Job Description

Overview

At Universal Medicines we are focused on:

(1)

keeping old well-established medicines and unloved consumer brands on the market, safeguarding future availability for patients and customers alike; and

(2)

reverse engineering high cost medicines, to improve future patient access by offering the same quality medicine at a cheaper price.

Universal Medicines is backed by the Founder and ex-CEO of Essential Pharma Group, scaling the business from 2 to 28 countries spanning Europe, Middle East, and Asia; achieving this independent of any financial institutions or bank loans within 10 years, before selling the business to a large global strategic buyer who further expanded the business to over 100 countries.

As the project manager of development and commercialisation (1 year FTC with the possibility of extend, you will be responsible for overseeing and executing projects related to the development, manufacturing, and commercialisation of generic drug products (oral, topical, IV dosage forms), ensuring projects are completed on time, within budget, and meet regulatory requirements.

Location

Egham, Surrey, UK (Hybrid role, working 3 days in the office)

Core Responsibilities

Formulation Development: Overseeing early phase pharmaceutical development of generic drug products, including analytical method and formulation development activities.

Manufacturing: Overseeing the manufacturing of generic drugs, including scale-up, process optimization, and validation.

Quality Control: Ensuring all products meet quality standards, regulations, and safety requirements throughout the product lifecycle

Regulatory Submissions: Overseeing submissions to scientific advice committees and involvement in generic drug applications to regulatory bodies, such as the EMA/ MHRA.

Commercialisation: Leading projects related to the commercialization of generic drugs, including marketing, sales, and distribution.

Qualifications

Pharmacy, chemistry or relevant life sciences degree.

Skills

Project Management: Strong project management skills, including planning, execution, monitoring, and control.

Technical Knowledge: A solid understanding of pharmaceutical development, manufacturing, and quality control processes.

Communication and Collaboration: Excellent communication, interpersonal, and collaboration skills.

Problem-Solving: Strong problem-solving and critical thinking skills.

Compliance: Knowledge of relevant regulatory requirements (GMP, GDP) and industry standards.

Teamwork: Must be a team player.

If you are passionate about driving pharmaceutical product success through strategic thinking and effective management, we encourage you to apply for this exciting opportunity.

Job Types: Full-time, Fixed term contract
Contract length: 12 months

Pay: 40,000.00-60,000.00 per year

Benefits:

Company pension On-site parking Work from home
Schedule:

Monday to Friday
Work authorisation:

United Kingdom (required)
Work Location: Hybrid remote in Egham TW20 8RY