Supervisor QC Chemistry

Kindeva Drug Delivery•Lexington, KY

1d•Onsite

About The Position

QC Chemistry Supervisor Our Work Matters At Kindeva we make products that save lives, ensuring better health and well-being for patients around the world. Why Kindeva? Purpose-driven work environment Significant growth potential Collaborative team culture Direct impact on patient care Industry-leading innovation At Kindeva – Lexington, KY, we're not just making products – we're manufacturing life-saving nasal spray medications that make a difference. The Impact You Will Make: The QC Chemistry Supervisor will be responsible for using their skills to lead and develop a team of highly talented QC Chemists and Technicians in maintaining the highest level of quality, safety, and compliance for incoming materials, drug product release, and stability testing in a rewarding fast-paced CDMO environment. The ideal candidate will have proven leadership abilities, strong problem-solving skills, a strong understanding of method validation requirements, and a deep knowledge of analytical techniques and pharmacopeial requirements Growth Opportunity Our Lexington facility is experiencing exponential growth, offering exceptional opportunities for professional development and advancement. Join us during this exciting expansion phase and grow your career while contributing to meaningful healthcare solutions.

Requirements

Bachelor’s degree in Chemistry or related field with minimum of 6 years or 6+ years pharmaceutical industry experience.
Master’s degree in Chemistry or related field with minimum of 4 years or 4+ years pharmaceutical industry experience.
PhD in Chemistry or related field with minimum of 2 years or 2+ years pharmaceutical industry experience.
Proven experience in a supervisory or team lead role.
Exceptional leadership, communication, and interpersonal skills.
Strong analytical, organizational, and problem-solving skills with high attention to detail.
Ability to manage multiple projects in a fast-paced environment.
Comprehensive knowledge of cGMP, ICH, and Pharmacopeia guidances.
Qualified to work with controlled substances.
Possess strong knowledge of analytical techniques. For example, HPLC, GC, UV- Vis, FTIR, Osmolarity, pH

Nice To Haves

Associate’s degree with 5+ years of administrative experience.
Experience supporting senior-level leadership.
Demonstrated ability to independently determine work methods and procedures in complex situations.
Experience contributing to process improvement initiatives.
Strong attention to detail and analytical capability.

Responsibilities

Supervise, mentor and provide technical guidance to a team of chemists and lab technicians
Manage direct reports scheduling
Conduct performance reviews for direct reports
Foster a positive and collaborative team environment
Oversee daily laboratory activities
Prioritize activities to meet project timelines and production schedules
Ensure all lab activities and documentation adhere to cGMP requirements
Lead investigations for Out of Specifications, Out of Trends, and Deviations
Support internal, customer, and regulatory audits as a subject matter expert for the QC Chemistry lab
Evaluate and implement opportunities for continuous improvement in lab processes for efficiency, compliance, and safety
Ensure that all safety policies are adhered to in the lab