Date: Feb 18, 2025
Location: Khandala-Satara, MH, IN, 412801
Company: Datwyler
In billions of syringes and in every second car worldwide, Datwyler components make an important contribution to the safety of patients and drivers. The high-tech company focuses on high-quality, system-critical elastomer components and holds leading positions in attractive global markets such as healthcare, mobility, connectivity, general industry and food & beverage. With over 25 production sites on four continents, sales in more than 100 countries and over 8,000 employees, the company, headquartered in Switzerland, generates annual sales of more than CHF 1,000 million.
Our employees are the heart of Datwyler - we treat each other with respect, trust and appreciation. We have strong roots and values that have been well established in our 100-year corporate history. Become part of our great team as a...
Key Skills:
- Familiar with cGMP and regulatory guidelines
- Review/approve the documents (SOP/WI/specification/validation document)
- Managing the QMS system (LCR/Deviation/CAPA/Market complaint/training)
- Participate in ISO/Customer audits and related compliance activities.
- Lead internal audit activities.
- Coordinate and support to RCA/FMEA activities
- Evaluate the adequacy of Quality standards as per applicable guidelines.
- Review and approve supplier/customer specifications and quality agreements.
- Lead/Participate supplier audits.
Experience: Minimum 15 years in pharmaceutical.
Qualification: B. Pharm/M. Pharm/M.Sc.
Job Title: ASSISTANT MANAGER - QUALITY ASSURANCE
In billions of syringes and in every second car worldwide, Datwyler components make an important contribution to the safety of patients and drivers. The high-tech company focuses on high-quality, system-critical elastomer components and holds leading positions in attractive global markets such as healthcare, mobility, connectivity, general industry and food & beverage. With over 25 production sites on four continents, sales in more than 100 countries and over 8,000 employees, the company, headquartered in Switzerland, generates annual sales of more than CHF 1,000 million.
Our employees are the heart of Datwyler - we treat each other with respect, trust and appreciation. We have strong roots and values that have been well established in our 100-year corporate history. Become part of our great team as a...
Key Skills:
- Familiar with cGMP and regulatory guidelines
- Review/approve the documents (SOP/WI/specification/validation document)
- Managing the QMS system (LCR/Deviation/CAPA/Market complaint/training)
- Participate in ISO/Customer audits and related compliance activities.
- Lead internal audit activities.
- Coordinate and support to RCA/FMEA activities
- Evaluate the adequacy of Quality standards as per applicable guidelines.
- Review and approve supplier/customer specifications and quality agreements.
- Lead/Participate supplier audits.
Experience: Minimum 15 years in pharmaceutical.
Qualification: B. Pharm/M. Pharm/M.Sc.
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Be yourself at Datwyler
We are convinced that people make the difference. At Datwyler, you will experience diversity and a wide range of career opportunities that only an international company can provide. Together, we are increasing our agility, accelerating digitalization and fostering sustainability. For motivated and talented employees, we offer interesting development opportunities with training and assignments in a global environment. With us, you can contribute with all of your creativity and all your ideas.
Be yourself at Datwyler
We are convinced that people make the difference. At Datwyler, you will experience diversity and a wide range of career opportunities that only an international company can provide. Together, we are increasing our agility, accelerating digitalization and fostering sustainability. For motivated and talented employees, we offer interesting development opportunities with training and assignments in a global environment. With us, you can contribute with all of your creativity and all your ideas.