Industry X MES Sr. Analyst (PharmaSuite)

Accenture; Calgary; On-site; CAD 80,000 - 110,000; Full time

Job summary

Accenture is seeking an Industry X MES Sr. Analyst to leverage digital capabilities in manufacturing. The role involves developing MES solutions and collaborating with multidisciplinary teams. Candidates should possess strong communication skills and experience in automated life sciences environments.

Qualifications

• Minimum of 1 year of experience with life sciences compatible MES solutions.
• Knowledge of FDA and GMP guidelines.
• Fluency in English is required.

Responsibilities

• Design/Develop/Configure Electronic Batch Records.
• Implement MES solutions and integrate with ERP.
• Gather user requirements for manufacturing activities.

Skills

Strong written and oral communication skills

Ability to work in a team-oriented environment

Education

Bachelor’s Degree or equivalent work experience

Job description

Industry X MES Sr. Analyst (PharmaSuite)

We are Industry X:

Looking to be part of a transformational digital engineering and manufacturing practice? How about an opportunity to help world-class clients solve their biggest challenges and create products and services that customers love - quickly, efficiently and sustainably?

Industry X combines Accenture’s powerful digital capabilities with deep engineering and manufacturing expertise.We use the power of data and digital to help our clients reimagine the products they make, and how they make them. By connecting engineering and manufacturing operations every step of the way - from how products are designed and engineered, sourced and supplied, manufactured, to how they are serviced and renewed, we help them achieve greater productivity, drive growth and meet their sustainability commitments.Find out more about Industry X.

You are:

An ambitious Manufacturing Execution Systems (MES) professional ready to take on new challenges. As industries head towards Manufacturing and Factory Digitalization, MES stands in the center of manufacturing excellence.

The Work:

• Design/Author/Develop/Configure Electronic Batch Records (EBR)
• Implement MES solutions and integrate with ERP and control equipment
• Documentation of MES configuration and validation of EBRs
• Provide organizational oversight for complex systems involving the development of MES
• Work closely with business management and users to strategically define the needs and design solutions that add value, gathering user requirements in relation to controlling and recording manufacturing activities

Here's What You Need:

• Minimum of 1 year of experience with PAS-X Syncade, PharmaSuite, XFP, POMS, Camstar, Simatic-IT or other life sciences compatible MES solutions in a highly automated Life Sciences manufacturing environment
• Knowledge of FDA and GMP guidelines
• Bachelor’s Degree or equivalent work experience
• English is required for this position as this role will be aligned to multi-national teams where English is the common language across our North America Market. Due to the significant high volume of interactions with these English-speaking multi-national teams, which is inherent to this position, it is not possible to reorganize the company's activities to avoid this requirement.
• Travel may be required for this role. The amount of travel will vary from 0 to 100% depending on business need and client requirements.

Set Yourself Apart:

• Strong written and oral communication skills
• Ability to work in a team-oriented, collaborative environment
• Understanding of Life Sciences validation processes

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