Join to apply for the R&D and Product Development role at Michael Page.
Get AI-powered advice on this job and more exclusive features.
About Our Client
Multinational Pharmaceutical Company.
Job Description
1. Lead co-development activities with external partners, ensuring product transition to commercial manufacturing and collaborating with internal teams for seamless product integration;
2. Develop and improve analytical methods for products, following international standards and regulatory expectations, up to validation;
3. Support technology transfer of registered products between manufacturing sites and partners;
4. Work with various oral dosage forms, with additional knowledge of other pharmaceutical dosage forms being a plus;
5. Implement and draft validation procedures and documentation, in collaboration with manufacturing, regulatory, and quality teams;
6. Provide technical support for registration and submissions, including resolving deficiencies until approval;
7. Troubleshoot and recommend modifications to formulas and processes to improve productivity, quality, and cost;
8. Ensure quality and compliance in R&D activities, safeguarding intellectual property and driving continuous process improvement;
9. Oversee knowledge and process transfer between R&D teams, accelerating time-to-market for products;
10. Manage the technology transfer lifecycle, including planning, execution, and monitoring;
11. Supervise equipment selection, sizing calculations, and P&ID development based on client requirements;
12. Prepare operational documentation (e.g., batch records, SOPs) and support capacity planning activities.
The Successful Applicant
* University degree, preferably in Pharmacy, Chemistry or Engineering;
* Strong project management skills and process development or technology transfer skills with 3 years of current work experience;
* A minimum of 5 years of experience in the pharmaceutical industry, with a strong background in research and development;
* Proven expertise in technical transfer processes, ensuring the transition of knowledge and processes;
* Experience executing projects in a GMP-regulated environment is considered a strong asset;
* Management of projects, systems, clients, and business relationships;
* Excellent collaboration and communication skills to work effectively with cross-functional teams;
* Proficiency in written and spoken English with the ability to communicate clearly with clients.
What's On Offer
A collaborative and friendly environment.
Contact
Pedro Justo
Quote job ref: JN-052025-6733771
Seniority level
* Mid-Senior level
Employment type
* Full-time
Job function
* Research, Analyst, and Information Technology
Industries
* Staffing and Recruiting
#J-18808-Ljbffr