Senior Consultant, Pharma/ Medical Device

1 month ago

Chicago, United States Kamet Consulting Group Full time

Role: Senior Consultant, Pharma/ Medical Device (Regulatory and M&A Consulting Solutions)

Locations: CA, TX, PA, IL, MA (other locations will be considered for the right candidate)


Company Description:


Kamet Consulting Group is a Healthcare Management Consulting firm providing Strategic Advisory, Implementation, Capability Building, and Outsourced Services to Pharmaceuticals, Medical Devices, Digital Health, and Consumer Health companies across their value chain.


Our expertise spans across organizational and functional areas of Deals, R&D, Clinical, Regulatory, Quality, Labeling, Safety, Supply Chain, and Commercial. We pride ourselves in bringing extensive experience and professionalism to every engagement and customize our support to our client’s individual needs and opportunities. We encourage entrepreneurial culture, spirit, which empowers individuals to think creatively, take initiatives, and drive innovative solutions.


At Kamet Consulting Group, we strive to create a strong and inclusive workforce by actively seeking a diverse pool of applicants. We firmly believe in providing equal opportunities to all qualified candidates, without any discrimination based on factors such as race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.


Role Description:


We are looking for a Senior Consultant ready to join our life sciences practice with a unique growth opportunity. This is a hybrid role and open for candidates based in California, Illinois, Massachusetts, or Pennsylvania. Candidates must have the ability to travel as necessary. Other locations will be considered for qualified candidates. The Senior Consultant will work with clients to deliver customized solutions, manage project timelines and budgets, conduct research and analysis, and develop recommendations for improving organizational performance. The Senior Consultant will also lead project teams and mentor junior consultants.


Please note this is a remote role in the US, however the candidate must be OK with 40-50% travel to client sites or internal firm trips.


Qualifications:

  • Experience in management consulting or related field
  • Expertise in at least one of the following domains: Deals, Regulatory, Quality, Labeling, or Supply Chain
  • Experience leading projects and managing project teams
  • Strong analytical and problem-solving skills
  • Excellent written and verbal communication skills
  • Ability to work independently and as part of a team
  • Bachelor's degree in Business, Life Sciences, or related field (Master's degree preferred)
  • Proficiency in MS Office and other analytical tools
  • Experience working in the Life Sciences, Medical Devices, Pharmaceutical or Consumer Health industry is required
  • Ability to travel domestically and internationally as needed
  • Facilitate engagement decisions, including work plan and timeline, project management, resource allocation, and career development of team members
  • Manage projects related to process transformation, operational improvements, and organizational redesign


Key Skills:

  • Experience with operational process improvement, M&A, or organizational transformation initiatives in pharmaceutical and/or medical device industry is preferred
  • Strong understanding of Regulatory Affairs, Supply Chain, and Labeling related data models and document structures is preferred
  • Understanding of data visualization best practices
  • Ability to work in an agile environment and critical thinking while working with customers to deliver the final solution
  • Adept at conducting research
  • Competencies with Powerpoint and advanced Excel
  • Self motivated


Required Qualifications: 

  • Minimum of five years of work experience related to the Regulatory Affairs, Regulatory Operations, Supply Chain, or Labeling Operations within the pharmaceutical and/or medical device industry
  • Prior consulting experience especially leading projects within M&A, Regulatory Affairs, Labeling, and Supply Chain is preferred
  • Applicants must be currently authorized to work in the United States without the need for sponsorship now or in the future
  • Ability to alteast travel 40% as necessary


Benefits: 

  • Competitive salary and benefits package (Medical, Rx, Dental, Vision, and 401(k) safe harbor, profit sharing)
  • Opportunity to work on groundbreaking projects with Top Organizations
  • Professional development and growth opportunities
  • Hybrid work options


How to Apply:

Interested candidates should submit their resume with this job posting. We thank all applicants for their interest; however, only those selected for an interview will be contacted.


Base Salary: $85k - $120k

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