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Showing posts with label Manufacturing. Show all posts
Showing posts with label Manufacturing. Show all posts

Monday, 14 October 2024

STRIDES WALK-IN DRIVE or Manufacturing and Engineering

October 14, 2024 0
STRIDES WALK-IN DRIVE
For Manufacturing and Engineering

Interview Location
Hotel Ibis, Hosur Road, 26/1, next to Hongasandra Metro Station, Bommanahalli, Bengaluru, Karnataka 560068

Walk in Time: 10:00AM to 03:00PM

Date: Sunday, 20th October 2024

Packing (OSD)
Planning and execution of batch packing activities such as Dispensing & Line clearance.

Expertise in handling Blister, Bottle and Sachet packing machineries like BQS, CAM, Maspack, Auto Cartonator etc.

Experience:
2-5years in Oral Solid Dosage

Qualification:
B.Pharm/M.Pharm

Job Location: Bangalore/Chennai

Maintenance Engineering

Responsible to conduct Preventive and Breakdown maintenance of production and packing equipment's.
Expertise in handling RMG, FBD, Compression machines, Coating machines, Blenders, Capsule filling machines, Blister packing, Serialization equipment's & inspection systems.

Experience:
2-5years

Qualification:
Engineering in Mechanical/Electrical

Job Location: Bangalore/Chennai/ Pondicherry
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Saturday, 21 September 2024

Walk-in Interview For QA,IPQA And Manufacturing Departments At Amneal Pharmaceuticals Pvt.

September 21, 2024 0
WE ARE HIRING
Walk-in Drive for Injectable Plant
☑ Manufacturing
Engineering
QA-IPQA
◎ Location: Pipan

Injectable Manufacturing Department
Designation: Officer/ Executive
Qualification: B.Pharma/ B.E/B.Tech
Experience:
Candidate must have 1 to 5 years of hands on experience in aseptic & controlled area of injectable / sterile manufacturing & packing.

Injectable Manufacturing Department
Designation: Assistant/ Associate
Qualification: ITI/ Diploma/ B.Sc
Experience:
Candidate must have 1 to 5 years of hands on experience in aseptic & controlled area of injectable/ sterile manufacturing & packing

Injectable Engineering Department
Designation: Officer / Executive/ Sr. Executive
Qualification: BE/B. Tech
Experience:
Candidate must have 1 to 5 years of experience in handling maintenance of vial washing, tunnel, vial filling, vial capping machine, sealing machine, Lyo, autoclave, steam sterilizer etc.

Injectable Engineering Department
Designation: Assistant/ Associate
Qualifications: ITI/ Diploma
Experienced:
Candidate must have 1 to 5 years of experience of handling maintenance of vial washing, tunnel, filling & capping machine, sealing machine, Lyo, autoclave, steam sterilizer etc. & RO water plant.


Injectable QA - IPQA Department
Designation: Officer / Executive/ Sr. Executive
Qualification: B. Pharma/ M. Pharma
Experience:
Candidate must have 1 to 5 years of experience to perform line clearance activity before starting of different operations like dispensing, manufacturing, filling, inspection, sealing, labelling & packing

Injectable QA - IPQA Department
Designation: Officer / Executive/ Sr. Executive
Qualification: B. Pharma/ M. Pharma
Experience:
Candidate must have 1 to 5 years of experience to perform line clearance activity before starting of different operations like dispensing, manufacturing, filling, inspection, sealing, labelling & packing.

Interview Venue:
Amneal Pharmaceuticals Pvt. Ltd.

Plot No: 161/1, Sanand Bavla Highway Road, Village: Pipan, Sanand, Ahmedabad, Gujarat - 382110

Date: 22nd Sept 2024 (Sunday)
Time: 9:00 AM to 1:00 PM
Unable to attend the walk-in interview? Share your CV on riddhi.patel@amneal.com
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Wednesday, 10 January 2024

Encube Ethical Hiring For Fresher And Experience Candidates For Quality Control, Formulation & Development, IVRT,Analytical Development, QA,Production, Manufacturing Departments

January 10, 2024 0
1. Quality Control (QC):
   Quality Control is a critical department responsible for ensuring that pharmaceutical products meet established quality standards. QC professionals perform various tests and inspections throughout the manufacturing process. This includes raw material testing, in-process checks, and final product analysis. They use a range of analytical techniques to verify the identity, purity, and potency of drug substances. By maintaining rigorous quality control measures, this department ensures that only products meeting predefined specifications reach the market.

2. Formulation & Development:
   Formulation and Development teams focus on designing and optimizing drug formulations. Their goal is to create a stable, effective, and patient-friendly product. This involves selecting suitable excipients, determining the optimal dosage form (tablets, capsules, injections, etc.), and addressing factors like bioavailability. These teams collaborate closely with researchers, utilizing scientific knowledge to create formulations that balance therapeutic efficacy, safety, and manufacturability.

3. In Vitro Release Testing (IVRT):
   In Vitro Release Testing is a specialized area that involves studying the release of drug substances from formulations in a controlled laboratory setting. This is crucial for understanding how a drug is released over time and under various conditions, providing insights into its behavior within the body. IVRT helps assess the performance of different formulations, aiding in the development of products with optimal release profiles.

4. Analytical Development:
   Analytical Development plays a pivotal role in developing and validating methods for analyzing pharmaceutical compounds. This includes techniques such as chromatography, spectroscopy, and mass spectrometry. The department ensures that these methods are accurate, reliable, and compliant with regulatory requirements. Analytical methods are essential for quality control, formulation development, and ongoing manufacturing processes.

5. Quality Assurance (QA):
   Quality Assurance is responsible for establishing and maintaining systems to ensure that pharmaceutical products comply with regulatory standards and internal quality processes. QA professionals oversee Good Manufacturing Practice (GMP) adherence, conduct audits, and manage documentation to guarantee product quality. This department acts as a regulatory liaison, ensuring that the company meets the standards set by health authorities.

6. Production:
   The Production department is involved in the actual manufacturing of pharmaceutical products on a larger scale. It transforms raw materials into finished dosage forms. This process requires strict adherence to established protocols, ensuring consistency and reproducibility. Production teams operate manufacturing equipment, monitor processes, and collaborate with other departments to ensure the efficient and compliant production of pharmaceuticals.

7. Manufacturing:
   Manufacturing encompasses the broader aspects of producing pharmaceuticals. This includes facility management, process optimization, and technology transfer. The Manufacturing department coordinates with various teams to streamline production workflows. Continuous improvement initiatives are implemented to enhance efficiency, reduce costs, and maintain a state of control in the manufacturing environment.

In summary, the synergy between these departments is crucial for the successful development, production, and quality assurance of pharmaceutical products. Each department contributes its specialized expertise to ensure that the end products are safe, effective, and meet regulatory standards.
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