Zenotech Laboratories Limited, a Sun Pharma company, has announced a hiring drive for experienced pharmaceutical professionals in the Microbiology and Quality Control (QC) departments. This recruitment initiative is focused on candidates with expertise in sterile manufacturing, analytical testing, GMP compliance, and quality systems within pharmaceutical manufacturing environments.

The organization is looking for qualified professionals who can contribute to its Injectable and OSD (Oral Solid Dosage) operations while maintaining the highest standards of quality, regulatory compliance, and operational excellence.

Available Departments and Positions

1. Microbiology Department

Sub Department: General Injectable

Designation: Senior Officer / Executive

Qualification: M.Sc. Microbiology

Experience: 2–7 Years

Key Responsibilities

Hands-on experience in aseptic practices and aseptic behavior.

Routine Environmental Monitoring (EM) activities in sterile manufacturing areas.

Microbiological testing and monitoring of controlled environments.

Participation in Media Fill validation activities.

Preparation, review, and trending of Environmental Monitoring data.

Compliance with GMP documentation requirements.

Support investigations related to microbiological deviations and contamination control.

2. Quality Control (QC) Department

Sub Department: Analyst (General Injectable & OSD)

Designation: Senior Officer / Executive

Qualification:

M.Pharm

B.Pharm

M.Sc. Organic Chemistry

Experience: 3–8 Years

Key Responsibilities

Operation, calibration, and maintenance of HPLC, GC, and analytical instruments.

Analysis of raw materials, finished products, cleaning validation samples, and stability samples.

Preparation and upkeep of working standards and reference standards.

Execution of AMV (Analytical Method Validation) and ATV (Analytical Method Verification) activities.

Review and interpretation of analytical data.

Preparation of Certificates of Analysis (COA).

Investigation and handling of OOS (Out of Specification) and OOT (Out of Trend) results.

Management of deviations, incidents, and document control activities.

Ensuring compliance with GLP and cGMP requirements.

Desired Candidate Profile

Candidates applying for these positions should possess:

Strong understanding of GMP, GLP, and pharmaceutical regulatory requirements.

Experience in injectable manufacturing or analytical laboratories.

Excellent documentation and investigation skills.

Ability to work in a highly regulated pharmaceutical environment.

Strong technical knowledge related to microbiology or analytical chemistry.

Effective communication and teamwork capabilities.

Work Location

Zenotech Laboratories Limited

Turkapally Village, Shamirpet Mandal,

Medchal–Malkajgiri District,

Hyderabad – 500101, Telangana, India.

Application Process

Interested candidates can apply through the official application form and submit their details to the company.

Email: hr1@zenotech.co.in

Applicants are advised to keep their updated resume, educational certificates, experience documents, and recent passport-size photographs ready before applying.

Technical FAQs

1. What is Environmental Monitoring (EM) in pharmaceutical manufacturing?

Environmental Monitoring is a systematic process used to assess the cleanliness and microbiological quality of controlled manufacturing environments. It includes air sampling, surface monitoring, personnel monitoring, and particulate monitoring to ensure aseptic manufacturing conditions remain compliant with regulatory standards.

2. Why is Media Fill important in sterile injectable manufacturing?

Media Fill is a simulation study used to validate aseptic manufacturing processes. It demonstrates that the manufacturing process can consistently produce sterile products without contamination under normal operating conditions.

3. What is the role of HPLC and GC in Quality Control laboratories?

HPLC (High Performance Liquid Chromatography) and GC (Gas Chromatography) are analytical techniques used to identify, quantify, and assess the purity of pharmaceutical substances, finished products, impurities, and residual solvents to ensure product quality and compliance.

4. What are OOS and OOT investigations?

OOS (Out of Specification): Results that fall outside predefined acceptance criteria.

OOT (Out of Trend): Results that deviate significantly from historical trends despite remaining within specifications.

Both require detailed investigation to identify root causes and implement corrective actions.

5. What is the significance of cGMP and GLP compliance?

Current Good Manufacturing Practices (cGMP) and Good Laboratory Practices (GLP) ensure that pharmaceutical products are consistently manufactured, tested, and controlled according to quality standards. Compliance helps maintain product safety, efficacy, data integrity, and regulatory acceptance.

Conclusion

The Zenotech Laboratories and Sun Pharma hiring drive presents an excellent opportunity for experienced Microbiology and Quality Control professionals seeking career growth in the pharmaceutical industry. Candidates with expertise in aseptic processing, environmental monitoring, analytical testing, and regulatory compliance are encouraged to apply and become part of a leading pharmaceutical organization dedicated to quality and innovation.