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A total of 5 vacancies are available for candidates with experience in pharmaceutical Quality Control (QC), analytical testing, microbiological analysis, stability studies, and laboratory compliance.
Zydus Healthcare Recruitment Oct, 2026- QC Analyst Jobs in Sikkim- Deails Table
| Particulars | Details |
|---|---|
| Company Name | Zydus Healthcare Limited |
| Industry | Pharmaceuticals |
| Job Role | QC Analyst |
| Designation | Officer / Executive |
| Department | Quality Control (QC) |
| Total Vacancies | 5 |
| Job Location | Sikkim Unit I & Unit II |
| Qualification | B.Sc. / M.Sc. in Chemistry, Microbiology or Biotechnology |
| Experience Required | 1-4 Years |
| Recruitment Type | Experienced Candidates |
| Job Announcement Date | 09-10-2026 |
| Application Mode | |
| Email Address | Bishnu.M.Bhujel@zyduslife.com |
| Company Website | Visit Official Website |
Job Position and Eligibility Criteria
QC Analyst – Officer / Executive
Zydus Healthcare Limited is seeking candidates for Quality Control laboratory operations at its Sikkim manufacturing units.Educational Qualifications:
- B.Sc. or M.Sc. in Chemistry.
- B.Sc. or M.Sc. in Microbiology.
- B.Sc. or M.Sc. in Biotechnology.
Experience: 1-4 years of relevant experience in pharmaceutical Quality Control laboratories.
Vacancies: 5 positions.
Candidates with hands-on experience in analytical instruments, pharmaceutical testing, microbiological analysis, stability studies, and GMP-compliant laboratory operations are encouraged to apply.
Key Responsibilities:
- Selected candidates will be responsible for the following activities:
- Perform testing of raw materials, finished products, stability samples, water samples, and microbiological samples according to approved specifications and test methods.
- Operate analytical instruments such as HPLC, GC, UV-Visible spectrophotometers, FTIR, and dissolution testing equipment.
- Conduct microbiological testing, including environmental monitoring, water testing, bioburden testing, and microbial limit testing.
- Monitor stability studies and perform testing according to approved stability protocols and applicable ICH guidelines.
- Prepare and standardize reagents, volumetric solutions, culture media, and reference standards.
- Review analytical and microbiological data to ensure compliance with established specifications.
- Maintain laboratory records, logbooks, worksheets, and analytical reports in accordance with GMP and GLP requirements.
- Investigate out-of-specification (OOS) and out-of-trend (OOT) results, laboratory incidents, and microbiological deviations.
- Ensure compliance with GMP, GLP, data integrity, and laboratory safety requirements.
- Support analytical method validation, method transfer, instrument qualification, and calibration activities.
- Participate in internal audits, regulatory inspections, and other compliance-related activities.
- Coordinate with Quality Assurance, Production, Engineering, and Regulatory Affairs teams.
- Ensure the proper operation, maintenance, and calibration of laboratory instruments and equipment.
Required Skills:
- Candidates should possess the following technical knowledge and professional skills:
- Hands-on experience with HPLC, GC, UV-Visible spectroscopy, FTIR, dissolution testing, and other analytical instruments.
- Knowledge of microbiological testing, environmental monitoring, and water analysis.
- Understanding of GMP, GLP, data integrity, and laboratory compliance requirements.
- Familiarity with pharmacopoeial standards, including IP, USP, BP, and EP.
- Knowledge of OOS, OOT, CAPA, deviation management, change control, and Quality Management System (QMS) processes.
- Strong analytical, troubleshooting, documentation, and communication skills.
- Ability to maintain laboratory documentation and perform analytical data reviews.
- Preferred Experience
- Candidates with the following experience may have an advantage:
- Pharmaceutical QC laboratory experience involving raw materials, finished products, stability samples, and microbiological testing.
- Experience working in GMP-compliant laboratories and participating in regulatory audits.
- Exposure to analytical method validation, stability studies, and microbiological testing.
- Familiarity with laboratory software, chromatography data systems, and electronic documentation.
- Experience in regulated pharmaceutical manufacturing environments and quality systems.
How to Apply for Zydus Healthcare Recruitment 2026
Interested and eligible candidates can apply by sending their updated CV to the recruitment contact below.
How to Apply?
Subject Line: Application for QC Analyst- Officer / Executive- Sikkim
Candidates should mention their relevant experience, educational qualifications, current designation, and preferred location in their CV.
Applicants are advised to ensure that their contact details and professional experience are up to date before submitting their applications.
Frequently Asked Questions (FAQs)
1. What positions are available at Zydus Healthcare Limited?
The company is inviting applications for QC Analyst positions at the Officer / Executive level.
2. How many vacancies are available?
A total of 5 vacancies have been specified.
3. What qualifications are required?
Candidates should hold a B.Sc. or M.Sc. in Chemistry, Microbiology, or Biotechnology.
4. How much experience is required?
Applicants should have 1–4 years of relevant experience.
5. Where are the jobs located?
The positions are located at Sikkim Unit I and Unit II.
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