Regulatory Affairs Pharmacist
Dasmariñas, Cavite
Posted 15 days ago
- Company:
- Sydenham Laboratories Inc
- Company Description:
- Sydenham Laboratories, Inc. (SLI) is an ISO 9001:2008, HACCP Certified, PIC/s GMP compliant pharmaceutical company that develops and manufactures healthcare products. SLI manufactures oral drug preparations in dosage forms of tablet, capsule, syrup, and powder for suspension. Non-penicillin, penicillin and cephalexin-based products are manufactured in separate buildings with 'clean room hepa-filtered' exclusive air-handling systems to ensure zero-cross contamination. SLI also manufactures food supplements in the above dosage forms. SLI is founded in 1971 by Dr. Eduardo R. dela Cruz, MD, a cardiologist and a former president of Philippine Medical Association. SLI derived its name from one of the great British physicians, Dr. Thomas Sydenham, known as the English Hippocrates, the founder of clinical medicine, and an advocate of effective management of illness that emphasized detailed observation and maintained patient records.
- Contract Type:
- Full Time
- Experience Required:
- 3 to 4 years
- Education Level:
- Bachelor’s Degree
- Number of vacancies:
- 2
Job Description
Staying up-to-date with changing regulatory requirements and guidelines in the pharmaceutical and medical device industries
Preparing and submitting regulatory documentation such as marketing authorisation applications, clinical trial applications, and post-approval variations
Liaising with regulatory authorities to address queries and secure approvals for our products
Providing regulatory guidance and support to the research and development, manufacturing, and quality assurance teams
Maintaining comprehensive records and databases to track the regulatory status of our product portfolio
Identifying and mitigating potential regulatory risks to the business
Contributing to the development and implementation of regulatory strategies aligned with the company's commercial objectives
What we're looking for
Pharmacy degree and valid registration as a pharmacist
Minimum 5 years' experience in a regulatory affairs role within the pharmaceutical or medical device industry
In-depth knowledge of regulatory requirements and guidelines in the Philippines and other key markets
Excellent written and verbal communication skills, with the ability to liaise effectively with both internal and external stakeholders
Strong attention to detail and problem-solving skills
Ability to work independently and as part of a cross-functional team
Proficiency in using regulatory information management systems and databases