pharmaceutical job, project manager, process engineer, aseptic

Project Manager / Program Manager - Pharmaceuticals

Global leader in the development of life saving pharmaceuticals seeks a Project Manager to oversee multiple major projects at the company's flagship site in suburban St. Louis, MO.

This person will be working with project managers to development and adhere to milestones and provide necessary leadership in resourcing tasks and assuring accountability.

The Project Manager should have extensive experience managing major projects exceeding $1MM.

Project activities might include some of the following activities: Master Validation Plan development, SOP and Batch Record Development, FAT and Validation activities including document review and approval, Equipment and Instrument calibration, Operator and Technician training, Resource Planning.

Job Requirements

Bachelor's degree in engineering or a scientific discipline
8+ years experience in project management in a cGMP pharmaceutical manufacturing environment
Documented experience managing multiple projects with budgets in excess of 1MM
Working knowledge of FDA and cGMP regulations
Experience managing and mentoring cross functional teams, including R&D, engineering, regulatory and quality
Strong leadership skills with the ability to drive change
Formal project management training
Lean certification, PMP certification strongly preferred
The ability to prioritize and multitask in a highly charged pharmaceutical manufacturing environment
Excellent communications skills, oral, written and electronic;
Strong analytical abilities





		Program Manager / Project Manager Pharmaceutical Manufacturing St. Louis MO Excellent Engineering Opportunity with Global Pharmaceutical Leader! Project Manager / Program Manager - Pharmaceuticals Global leader in the development of life saving pharmaceuticals seeks a Project Manager to oversee multiple major projects at the company's flagship site in suburban St. Louis, MO. This person will be working with project managers to development and adhere to milestones and provide necessary leadership in resourcing tasks and assuring accountability. The Project Manager should have extensive experience managing major projects exceeding $1MM. Project activities might include some of the following activities: Master Validation Plan development, SOP and Batch Record Development, FAT and Validation activities including document review and approval, Equipment and Instrument calibration, Operator and Technician training, Resource Planning. Job Requirements Bachelor's degree in engineering or a scientific discipline 8+ years experience in project management in a cGMP pharmaceutical manufacturing environment Documented experience managing multiple projects with budgets in excess of 1MM Working knowledge of FDA and cGMP regulations Experience managing and mentoring cross functional teams, including R&D, engineering, regulatory and quality Strong leadership skills with the ability to drive change Formal project management training Lean certification, PMP certification strongly preferred The ability to prioritize and multitask in a highly charged pharmaceutical manufacturing environment Excellent communications skills, oral, written and electronic; Strong analytical abilities Candidates should submit resumes in WORD. Submit Resume Resume Tips Send your resume as a Word Document attachment in an email. Do not put your name and contact information in the header of a document. Using a header makes it difficult to scan the resume into our clients HR tracking software. Read the job description and tailor your resume to feature your skills as they relate to the job. Focus on accomplishments rather than activities. Be specific when describing your experience. When listing accomplishments on a resume include the results: how did you save the company time or money. Don’t worry too much about length. Each position should include a brief description of the company, job, and at least 2-3 accomplishments. Proofread! Do not lie on your resume! Use a font that is easy to read. Be concise and clear. Use bullets for accomplishments. Do not include personal information like date of birth, marriage status or pictures. Write in the first person but remove the “I” from your statements. Use an active voice — it is more effective making you the subject of your statements rather than the object.


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