Evotec

QA Specialist - Lot Disposition, Site Based, Redmond, WA

Evotec$90K — $100K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor’s degree in biological or engineering science
  • Minimum of 3 years relevant experience in a biopharmaceutical/pharmaceutical cGMP manufacturing environment
  • Ability to collaborate and communicate cross-functionally
  • Proven attention to detail

Responsibilities

  • Compile lot release documentation for product disposition
  • Ensure lot release deliverables are received from key stakeholders before product disposition
  • Facilitate weekly lot disposition meetings with QA, Manufacturing, and QC
  • Review deviations, OOS, and change control records to ensure no impact to product
  • Partner with other QA peers for consistency and efficiency in the department
  • Alert senior management of significant quality and compliance risks

Benefits

  • Growth opportunities through professional courses and mentorship
  • Flexible work environment to balance professional and personal life
  • Inclusive culture that values diverse voices
  • Opportunity to work on innovative projects with cutting-edge technology
  • Encouragement for big ideas and creative thinking
Full Job Description

Location: Seattle, WA

Department: Quality

Shift: Monday-Friday, 8am-5pm

The Role: / your challenge, in our journey

Were looking for a passionate and curious QA Specialist to join our team. If youre excited by new challenges, solving complex problems, and learning every step of the way, you might just be the perfect fit. In this role, youll have the opportunity to drive impactful projects, collaborate with bright minds, and explore uncharted territories.

As a QA Specialist at Just Evotec Biologic., youll have the freedom to ask the hard questions, think outside the box, and find creative solutions that push us forward. Its a role where your curiosity will fuel both your personal growth and the success of the team.

Just-Evotec Biologics is seeking a highly motivated QA Specialist that desires a significant opportunity to improve worldwide access to biotherapeutics. This team member will be responsible forthe execution of day-to-day QA responsibilities for GMP manufacturing, along with building and enhancingthe qualityassurance systems.The role incumbent works both independently and collaboratively with Manufacturing, Quality and Facilities staff to ensure compliance withcGMPsand internal procedures.

What Youll Do:

  • Compile lot release documentation for productdisposition

  • Ensure lot release deliverables are received from key stakeholders prior to Productdisposition

  • Facilitate weekly lot disposition meeting with QA, Manufacturing, QC,etc

  • Review Deviations, OOS, and Change control records to ensure no impacttoProduct

  • Partner with other QA peers to ensure consistency and efficiency within the QA department.

  • Alert senior management of significant quality, compliance, supply, and safety risks.

Who You Are:

  • Candidate must possess strong focus on right the first time and attention to detail

  • Possess effective task/time management organizational skills

  • Capacity to develop solutions to technical issues of moderate scope

  • Ability to organize, analyze/interpret, and effectively communicate individual results

  • Motivated, self-starter with strong mechanical aptitude

  • Good interpersonal, team, and communication skills are a must

  • Excellent oral and written communication skills

Qualifications:

  • Bachelors degree in biological or engineering science

  • Minimum of 3 years relevant experience in a biopharmaceutical/Pharmaceutical cGMP manufacturing or similar environment.

  • Ability to collaborate and communicate cross-functionally.

  • Proven attention to detail

Why Join Us:

  • Growth Opportunities: Were a company that believes in continuous learning and development. Whether its professional courses, mentorship, or new projects, well help you grow.

  • Flexible Work Environment: We offer flexible work options to help you balance your professional and personal life. This is a site based role.

  • Inclusive Culture: Were committed to building a diverse and inclusive environment where everyones voice is valued, and curiosity is encouraged.

  • Innovative Projects: Youll have the chance to work on groundbreaking initiatives and cutting-edge technology in an atmosphere where your curiosity is the key to success.

  • A Place for Big Ideas: We dont just talk about thinking outside the boxwe throw the box away. If youve got ideas, we want to hear them.

Are You Still Curious?

If youve read this far, then chances are youve got a curious mindjust like us. So, what are you waiting for? Take the leap and apply today. We cant wait to see where your curiosity leads youand how it will shape the future of Just Evotec Biologic.

Let your curiosity guide your career#BeCurious and explore the endless possibilities at Just Evotec Biologic!

The base pay range for this position at commencement of employment is expected to be $90,000 to $100,000; Base salary, exempt, offered may vary depending on individuals skills, experience and competitive market value. Additional total rewards include discretionary annual bonus, comprehensive benefits to include Medical, Dental and Vision and 401k company match, flexible paid time off and paid holiday, wellness and transportation benefits.

About Evotec

Evotec is a drug discovery and development company that provides services to pharmaceutical and biotechnology companies. The company's services include drug discovery, preclinical development, and clinical development. Evotec was founded in 1993 and is headquartered in Hamburg, Germany.
Learn more about Evotec
Size
3,000 employees
Industry
Founded
1993

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