job description
Join The GMP Group as a Quality Validation Officer in the pharmaceutical manufacturing sector and play a pivotal role in ensuring product quality and compliance with regulatory standards. This contract position offers a completion bonus, excellent work-life balance, and the opportunity to enhance your expertise in a high-impact role.
Based in beautiful Bali, you'll work in a dynamic environment while contributing to critical validation processes that uphold the highest industry standards. This role is ideal for professionals seeking to strengthen their resume with valuable experience in pharmaceutical quality assurance.
At The GMP Group, we value precision, integrity, and continuous improvement. If you're passionate about quality control and eager to make a difference in pharmaceutical manufacturing, we invite you to apply and grow with us.
Responsibility
- Conduct validation activities for pharmaceutical manufacturing equipment, processes, and systems in accordance with GMP guidelines.
- Develop, review, and execute validation protocols, including Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ).
- Perform risk assessments and implement corrective actions to ensure compliance with regulatory requirements.
- Collaborate with cross-functional teams to ensure validation activities align with project timelines and quality standards.
- Maintain accurate documentation of validation activities, including reports, deviations, and change controls.
- Participate in internal and external audits to ensure adherence to quality systems and regulatory expectations.
- Provide training and guidance to team members on validation procedures and best practices.
- Stay updated on industry trends, regulatory changes, and emerging technologies in pharmaceutical validation.
Qualifications
- Bachelor's degree in Pharmacy, Chemistry, Biotechnology, or a related field.
- Minimum of 2 years of experience in pharmaceutical validation, quality assurance, or a related role.
- Strong knowledge of GMP, GLP, and other regulatory guidelines (e.g., FDA, EMA, PIC/S).
- Experience with validation protocols, risk assessments, and compliance documentation.
- Excellent analytical and problem-solving skills with keen attention to detail.
- Proficient in Microsoft Office and validation software tools.
- Strong communication and interpersonal skills for effective collaboration.
- Ability to work independently and manage multiple priorities in a fast-paced environment.