MES Consultants
AMARIS GROUP SA
Boston, MA
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JOB DETAILS
LOCATION
Boston, MA
POSTED
6 days ago
Who are we?
Amaris Consulting is an independent technology consulting firm providing guidance and solutions to businesses. With more than 1000 clients across the globe, we have been implementing solutions in major projects for over a decade. This success is supported by an international team of 7,600 people spread across 5 continents and more than 60 countries. Our solutions focus on four Business Lines: Information System & Digital, Telecom, Life Sciences, and Engineering. We are committed to building and nurturing a top talent community where all team members can reach their full potential. Amaris is your stepping stone to navigating change, meeting challenges, and successfully completing projects.At Amaris, we aim to provide candidates with the best recruitment experience. We seek to understand our candidates, challenge them, and provide prompt, constructive feedback. Our typical recruitment process includes:
Brief Call: An initial virtual or phone conversation to learn about you, understand your motivations, and find the right role.
Interviews: Usually around three, involving meetings with your future team members and managers to discuss your experience, skills, the role, and our company culture.
Case Study: Depending on the role, you may be asked to complete a test or practical exercise.
We recognize that each person and role is unique, and our process is adaptable to ensure a positive candidate experience. We look forward to meeting you!
Job Description
We are seeking a talented and motivated MES PAS|X Consultant to join our team in Boston, USA, working on a hybrid model. You will be instrumental in designing, configuring, and optimizing manufacturing processes within the PAS|X MES system to support high-quality pharmaceutical production.
Key Responsibilities:
- Facilitate workshops to gather and define user requirements.
- Design manufacturing processes within the PAS|X MES system.
- Translate business needs and operational processes into system functionalities and configurations.
- Identify process gaps and system limitations, propose, and implement effective solutions.
- Oversee system configuration activities and manage master data setup.
- Develop comprehensive test cases based on system functional specifications.
- Provide system training and support to end users.
Requirements:
- Minimum of 4 years of relevant experience.
- University degree (Bachelor's or higher) in a related field.
- At least 1 year of experience with document management, electronic systems (E-systems), and quality/compliance requirements.
- At least 3 years of experience in the pharmaceutical or related industries, with a strong understanding of GMP, Health and Safety, and Quality standards.
- Proven experience leading or supporting projects in a project-based environment.
- Hands-on experience with execution systems (MES, PCS, Data Historian, PAS|X) is highly valuable.
- Ability to train users effectively on system functionalities.
- Strong technical knowledge of GAMP, ISA 95, ISA 88, and CFR Part 11 regulations is preferred.
- Ability to translate complex technical concepts into clear business language.
- Ability to work independently in a dynamic, project-driven matrix organization.
About the Company
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