- 経験
- 4–6 yrs
- 給料
- —
- 求人情報
- 1
- 投稿済み
- 4時間前
- Work mode
- 在任中
- 教育
- Pharmacy graduate
- Eligibility
- Candidates with a pharmacy degree and 4 to 6 years of relevant experience can apply.
- Resume
- Required to apply
Where you'll work
仕事内容
Role Overview
This position involves supporting quality and compliance activities at the Goa site, with a focus on document review and adherence to pharmaceutical standards.
Key Duties
- Ensure compliance with current Good Manufacturing Practices, Good Practices, and any other applicable regulatory expectations, including environmental, health, and safety requirements.
- Carry out assigned work and oversee related activities in line with the relevant standard operating procedures.
- Stay current with required training and help ensure team members are trained on applicable SOPs.
- Complete the mandatory learning assigned for the workgroup “QA - Document review -GOA” in L2LMS (SABA).
- Draft and update standard operating procedures as needed.
- Handle customer requirements and notifications.
- Manage market complaints, out-of-specification cases, CAPA, change controls, and deviations.
- Investigate and close market complaints, adverse drug events, out-of-specification incidents, failures, and deviations.
- Escalate quality concerns and improvement suggestions to managers.
Experience Required
Relevant experience of 4 to 6 years is required.
Education
Graduation in Pharmacy is required.
Additional Information
The source text does not provide details on perks, salary, notice period, number of openings, or a separate eligibility note.
Competencies
The source mentions competencies, but specific details are not provided.