For more than 40 years, Leben Life Sciences has been a cornerstone of the pharmaceutical formulation industry. Our commitment to “Responsible Healthcare” is the driving force behind everything we do. We take pride in our EU-GMP Approved Global Standard manufacturing facility in Akola, which specializes in the production of OSD (Oral Solid Dosage) and Semi-solid formulations.
This certification is a testament to our unwavering dedication to quality, safety, and efficacy, meeting the stringent regulatory requirements of international markets. By joining LLS, you become part of a legacy that impacts global health.
Job Description: Officer/Sr. Officer – Quality Control
This is a hands-on role critical to maintaining the integrity and quality of our pharmaceutical products. The selected candidate will be an integral part of our QC team, ensuring all processes and products comply with established global standards.
Key Details:
- Designation: Officer / Sr. Officer
- Department: Quality Control (QC)
- Section: GLP (Good Laboratory Practice)
- Work Location: Akola, Maharashtra (MS)
- Experience Required: 2 to 4 Years in a pharmaceutical QC laboratory.
Key Responsibilities:
As a QC Officer at our EU-GMP facility, your responsibilities will include, but are not limited to:
- Performing analytical testing of raw materials, in-process samples, and finished products (OSD & Semi-solids).
- Strictly adhering to Good Laboratory Practices (GLP) and standard operating procedures (SOPs).
- Operating and maintaining sophisticated analytical instruments like HPLC, GC, UV-Vis Spectrophotometer, etc.
- Accurately documenting all analytical data and ensuring its integrity.
- Participating in method verification and validation activities.
- Ensuring the laboratory is compliant with cGMP and EU-GMP guidelines.
- Contributing to laboratory investigations and deviation management.
Desired Candidate Profile:
- Qualification: M.Sc. in Chemistry / Biotechnology or B.Pharm / M.Pharm from a recognized university.
- Experience: 2 to 4 years of relevant experience in the Quality Control department of a pharmaceutical company.
- Technical Skills: Hands-on experience with analytical instruments and a strong understanding of GLP/cGMP norms.
- Personal Attributes: High attention to detail, excellent documentation skills, and a strong sense of responsibility.
How to Apply
Ready to take the next step in your pharmaceutical career with a leading company?
Interested and eligible candidates are requested to mail their updated resume to:
Email: career@lebenlifesciences.com
Contact Number: 7498035480 (For queries)