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Catalent · 1 day ago

Manager, Facilities

Harmans, MD

Full-time

Onsite

Mid, Senior Level

5+ years exp

Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, manufacture, and supply products that help people live better and healthier lives. The Facilities Manager will support the manufacturing and process development organizations by developing and implementing maintenance and engineering best practices resulting in robust, sustainable, integrated manufacturing processes.

BiotechnologyHealth CareManufacturingPharmaceutical

Responsibilities

Provide leadership for site FM strategy for facilities processes

Direct internal and external teams to execute activities supporting facility per cGMP requirements

Assemble the appropriate set of multidisciplinary professionals which integrates support of people, process and technology to ensure the safe, secure and sustainable functionality of the built environment

Formulate operational procedures and organization to build a team that contributes to the success at the BWI site and corporation

This includes assessing, repairing and upgrading facilities, systems and utilities to ensure the facility and services fully support the occupants and functions housed within them

Identify and evaluate solutions to support change to create a robust/reliable environment

Develop, programs to improve efficiency, heighten performance and ensure the facility meets OSHA health and safety requirements

Qualification

Engineering degreeGMP complianceEnvironmental HealthSafetyTechnical engineering managementLeadership experienceOperational proceduresContinuous Improvement Processes

Required

Bachelor's degree in Engineering is preferred; (Engineering, Engineering Management, or Engineering Technology). But additional experience can be accepted in lieu of degree

Minimum of 5 years of experience implementing engineering best practices, as well as experience in managing technical engineering functions. Experience in hands on implementation and support of utility/manufacturing systems within a highly regulated cleanroom manufacturing environment is required

Experience in compliance Regulations that apply to Quality, Regulatory Compliance (21 CFR Part 11), Environmental Health and Safety, as well as have knowledge of standards related to maintenance processes, construction, equipment design and implementation into global medical device manufacturing facilities

5+ years of related work experience, prefer in GMP/Bio-Pharma maintenance/engineering environments

Demonstrable leadership experience at Catalent (including but not limited to participation in Catalent-sponsored leadership programs such as NGGL, GOLD, GM Excellence, and GROW) may be considered in place of external experience

Benefits

Competitive medical benefits and 401K

152 hours PTO + 8 Paid Holidays

Company

Catalent

Catalent - Blow-Fill-Seal Sterile CDMO Business is focusing on complex clinical to commercial stage formulation and manufacturing. It is a sub-organization of Catalent Pharma Solutions.

Founded in 2007

Somerset, New Jersey, USA

10001+ employees