Adress Veritaz is a leading IT staffing solutions provider in Sweden, committed to advancing individual careers and aiding employers in securing the perfect talent fit. With a proven track record of successful partnerships with top companies, we have rapidly grown our presence in the USA, Europe, and Sweden as a dependable and trusted resource within the IT industry.
Assignment Description:
We are looking for a Senior Process Engineer or Validation Engineer to join our dynamic team
What You Will Work On:
Engage as a Process Engineer or Validation Engineer within pharmaceutical manufacturing operations.
Contribute to the development, optimization, and validation of manufacturing processes and equipment.
Collaborate with cross-functional teams to ensure compliance with regulatory requirements and industry standards.
Participate in the design, execution, and analysis of validation protocols and reports.
Provide technical support and troubleshooting expertise to resolve manufacturing issues.
Assist in the implementation of process improvements and efficiency enhancements.
What You Bring:
Minimum of 3 years of university studies with a focus on disciplines such as mechanical engineering, biotechnology, or chemistry.
Practical experience of at least 1 year in pharmaceutical manufacturing or an equivalent field.
Hands-on experience of at least 1 year in the validation of equipment used in pharmaceutical manufacturing processes.
Strong understanding of pharmaceutical manufacturing processes and regulatory requirements.
Proficiency in conducting validation activities and interpreting validation data.
Excellent problem-solving skills and attention to detail.
Ability to work effectively in a cross-functional team environment.
Strong communication and interpersonal skills.
Adherence to high ethical standards and a commitment to quality and compliance.
Fluent in Swedish and English.
