JOB TITLE |
TRAINING AND REGULATORY OFFICER (PHARMACEUTICAL COMPANY) |
NATURE OF JOB |
FULL TIME |
INDUSTRY |
PHARMACEUTICAL MANUFACTURING & DISTRIBUTION |
SALARY |
KSHS. 100,000 NET |
JOB LOCATION |
MOMBASA ROAD |
DUTIES AND RESPONSIBILITIES
- Manage activities such as audits, regulatory agency inspections, or product recalls.
- Develop regulatory strategies and implementation plans for the preparation and submission of new products.
- Provide responses to regulatory agencies regarding product information or issues.
- Oversees all regulatory matters and executes the strategy to ensure the organization complies with applicable regulations.
- Develops processes and systems to ensure that all necessary licensing, filings, certifications, and permits are processed and monitored.
- Reviews existing training programs; suggests enhancements and modifications to improve engagement, learning, and retention and/or to meet the changing needs of clientele, the organization, or the industry.
- Ensures that training materials and programs are current, accurate, and effective.
- Responsible for new employee team training, covering sales skills
- Maintains knowledge of new methods and techniques for training, and training requirements applicable to the organization and/or industry.
- Identifies problems and opportunities such as operational changes or industry developments that training could improve.
- Conducts or facilitates required and recommended training sessions.
- Collaborates with vendors and third-party training providers to arrange employee registration for and participation in outside training programs.
- Ensures that training milestones and goals are met while adhering to approved training budget.
- Prepares and implements training budget.
- Performs other related duties as assigned
KEY REQUIREMENT SKILLS AND QUALIFICATION
- Degree in Pharmacy, Pharmaceutical Science, Biochemistry, or related Life Sciences field
- At least 3–5 years’ experience in a regulatory affairs or training role within a pharmaceutical company
- In-depth knowledge of PPB regulations, GMP/GDP guidelines, and pharmaceutical quality systems
- Proven experience preparing and submitting regulatory filings and handling audits/inspections
- Certification in Regulatory Affairs, Training & Development, or Quality Assurance will be an added advantage
HOW TO APPLY
- If you meet the above qualifications, skills and experience share CV on
This email address is being protected from spambots. You need JavaScript enabled to view it. - Interviews will be carried out on a rolling basis until the position is filled.
- Only the shortlisted candidates will be contacted.