Pharmaceutical Project Manager

posted:
Location
Punta Gorda, Florida
Industry
Manufacturing & Production (Production Occupations)
Job Type
Temp to Perm
Working Hours
8:00 AM - 4:00 PM
Salary
US$ 25.00 per hour
Ref. Number
S_48185
Contact
Weinberg,Brooke, Spherion
Phone
239-939-9999
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Job Description

Spherion is seeking a Project Manager for a pharma company in Punta Gorda. This person needs to have a Chemistry or Biology background as well as the capability to manage multiple projects. This is a temp to hire opportunity and the company offers an excellent benefits package once you have worked the probationary period.

Responsibilities:
The Project Manager role serves as a liaison between the customer and management for new product development and integration of process schemes within the plant. The project manager develops relationships with customers, manages and communicates project status and performance, and ensures alignment with production activities and corporate objectives. Responsible for successful execution of multiple projects that support manufacturing and packaging of bulk, injectables, oral formulation, fluid delivery, printed packaging materials, and warehousing.
- Coordinate preproduction administration to meet customer requirements and operational goals
-Develop and write batch records, SOPs, and training materials that support production activities
-Ability to operate in a flexible plant that produces multiple products simultaneously for scientific, technical, research-based environments
-Develop clear and effective written proposals and quotations (RFQ) for current and prospective customers and coordinate with management, R&D, and manufacturing
-Respond quickly to the customer, expediting the resolution of customer questions, concerns, and problems
-Develop training programs and train employees on unit operations, safety, and compliance
-Work with technical personnel to resolve capacity issues and unplanned downtime
-Perform Root Cause Analysis on deviations, product complaints, and suspect results; develop and implement countermeasures to prevent recurrence and improve reliability
-Maintain an organized and safe work environment and compliance with training, SOPs, and safe work practices
-Develop quality systems that ensure conformance to established standards such as batch records, good documentation, site plan, employee checklist, facilities, and equipment, etc.
-Understanding of cGMP and cGLP
-Review batch records and procedures and perform lot disposition; coordinate project completion with metrics analysis and performance evaluation
- Respond quickly to the customer, expediting the resolution of customer questions, concerns, and requests
-Other duties as assigned

Working hours: 8:00 AM - 4:00 PM

Skills:
- Knowledge/experience in manufacturing, packaging, and/or project management
- Knowledge of cGLP, cGMP, FDA and USP, regulatory requirements
- Strong project management skills and highly organized; ability to manage multiple tasks and multiple projects simultaneously
- Strong work ethic, detail and results orientated
- Customer focused
- Proficient in computer skills and desktop office products
- Basic Adobe products skills preferred (e.g. Illustrator)
- Familiar with web development and desktop publishing preferred
- Excellent interpersonal oral and written communication skills
- May need to be available off shift and respond to production issues
- Some travel may be required
- Applicant will work within a production plant. Some chemicals and allergens may be present. Mobility requirements and potential exposure to allergens should be considered when applying for this position

Education:
Bachelors

Experience:
4-7 years

Qualifications:
Bachelor's degree in a Chemistry, Engineering, or other technical related field and 1-3 years work experience preferred
Valid Driver's License


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