Location: On-site Nalagarh, Himachal Pradesh
Experience: 12 years (Mandatory)
Qualification: . in Chemistry / Microbiology / Biotechnology / Life Sciences
About the Role:
We are looking for a dedicated Quality Control (QC) Officer to join our pharmaceutical manufacturing team at our Nalagarh facility. The ideal candidate will have hands-on experience with laboratory testing and strong documentation practices in a GMP-regulated environment.
Key Responsibilities:
Conduct testing of raw materials, in-process samples, and finished products.
Operate and maintain analytical instruments like HPLC, UV, IR, pH meter, etc.
Ensure accurate and timely documentation as per cGMP and GLP guidelines.
Perform stability studies and environmental monitoring (if required).
Participate in lab audits, calibration, and equipment qualification.
Maintain safety and hygiene in the lab environment.
Desired Profile:
. in Chemistry / Microbiology / Biotechnology or relevant field
12 years of QC experience in a pharmaceutical formulation unit (mandatory)
Sound knowledge of GMP practices and analytical techniques
Attention to detail, good documentation habits, and strong analytical skills
Mandatory Proficiency in written and verbal English
Join a team committed to delivering high-quality, affordable medicines.
Apply now to become part of our quality-driven organization!
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Experience
3 Years
No. of Openings
5
Education
B.Pharma, B.Sc, M.Pharma, M.Sc
Role
Quality Control Officer
Industry Type
Manufacturing / Production / Quality
Gender
[ Male / Female ]
Job Country
India
Type of Job
Full Time
Work Location Type
Work from Office
Walk-in interview location
Village Mehsa Tibba, P.O. Manjholi, Tehsil Nalagarh, Distt, Solan, HP,INDIA , 174101