JanSat Labs Walk-in Interview.JanSat Labs Notification full details below. Interested and eligible candidates can attend Interview on scheduled time and venue.
Vacancy details:
- Department: Qc Executive
- Qualification : B.Sc / M.Sc in Chemistry / Pharmaceutical Sciences or related field./Bphar/Mpharm
- Experience: 4 – 9 years
Important Details :
- Selection Process: The selection will be on the basis of Interview.
- Mode of Interview: Face to face
- Interview Rounds of Interview: HR
QC Reviewer / Sr. Research Associate:
Role & responsibilities
- Review analytical raw data, calculations, and reports for accuracy, completeness, and compliance with approved specifications and methods.
- Ensure all laboratory documentation meets regulatory and internal quality standards (e.g., USFDA, EU-GMP, ICH, WHO, etc.).
- Review chromatographic data (HPLC, GC), wet chemistry reports, and other analytical test results.
- Verify results for routine analysis, stability studies, and validation reports.
- Check instrument calibration records and ensure compliance before reviewing analytical results.
- Identify and report any data discrepancies, deviations, or non-conformities.
- Review and verify entries in logbooks, worksheets, and other controlled documents.
- Assist in investigations related to out-of-specification (OOS), deviations, and laboratory incidents.
- Coordinate with analysts and the QA team to ensure timely corrections or clarifications.
- Ensure timely completion and archival of reviewed documents.
- Provide support during internal and external audits (regulatory and customer).
- Participate in continuous improvement initiatives within the QC function.
Time and Venue
25 June – 4th July , 9.30 AM – 5.30 PM
JanSat Labs Private Limited Plot No:135B, Road No. 2, First floor, ALEAP Industrial Estate, Gajularamaram Village, Qutubullapur Mandal, Hyderabad-500090, Medchal-Malkajgiri district, Telangana. (View on map)
Contact – HR ( 8500807063 )
Preferred candidate profile
Education: B.Sc / M.Sc in Chemistry / Pharmaceutical Sciences or related field.
Experience: 4-8 years of experience in Quality Control, preferably in API manufacturing. At least 2 years in a QC Reviewer role.
Technical Skills:
Hands-on experience and data interpretation of analytical instruments like HPLC, GC, FTIR, UV, KF, etc.
Thorough understanding of cGMP, GLP, and regulatory requirements.
Good documentation and analytical skills.
Key Competencies:
Attention to detail.
Strong analytical and problem-solving skills
Good communication and interpersonal skills
Ability to manage priorities and meet deadlines
High integrity and compliance mindset
ABAC
