- 경험
- 3–5 yrs
- 샐러리
- —
- 채용 공고
- 1
- 게시됨
- 3시간 전
Where you'll work
직무 설명
Role Overview
This position is for a Quality Assurance professional to support GMP compliance across manufacturing and warehouse operations in Pune/Pimpri-Chinchwad. The role focuses on documentation review, validation oversight, investigation support, and quality system upkeep in line with regulatory expectations and approved procedures.
Key Duties
- Carry out site visits to DS manufacturing and warehouse facilities to confirm that operations are aligned with GMP standards, regulatory needs, and approved procedures.
- Take part in manufacturing investigations and help close CAPA actions.
- Draft and review risk assessments along with mitigation plans.
- Monitor process validation and cleaning validation work to ensure execution matches approved protocols.
- Examine core master documents such as study protocols, BPRs, and MFRs.
- Check executed Batch Processing Records to support batch release decisions.
- Review Batch Dispatch Records and confirm warehouse dispatch activities.
- Coordinate the collection and compilation of APQR data and support preparation of the APQR.
- Prepare and review SOPs and other quality system documents.
- Review departmental SOPs to verify GMP compliance across functions.
Experience Required
The role calls for 3 to 5 years of relevant experience.
Education Required
Candidates should have a Master’s degree in Biotechnology, or a postgraduate qualification in Pharmacy or Pharmaceutical Technology.
Competencies
- Innovation and creative thinking
- Customer focus
- Talent development mindset
- Results-driven approach
기술
품질 보증
위험 평가
Regulatory Compliance
CAPA Management
Good Manufacturing Practice (GMP)
Validation Review
Batch Record Review
SOP Documentation
APQR Preparation
Pharmaceutical Quality Systems