On-Site Trainee: Technical Affairs Scientist (GMP/Regulatory)

Hikma Pharmaceuticals; Viseu; On-site; EUR 20,000 - 28,000; Full time

Job summary

Hikma Pharmaceuticals in Portugal is seeking a Trainee, Technical Affairs Scientist (m/f) to join the Technical Affairs department on an on-site basis. You will support technology transfer related GMP documents and regulatory filings, and assist with process validation activities for injectable products.

The ideal candidate holds a Master's in Pharmaceutical Sciences with 0-2 years' experience, fluent in English, and demonstrates strong presentation, communication, and teamwork skills.

Qualifications

• Master's in Pharmaceutical Sciences is required.
• 0-2 years' experience relevant to pharmaceutical sciences.
• Fluent in English; strong presentation, communication and teamwork skills expected.

Responsibilities

• Support technology transfer related GMP documents and regulatory filings.
• Assist with process validation activities for injectable products.
• Participate in on-site activities at Sintra, Portugal, as part of the Technical Affairs team.

Skills

Presentation skills

Communication skills

Teamwork

Education

Master's in Pharmaceutical Sciences

Job description

Hikma Pharmaceuticals in Portugal is seeking a Trainee, Technical Affairs Scientist (m/f) to join the Technical Affairs department on an on-site basis. You will support technology transfer related GMP documents and regulatory filings, and assist with process validation activities for injectable products.

The ideal candidate holds a Master's in Pharmaceutical Sciences with 0-2 years' experience, fluent in English, and demonstrates strong presentation, communication, and teamwork skills.