Cronus Pharma QC Jobs for Career-Break Returnees

Cronus Pharma Specialties India Pvt. Ltd. is inviting applications for 15 vacancies in its Quality Control (QC) Department, specifically targeting experienced professionals looking to restart their careers after a break. Candidates with M.Sc. or B.Pharm. qualifications and 2–5 years of relevant QC experience are eligible to apply. The openings cover Analytical Method Validation (AMV), QC Microbiology, Environmental Monitoring, BET, and Water Analysis. Selected candidates will initially be engaged through third-party contract payroll for six months, which may be extended.

Company Overview

Cronus Pharma Specialties India Pvt. Ltd. is inviting experienced pharmaceutical quality control professionals to return to the workforce through its latest recruitment initiative.

The company is particularly interested in candidates who have taken a career break but possess relevant experience in pharmaceutical Quality Control operations. This opportunity allows professionals to resume their careers and contribute their technical knowledge to laboratory and quality operations.

Cronus Pharma Quality Control Vacancies and Job Roles

Required Qualification: M.Sc. / B.Pharm.

Required Experience: 2–5 Years

1. QC – Analytical Method Validation (AMV)

The AMV section involves analytical method validation, laboratory testing, documentation, and general Quality Control activities.

Key Responsibilities:

• Perform analytical method validation in accordance with ICH guidelines.

• Prepare and review validation protocols and reports.

• Handle analytical instruments such as HPLC, GC, and UV systems.

• Perform data analysis and interpretation.

• Prepare SOPs and related documentation.

• Conduct routine analysis and support activities as assigned.

Other QC Responsibilities:

• Raw material testing.

• Finished product testing.

• Stability studies.

• Analytical support for regulatory audits.

• Documentation and record management.

• Ensure compliance with cGMP and GLP requirements.

2. QC – Microbiology

Key Responsibilities:

Environmental Monitoring (EM)

• Air monitoring.

• Surface monitoring.

• Personnel monitoring.

• Trend analysis and reporting.

Bioburden / Endotoxin Testing (BET)

• Sterility testing.

• Bacterial endotoxin testing.

Water Analysis

• Purified Water (PW) analysis.

• Water for Injection (WFI) analysis.

• Testing and monitoring activities.

Additional Responsibilities:

• Microbial limit testing.

• Media fill studies.

• Documentation and compliance as per Pharmacopoeia requirements and cGMP.

Eligibility & Qualifications

Educational Qualifications

Candidates must possess one of the following qualifications:

• M.Sc. (Master of Science)

• B.Pharm. (Bachelor of Pharmacy)

Experience Requirements

• Required experience: 2–5 years.

• Relevant experience in pharmaceutical Quality Control operations.

• Previous experience in Analytical Method Validation or QC Microbiology is relevant to the respective sections.

• Candidates returning to work after a career break are encouraged to apply.

Required Skills

• Knowledge of analytical method validation and ICH guidelines.

• Hands-on experience with HPLC, GC, and UV instruments.

• Understanding of laboratory testing and analytical data interpretation.

• Knowledge of Environmental Monitoring and microbiological testing.

• Understanding of sterility testing, BET, and water analysis.

• Familiarity with SOPs and laboratory documentation.

• Knowledge of cGMP, GLP, and applicable Pharmacopoeia requirements.

Location & Salary

The recruitment advertisement does not specify the exact work location or salary package. Interested candidates can contact the recruitment team for further information.

Employment Type: Third-party contract payroll for six months, which may be extended.

Payroll Conversion: After completion of the contract, candidates may be considered for company payroll based on their performance and available vacancies.

How to Apply

Interested and eligible candidates can share their updated resumes through the official recruitment email address.

Application Instructions

• Send your updated resume to the recruitment email address.

• Clearly mention your relevant Quality Control experience.

• Highlight your expertise in Analytical Method Validation, QC Microbiology, or general QC activities.

• Mention your previous employment details and career-break duration.

• Ensure your technical experience matches the advertised requirements.

Important Recruitment Details

• Total vacancies: 15.

• Department: Quality Control.

• Qualification: M.Sc. / B.Pharm.

• Experience: 2–5 years.

• Target candidates: Experienced professionals returning after a career break.

• Initial employment arrangement: Third-party contract payroll for six months.

• Contract extension may be considered.

• Company payroll conversion depends on performance and available vacancies.

Frequently Asked Questions

1. Who can apply for Cronus Pharma Quality Control jobs?

Candidates with M.Sc. or B.Pharm. qualifications and 2–5 years of relevant Quality Control experience can apply.

2. Are these vacancies suitable for career-break candidates?

Yes. The recruitment specifically encourages experienced professionals who have taken a career break and want to return to the pharmaceutical industry.

3. How many vacancies are available?

There are 15 vacancies in the Quality Control Department.

4. Which QC specializations are covered?

The openings cover Analytical Method Validation (AMV), QC Microbiology, Environmental Monitoring, BET, Water Analysis, and general QC activities.

5. What is the employment arrangement?

Candidates will initially work on third-party contract payroll for six months. The contract may be extended, and company payroll conversion may be considered based on performance and available vacancies.

6. How can candidates apply?

Candidates can submit their updated resumes to eravi@cronuspharma.com.

Job Summary