Analytical Chemistry Specialist

2 weeks ago


Charlotte, North Carolina, United States Blue Signal Search Full time

Company Overview: Blue Signal Search is a recognized executive search firm with a proven history of connecting exceptional talent with leading organizations in the manufacturing and industrial sectors.

Position Summary: Our client, a prominent manufacturing entity collaborating with major Fortune 500 companies, is in search of a skilled Quality Control Chemist. This role is integral to the formulation and verification of analytical methodologies, establishment of specifications, and testing of pharmaceutical products.

Key Responsibilities:

  • Engage with Innovation, Production, and Marketing teams to spearhead project development, ensuring deadlines are met.
  • Conduct thorough reviews of analytical results and provide necessary feedback.
  • Oversee instrument troubleshooting, preventive maintenance, and operational qualification of laboratory equipment.
  • Lead analytical initiatives related to product development and communicate updates to relevant teams.
  • Draft specifications and standard operating procedures (SOPs), generating necessary protocols and reports.
  • Facilitate training for laboratory analysts during method transfer processes.
  • Maintain a clean and organized laboratory to ensure adherence to regulatory standards.
  • Actively participate in cross-departmental meetings, offering insights as needed.
  • Review laboratory notebooks, providing constructive feedback to ensure compliance with internal protocols.
  • Design and execute method validation protocols for drug substances and dosage forms.
  • Analyze experimental data, draw conclusions, and make informed recommendations.
  • Contribute to the evaluation of innovation capabilities and identify potential new product opportunities.

Qualifications:

  • Bachelor's, Master's, or PhD in Chemistry or a related scientific discipline.
  • A minimum of 5 years of experience in a regulated manufacturing setting.
  • Experience in dissolution, drug impurity method development, and/or method validation is preferred.
  • Familiarity with ICH guidelines for drug product analysis and knowledge of analytical data regulatory submission requirements.
  • Proficiency in chromatography techniques, including gas chromatography (GC) and high-performance liquid chromatography (HPLC).
  • Strong understanding of cGMPs and GLPs, with experience in solid analytical techniques.
  • Ability to work independently and collaboratively within a team, demonstrating excellent communication skills.
  • Exceptional creativity, innovation, and decision-making capabilities.
  • Proficiency in Microsoft Office and relevant software applications.
  • Willingness to work flexible hours as necessary.

What We Offer:

  • Competitive salary and bonus structure, along with comprehensive benefits including medical, dental, and vision coverage.
  • A workplace culture that promotes high employee retention and minimizes bureaucratic obstacles.
  • Stable financial standing with a significant market presence.
  • A commitment to innovation, with dedicated resources for new product development and support for existing brands.
  • Unmatched autonomy to influence your career path.


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