a. Responsible for receive sample from production, make inward entry received from production department, co-ordinate with QA for AWR & relevant formats, sampling of material.
b. Responsible for daily calibration of Weighing balance, PH meter, Karl fisher etc. and instrument calibration
c. Responsible to prepare desk reagents, volumetric solution by using primary standards, sample analysis which is allotted by seniors.
d. Responsible for proper documentation / record keeping like ensure attachment of all analytical related results as per SOP.
e. Log books management for various activities.
f. Responsible for maintain good housekeeping, work with safety by using PPEs.
Qualification and Experiences
a. Post-Graduation in Chemistry.
b. Knowledge of cGMP & GLP guidelines, ICH/ USFDA guidelines.
c. Working knowledge of Method development and validation.
d. Handling of instruments like HPLC/GC/GCHS/Spectrophotometer etc.
e.
Minimum 7 years of experience in Pharmaceutical industry and extensive Quality control experience in API manufacturing industry.
Competencies / Skills
a. Well versed with industry specific products and its application
b. Strong analytical skills
c. High Emotional Quotient
d. Strong communication and collaboration skill
e. Conflict resolution and problem resolution skills
Mandatory
a. Well versed with industry specific products and its application
- What is your total experience ?
- Mention Your current CTC ?
- Mention Your expected CTC ?
- If Selected, How soon you can join ?
- Do you have experience in API industry ?
Experience:
- HPLC: 3 years (Required)
Location:
- Vapi, Gujarat (Required)
Work Location: In person
📌 Sr. QC Officer (Vapi)
🏢 Vital Laboratories
📍 Vapi
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