Website Quality Control / Pharmaceutical
Job Description
A pharmaceutical organization is looking for experienced professionals for multiple positions in the Quality Control (QC) department at Roorkee, Uttarakhand.
The available positions are for candidates with 2–5 years of relevant experience in areas such as Finished Goods, Stability and Raw Material Quality Control.
The ideal candidate should have a good understanding of pharmaceutical quality control processes, laboratory testing, documentation and regulatory requirements. Candidates with USFDA regulatory exposure will be preferred.
Key Responsibilities
Quality Control – Finished Goods
Perform quality control activities related to finished pharmaceutical products.
Conduct testing and analysis as per approved specifications and procedures.
Review laboratory results and ensure accurate documentation.
Support investigation of out-of-specification or atypical results, as applicable.
Ensure laboratory activities are performed in accordance with established quality procedures.
Quality Control – Stability
Support stability testing activities for pharmaceutical products.
Perform testing according to approved stability protocols and schedules.
Maintain accurate records of stability samples, test results and observations.
Ensure stability-related documentation is complete and maintained properly.
Coordinate with relevant departments regarding stability testing requirements.
Quality Control – Raw Materials
Perform quality testing and analysis of incoming raw materials as per approved specifications.
Review analytical results and maintain appropriate laboratory records.
Support sampling, testing and release-related activities for raw materials.
Ensure testing is performed according to approved Standard Operating Procedures (SOPs).
Documentation & Compliance
Maintain accurate and complete QC laboratory documentation.
Follow applicable SOPs, specifications, test methods and quality procedures.
Ensure laboratory records are properly maintained and traceable.
Support internal and external audits when required.
Follow applicable Good Laboratory Practices (GLP) and pharmaceutical quality standards.
Desired Candidate Profile
Experience: 2–5 years in Pharmaceutical Quality Control.
Qualification: B.Pharm / B.Sc / M.Sc.
Relevant experience in Finished Goods, Stability or Raw Material QC will be preferred.
Good understanding of pharmaceutical laboratory testing and documentation.
Knowledge of SOPs, specifications and quality control procedures.
Candidates with USFDA regulatory exposure will be preferred.
Good analytical, documentation and communication skills.
Ability to work effectively within a quality-focused pharmaceutical environment.
Key Skills
Quality Control, Pharmaceutical QC, Finished Goods Testing, Stability Testing, Raw Material Testing, Laboratory Analysis, Quality Documentation, SOP, GLP, Pharmaceutical Quality, USFDA, Laboratory Testing, Compliance, Quality Assurance.
Number of Openings
Multiple Positions
How to Apply
Interested and eligible candidates can share their updated resume at:
Email: niketa.chauhan1@jubl.com
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To apply for this job email your details to niketa.chauhan1@jubl.com