
- Create clinical trial packaging documentation including packaging specification, labels, blinding strategies, randomisation, batch packaging records, dispatch and returns.
- Manage timely receipt and release of starting materials, bulk, and components.
- Ensure IMPs, NIMPs and Comparators are received and stored according to the SOPs and the sponsor requirements.
- Supervise clinical trial packaging operations that include directly working in clinical trial packaging operations when required.
- Support timely completion of QP Certification of clinical trial supplies.
- Maintain finished goods inventories and ensure timely distribution of trial materials to the clinical sites.
- Resolves clinical trial product distribution issues by working closely with couriers, customer, and clinical sites.
- To complete reconciliation and agree with the customer on product disposition, destruction and or returns at the end of study.
- Host and manage customer visits along with the QA Teams.
- Support assigned customer meetings, teleconference, and internal meetings.
- Customer point of contact for clinical packaging, storage, and distribution as assigned.
- Manage sourcing and supply of Comparator products as required for the clinical trials.
- Ensure compliance with the company Pharmaceutical Quality Management System in accordance with relevant SOPs and instructions.

**Job Qualification & Requirements**
- Ideally have a degree in Pharmaceutical Sciences, Clinical Supplies, or similar disciplines.
- Must have 5+ years on-the-job experience in a clinical manufacturing and or packaging environment.
- Have in-depth understanding of clinical trials and supplies.
- Knowledge of QMS Quality Standards including GMP, GCP and GDP
- Experience in clinical supply field and a contract manufacturing organisation works.

Pay: £32,000.00-£46,000.00 per year

**Benefits**:

- Company pension
- On-site parking
- Referral programme

Schedule:

- Day shift
- Monday to Friday

Supplemental pay types:

- Performance bonus

Work Location: In person

Application deadline: 04/06/2024
Reference ID: QCS


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