Arbetsbeskrivning

Veritaz is a leading IT staffing solutions provider in Sweden, committed to advancing individual careers and aiding employers in ensuring 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 seeking an Analytical Chemist

What You Will Work On

• Represent Quality Control (QC) in projects related to new product introductions.
• Act as QC representative in projects and take responsibility for strategy, documentation, and follow-up of analytical technology transfer.
• Lead and manage investigations related to product care issues.
• Prepare and submit material for product review and Continuous Process Verification (CPV).
• Ensure alignment between internal analytical methods and registered methods.
• Provide expert support and guidance during method validation activities.
• Review pharmacopoeia updates and ensure they are correctly implemented.
• Review and approve regulatory documentation.
• Drive and manage change control activities.
• Issue, review, and technically approve governing and controlled documents.

What You Bring

• University degree in Natural Sciences, preferably with specialization in Analytical Chemistry, or equivalent.
• Several years of experience in qualified Quality Control work, including hands-on laboratory experience.
• Strong experience working under Good Manufacturing Practice (GMP) conditions.
• Good understanding of regulatory requirements, including SUPAC, EU, and ICH guidelines.
• Excellent communication skills in Swedish and English, both written and spoken.