Steribio Lifesciences Private Limited is hiring for a QC Chemical – Injectable Formulation (LVP) role for a Greenfield Pharma Project in Patas. This is an excellent opportunity for professionals with experience in sterile injectable manufacturing.
Key Responsibilities:
- Support QC Chemical activities in document preparation and sample collection.
- Preparation of SOPs, STPs, and Protocols for injectable formulations.
- Ensure compliance with GMP, GLP, and regulatory standards.
- Perform chemical testing and analysis of raw materials and finished products.
- Maintain accurate documentation and records for quality control processes.
Must-Have Requirements:
- 1.5 to 3 years of experience in Injectable Formulation (LVP/SVP).
- B.Pharma / M.Sc / M.Pharma qualification.
- Male candidates only (due to work environment constraints).
- Experience in Greenfield Pharma Projects is mandatory.
Why Join Steribio Lifesciences?
- Work on a high-profile injectable formulation project.
- Gain exposure in a sterile manufacturing environment.
- Competitive salary and growth opportunities.
About Steribio Lifesciences Private Limited
Steribio Lifesciences is a leading pharmaceutical company specializing in sterile injectable formulations. With a strong focus on quality and compliance, the company is expanding its operations with a new Greenfield project in Patas.
How to Apply?
Interested and eligible candidates can fill out the Google Form before the deadline:
👉 Apply Here
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Note: Only shortlisted candidates will be contacted. Freshers & Female candidates please do not apply.
