JOBS

Available Positions:

Sales – Business Development Representative/Manager (Several Openings)

As a Business Development Representative/Manager with REJIMUS, a preeminent regulatory management consulting firm to companies the Food/Beverage, Dietary Supplement, Cosmetic and OTC/Homeopathic industries, you will be responsible for growth of company, territories and driving new business development activities associated with your assigned accounts/territory, including reporting and the provision of support to the executive management team, other team members and/or prospective clients for the designated service offerings provided by REJIMUS in order to achieve or exceed the monthly, quarterly and/or annual sales goals. You will study up, learn from mistakes and seek to continually learn and understand the industries to which we support, and most importantly your clients’ businesses so as to leverage all available service offerings provided by REJIMUS for your clients. You will keep current and organize and manage client information and project opportunities at all times, and related information using the designated sales systems, sales guidances/support and education to ensure accuracy of project information and opportunities, manage personal time maximize sales performance, including the delivery of deliverables, reports, quotations or other assigned tasks and overall sale effectiveness. You will function as the point person for new business inquiries to drive growth for the company in a timely manner for prospecting, qualifying new opportunities and establishing business accounts as required, in order to transact business with REJIMUS as well as ensure confidentiality at every stage.

QDS – Regulatory Manager/Regulatory Specialist

Several full-time salaried positions are now open in our Regulatory Operations team, within the Quality Development Services (QDS) department at REJIMUS, INC., a preeminent regulatory management consulting firm to the Food & Beverage, Dietary Supplement, Cosmetic and Homeopathic industries. Job title and performance-oriented compensation plan for key regulatory personnel member depend on the experience levels, education, and applicable skillset(s) as well as how well the interviewee does with the REJIMUS team and on the written regulatory exam. We seek to gauge your regulatory knowledge, writing ability, approach to evaluation of quality and compliance challenges through real-life scenarios that we face with our clients on a daily basis. In the QDS department you will be responsible for task and project ownership, client support in areas of regulatory compliance, including by not limited to manufacturing operations, standard operating procedure writing/optimization, specification writing, auditing, training, product development support, regulatory due diligence, formulation reviews, operational compliance, quality documentation review/development, FSMA/HARPC Plan writing/reviews, etc. Additional responsibilities will include cGMP Facility Audits, GMP training, safety data sheets, registrations in US markets, support for report drafting and reviews of reports and marketing copy, and aid the design and development of controlled documentation, as well as providing other support to colleagues as your skills permits and as required. You will work with integrity, ethics and honesty to organize project and regulatory information, track and control documentation, tasks, proof-read and provide input on compliance work in accordance with the practices and standards set forth by REJIMUS, including managing of daily work schedule, team communications, and accountability to all work, work products submitted, billable records, computer activity and productivity metrics.

If you are interested in applying for any of our positions, please email your resume to info@rejimus.com.