Cronus Pharma is hiring for its Quality Control (QC) Department, with 15 vacancies across analytical method validation, general quality control, and microbiology. The recruitment is open to M.Sc. and B.Pharm candidates with 2–5 years of QC experience, particularly professionals on a career break who are ready to return to the workforce.
Job Details
| Particulars | Details |
|---|---|
| Company | Cronus Pharma |
| Department | Quality Control (QC) |
| Total Vacancies | 15 |
| Qualification | M.Sc., B.Pharm |
| Required Experience | 2–5 years |
| Eligible Candidates | QC professionals on a career break who are ready to rejoin |
| Application Mode | |
| Email Address | eravi@cronuspharma.com |
| Employment Opportunity | Potential conversion to a company role after contract completion, based on performance and vacancies |
Positions and QC Sections
1. QC – Analytical Method Validation (AMV)
The AMV section involves analytical method validation, documentation, instrument handling, and routine analytical support.
Key Responsibilities:
- Perform method validation in accordance with ICH guidelines.
- Prepare and review validation protocols and reports.
- Handle analytical instruments such as HPLC, GC, and UV.
- Conduct data analysis and interpretation.
- Prepare SOPs and related documentation.
- Provide routine analytical support as per section allocation.
2. Other QC Sections – General Quality Control
Key Responsibilities:
- Perform raw material testing.
- Conduct finished product testing.
- Support stability studies.
- Provide analytical support during regulatory audits.
- Maintain documentation and records.
- Ensure compliance with cGMP and GLP requirements.
3. QC – Microbiology
The microbiology section includes Environmental Monitoring (EM), Bioburden/Endotoxin Testing (BET), and Water Analysis.
Environmental Monitoring (EM):
- Conduct air, surface, and personnel monitoring.
- Perform trend analysis and reporting.
Bioburden/Endotoxin Testing (BET):
- Perform sterility testing.
- Conduct endotoxin testing using the LAL method.
Water Analysis:
- Test and monitor Purified Water (PW) and Water for Injection (WFI).
- Perform microbial limit testing.
- Support media fill studies.
- Maintain documentation and compliance with pharmacopoeial and cGMP requirements.
Eligibility and Qualifications
Candidates applying for Cronus Pharma QC jobs must meet the following criteria:
- Educational Qualification: M.Sc. or B.Pharm.
- Experience: 2–5 years of Quality Control experience.
- Career Break: Professionals currently on a career break and ready to rejoin the workforce are encouraged to apply.
- Technical Background: Relevant QC experience aligned with analytical method validation, general QC, or microbiology requirements.
Required Skills and Technical Knowledge
Depending on the QC section, relevant technical knowledge includes:
- Analytical method validation and ICH guidelines.
- Handling HPLC, GC, and UV instruments.
- Validation protocols, reports, and SOP documentation.
- Raw material and finished product testing.
- Stability studies and regulatory audit support.
- Environmental monitoring and trend analysis.
- Sterility testing and LAL endotoxin testing.
- Purified Water and Water for Injection analysis.
- Microbial limit testing, media fill studies, cGMP, and GLP compliance.
How to Apply for Cronus Pharma QC Recruitment
Eligible candidates should email their updated resume to the following address:
Email: eravi@cronuspharma.com