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Title
Text copied to clipboard!Pharmaceutical Compliance Specialist
Description
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We are looking for a Pharmaceutical Compliance Specialist to join our team to ensure the quality, safety, and regulatory compliance of pharmaceutical products. This role is critical in guaranteeing that all medications and pharmaceutical goods are manufactured, stored, and distributed in accordance with local and international standards. The Pharmaceutical Compliance Specialist works closely with manufacturing, quality control, and regulatory affairs teams to ensure adherence to all requirements.
Key responsibilities include overseeing pharmaceutical processes, reviewing documentation, assessing quality, and conducting internal audits. The candidate must have strong analytical skills, an understanding of the pharmaceutical regulatory environment, and the ability to work collaboratively. This position requires a high level of responsibility and accuracy, as errors can impact patient health and company reputation.
The ideal candidate holds a degree in pharmacy, chemistry, or a related field and has experience in the pharmaceutical industry. The ability to analyze data, interpret regulatory documents, and prepare reports is essential. We offer a dynamic work environment, opportunities for professional growth, and a competitive salary.
Responsibilities
Text copied to clipboard!- Monitor pharmaceutical manufacturing processes
- Conduct quality control inspections
- Ensure compliance with regulatory requirements
- Prepare and review documentation
- Coordinate internal and external audits
- Collaborate with quality and regulatory affairs teams
- Investigate quality deviations and propose corrective actions
- Maintain compliance with GMP (Good Manufacturing Practices)
- Collect and analyze quality data
- Develop and implement quality improvement plans
Requirements
Text copied to clipboard!- Degree in pharmacy, chemistry, or related field
- At least 2 years of experience in the pharmaceutical industry
- Knowledge of GMP and other regulatory standards
- Ability to analyze and interpret technical documentation
- Strong communication and collaboration skills
- Attention to detail and accuracy
- Ability to work independently and in a team
- Good computer skills (MS Office, quality management systems)
- Proficiency in Latvian and English
- Experience conducting audits is a plus
Potential interview questions
Text copied to clipboard!- What is your experience in pharmaceutical quality control?
- Do you have experience working with GMP standards?
- How do you handle quality deviations?
- Have you participated in internal or external audits?
- What software do you use for quality management?
- How do you ensure documentation accuracy?
- Do you have experience working with regulatory authorities?
- How do you stay updated on regulatory changes?
- How do you manage your workload to meet deadlines?
- Do you have experience with the CAPA process?
