Analytical Development Coordination - LCM

About Adecco:

A World Leader in Human Resources, Adecco is present in 60 countries through a network of 5,500 branches, which provide employment daily to 700,000 people and serve more than 100,000 companies. It is part of the Fortune Global 500 list and is listed on the Zurich stock exchange. Adecco presents a global structure oriented towards providing an integrated service in the Human Resources area, with a commitment to continuous development of effective and competitive solutions for its clients.

We are advising an important company in the health and pharmaceuticals segment.

Position Objective

Coordinate the Analytical Development team and activities, ensuring the creation, validation, transfer, and maintenance of analytical methods necessary for the development, launch, and lifecycle of medicines.

Main Responsibilities:

• Coordinate the development of analytical methods.
• Coordinate method validations.
• Manage analytical transfers.
• Support product launches and transfers.
• Coordinate stability studies.
• Monitor laboratory issues and investigations.
• Review technical documents.
• Participate in committees and meetings.
• Evaluate analysis results.
• Ensure compliance with deadlines and regulatory requirements.
• Distribute and prioritize team activities.
• Lead a team of approximately ten professionals.
• Ensure the technical quality of deliverables.
• Support discussions on deviations, out-of-specification results, and laboratory issues.
• Interact with Pharmaceutics Development, Quality, Regulatory Affairs, Production, and Quality Control.
• Coordinate activities related to the launch and transfer of medicines.

Requirements

Academic Background

• Completed degree in Pharmacy, Chemistry, or related fields.
• Postgraduate degree will be considered a differential.

Technical Experience

• Solid experience in analytical development, analytical validation, and method transfer.
• Experience in stability studies and laboratory routine (bench work).
• Proficiency in instrumental techniques and physicochemical analyses.
• Hands-on experience with HPLC, spectrometry, and other analytical equipment.
• Knowledge in analytical method review, preparation, and review of technical documentation.
• Experience in investigating deviations and laboratory issues.
• Experience in evaluating drug product compliance.
• Knowledge of Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP).
• It is essential that the professional has recent technical laboratory experience, deeply understanding bench routine, analytical equipment, and method validation, with solely managerial experience not being sufficient.

Benefits

- Medical Assistance

- Dental Assistance

- Life Insurance

- Food Voucher

- Meal Voucher

- Transportation Voucher