Catalent Pharma Solutions
Specialist III, Form/Fill
Catalent Pharma Solutions, Bloomington, Indiana, United States, 47401
Catalent Pharma Solutions - Specialist III, Form/Fill - 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’s facility in Bloomington provides a fully integrated and unique model for process development, clinical and commercial mammalian cell culture manufacturing, formulation, parenteral drug manufacturing and packaging under one roof.The Specialist III, Form/Fill role
provides direct technical support to operations area as it relates to documentation, equipment procurement, testing, operational excellence, and training. This role works collaboratively with multiple company functions to ensure production systems operate in a safe, and quality-oriented manner.This is a fulltime, onsite role, working days; Monday – Friday.The RoleServes as the Subject Matter Expert (SME) for processes and procedures within primary manufacturing, completing work autonomously.Proposes, develops and owns process improvements related to equipment and processes.Collaborates with Production Supervisors, Room Leads, and QA floor support to solve issues real time.Acts as a technical expert for machine setup, troubleshooting, and maintaining overall efficiency; serves as the technical representative of Primary Manufacturing in audit activities.Develops training strategies for Primary Operations and provides coaching and training related to floor operations in all aspects of primary manufacturing.Reviews and approves documents in EDMS; owns, revises, and routes documents through EDMS.Executes other duties as assigned.The CandidateHigh School/GED required.8 years’ of GMP in a pharmaceutical and/or manufacturing environment, required.Why You Should Join CatalentCompetitive medical benefits and 401K.152 hours of PTO + 8 Paid Holidays.Dynamic, fast-paced work environment.Opportunity to work on Continuous Improvement Processes.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.Catalent is an Equal Opportunity Employer, including disability and veterans.
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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’s facility in Bloomington provides a fully integrated and unique model for process development, clinical and commercial mammalian cell culture manufacturing, formulation, parenteral drug manufacturing and packaging under one roof.The Specialist III, Form/Fill role
provides direct technical support to operations area as it relates to documentation, equipment procurement, testing, operational excellence, and training. This role works collaboratively with multiple company functions to ensure production systems operate in a safe, and quality-oriented manner.This is a fulltime, onsite role, working days; Monday – Friday.The RoleServes as the Subject Matter Expert (SME) for processes and procedures within primary manufacturing, completing work autonomously.Proposes, develops and owns process improvements related to equipment and processes.Collaborates with Production Supervisors, Room Leads, and QA floor support to solve issues real time.Acts as a technical expert for machine setup, troubleshooting, and maintaining overall efficiency; serves as the technical representative of Primary Manufacturing in audit activities.Develops training strategies for Primary Operations and provides coaching and training related to floor operations in all aspects of primary manufacturing.Reviews and approves documents in EDMS; owns, revises, and routes documents through EDMS.Executes other duties as assigned.The CandidateHigh School/GED required.8 years’ of GMP in a pharmaceutical and/or manufacturing environment, required.Why You Should Join CatalentCompetitive medical benefits and 401K.152 hours of PTO + 8 Paid Holidays.Dynamic, fast-paced work environment.Opportunity to work on Continuous Improvement Processes.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.Catalent is an Equal Opportunity Employer, including disability and veterans.
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