Synokem Pharmaceuticals is Established in 1983 with the core mission of protecting consumers’ health and wellbeing, Synokem Pharmaceuticals is making rapid growth with proven expertise in the field of manufacturing and marketing premium quality pharmaceutical products.
Urgent Hiring Synokem Pharmaceuticals Ltd
Department : Quality Assurance (IPQA)
- Position : Senior Executive / Assistant Manager (1 Nos)
- Experience : 06 – 09 Years.
- Qualification : B.Pharma / M.Pharma.
Exposure of area:
- Deep Process Knowledge: Develop a comprehensive understanding of the production and quality processes, including raw material inspection, in-process checks, and final product quality checks.
- Deviation Management: Gain experience in identifying, analyzing, and resolving process deviations. Work on documentation and root cause analysis.
- Control Strategy: Assist in the implementation of control strategies that ensure product quality at each stage of the manufacturing process.
- SOP Development: Exposure to writing, reviewing, and updating Standard Operating Procedures (SOPs) in line with regulatory and organizational changes.
- Documentation & Data Integrity: Ensure accurate and timely documentation of in-process checks, CAPA (Corrective and Preventive Actions), and batch records to maintain data integrity and compliance.
- Innovation in IPQA: Explore and implement new technologies or automation tools that can enhance the quality assurance process, ensuring efficiency and reliability.
How to Apply:
- Job Location : Sidcul Haridwar Uttarakhand.
- Drop your resume at hr3.p3@synokempharma.com or What’s app at +91 9760146288 with subject line “Resume for Quality Assurance Department”.
Urgent Hiring Synokem Pharmaceuticals Ltd
- Department: Quality Assurance (Process Validation & Cleaning Validation)
- Position : Senior Executive / Assistant Manager (1 Nos)
- Experience : 07 – 10 Years.
- Qualification : B.Pharma / M.Pharma.
Exposure of area:
- Comprehensive Process Understanding: Gain a deep understanding of the entire manufacturing process, including critical process parameters (CPP) and critical quality attributes (CQA).
- Validation Master Plan (VMP): Get involved in developing and updating the Validation Master Plan, ensuring that all process validation activities are aligned with regulatory guidelines and company standards.
- Protocol & Report Preparation: Lead the drafting, reviewing, and approval of process validation protocols and reports, ensuring they meet both regulatory requirements and internal quality standards.
- Execution of Validation Batches: Supervise the execution of validation batches for new or modified processes, ensuring adherence to protocols and proper documentation of results.
- GMP and Regulatory Guidelines: Strengthen knowledge of Good Manufacturing Practices (GMP), ICH, FDA, EMA, and WHO guidelines as they pertain to both process validation and cleaning validation.
- Root Cause Analysis: Lead or assist in conducting root cause analysis for validation failures or deviations, and ensure implementation of corrective actions to maintain process control.
How to Apply:
- Job Location : Sidcul Haridwar Uttarakhand.
- Drop your resume at hr3.p3@synokempharma.com or What’s app at +91 9760146288 with subject line “Resume for Quality Assurance Department”.
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