1 Opening(s)
15.0 Year(s) To 20.0 Year(s)
15.00 LPA TO 20.00 LPA
Job Title: Production 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)
12.0 Year(s) To 20.0 Year(s)
8.00 LPA TO 10.00 LPA
Qualification: Graduate first Class and Material management diploma first class can be preferable.Relevant experience: min 12 to 20 Years Experience stores functioning from Chemical, Paint, Resins, Additives Industries.Work location: Nerul in Mumbai
Job description:➢ Ensure availability of required raw materials by continuous follow up with Purchase as per production plan so ...
1 Opening(s)
1.0 Year(s) To 2.0 Year(s)
2.50 LPA TO 3.00 LPA
Role: Production ExecutiveLocation: Dundigal, Medchal Experience: 1-2 years in manufacturing Salary: Up to 3 LPA Industry: Pharma Manufacturing (Preferred) Qualification: Undergraduate / Graduate Working Days: 6 days a week
Key Responsibilities:* Handle cGMP & GDP practices in manufacturing.* Coordinate and manage a cross-functional team.* Oversee manufacturing processes, dispensing, and excess material ...
1 Opening(s)
15.0 Year(s) To 17.0 Year(s)
15.00 LPA TO 17.00 LPA
Sr. Manager- Quality Assurance (QA QC)
Job Responsibilities?:-
Planning and execution of daily QA, QC operation activities for production in Injectable section to smooth Functioning work culture.
To prepare and review the SOPs of QA QC departments. Ensure qualification/ validation status of equipment’s
QA, QC of Internal and external Manufacturing as per SOP.
Experience of handling ...
1 Opening(s)
8.0 Year(s) To 15.0 Year(s)
10.00 LPA TO 20.00 LPA
Technical Function – Operation Of Distillation / MEE/ Filtration
Area Responsibility – Recovery Plant 1. Verification of Distillation / Verification MEE/ Verification Filtration 2. Verification of Document Process 3. Plant document as per CGMP.
Technical Function – Operation Of Distillation / MEE/ Filtration
Area Responsibility – Recovery Plant 1. Verification of Distillation / ...
1 Opening(s)
7.0 Year(s) To 8.0 Year(s)
8.00 LPA TO 10.00 LPA
Position: Packing Incharge(U1)
Location: Daman
Experience: 7 - 8 Years
Industries: Pharma
Responsibilities:
To finalize Packing plan for weekly and monthly.
To allocate work to workforce and perform the critical checks and ensure line clearance at all stages of Packing to implement Current good manufacturing practice.
Preparation and review ...
4 Opening(s)
2.0 Year(s) To 4.0 Year(s)
3.00 LPA TO 4.00 LPA
Job Summary:
The Granulation Operator is responsible for operating and monitoring granulation equipment used in the pharmaceutical manufacturing process. This role ensures that raw materials are processed according to standard operating procedures (SOPs) and current Good Manufacturing Practices (cGMP) to produce high-quality granules used in tablet or capsule formulations.
Key Responsibilities:
Granulation Process ...
5 Opening(s)
7.0 Year(s) To 15.0 Year(s)
6.00 LPA TO 8.00 LPA
JOB PURPOSE:
Design, Implement & Monitor Organizational processes intended to yield consistency or improvement in operational results. It is the responsibility of the Asst. Manager QA to ensure that the systems in the plants are to be maintained according to current and approved specifications, as per approved SOP’s.
Also ensure that all ...
1 Opening(s)
15.0 Year(s) To 20.0 Year(s)
15.00 LPA TO 20.00 LPA
A "QC Manager - Sterile Formulation" job description entails overseeing all quality control operations within a sterile injectable drug manufacturing facility, ensuring that all products meet stringent regulatory standards by managing testing procedures for raw materials, in-process samples, and finished products, while maintaining compliance with cGMP guidelines and conducting thorough ...
3 Opening(s)
0 To 2.0 Year(s)
0.00 LPA TO 2.00 LPA
Internal Job Description
Education / Experience
M.Sc. Analytical/Organic Chemistry/Inorganic Chemistry
Min. 5 years’ Experience in a Quality Control/Analysis laboratory in a cGMP/ISO environment, with exposure to method development and validation activities
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 ...