Group Leader, Analytical Characterization, Biologics

Catalent Pharma Solutions•Kansas City, MO

5d•Onsite

About The Position

We have an opportunity for a Group Leader, Analytical Characterization, Biologics to join our team. This role focuses on managing a sub-team of junior scientists and serving as a technical expert on projects. You will act as a liaison between teams, mentor associates, and support client audits and visits. The position involves working on analytical activities for Biopharma product development under cGMP regulatory guidance for large molecules and biologics.

Requirements

Bachelor’s degree with more than 4 years of relevant experience in department-specific techniques or based on performance at Catalent, OR
Master’s degree with more than 2 years of relevant experience in department-specific techniques or based on performance at Catalent, OR
Doctorate degree with more than 1 year of relevant experience in department-specific techniques or based on performance at Catalent
Individual may be required to sit, stand, walk regularly and occasionally lift, pull or push 0-40 pounds.

Nice To Haves

Demonstrable leadership experience at Catalent (including but not limited to participation in Catalent-sponsored leadership programs such as NGGL, GOLD, LEAD Now, GM Excellence, and GROW) may be considered in place of external experience.
Knowledge of principles, theories, and concepts in disciplines such as Biology, Chemistry, and Biochemistry, with broad knowledge of related areas.
Able to lead difficult discussions with customers and drive them to an acceptable resolution.
Well organized with ability to multitask and complete multiple tasks efficiently within given timeframes.
Coaching skills to train junior scientists.
Good project management skills for multiple concurrent projects of moderate to high complexity.
High personal credibility with peers and subordinates.
Motivator and experienced in team development.
Lead by example according to Catalent's values and culture.

Responsibilities

Plan, prioritize, organize, and execute analytical work in the laboratory according to client contracts and technical agreements.
Ensure cGMP practices are implemented and followed by the team and self.
Adopt safe working practices in the laboratory and comply with in-house SOPs and safety legislation.
Establish and maintain technical communications with other groups and clients as needed.
Carry out performance reviews and HR activities such as time entry approval, PTO approval, and salary adjustments in line with company policy.
Maintain team engagement and foster a learning and growth culture.
Advocate and model Catalent’s culture of quality, safety, and ethics.
All other duties as assigned.