JOBS

Available Positions:

QDS – QA Regulatory Manager & Sr. QA Regulatory Manager

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. Final job title and compensation plan as a key regulatory personnel member depend on the experience, applicable skillset(s) and how well the interviewee does during the course of the interviews with the team here at REJIMUS and on the written assessment. We seek to gauge your regulatory knowledge, writing ability, approach to evaluation of compliance, and more through real-life scenario applications that we face with our clients. In the QDS department you will be responsible for project ownership, clients’ support, as directed in areas of regulatory compliance: manufacturing operations, standard operating procedure writing/optimization, specification writing, auditing, training, product development support, regulatory due diligence, formulation reviews, regulatory operations compliance, quality documentation review/development, FSMA/HARPC Plan writing/reviews, cGMP Facility Audits as directed, 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 organize regulatory information, track and control documentation, proof-read and provide input on compliance works in accordance with daily operating practices and the regulations as cited under the applicable regulations relevant to the assigned projects.

MRS – Specialist, Sr. Specialist, Manager, Sr. Manager

Several full-time salaried positions are now open in our Regulatory Operations team, within the Marketing Review Services (MRS) department at REJIMUS, INC., a preeminent regulatory management consulting firm to the Food & Beverage, Dietary Supplement, Cosmetic and Homeopathic industries. Final job title and compensation plan as a key regulatory personnel member depend on the experience, applicable skillset(s) and how well the interviewee does during the course of the interviews with the team here at REJIMUS and on the written assessment. We seek to gauge your regulatory knowledge, writing ability, approach to evaluation of compliance, and more through real-life scenario applications that we face with our clients. In the MRS department, you will be responsible for providing regulatory review expertise and execution of tasks or projects in accordance with a multitude of regulations including but not limited to project/task ownership, marketing development support for clients, labeling and marketing reviews, claim substantiation, claims reviews/development, accreditation/certification support, labeling design/development support, scientific research, regulatory due diligence, formulation reviews, quality documentation review/development, and support for report drafting and reviews of reports and any other regulated marketing copy. You will organize regulatory information, track and control documentation, develop and management team/service specific documentation controls, proof-read and provide other strategic compliance input on works in accordance with daily operating practices of REJIMUS and the regulations as cited under the applicable regulations relevant to the task(s)/project(s) assigned.

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