Cubit Lifesciences LLP, a rapidly growing pharmaceutical organization committed to quality healthcare solutions, has announced a Walk-In Interview Drive for experienced pharmaceutical professionals. The company is inviting talented candidates to join its Quality Assurance (QA) and Quality Control (QC) departments at its manufacturing facility in Gujarat.
This recruitment drive offers an excellent opportunity for candidates seeking career growth in a professional and quality-driven pharmaceutical environment.
About Cubit Lifesciences LLP
Cubit Lifesciences LLP is a pharmaceutical company dedicated to delivering high-quality healthcare products while maintaining global quality standards. The organization focuses on innovation, regulatory compliance, and continuous improvement across its operations.
Walk-In Interview Details
Particulars Details
Company Name
Cubit Lifesciences LLP
Interview Type
Walk-In Interview
Interview Date
23rd June 2026 (Tuesday)
Interview Time
11:00 AM to 03:00 PM
Job Location
Ahmedabad, Gujarat
Industry
Pharmaceuticals
Open Positions
1. Quality Assurance (QA)
Designation: Officer to Assistant Manager
Qualification:
B.Pharm
M.Pharm
B.Sc
M.Sc
Experience Required:
1 to 12 Years
2. Quality Control (QC)
Designation: Officer
Qualification:
B.Pharm
M.Pharm
B.Sc
M.Sc
Experience Required:
1 to 3 Years
Interview Venue
Cubit Lifesciences LLP
Plot No. 39-40, Ozone Industrial Park,
Near Kerala GIDC, Village Bhayla,
Bavla-Rajkot Highway, Taluka Bavla,
Dist. Ahmedabad – 382220, Gujarat.
Documents Required
Candidates attending the interview should carry:
Updated Resume/CV
Educational Certificates
Experience Certificates
Latest Salary Slip
Government Photo ID Proof
Passport Size Photographs
Application Process
Interested candidates who are unable to attend the walk-in interview may share their updated CV along with:
Total Years of Experience
Current CTC
Expected CTC
Notice Period
Preferred Date for Face-to-Face Interview
WhatsApp CV: +91 78598 00724
Why Join Cubit Lifesciences?
Career growth opportunities
Exposure to pharmaceutical quality systems
Professional work environment
Learning and development programs
Commitment to quality and innovation
Technical FAQs
1. What are the key responsibilities of a QA Officer in a pharmaceutical company?
A Quality Assurance Officer is responsible for ensuring compliance with GMP guidelines, reviewing batch manufacturing records, handling deviations, CAPA management, change controls, document review, internal audits, and maintaining regulatory compliance.
2. What instruments and tests are commonly handled by QC professionals?
QC professionals work with analytical instruments such as:
HPLC (High Performance Liquid Chromatography)
GC (Gas Chromatography)
UV Spectrophotometer
FTIR
Dissolution Apparatus
pH Meter
Karl Fischer Titrator
These instruments are used for raw material, in-process, and finished product testing.
3. What is GMP and why is it important in pharmaceuticals?
Good Manufacturing Practices (GMP) are regulatory guidelines that ensure pharmaceutical products are consistently manufactured and controlled according to quality standards. GMP helps ensure product safety, efficacy, and compliance with regulatory authorities.
4. What is CAPA in pharmaceutical quality systems?
CAPA (Corrective and Preventive Action) is a systematic approach used to investigate quality issues, identify root causes, implement corrective measures, and prevent recurrence. CAPA is a critical component of pharmaceutical quality management systems.
5. What technical questions can be asked during a QA/QC interview?
Common technical interview questions include:
Explain OOS (Out of Specification) and OOT (Out of Trend).
What is data integrity and ALCOA+?
How does HPLC work?
What is a deviation and change control?
Explain analytical method validation parameters.
What are GMP and GDP requirements?
How do you handle laboratory investigations?
Conclusion
Cubit Lifesciences LLP’s Walk-In Interview on 23 June 2026 presents an excellent opportunity for QA and QC professionals to advance their pharmaceutical careers. Candidates with relevant qualifications and experience are encouraged to attend the interview with the required documents and explore rewarding career opportunities with a growing pharmaceutical organization.

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