QC Scientist - Raw Materials, Site Based, Redmond, WA

Evotec•Redmond, WA

10d•$82,000 - $86,250•Onsite

About The Position

We’re looking for a passionate and curious QC Scientist, Raw Materials 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 Scientist, Raw Materials at Just Evotec Biologics, 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 QC 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.

Requirements

BS Chemistry or related science with 3+ years related experience
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
Ability to understand and follow compendial (USP, EP) testing instructions and in-house procedures
Strong adherence to data integrity requirements
Knowledge of current instrumentation and procedures used in an analytical laboratory
Knowledge of Material Safety Data Sheets and safety precautions
Legible penmanship
Ability to perform multiple tasks simultaneously, manage time effectively, and adapt to changing priorities
Ability to succeed with minimal supervision
Excellent oral and written communication skills
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

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 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
Write, revise, or review SOPSs and job aids
Perform primary review of laboratory data and documentation
Train and mentor junior colleagues
Be proficient in aseptic sampling techniques and ensure all cGMP documentation is ALCOA