44 Quality Control Specialists jobs in Baddi
Quality Control
Posted 1 day ago
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Role & responsibilities :-
Proficiency in using laboratory instruments like HPLC, UV-Vis spectroscopy, KF apparatus and other analytical tools for testing of finished products and stability samples.
Analytical Testing: Proficiency in using laboratory instruments like HPLC (High-Performance Liquid Chromatography), GC (Gas Chromatography), UV-Vis spectroscopy, and other analytical tools for testing Stability sample and finished products.
Troubleshooting Analytical Instruments: Skill in identifying and addressing technical issues with laboratory equipment.
Must have knowledge of ALCOA+ principals.
Good Laboratory Practices (GLP): Familiarity with GLP guidelines for maintaining the quality and integrity of lab tests and results.
Communication Skills: Ability to communicate effectively with cross-functional teams, including R&D, production, and regulatory affairs.
Familiarity with GLP guidelines for maintaining the quality and integrity of lab tests and results.
Familiarity with global regulatory guidelines for pharmaceutical testing and quality control.
Preferred candidate profile
Perks and benefits
Quality Control
Posted today
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**Location: Nayagarh, Himachal Pradesh (On-site)**
**Company: Elfin Drugs Private Limited**
Elfin Drugs Private Limited, a GMP-certified pharmaceutical company, is looking for a **Head of Quality Control** with a minimum of **1 to 5 years of experience** in the pharmaceutical industry.
if u are interested - contact person - HR Shubham - Call and Whats app
**Job Types**: Full-time, Permanent
Pay: ₹14,000.00 - ₹30,000.00 per month
**Benefits**:
- Food provided
- Health insurance
- Paid sick time
Schedule:
- Day shift
- Rotational shift
Supplemental Pay:
- Performance bonus
- Yearly bonus
Work Location: In person
Executive Quality Control
Posted 4 days ago
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Job Description
2. Having adequate knowledge of Laboratory Instruments and equipment's Calibration, Maintenance/External calibration.
3. Having adequate knowledge of Preparation of laboratory chemicals, Reagents, test solution, and Volumetric solution.
4. Having adequate knowledge of Reference, Chemical and Working standard management i.e., Working Standard qualification and support in working standard management.
5. Having adequate knowledge of Data entry in SAP.
6. Having adequate knowledge of operation and trouble shoot of HPLC/GC/AAS/UV/IR/Dissolution and other QC analytical instruments and its software.
7. Having adequate knowledge of data entry management in inventory/Information management software of QC like LIMS software.
8. Having adequate knowledge of preparation of the QC documents like SOPs, Protocols and general documentation.
9. Having adequate knowledge of Pharma Industry Guidelines and Pharmacopoeias.
10. Having exposure of regulatory audit and GDP/DI compliance.
11. Having adequate knowledge of GLP / GMP requirements.
An Equal Opportunity Employer
Abbot welcomes and encourages diversity in our workforce.
We provide reasonable accommodation to qualified individuals with disabilities.
To request accommodation, please call or email
Quality Control Officer
Posted 1 day ago
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Hi we are hiring
Position;- QC Officer & Executives
QC Officer & Executives
Location- Baddi
Experience- 2-6 years (HPLC analyst )
Salary Range K
Interested candidate Apply
Mail ;-
Contact No;
Executive Quality Control
Posted 1 day ago
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Job Description
Job Description
The Job Responsibilities of the position holder are :
Responsible for performing the analytical activities as per Analytical competency matrix (Format No.BDI-QCSG004F23) and On job training and Practical Demonstration for Chemical and Instrumentation (Format No.BDI-QCSG004F19).
Analysis of In process, SFG, Finished Goods, Raw material & stability sample, Analytical method validation/Verification, of OSD and LVP as per defined Protocol or procedure and related documentation as per GLP and GMP in time.
Responsible for receiving sample and their documentation.
Responsible Data entry in SAP.
Responsible for sending the sample to outside laboratory and ensure their analysis as per requirement from Outside Commercial Lab as and when required.
Calibration of instruments, as and when required.
Preparation of volumetric solution, reagent, and test solution, as and when required.
Ensuring the timely updation in the documents as per the Pharmacopeial amendments.
Responsible for maintaining the resource in the quality control department.
To ensure the compliance of the requirement of cGDP/cGDP and Data integrity while performing all activities in the laboratory.
Ensuring the Compliance to EPD Global Guidelines.
Facing internal and external audits and ensuring compliance.
Implementation of GLP / GMP requirements.
Coordinating and aligning the practices and procedures in line with the COBC requirements.
SOP training in Isotrain of self-train within stipulated time.
Any other task assigned by reporting manager.
In absence of the position holder, the sub-ordinate Executive / Manager working in the section, or the authorized designee (as applicable) shall be responsible for day to day working.
Executive Quality Control
Posted today
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Job Description
- Analysis of Stability Samples/ Finished Products as per respective STP/Specification in Quality Control of Hormone block.
- Calibration of routine usage instruments such as Balance, pH meter and Conductivity meter, as and when required.
- Timely analysis of stability sample (Hormone block) and report if any abnormality observed.
- Timely Charging & withdrawal of samples from Stability Chambers & their documentation within the time frame.
- Sample reconciliation and destruction record of stability sample.
- Implementation of GLP / GMP requirements.
- Coordinating and aligning the practices and procedures in line with the COBC requirements
- Stability sample charging, Withdrawal, Reconciliation and data entry in software such as LIMS.
- Completion of assigned trainings of GLP/GMP on time
- Reporting of stability/Finished product sample as per report received from outside Laboratory and check the compliance against respective specifications.
- Evaluates the analysis results as per SOP and report to the supervisor for any abnormality.
Executive Quality Control
Posted today
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Job Description
1. Analysis of Stability Samples/ Finished Products as per respective STP/Specification in Quality Control of Hormone block.
2. Calibration of routine usage instruments such as Balance, pH meter and Conductivity meter, as and when required.
3. Timely analysis of stability sample (Hormone block) and report if any abnormality observed.
4. Timely Charging & withdrawal of samples from Stability Chambers & their documentation within the time frame.
5. Sample reconciliation and destruction record of stability sample.
6. Implementation of GLP / GMP requirements.
7. Coordinating and aligning the practices and procedures in line with the COBC requirements
8. Stability sample charging, Withdrawal, Reconciliation and data entry in software such as LIMS.
9. Completion of assigned trainings of GLP/GMP on time
10. Reporting of stability/Finished product sample as per report received from outside Laboratory and check the compliance against respective specifications.
11. Evalutates the analysis results as per SOP and report to the supervisor for any abnormality.
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Executive Quality Control
Posted today
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1. Sampling of raw material (Exposure to sampling in Isolator) as per defined procedure of Quality Control Lab of Hormone block.
2. To ensure the proper cleaning of sampling booth, sampling utensil and compilation of its records.
3. Analysis of Vendor Approval Samples.
4. Raw material samples sent to outside laboratories with proper documentation and its receiving compliance.
5. Analysis of Raw material, Finished Goods, & stability samples as per defined STP.
6. Preparation of volumetric solution & standardization, preparation of reagent and indicator as and when required.
7. Labeling on approved RM, Rejected RM and related to documentation.
8. Data entry in SAP system.
9. Coordinating and aligning the practices and procedures in line with the COBC requirements
Executive Quality Control
Posted today
Job Viewed
Job Description
The Job Responsibilities of the position holder are:
1. Responsible for performing the analytical activities as per Analytical competency matrix (Format No.BDI-QCSG004F23) and On job training and Practical Demonstration for Chemical and Instrumentation (Format No.BDI-QCSG004F19).
2. Analysis of In process, SFG, Finished Goods, Raw material & stability sample, Analytical method validation/Verification, of OSD and LVP as per defined Protocol or procedure and related documentation as per GLP and GMP in time.
3. Responsible for receiving sample and their documentation.
4. Responsible Data entry in SAP.
5. Responsible for sending the sample to outside laboratory and ensure their analysis as per requirement from Outside Commercial Lab as and when required.
6. Calibration of instruments, as and when required.
7. Preparation of volumetric solution, reagent, and test solution, as and when required.
8. Ensuring the timely updation in the documents as per the Pharmacopeial amendments.
9. Responsible for maintaining the resource in the quality control department.
10. To ensure the compliance of the requirement of cGDP/cGDP and Data integrity while performing all activities in the laboratory.
11. Ensuring the Compliance to EPD Global Guidelines.
12. Facing internal and external audits and ensuring compliance.
13. Implementation of GLP / GMP requirements.
14. Coordinating and aligning the practices and procedures in line with the COBC requirements.
15. SOP training in Isotrain of self-train within stipulated time.
16. Any other task assigned by reporting manager.
In absence of the position holder, the sub-ordinate Executive / Manager working in the section, or the authorized designee (as applicable) shall be responsible for day to day working.
Quality Control Assistant Manager
Posted 1 day ago
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Job Description
Roles and Responsibilities
- Conduct quality control activities such as raw material inspection, finished product testing, and sample analysis using HPLC and other relevant methods.
- Ensure compliance with USFDA regulations by performing chemical testing and material verification.
- Develop and implement quality control procedures to maintain high-quality standards in the manufacturing process.
- Collaborate with cross-functional teams to resolve quality issues and improve overall process efficiency.
- Maintain accurate records of all quality-related activities, including test results, inspection reports, and documentation.
Desired Candidate Profile
- 9-14 years of experience in Quality Control or related field (Pharmaceutical industry).
- B.Sc degree in Any Specialization; MS/M.Sc(Science) preferred but not mandatory.
- Strong knowledge of Chemical Analysis, Chemical Testing, HPLC, Material Testing, Materialize CSS, Raw Material Inspection, Sample Inspection, Quality Inspection & Quality Control principles.