Pharmaceutical Process Development Specialist
vor 2 Wochen
**About Us:**
Siegfried AG is a leading Custom Development and Manufacturing Organization (CDMO) that develops and produces active pharmaceutical ingredients (APIs), intermediates, and finished dosage forms.
We operate in a future-oriented business field with a highly professional and motivated team. Our unique culture leverages cultural differences to create a competitive advantage.
We place high priority on providing a flexible, diverse, and discrimination-free working environment where employees can develop personally and professionally, advance innovation, and deliver superior performance.
**Job Description:**
We are seeking a skilled Pharmaceutical Process Development Specialist to join our team in Zofingen, Switzerland. As a key member of our development team, you will be responsible for the development and commercial manufacture of APIs and corresponding intermediates.
You will work closely with our cross-functional teams to ensure seamless integration of chemical and pharmaceutical capabilities into a single business model.
The successful candidate will have a strong background in process development, with experience in developing and scaling up API processes. You will also have excellent knowledge of GMP regulations and guidelines.
**Key Responsibilities:**
- Develop and commercialize APIs and corresponding intermediates
- Collaborate with cross-functional teams to ensure seamless integration of chemical and pharmaceutical capabilities
- Ensure compliance with cGMP and SHE standards
- Manage and maintain documentation, including batch records and standard operating procedures
- Troubleshoot and resolve issues related to process development and manufacturing
- Communicate effectively with stakeholders, including production personnel, quality assurance, and regulatory authorities
**Requirements:**
- Bachelor's degree in Chemical Engineering or a related field
- Minimum 5 years of experience in process development and commercialization
- Strong knowledge of GMP regulations and guidelines
- Excellent communication and collaboration skills
- Ability to work in a fast-paced environment and prioritize tasks effectively
- Proficiency in MS Office and ability to learn new software applications quickly
**Benefits:**
- Competitive salary: CHF 80,000 - CHF 120,000 per year
- Comprehensive benefits package, including health insurance, retirement plan, and paid time off
- Opportunities for career growth and professional development
- Collaborative and dynamic work environment
- Access to cutting-edge technology and equipment
**What We Offer:**
We offer a challenging and rewarding work environment with opportunities for career growth and professional development. Our company is committed to fostering a culture of excellence, diversity, and inclusion.
If you are a motivated and experienced professional looking for a new challenge, we encourage you to apply for this exciting opportunity.
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