Pharmaceutical Labelling Specialist

Job content

Bachelors degree or equivalent in pharmacy, engineering, business or life sciences Relevant Extensive experience in the pharmaceutical industry or related healthcare environment. Labelling experience in the pharmaceutical industry is highly desired
Position Description:

• Supports timely delivery of clinical supplies through effective management of assigned projects.

• Manages multiple projects and tracks all activities and milestones related to assigned projects. Identifies and reports issues to appropriate levels of management in a timely manner.

• Generates label vendor specifications in accordance with relevant regulatory requirements for assigned projects.

• Works with external partners to ensure clinical labels are created with exacting specification.

• Generates clinical labeling source documentation as required.

• Reviews and approves vendor generated label proofs/specifications and other related documents.

• Utilizes electronic verification software to perform check on label proof. Routes final label for review and approval accordingly.

• Works cross-functionally with individuals and project teams in various areas.

• Participates in assigned training including cGMP and safety training

• Ensures regulatory, cGMP, GDP compliance of activities in assigned areas of responsibility. Reports any deviations to the appropriate management.

• Liaises with responsible Trial Supplies Manager on aspects of clinical supplies packaging and labelling design and study requirements and resolves issues.

Competencies Required:

• Ability to plan, manage and execute multiple projects and to deliver against critical timelines in a fast-paced, rapidly changing environment.
• Exceptional project management skills and detail oriented.
• Possesses solid oral and written communication skills.
• Good decision making and organizational skills.
• Ability to effectively communicate ideas and to influence others to achieve results.
• Ability to understand and apply regulatory and CGMP principles.
• Good understanding of pharmaceutical or medical terminology
• Proficiency in standard office technology, including Microsoft Suite (Outlook, PowerPoint, Excel) Additional applications such as Adobe. Willing to learn additional applications as needed
• Experience working on multi-disciplinary teams and projects
• Good knowledge of rigorous pharmaceutical and/or scientific documentation practices and change control processes (e.g. revision control) is preferred

Job Type: Freelance

Salary: £28.00-£32.00 per hour

Expected hours: 35 per week

Benefits:

• Company pension
• Free parking
• On-site parking

Ability to commute/relocate:

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

Licence/Certification:

• Driving Licence (preferred)

Work Location: In person