Joulé
Director of Site Operations - Pharmaceutical Manufacturing
Joulé, Allentown, Pennsylvania, United States, 18106
Title: Director of Site Operations - Pharmaceutical Manufacturing
Making sure you fit the guidelines as an applicant for this role is essential, please read the below carefully.Location: Lehigh Valley, PAType: Direct HireSalary: $150,000-$175,000/year, plus bonus
Overview:Pharmaceutical Manufacturing Company is seeking an experienced Operations Leader to oversee and manage all site operations and teams. In this highly visible role, you will be driving business changes, maintain a positive company culture and enforcing FDA GMP regulations.
Responsibilities:
Planning, directing and managing all aspects of the manufacturing operations, adhering to regulatory requirementsResponsible for the financial performance of site; establishing annual financial plan and forecast financial and operational performance to meet corporate revenue goals and product cost goals?????Prepare and present financial, performance and operating reports and recommendations to executive managementMeet all manufacturing goals to support the customer demands and responsible for facility production goals.Develop and train staff of business unit leaders to establish shift production schedules and goals. Plan labor capacity and manage physical assets.Administer cooperation with the various departments to establish teamwork from the purchasing, production, and distribution departments.Collaboratively work with quality heads to maintain an active role in review and revision of standard operating procedures and development and implementation of new procedures.Plans, inspects and monitors facility operations to ensure safe and efficient operation.Establish and maintain relationships with key customers, suppliers, staff, vendors, contractors and company executive personnel.
Requirements: Bachelor's Degree Required10 years in GMP pharmaceutical manufacturing environment in operations managementStrong leadership skills; People management experience with direct reports of Managers and Leads as well as indirect reportsExpert in FDA GMP regulations
#M3#LI-GS1
Making sure you fit the guidelines as an applicant for this role is essential, please read the below carefully.Location: Lehigh Valley, PAType: Direct HireSalary: $150,000-$175,000/year, plus bonus
Overview:Pharmaceutical Manufacturing Company is seeking an experienced Operations Leader to oversee and manage all site operations and teams. In this highly visible role, you will be driving business changes, maintain a positive company culture and enforcing FDA GMP regulations.
Responsibilities:
Planning, directing and managing all aspects of the manufacturing operations, adhering to regulatory requirementsResponsible for the financial performance of site; establishing annual financial plan and forecast financial and operational performance to meet corporate revenue goals and product cost goals?????Prepare and present financial, performance and operating reports and recommendations to executive managementMeet all manufacturing goals to support the customer demands and responsible for facility production goals.Develop and train staff of business unit leaders to establish shift production schedules and goals. Plan labor capacity and manage physical assets.Administer cooperation with the various departments to establish teamwork from the purchasing, production, and distribution departments.Collaboratively work with quality heads to maintain an active role in review and revision of standard operating procedures and development and implementation of new procedures.Plans, inspects and monitors facility operations to ensure safe and efficient operation.Establish and maintain relationships with key customers, suppliers, staff, vendors, contractors and company executive personnel.
Requirements: Bachelor's Degree Required10 years in GMP pharmaceutical manufacturing environment in operations managementStrong leadership skills; People management experience with direct reports of Managers and Leads as well as indirect reportsExpert in FDA GMP regulations
#M3#LI-GS1