Group Leader, Analytical Characterization, Biologics

Catalent Pharma Solutions; Kansas City (MO); On-site; USD 120,000 - 150,000; Full time

Benefits offered by this job

Competitive PTO

8 paid holidays

Tuition reimbursement

Medical, dental and vision coverage

Job summary

Catalent Kansas City seeks a Group Leader for Analytical Characterization in Biologics. The role manages a sub-team of scientists and serves as technical expert on projects, liaising with teams and supporting client audits.

You will mentor associates, drive cGMP compliance, and lead performance reviews while advancing Biologics analytical programs under regulatory guidelines. This onsite role requires strong leadership and collaboration.

Qualifications

• Bachelor's degree with 4+ years in relevant techniques, or equivalent advanced degree with related experience.
• Ability to mentor junior scientists and manage a sub-team.
• Strong understanding of cGMP for biologics and biopharma workflows.

Responsibilities

• Plan, prioritize, and execute analytical work in the laboratory per contracts.
• Lead a sub-team of junior scientists and provide technical guidance.
• Ensure cGMP practices are followed by the team and self.
• Coordinate with other groups and clients on project needs.
• Conduct performance reviews and HR activities per policy.
• Foster engagement and a learning culture within the team.

Skills

Leadership & coaching

cGMP compliance

Analytical characterization

Project management

Cross-functional collaboration

Education

Bachelor's degree in a relevant field

Master's degree in a relevant field

Doctorate degree in a relevant field

Job description

Group Leader, Analytical Characterization, Biologics

About Site Catalent's Kansas City facility is home to our Oral & Specialty Drug Delivery, Biologics Analytical Services and Clinical Supply Services businesses.

Position Summary

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.

Shift: Monday - Friday, 1st shift 8-4:30 pm. Location: Kansas City, MO 100% Onsite.

Role

• 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.

Candidate Minimum 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.
• 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.
• Individual may be required to sit, stand, walk regularly and occasionally lift, pull or push 0-40 pounds.

Preferred Skills & Background

• 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.

Why You Should Join Catalent

• Defined career path with annual performance reviews and feedback process.
• Diverse and inclusive culture.
• Potential for career growth on an expanding team within an organization dedicated to preserving and bettering lives.
• Competitive paid time off plus 8 paid holidays.
• Community engagement and green initiatives.
• Medical, dental, and vision benefits effective day one of employment.
• Tuition reimbursement.

Catalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000 life‑saving and life‑enhancing products to patients around the world.

Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference. personal initiative. dynamic pace. meaningful work.

Catalent is an Equal Opportunity Employer, including disability and veterans.

If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to [e-mail]. This option is reserved for individuals who require accommodation due to a disability.