The shift is Monday-Friday 7:00 am- 3:30pm
A Quality Control (QC) Supervisor's primary duty is to plan, organize, direct and evaluate the routine activities and project deliverables of the QC laboratories to ensure the safety and reliability of products produced in compliance with quality and regulatory requirements. Responsibilities include overseeing the scheduling of daily activities for QC personnel, interpreting applicable quality and regulatory requirements and develop associated policies and procedures for the laboratories operations, interfacing with investigators during both internal and external inspections, evaluating audit observations and developing responses and oversight for related action plans, making critical decisions concerning testing operations, working collaboratively with manufacturing, technical and product development teams to improve quality, increase efficiency, solve problems, generate cost savings, and provide new product support, managing operations for the QC laboratories and supporting the QC documentation and LIMS activities.
This is a permanent, full time position. It is a salaried role. The shift is Monday-Friday 7:00 am- 3:30pm. This position offers a sign on bonus and relocation.
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.
Supervises the daily activities of business or technical support or production team
Typically manages 5-25+ employees
Sets priorities for the team to ensure task completion; coordinates work activities with other supervisors for up to 2+ months in advance
Decisions are guided by policies, procedures and business plan; receives guidance and oversight from manager
Typically does not perform the work supervised
Bachelor's degree preferred
2 years laboratory experience
2 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
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 ~~~ . 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 ~~~ for us to investigate with local authorities.