Unichem Walk-In Quality Control
- H2: Company Overview
- H2: Job Role & Responsibilities
- H3: Quality Control
- Key Responsibilities
- H2: Eligibility / Qualifications
- Educational Qualification
- Relevant Courses
- Experience Required
- Required Technical Skills
- H2: Location & Salary
- H2: Application Process
- Walk-In Interview Details
- Email Application
- H2: Frequently Asked Questions (FAQs)
- 1. Who can apply for Unichem Laboratories Quality Control vacancies?
- 2. Is pharmaceutical industry experience mandatory?
- 3. What analytical instruments should candidates know?
- 4. Is shift work required for this role?
- 5. Is regulatory exposure mandatory?
- 6. How can candidates apply?
- Summary
Unichem Labs QC Jobs Goa | BSc M.Sc B.Pharm
Unichem Laboratories hiring Quality Control professionals in Goa. M.Sc, B.Sc, B.Pharm candidates with 1–4 years pharma experience can apply.
Unichem Laboratories Ltd. is conducting a walk-in interview drive for Quality Control professionals at its pharmaceutical manufacturing facility in Pilerne, Goa. The company is looking for candidates with pharmaceutical industry experience who have hands-on exposure to analytical instruments, laboratory testing, regulatory compliance, and cGMP environments.
This opportunity is suitable for candidates seeking Quality Control jobs in pharma, analytical laboratory careers, HPLC analyst positions, pharmaceutical testing roles, and regulatory-compliant manufacturing opportunities within a reputed pharmaceutical company.
Candidates with experience in handling HPLC, UV, IR, Karl Fischer, GC, Dissolution, and LCMS instruments are encouraged to participate in the walk-in drive.
H2: Company Overview
Unichem Laboratories Ltd. is a well-established pharmaceutical company with a strong presence in domestic and international markets. The company manufactures a wide range of pharmaceutical formulations and operates facilities that follow stringent quality systems and global regulatory standards.
The Goa manufacturing site focuses on maintaining high-quality manufacturing and laboratory practices while complying with cGMP requirements and regulatory expectations. Employees gain valuable exposure to pharmaceutical quality systems, analytical testing, data integrity practices, and regulated market manufacturing environments.
H2: Job Role & Responsibilities
H3: Quality Control
Designation: Quality Control Executive / Analyst
Candidates selected for the Quality Control department will be responsible for supporting analytical testing activities and ensuring compliance with pharmaceutical quality standards.
Key Responsibilities
- Perform routine analysis of raw materials, in-process samples, and finished products.
- Operate analytical instruments such as HPLC, UV, IR, GC, Karl Fischer, Dissolution, and LCMS.
- Ensure compliance with current Good Manufacturing Practices (cGMP).
- Maintain laboratory documentation and analytical records.
- Follow Good Laboratory Practices (GLP) and data integrity requirements.
- Participate in laboratory investigations and quality improvement activities.
- Support regulatory compliance and audit readiness initiatives.
- Review analytical results and ensure timely reporting.
- Work effectively in shift-based laboratory operations.
- Follow company quality policies and standard operating procedures.
H2: Eligibility / Qualifications
Educational Qualification
Candidates possessing any of the following qualifications are eligible to apply:
- M.Sc
- B.Sc
- B.Pharm
Relevant Courses
Pharmacy, Pharmaceutical Sciences, Pharmaceutical Analysis, Analytical Chemistry, Organic Chemistry, Industrial Chemistry, Microbiology, Biochemistry, Quality Control, Pharmaceutical Quality Assurance
Experience Required
- 1 to 4 Years
- Candidates must have a pharmaceutical industry background.
- Exposure to regulated pharmaceutical environments is mandatory.
- Knowledge of analytical laboratory operations and quality systems is preferred.
Required Technical Skills
Candidates should be familiar with:
- HPLC Analysis
- UV Spectroscopy
- Infrared Spectroscopy (IR)
- Karl Fischer Titration
- Gas Chromatography (GC)
- Dissolution Testing
- LCMS Analysis
- cGMP Compliance
- Pharmaceutical Documentation
- Regulatory Environment Requirements
H2: Location & Salary
Location: Pilerne, Goa
Salary: Approx. ₹2.5 LPA – ₹5.5 LPA (Based on qualification, technical skills, and experience)
H2: Application Process
Walk-In Interview Details
Interview Dates: 25 May 2026 to 30 May 2026
Interview Time: 10:00 AM to 05:00 PM
Interview Venue: Unichem Laboratories Ltd., Pilerne, Bardez, Goa
Email Application
Candidates who are unable to attend the walk-in interview can send their updated resume to:
Email: hrgoa@unichemlabs.com
Candidates should mention “Quality Control Application” in the subject line while applying.
H2: Frequently Asked Questions (FAQs)
1. Who can apply for Unichem Laboratories Quality Control vacancies?
Candidates with B.Sc, M.Sc, or B.Pharm qualifications and 1–4 years of pharmaceutical industry experience can apply.
2. Is pharmaceutical industry experience mandatory?
Yes. Candidates should have relevant pharmaceutical industry exposure and understanding of laboratory operations.
3. What analytical instruments should candidates know?
Applicants should have working knowledge of HPLC, UV, IR, Karl Fischer, GC, Dissolution, and LCMS instruments.
4. Is shift work required for this role?
Yes. The Quality Control role involves shift-based working.
5. Is regulatory exposure mandatory?
Yes. Candidates should have exposure to regulated pharmaceutical environments and cGMP requirements.
6. How can candidates apply?
Candidates can attend the walk-in interview directly or email their updated CV to hrgoa@unichemlabs.com.
Summary
| Company | Unichem Laboratories Ltd. |
| Department Vacancies | Quality Control |
| Qualification | M.Sc, B.Sc, B.Pharm |
| Experience | 1–4 Years |
| Location | Goa |

To apply for this job please visit unichemlabs.com.