Operations Integration Scientist
Millipore Corporation

Job Info

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Work Location: St. Louis, Missouri
Shift:
Department: LS-SC-POKM-A1 Cherokee STL Technical Operations 2
Recruiter: Guadalupe Barragan

Hiring Manager: Kevin Messick

This information is for internals only. Please do not share outside of the organization.

Your Role:

At MilliporeSigma, as the Operations Integration Scientist, at our Cherokee/ 3300 S. Second Ave location in St. Louis, you will lead the integration and implementation of new custom manufacturing products into the GMP manufacturing facilities. This technically sound position works cross-functionally at multiple manufacturing facilities with Project Management, Quality, Manufacturing, Process and Analytical Development, and the customer. You manage the technology transfer into GMP by authoring technical documents such as specifications and risk assessments, driving Change Control for new and existing custom manufacturing projects and planning for operational requirements. We're looking for a candidate with strong technical skills, demonstrated ability to work within a cross- functional team, and excellent interpersonal and team building skills.

• Manage change control deliverables and timelines, creation, and management of project timelines
• Present to customers and leadership and attending numerous project meetings
• Uncover potential roadblocks and problem solve to find solutions to ensure GMP timelines are met
• Manage product commercialization activities and review of impact of process scale changes
• Set up and tracking of GMP raw materials and equipment for purchase
• Review of GMP documents for manufacturing, packaging, and quality control
• Lead, develop, and implement process improvement initiatives via evaluation of current chemical raw materials, practices, and process history

Who you are:

Minimum Qualifications:

• Bachelor's Degree in a scientific discipline (e.g., Biology, Chemistry, Biotechnology, etc.)
• 1+ years working experience in GMP Operations or life science field

Preferred Qualifications:

• 3+ years working experience in GMP Operations or life science field
• Ability to effectively communicate with internal and external customers
• Ability to effectively manage numerous projects at different stages
• Experience with SAP and Trackwise systems
• Familiar with FDA, EMA, and other regulatory standards
• Familiar with biologic drug substance/product manufacturing
• High level of demonstrated initiative and strong follow through and accountability
• Able to think about a task or a problem in a new or different way, question conventional thought patterns

The Company is an Equal Employment Opportunity employer. No employee or applicant for employment will be discriminated against on the basis of race, color, religion, age, sex, sexual orientation, national origin, ancestry, disability, military or veteran status, genetic information, gender identity, transgender status, marital status, or any other classification protected by applicable federal, state, or local law. This policy of Equal Employment Opportunity applies to all policies and programs relating to recruitment and hiring, promotion, compensation, benefits, discipline, termination, and all other terms and conditions of employment. Any applicant or employee who believes they have been discriminated against by the Company or anyone acting on behalf of the Company must report any concerns to their Human Resources Business Partner, Legal, or Compliance immediately. The Company will not retaliate against any individual because they made a good faith report of discrimination.

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