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Analytical Chemistry Specialist
2 months ago
Company Overview:
Blue Signal Search is a renowned executive search firm with a proven history of connecting top talent in the manufacturing and industrial sectors. Our expertise spans across various roles including manufacturing leadership, engineering, supply chain, and logistics.
Position Summary:
We are currently seeking a Quality Control Chemist for a prominent manufacturing organization that collaborates with major corporations and well-known brands to create successful products.
The Quality Control Chemist is essential in the establishment and validation of analytical methodologies, specification setting, and testing of pharmaceutical products. This position requires a unique combination of creativity, analytical skills, and teamwork to ensure project success within a regulated manufacturing setting.
What We Offer:
- Attractive salary package, including bonuses and comprehensive benefits such as medical, dental, and vision coverage, along with a 401(K) match.
- A workplace culture that promotes high employee retention and minimizes bureaucratic obstacles.
- Strong financial stability, with the company holding a significant share in the market.
- A commitment to innovation, with dedicated resources for new product development and support for existing brands.
- Exceptional autonomy, allowing you to influence your career path.
Key Responsibilities:
- Collaborate with Innovation, Production, and Marketing teams to drive project development and ensure timely completion.
- Conduct thorough reviews of analytical results and provide constructive feedback.
- Perform troubleshooting, preventive maintenance, and operational qualification of laboratory instruments.
- Lead analytical tasks related to product development and communicate updates to relevant teams.
- Draft specifications and standard operating procedures (SOPs), and generate necessary protocols and reports.
- Facilitate training for laboratory analysts during method transfers.
- Maintain a clean and organized laboratory to comply with regulatory standards.
- Actively participate in cross-departmental meetings and contribute valuable insights.
- Review laboratory notebooks, ensuring compliance with internal protocols and providing feedback.
- Design and execute method validation protocols for drug substances and dosage forms.
- Analyze experimental data, draw conclusions, and make informed recommendations.
- Engage in evaluating innovation capabilities and identifying 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 environment.
- Experience in dissolution, drug impurity method development, and/or method validation is preferred.
- Familiarity with ICH guidelines for drug product analysis and knowledge of regulatory submission requirements is advantageous.
- Proficiency in chromatography techniques, including gas chromatography (GC) and high-performance liquid chromatography (HPLC).
- Strong understanding of cGMPs and GLPs, along with familiarity in solid analytical techniques.
- Demonstrated ability to work both independently and collaboratively, with excellent communication skills.
- Exceptional creativity, innovation, and decision-making capabilities.
- Proficiency in Microsoft Office and relevant software applications.
- Willingness to work flexible hours as needed.
