Zenotech Hiring QC Analyst, Sr. Officer , Executive
- Company Overview
- Job Role & Responsibilities
- Quality Control Analyst – General Injectables
- Eligibility / Qualifications
- Location & Salary
- Application Process
- Why This Opportunity Stands Out
- FAQs
- Summary Table
MPharm BPharm QC Jobs Zenotech Hyderabad Hiring
Zenotech hiring QC Analysts in Hyderabad. MPharm, BPharm, MSc candidates with 3–8 yrs experience eligible for multiple vacancies.
Zenotech Laboratories Limited is actively hiring experienced candidates for multiple vacancies in the Quality Control (QC) department, specifically for Analyst – General Injectables roles at its Hyderabad manufacturing facility. This opportunity is ideal for professionals with 3 to 8 years of experience in pharmaceutical quality control, analytical testing, and regulatory-compliant laboratory environments.
The company is looking for qualified candidates from M.Pharm, B.Pharm, and M.Sc Organic Chemistry backgrounds who have hands-on experience in analytical instruments such as HPLC and GC. These roles are critical in ensuring product quality, regulatory compliance, and safety in injectable pharmaceutical manufacturing.
Company Overview
Zenotech Laboratories Limited is a well-established pharmaceutical company specializing in oncology products, biotechnology solutions, and sterile injectable manufacturing. The company operates with a strong focus on innovation, regulatory compliance, and high-quality production standards aligned with global guidelines such as USFDA, cGMP, and GLP.
With advanced manufacturing capabilities and a commitment to scientific excellence, Zenotech plays a key role in delivering safe and effective medicines. The company’s Hyderabad facility is equipped with modern analytical laboratories and quality systems, making it an ideal workplace for professionals in pharmaceutical quality control and analytical research.
Job Role & Responsibilities
Quality Control Analyst – General Injectables
As a Quality Control Analyst, you will be responsible for ensuring the quality and compliance of pharmaceutical products through analytical testing, documentation, and regulatory adherence.
Key responsibilities include:
- Perform operation, calibration, and maintenance of analytical instruments such as HPLC, GC, and other laboratory equipment
- Conduct analysis of raw materials, finished products, cleaning validation samples, and stability samples
- Prepare and maintain working standards, reference standards, and specifications
- Execute analytical method validation (AMV) and analytical method transfer (ATV) activities
- Review analytical data, generate Certificates of Analysis (COA), and ensure data integrity
- Handle deviations, OOS (Out of Specification), OOT (Out of Trend), and incident investigations
- Maintain documentation in compliance with GLP and cGMP guidelines
- Support regulatory audits and inspections by ensuring proper documentation and compliance
This role is essential in maintaining product quality and ensuring that pharmaceutical products meet stringent regulatory standards before reaching patients.
Eligibility / Qualifications
Candidates must meet the following educational criteria:
M.Pharm, B.Pharm, M.Sc Organic Chemistry
Relevant courses include: Pharmaceutical Analysis, Organic Chemistry, Analytical Chemistry, Quality Assurance, Drug Regulatory Affairs, Medicinal Chemistry, Industrial Pharmacy
- Experience: 3 to 8 years in pharmaceutical quality control or analytical laboratories
- Hands-on experience with HPLC, GC, and analytical techniques is mandatory
- Strong knowledge of GLP, cGMP, and regulatory compliance requirements
- Experience in injectable manufacturing is preferred
- Good documentation and analytical skills required
Location & Salary
- Job Location: Zenotech Laboratories Limited, Turkapally, Shamirpet, Hyderabad, Telangana
- Salary: Competitive and aligned with industry standards based on experience
Application Process
Candidates must follow the two-step application process:
Step 1: Submit your details through the official form:
https://forms.office.com/r/Y5XkYcUKKY
Step 2: Send your updated resume to:
hr1@zenotech.co.in
Ensure your resume clearly highlights your experience in analytical testing, quality control, and regulatory compliance to improve your chances of selection.
Why This Opportunity Stands Out
- Opportunity to work in injectable pharmaceutical quality control
- Exposure to advanced analytical instruments like HPLC and GC
- Experience in regulatory-compliant environments including USFDA standards
- Career growth in high-demand QC and analytical roles
- Contribution to ensuring safe and effective medicines for patients
FAQs
Who can apply for this QC Analyst role?
Candidates with M.Pharm, B.Pharm, or M.Sc Organic Chemistry and relevant experience can apply.
Is prior experience mandatory?
Yes, candidates must have 3–8 years of experience in QC or analytical roles.
What instruments should candidates be familiar with?
HPLC, GC, and other analytical laboratory equipment.
What kind of products will be handled?
Injectable pharmaceutical products including raw materials and finished formulations.
How to apply for this role?
Complete the online form and send your resume via email as mentioned.
Summary Table
| Category | Details |
|---|---|
| Company | Zenotech Laboratories Limited |
| Vacancies | QC Analyst, Sr. Officer QC, Executive QC |
| Required Education | M.Pharm, B.Pharm, M.Sc Organic Chemistry |
| Experience | 3 to 8 Years |

To apply for this job please visit forms.office.com.