Biophore india pharmaceuticals Walk-in On 30th Nov 2024 Msc,Bpharm,Mpharm for QC

Biophore is a research driven global pharmaceutical company focused on development, manufacturing and marketing of Active Pharmaceutical Ingredients (APIs) having its operations based in Hyderabad, India and also has a registered office in New Jersey, USA. Biophore has two dedicated R&D facilities in Hyderabad and Vishakapatnam. 

• Vacancy details:
• Department: Qc Analyst
• Experience: 03 to 7 Years
• Qualification: Bpharm/M.Pharma in Any Specialization, MS/M.Sc(Science) in Chemistry
• Salary:₹3.5-6.5 Lacs P.A.

Job Description: Greeting from Biophore india pharmaceuticals pvt ltd !!!

Important Details :

• Work Location: Visakhapatnam
• Post of date :26/11/2024
• Selection Process: The selection will be on the basis of Interview.
• Mode of Interview: Face to face
• Interview Rounds of Interview: HR

Walkin Interview Details:

Time and Venue

30 November , 9.30 AM – 1.30 PM

Biophore India Pharmaceuticals Pvt. Ltd. Plot No. 80-A, Road No: 5, JNPC, Parawada, E BONANGI Vill. Visakhapatnam Vizag – 531021.

Contact – ESWAR ( 07674014367 )

Roles and Responsibilities

Conduct stability analysis, method validation, instrument calibration, and GC/HPLC analysis to ensure compliance with regulatory requirements.

Perform quality control testing on pharmaceutical products using various analytical techniques such as UV spectrophotometry and dissolution testing.

Develop and maintain documentation for laboratory procedures, protocols, and reports in accordance with cGMP guidelines.

Collaborate with cross-functional teams to resolve issues related to product quality and process improvements.

Ensure accurate recording of data and maintenance of records according to company standards.

Desired Candidate Profile

3-7 years of experience in a similar role within the pharmaceutical industry.

Bachelor’s degree (B.Pharma) or Master’s degree (M.Pharma) in Any Specialization from a recognized institution.

Strong understanding of Good Laboratory Practices (GLP), Current Good Manufacturing Practice (cGMP), and regulations governing the pharmaceutical industry.

Proficiency in HPLC Analysis, GC Analysis, Stability Analysis, Method Validation, Instrument Calibration.