Senior Manager, QC

We're hiring for a Senior Manager, QC supporting the microbiology team in Bloomington, Indiana!

Catalent is a global, high-growth, public company, and a leading partner for the pharmaceutical industry in the development and manufacturing of new treatments for patients worldwide. Your talents, ideas, and passion are essential to our mission: to help people live better, healthier lives. Catalent is committed to a Patient First culture through excellence in quality and compliance, and to the safety of every patient, consumer, and Catalent employee.

Catalent Biologics in Bloomington, Indiana is a state-of-the art, GMP manufacturing facility, providing one million sq/ft of drug substance manufacturing, drug product manufacturing, and related pharmaceutical services. This award-winning facility helps customers accelerate biologic drug development programs and bring better treatments to help patients live better, healthier lives.

The Senior Manager, QC's primary role is directly responsible for organizing, overseeing, and evaluating routine activities on the microbiology team including analytical testing, data analysis, document writing, and data reporting to support the manufacturing and release of bulk drug substance and drug product. This is a full-time, salaried position and is 100% site based. The schedule is Monday - Friday, 1st shift.

The Role

• Accountable for daily operations to maintain Quality standards and project timelines, including execution of work, coordination with stakeholders, and communication with leadership.
• Accountable for collaboration with internal Catalent stakeholders to complete microbiological analyses, maintain effective and efficient processes, and ensure appropriate test directives are established and followed.
• Accountable for oversight of microbiological compendial method verification.
• Accountable for daily operations of the site's environmental monitoring program.
• Accountable for collaboration with internal Catalent stakeholders to complete in-process and finished product testing, maintain effective and efficient processes, and ensure appropriate test directives are established and followed.
• Accountable for trending and reporting of site microbiological data, including product testing data.
• Support instrument onboarding and maintenance.
• Other duties as assigned.

The Candidate

• Bachelor's degree in life sciences required.
• 2 years laboratory experience.
• 10 years GMP experience or other regulated industry.
• 5-8 years of management experience.
• Biologics experience highly preferred.
• Microbiology experience highly preferred.
• Must be able to read and understand English-written job instructions and safety requirements.

Why you should join Catalent:

• Defined career path and annual performance review and feedback process.
• Medical, dental and vision benefits effective on first day of employment.
• Potential for career growth on an expanding team and organization.
• 152 hours of paid time off annually plus 8 paid holidays.
• Community engagement and green initiatives.
• Competitive salary with bonus potential.
• Tuition reimbursement program.
• Diverse, inclusive culture.
• Generous 401K match.

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.

Catalent is committed to the health and safety of its employees, visitors and the customers and patients we serve. As a result of the global pandemic, we have modified many of our recruitment and on-boarding processes to maintain everyone's safety. The Human Resources teams will communicate all necessary safety processes and procedures throughout each stage.

personal initiative. dynamic pace. meaningful work.

Visit Catalent Careers to explore career opportunities.

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 [email protected]. This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process.

Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.

Important Security Notice to U.S. Job Seekers:

Catalent NEVER asks candidates to provide any type of payment, bank details, photocopies of identification, social security number or other highly sensitive personal information during the offer process, and we NEVER do so via email or social media. If you receive any such request, DO NOT respond- it is a fraudulent request. Please forward such requests to [email protected] for us to investigate with local authorities.

California Job Seekers can find our California Job Applicant Notice HERE.