INDOCO REMEDIES LIMITED Walk In Interview for Officer to Section Head QC department at Goa Plant III (OSD manufacturing facility) on 23rd, 24th & 25th July, 2022
A leading Pharma Company with global presence in 55 countries and approvals from USFDA, UKMHRA, etc.
WALK-IN
INTERVIEWS
Quality Control department at our Goa Plant III (OSD manufacturing facility)
Section Head – (RM & FP)
Qualification: M.Sc/B.Sc with 10-15 years’ experience in Quality Control department.
Candidate must be able to handle the section (RM/FP)
Planning of work, handling of manpower. Candidate should be well versed with latest version of software such as, Caliber Lims, Empower, Trackwise, Lab solutions, etc.
Handling of QMS like OOS/CCF/Deviations
Officer/Sr. Officer
Qualification: M.Sc/B.Sc (Chemistry/Analytical) /
B.Pharm with 3-5 years’ experience in:
Stability. Validation, Finished Products, In process, Raw material
Software requirement: Empower, Lab solution, Tiamo, Caliber LIMS.
Instruments handled: HPLC,UV,IR, KF GC, Malvern
• Exposure of Regulatory Audits USFDA/MHRA
Executive/Sr. Executive (Reviewers)
Qualification: M.Sc/ B.Sc (Chemistry/ Analytical) / B.Pharm with 5 to 10 years’ experience.
Should have experience in review (hard data and electronic review) of chromatographic and non chromatographic systems and software (Empower, Tiamo. Labsolutions, Caliber, etc.).
Should be involved in OOT/ OOS/incident investigation.
Sr. Officer/Executive (Reviewer) – Micro
Qualification: M.Sc/B.Sc (Microbiology) with 5 to 7 years’ experience:
• Have experience in reviewing of microbiology lab records. . Should have experience of MLT testing, Autoclave operations, Equipment Validations, MLT Method validations.
Handling of QMS like OOS / CCF / Deviations / SOP preparations.
VENUE: INDOCO REMEDIES LIMITED
Plot No. L-32,33, 34 (Plant III), Verna Industrial Estate, Verna, Goa 403 722
Candidates who are unable to attend personal interview can email their CVs to deepika.gayak@indoco.com. Contact no. 0832-6721627
Note: All above mentioned positions candidate must have exposure in facing various regulatory audits like USFDA, EU, MHRA, WHO, etc.
On Saturday, 23 July, 2022
Time: 09.30 am to 05.00 pm
Sunday, 24th July, 2022 Time: 09.00 am to 01.30 pm
AND
Monday, 25th July, 2022 Time: 02.00 pm to 05.30 pm
