1 Opening(s)
8.0 Year(s) To 10.0 Year(s)
10.00 LPA TO 15.00 LPA
Position: QC Manager (Biosimilars)
Location: Bhopal
Experience: 8 - 10 Year
Industries: Pharma
Responsibilities:
Manage QC activities raw materials, in-process, and finished biosimilar products.
Oversee analytical and microbiological testing (e.g., HPLC, ELISA, SDS-PAGE, Western Blot).
Ensure compliance with cGMP, GLP, ...
1 Opening(s)
4.0 Year(s) To 5.0 Year(s)
Not Disclosed by Recruiter
Job Description:
We are seeking a skilled and experienced microbiology professional to lead microbial testing and environmental monitoring activities in an API manufacturing setup. The Assistant Manager will ensure compliance with regulatory standards, supervise microbiological operations, and support quality systems in the microbiology lab.
Key Responsibilities:
Oversee routine microbiological testing of raw materials, ...
3 Opening(s)
0 To 1.0 Year(s)
Not Disclosed by Recruiter
1. Adhere to cGMP and GDP practices and perform activities as per SOP.
2. Verify documents and ensure all activities, activities are performed as per SOP.
3. Final Quality Check & Approval of the finished products (Components, assemblies/2D/3D bags/liners).
4. Execute shift production as per planning and verify Integrity report and sealing parameters
5. ...
15 Opening(s)
5.0 Year(s) To 10.0 Year(s)
5.00 LPA TO 7.00 LPA
Job Descripation
1. Responsible for Checking & distribution of approved artwork.2. Responsible for colour approval of the shade card.3. Responsible for the Allocation & Verification of the Pharma code.4. Responsible for the Allocation & Verification of GTIN numbers as per GS1 guidelines.5. Artwork management as per the product brief.6. To verify ...
1 Opening(s)
2.0 Year(s) To 6.0 Year(s)
Not Disclosed by Recruiter
6.1 Over all responsibility of Quality Assurance Department.
6.2 Vendors approval for RM & PM.
6.3 Periodical Quality Audit.
6.4 Activities related to Drug Control Authorities.
6.5 Evaluation of Product Complaints & Product Recall.
6.6 Validation and Qualification.
6.7 GMP Training to Staff.
6.8 GMP Implementation in the factory.
6.9 Co-ordination with various departments to implement cGMP in ...
1 Opening(s)
15.0 Year(s) To 20.0 Year(s)
15.00 LPA TO 20.00 LPA
Job Title: Plant Head - Pharma Pellet Manufacturing Facility
Location: SB Organics, Chandapur Village, Hathnoora Mandal, Sangareddy District, Telangana
Company Overview:SB Organics is a WHO-GMP accredited pharmaceutical pellet manufacturing facility dedicated to producinghigh-quality medicines. We are committed to adhering to the highest standards in manufacturing, ensuring the safety,efficacy, and compliance of our ...
1 Opening(s)
2.0 Year(s) To 6.0 Year(s)
3.00 LPA TO 4.00 LPA
Technical skills &
Competencies / Language
Technical competence.
Leadership skills.
Analytical ability.
Planning ability.
Communication skills.
Problem solving.
Team building.
KEY ACCOUNTABILITIES
Analysis and approval
Sampling, analysis and ascertaining quality of raw materials, packaging material, intermediates, In-process samples and API for Chemistry Ankleshwar.
Testing of the method validation samples and process validation samples and cleaning validation.
Perform analysis and documentation of API finished ...
1 Opening(s)
2.0 Year(s) To 5.0 Year(s)
2.00 LPA TO 6.00 LPA
Troubleshoot and repair equipment
Install and maintain heavy machinery, plant equipment, and tools
Use industrial technology to diagnose equipment failures
Create maintenance procedures
Optimize equipment, procedures, and budgets
Make production department smooth Handle manpower
Provide training to new employees
Work under the guidance of departmental manager
Following GMP
Following cGMP.
5 Opening(s)
2.0 Year(s) To 6.0 Year(s)
2.00 LPA TO 7.00 LPA
Job Title - QC Officer/Executive
Job Responsibilities and required key skills :
Titration method (Peroxide value, Free fatty Acid, chemicals Standardization)
Equipment Exposure ( HPLC, GC, pH meter)
Safety Compliance
GLP compliance
Good Communication Skills
Major Responsibilities: •On time analysis & release of raw material, in process samples & finished product samples • Ontime Training completion within predefined ...
5 Opening(s)
5.0 Year(s) To 15.0 Year(s)
4.00 LPA TO 15.00 LPA
Job Description:* To ensure all relevant quality related documents are prepared, approved, implemented and followed.* Assuring that the right quality products reach the customer.* To ensure critical deviations are investigated and resolved.* To lead the internal audits and external periodically and follow up actions for its Compliances.* To identify gaps ...