Quality Control Analyst Ii/iii (ipc Group)

Serán BioScience is looking for an experienced analysts to support manufacturing of novel pharmaceutical drug products within our In-Process Control group. As a QC Analyst II/III within the Quality Control department you will work alongside a team of analysts and operators to ensure the highest quality product by testing raw materials and production equipment within GMP clean spaces. Qualified candidates will demonstrate expertise in utilizing specialized laboratory equipment, techniques, and methodologies for technical assessments and data analysis purposes. Preference will be given to those with experience in GMP environments and technical data review specific to the pharmaceutical industry.

At Serán, everything that we do has the potential to changes lives. Knowing that we're bringing solutions to patients is what powers us every day. Knowing you're making a difference, is the difference.

Duties and Responsibilities

• Conducts appearance testing, solution preparation, and pH measurement
• Conducts raw material sampling, AQL, and Identification Testing (FT-IR)
• Enters clean spaces with appropriate PPE to collect various samples
• Is familiar with introductory analytical equipment (e.g., HPLC, GC-HS, TOC, FT-IR)
• Is familiar with raw materials testing requirements (compendial and client testing)
• Conducts technical data review
• Cleans lab and glassware
• Logs-in samples and standards
• Disposes of analytical waste appropriately
• All other related duties as assigned

Required Skills and Abilities

• Hands-on lab experience in HPLC, CG-HS, TOC, FT-IR
• Hands-on lab experience with raw materials testing
• Strong verbal and written communication skills
• Demonstrated ability to collaborate and work in cross-functional teams
• Strong organizational skills and attention to detail
• Strong time management skills with a proven ability to meet variable and competing deadlines
• Strong analytical and problem-solving skills
• Ability to prioritize tasks and to keep leadership apprised of performance to timelines
• Ability to function well in a high-paced and at times stressful environment
• Proficient with Microsoft Office Suite or related software

Education and Experience

• Bachelor's degree in related scientific discipline
• 3 years of hands-on laboratory experience
• Minimum of 2 years of GMP experience required

Physical Requirements

• Prolonged periods of sitting or standing at a desk and working on a computer
• Prolonged periods of sitting or standing in laboratory environment
• Must be able to lift up to 25 pounds at times
• Motor skills required for basic laboratory operations