Demo

Senior Quality Control Chemist

Actylis
Eugene, OR Full Time
POSTED ON 2/8/2025
AVAILABLE BEFORE 3/8/2025
Actylis is a global solutions provider with over 75 years of experience, specializing in streamlining the management of critical ingredients and raw materials for our business partners.

We offer both sourcing and manufacturing solutions tailored to meet diverse and evolving needs, ensuring a reliable, agile, and secure supply network. Our commitment to customization allows us to create flexible solutions, whether it’s a unique specification, custom packaging, or tailored logistics strategies.

With deep expertise in quality and regulatory compliance, sourcing and logistics management, analytical services, and R&D support, we reduce complexities and mitigate risks, empowering our partners to focus on growing their business.

In furtherance of that goal, Actylis is seeking new members of the team. This expansion, coupled with a comprehensive benefits package, and opportunities for challenge and growth, make Actylis the ideal place to work and thrive. We hope you’ll consider joining us!

Position Summary

We are seeking a motivated Senior Quality Control (QC) Chemist. This position requires utilizing analytical lab skills to test and measure materials in a manufacturing or pharmaceutical field. As someone whose work is generally part of a team effort, a QC chemist ensures that all QC operations are conducted following established Standard Operating Practices (SOP), Good Manufacturing Practices (GMP), and other applicable regulatory standards. This senior role will also provide guidance and support to other QC scientists in a mentoring capacity.

Responsibilities will include:

  • Independent execution of various standard laboratory techniques, including but not limited to HPLC, LC/MS, GC, GC/MS, FTIR, KF, LOD, and appearance assessment
  • Independent preparation of samples, solutions, instrument set-up and breakdown
  • Lead the transfer of analytical methods to QC from internal and external sources
  • Analysis of various sample types with approved prescribed test methods
  • Provide guidance and support on day-to-day tasks to QC personnel
  • Represent the Quality Control Department on internal and external matters as requested by QC Manager
  • Independent authoring, reviewing, and execution of analytical method validation protocols
  • Lead internal meetings as requested
  • Independent authoring, reviewing, and execution of stability study protocols
  • Independent preparation of data packets, stability reports, and certificates of analysis to summarize analytical testing
  • Participation in, or lead, Out of Specification investigations and the documentation of analytical deviations along with qualified investigators and management
  • A working knowledge of QC laboratory operating under US FDA/EU GMPs and ICH guidelines
  • Provide mentorship to co-workers as needed.

Required Experience & Knowledge

  • B.S. degree in Chemistry, Biochemistry, or relevant science field with a minimum of 7 years applicable laboratory experience, or M.S. degree with a minimum of 5 years of experience, or PhD. with a minimum of 1 year of experience.
  • GMP experience required
  • Proficient in a variety of analytical techniques including, but not necessarily limited to, analytical balances, pH meters, HPLC, HPLC/MS, GC, GC/MS, FTIR, KF, LOD, and UV/Vis spectroscopy.
  • Demonstrate ability to identify any performance issues with analytical instrumentation and to perform minor troubleshooting.
  • Must be willing to work both independently and as a team player with a positive attitude.
  • Detail-oriented mindset with excellent critical thinking, multi-tasking, and organizational skills.
  • Clear, effective, and professional communication with colleagues and contractors
  • Ability to communicate technical information to a nontechnical audience
  • Ability to organize meetings and present to groups

Work Environment/Physical Demand

  • Works in an office and laboratory environment
  • Must be able to work safely with chemicals and hazardous materials
  • May work at both Actylis sites in Eugene
  • May sit or stand for long periods of time
  • May lift up to 40 pounds with or without reasonable accommodation
  • May travel between facilities in Eugene as needed

Actylis is an Equal Opportunity Employer. Actylis US does not discriminate on the basis of race, religion, color, sex, gender identity or expression, sexual orientation, age, non-disqualifying physical or mental disability, national origin, veteran status or any other basis covered by appropriate law. All employment is decided based on qualifications, merit, and business need.

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Job openings at Actylis

Actylis
Hired Organization Address Port Washington, NY Full Time
Actylis is a global solutions provider with over 75 years of experience, specializing in streamlining the management of ...

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