Regulatory Consultant – Jamaica | Ryvis Pharma

Regulatory Consultant – Jamaica | Ryvis Pharma

• Company website link – https://ryvispharma.com

• Company name – Ryvis Pharma

• Location – Kingston, Jamaica

• Postal Code –

• Region – Jamaica

• Company Office local Address –

• Contact info –

• email address –

• Country – Jamaica

• Job Type – Full Time

• Job Average Salary rate – JMD 2,500,000–3,500,000 yearly

• Currency – Jamaican Dollar

Job description

🌍 Regulatory Consultant – Jamaica | Ryvis Pharma

Location: Jamaica

Industry: Pharmaceuticals | Regulatory Affairs

About Us

Ryvis Pharma, a Canadian multinational, is a fast-growing, export-focused pharmaceutical company. With 25 years of global operations, we are recognized as a Star Export House by the Government of India and trusted worldwide for high-quality formulations.

The Opportunity

We’re looking for an experienced Regulatory Consultant based in Jamaica to lead product registrations and compliance with the Ministry of Health and Wellness (MOH). If you have deep expertise in regulatory affairs and strong local knowledge, this role offers the chance to make an impact in a growing international organization.

What You’ll Do

✅ Review, submit and follow up on product registration dossiers with the Pharmaceutical and Regulatory Affairs Branch (PRAB), MOH in Jamaica.

✅ Manage post-submission queries and ensure timely approvals.

✅ Coordinate with Ryvis Pharma’s global regulatory team for dossiers, technical documents, and samples.

✅ Apply for Import Permits for registration samples and manage regulatory logistics.

✅ Review product label artworks and oversee legal licenses.

Excerpt from the official job listing
See full job description from the company website.

Job Summary

You will oversee regulatory submissions, maintain product dossiers, liaise with health authorities, and ensure compliance for pharmaceutical products across Jamaica and regional markets.

About Us

We are Ryvis Pharma, a Canadian-owned pharmaceutical company that develops, manufactures, and distributes high-quality OTC, prescription, and veterinary products globally. We operate under rigorous standards and commit to accessible, effective healthcare. Visit our site above to explore our mission, values, and operations.

Culture and Work Environment

We champion integrity, respect, and accountability. Our teams work cross-functionally with clarity and mutual support. Continuous learning, open feedback, and collaborative problem-solving guide daily interactions and growth.

Why Work With Us

You’ll join a company that values scientific rigor and ethical impact. Your regulatory contributions will directly influence public health. Work side by side with seasoned professionals, gain domain expertise, and enjoy meaningful responsibility in a global pharmaceutical setting.

Key Responsibilities

• Prepare and submit regulatory dossiers to Jamaican and regional authorities

• Maintain and update product registration files

• Monitor regulatory changes and align internal processes

• Coordinate with manufacturing, quality, and legal teams

• Respond to queries from regulators and ensure timely compliance

Key Qualifications

• Degree in pharmacy, regulatory affairs, life sciences, or related field

• Experience with regulatory submissions in Jamaica or CARICOM

• Strong written and verbal communication skills

• Meticulous attention to detail and project management ability

• Ability to interpret guidelines and enforce compliance

Benefits & Perks

• Health insurance and wellness benefits

• Professional development and training

• Performance bonuses

• Contribution to pension or retirement plan

• Flexible working options where feasible

Location Insights

Kingston, Jamaica operates as a vibrant pharmaceutical market hub, with regulatory bodies, manufacturing, and distribution networks concentrated in the capital. Familiarity with local systems and logistics offers clear advantages.

Common Interview Questions and Tips

1. How have you handled regulatory rejections in past roles? — Highlight resolution strategies.

2. Describe when you managed multiple concurrent submissions. — Show prioritization skills.

3. How do you stay current with regulatory guidelines? — Mention trusted sources or networks.

4. Give an example of cross-team regulatory coordination. — Emphasize communication.

5. How would you respond to a compliance audit issue? — Show corrective action mindset.

Tip: Use specific examples with metrics. Demonstrate your understanding of regulatory environments and your ability to deliver under deadlines.

Market-Based Salary Overview and Analysis

In Jamaica’s pharmaceutical industry, regulatory roles generally range from JMD 2.2M to 4.0M annually depending on experience and responsibility. Senior roles may add incentives or international allowances, making top compensation competitive regionally.

Disclaimer

We aggregate publicly available job listings and link to the original source. We are not the hiring company and do not manage the recruitment process. Please apply only through the official careers website above.
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