QC Associate Scientist, Raw Material Inspection and Sampling - Site Based, Redmond, WA

Evotec • Redmond, WA

1d • $78,000 - $83,000 • Onsite

About The Position

We’re looking for a passionate and curious QC Associate Scientist to join our team. If you’re excited by new challenges, solving complex problems, and learning every step of the way, you might just be the perfect fit. In this role, you’ll have the opportunity to drive impactful projects, collaborate with bright minds, and explore uncharted territories. As a QC Associate Scientist at Just Evotec Biologic , you'll have the freedom to ask the hard questions, think outside the box, and find creative solutions that push us forward. It’s a role where your curiosity will fuel both your personal growth and the success of the team. This role will be responsible for supporting the QC Raw Materials program by inspecting and sampling incoming GMP raw materials and manufacturing supplies, performing related equipment cleaning and maintenance, and providing documentation support. In addition, the Associate Scientist will partner with Manufacturing, Materials Management, Quality Assurance, Procurement, QC staff, and outsourced testing laboratories to meet business goals and compliance requirements. As a key member of the QC group, the successful candidate will have experience with good documentation practices (GDP), be detail oriented, internally motivated, and skilled at working independently. Experience with fume hoods, laminar flow hoods, balances, aseptic technique, and cleanroom gowning is highly desired. The ideal candidate has strong written and verbal communication skills, multitasks effectively, and works well both independently and in teams. This position reports directly to the Senior Manager of Quality Control Raw Materials.

Requirements

• BS Chemistry or related science with related experience, or AS Chemistry with 1 + years related experience
• Strong adherence to data integrity requirements
• Knowledge of current instrumentation and procedures used in an analytical laboratory
• Knowledge of Material Safety Data Sheets and appropriate safety precautions
• Ability to follow detailed written procedures
• Legible penmanship
• Ability to perform multiple tasks simultaneously, manage time effectively, and adapt to changing priorities
• Ability to succeed with minimal supervision
• Must demonstrate initiative, resourcefulness, and flexibility to work independently and as part of a team
• Ability to interact constructively with co-workers
• Demonstrated meticulous attention to detail and sense of craftsmanship
• Ability to lift up to 60 pounds; kneeling, crouching, twisting the upper body, walking, bending, stooping, pushing, pulling, and reaching without accommodation
• Ability to routinely wear applicable personal protective equipment (PPE)
• Ability to work with various laboratory cleaning agents and chemicals
• Ability to train on and wear a respirator, as applicable
• Tolerance of exposure to cold-room (2-8°C) conditions
• Tolerance of medium noise levels

Nice To Haves

• Experience in a quality control or production environment in a cGMP facility
• Experience in a raw materials testing or chemistry laboratory
• Experience with aseptic technique

Responsibilities

• Execute the daily activities (in warehouse, laboratory, and cleanroom environments) of the QC Raw Material group in support of inspection, sampling, and testing as per written specifications and compendial methods
• Inspect material containers, labels, and associated documentation for integrity and compliance with written specifications
• Initiate investigations for any container integrity or compliance issues found during the inspection/sampling process
• Manage inventory of raw material samples
• Coordinate attribute testing (internal or external) for batch release
• Maintain lab spaces and supply stocks
• Provide subject matter expertise during internal project team meetings
• Support investigation and closure of deviations, CAPAs, etc.
• Collaborate with Quality Assurance, Manufacturing, Materials Management, and other functions to ensure internal timelines, testing TAT, and team milestones are achieved
• Use various software tools to support tracking of material release status (Excel, SAP, LIMS, etc.)
• Safely use laboratory equipment and instruments (e.g., FTIR, pH meter, osmometer, etc.)
• Maintain a clean and organized work area to ensure material segregation and prevent cross contamination
• Assist senior colleagues with reagent preparation and equipment maintenance, as necessary

Benefits

• Growth Opportunities
• Flexible Work Environment
• Inclusive Culture
• Innovative Projects
• A Place for Big Ideas
• discretionary annual bonus
• comprehensive benefits to include Medical, Dental and Vision, short-term and long-term disability, company paid basic life insurance, 401k company match, generous paid time off and paid holiday, wellness and transportation benefits

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Education Level: Associate degree
• Number of Employees: 501-1,000 employees