Job Overview:
A Quality Assurance Specialist is responsible for ensuring product quality and safety in the pharmaceutical industry.
Key Responsibilities:
* Execute day-to-day activities while adhering to CGMP/GDP regulations.
* Escalate any potential violations or concerns affecting product quality or safety.
* Maintain a safe and compliant culture through collaborative efforts.
* Drive a high-performing culture, promoting personal growth and development.
* Responsible for resolving quality-related queries with QC Leads.
* Implement adequate processes for all quality activities.
* Support manufacturing and release activities in compliance with procedures.
Requirements:
* 1-3 years of experience in pharmaceuticals or a similar field.
* Previous analytical experience is required.
* Ability to work independently and lead improvement initiatives with moderate guidance.
* Excellent communication and interpersonal skills to work effectively across teams.
Work Schedule:
Monday-Friday, 40 hours/week.
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Benefits:
* Competitive compensation package
* Ongoing training and professional development opportunities
* Collaborative and dynamic work environment
Additional Information:
Applicants must have excellent problem-solving skills, attention to detail, and strong analytical skills. A strong understanding of pharmaceutical regulations and guidelines is also essential.