Senior Associate EDMS (Secondment - 12 Months)
On-siteGroton, Connecticut, United States
Job Summary
Manage moderately complex projects, resolve ambiguous problems, and oversee supplier relationships to ensure timely delivery and optimal quality of medicines. Act as the primary liaison between the company and contractors, coordinate external vendor activities, and support the execution of outsourced analytical development and GMP testing. Drive team objectives, foster consensus among stakeholders, and contribute to continuous improvement across EDMS workflows and vendor engagement models. This 12-month secondment requires permanent U.S. work authorization and involves flexible on-site attendance. The role supports Pfizer's global mission to improve patient health through precise medication delivery and innovative supply chain solutions.
Required Qualifications
- Bachelor's degree
- 3+ years of experience
- Experience in supply chain systems and projects requiring a collaborative approach
- Strong analytical skills to understand complex business issues and processes
- Extensive knowledge of data management systems
- Outstanding verbal and written communication skills in English
- Demonstrated ability to work in teams
- Excellent interpersonal skills
- Recent knowledge of ARD workflows, project interfaces, documentation expectations, and analytical deliverables
- Working knowledge of analytical techniques used for pharmaceutical development, such as chromatography, dissolution, Karl Fischer, particle size, spectroscopy, or related methods
- Strong communication, collaboration, organization, and stakeholder management skills
- Understanding of GMP laboratory expectations
- Ability to work effectively across internal functions and with external partners in a fast-paced dynamic project environment
- Must be authorized to be employed in the U.S. by any employer
- Permanent work authorization in the United States
Desired Qualifications
- Master's degree with more than 1+ year of experience
- An associate's degree with 6+ years of experience
- A high school diploma (or equivalent) and 8+ years of relevant experience
- Extensive experience in a planning environment within a production plant
- In-depth understanding of aseptic manufacturing processes
- Background in planning and production in a pharmaceutical setting
- Proficiency in managing supply chain agreements with markets
- Adept at coordinating all necessary activities for product launches
- Demonstrated problem-solving skills in a dynamic work environment
- Strong organizational abilities
- Experience using common AI tools, including generative technologies such as ChatGPT or Microsoft Copilot, to support problem solving and enhance productivity
- Demonstrated curiosity for exploring how these tools can improve outcomes and understanding of responsible AI practices, including risk management and ethical use
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