We're hiring for a Supervisor, QA 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.

　　A Supervisor, QA’s primary role is to support the quality function by overseeing GMP activities, documentation and reports. This is a full-time, salaried position and is 100% site based. The schedule is Monday – Friday, first shift.

　　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. 

　　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.

　　The Role

　　Accountable for daily operations to maintain Quality standards and project timelines, including execution of work, coordination with stakeholders, and communication with leadership.

　　Ensure employee training is executed according to defined training plans and maintain current training plans.

　　Identify, maintain, and report functional KPIs to site management.

　　Drive continuous improvement through leading cross function teams to address process improvement, system improvement, new regulations/expectations, new business needs, training improvements, and KPI performance improvements.

　　Conduct performance reviews and engage in employee hiring process.

　　Assist in customer audits and regulatory inspections.

　　Other duties as assigned.

　　The Candidate

　　Bachelor’s degree in life sciences or equivalent preferred or relevant experience

　　2 years quality assurance support in cGMP pharmaceutical production or other regulated industry

　　3 years GMP experience or other regulated industry

　　0-1 years of management experience

　　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

　　Diverse, inclusive culture

　　Potential for career growth on an expanding team within an organization dedicated to preserving and bettering lives

　　152 hours of paid time off annually + 8 paid holidays

　　Competitive salary with yearly bonus potential

　　Community engagement and green initiatives

　　Generous 401K match and Paid Time Off accrual

　　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.

　　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 (https://careers.catalent.com/us/en) 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 (https://cdn.catalent.com/files/legal/CCPA-Privacy-Notice-at-Collection-for-California-Employees-and-Applicants-English.pdf) .