Puerto Life Sciences Pvt. Ltd. is hiring experienced professionals for Quality Control (QC) Analytical positions at its facility in Neemrana, Rajasthan.
The recruitment drive includes openings for Reviewer & GLP and Officer – QC Analytical / HPLC.
Candidates with B.Pharm, M.Pharm, B.Sc., M.Sc., or other relevant qualifications can apply according to the requirements of each position.
The company is offering one vacancy for Reviewer & GLP and two vacancies for Officer – QC Analytical / HPLC, with relevant pharmaceutical QC and analytical experience required.
Company Overview
Puerto Life Sciences Pvt. Ltd. is recruiting professionals for its Quality Control Analytical department. The available positions focus on analytical data review, laboratory compliance, HPLC testing, and quality documentation.
The recruitment notice lists three vacancies across two roles. Candidates should review the qualifications, experience requirements, and technical skills before applying.
Puerto Life Sciences Reviewer & GLP Jobs in Neemrana
Position Details
- Department: Quality Control – Analytical
- Designation: Reviewer & GLP
- Vacancies: 1
- Qualification: B.Pharm / M.Pharm / M.Sc. or relevant qualification
- Experience: 6+ years
- Mandatory / Preferred Experience: Six or more years of pharmaceutical QC experience, with strong data review and GLP exposure.
Job Role & Responsibilities
- Review analytical raw data, chromatograms, worksheets, and calculations.
- Check system suitability, analytical reports, and data integrity.
- Review GLP/GMP documentation, OOS/OOT records, deviations, and CAPA.
- Review stability data for raw materials and finished products.
- Review method validation and verification documentation.
- Identify compliance gaps and support audits.
- Guide and train QC personnel.
- Ensure laboratory documentation and GLP compliance.
Technical Requirements
- Analytical raw data and chromatogram review.
- GLP, GMP, and data integrity knowledge, including ALCOA+.
- Method validation and verification.
- Stability studies involving raw materials and finished products.
- Deviation handling and CAPA/OOS/OOT management.
- Audit preparation and compliance support.
- Training and mentoring of QC team members.
- Strong documentation and reporting skills.
Puerto Life Sciences Officer – QC Analytical / HPLC Jobs in Neemrana
Position Details
- Department: Quality Control – Analytical
- Designation: Officer – QC Analytical / HPLC
- Vacancies: 2
- Qualification: B.Pharm / M.Pharm / B.Sc. / M.Sc. or relevant qualification
- Experience: 2+ years
- Mandatory Experience: Hands-on pharmaceutical HPLC experience.
Job Role & Responsibilities
- Operate and troubleshoot HPLC systems.
- Perform assay, related substances, and impurity testing.
- Conduct identification testing and sample and standard preparation.
- Handle chromatographic data and analytical method execution.
- Support method validation and verification.
- Perform stability testing of raw materials and finished products.
- Calibrate and qualify laboratory instruments.
- Maintain analytical documentation, including OOS/OOT records and CAPA.
- Follow GMP/GLP, ALCOA+, data integrity, and laboratory SOP requirements.
Technical Requirements
- HPLC operation and troubleshooting.
- Analytical method execution.
- Assay and impurity analysis.
- System suitability and chromatographic data handling.
- Method validation and verification support.
- Stability, raw material, and finished product testing.
- Instrument calibration and qualification.
- GMP/GLP compliance, ALCOA+, and data integrity.
- Documentation and compliance, including SOPs, OOS/OOT, and CAPA.
Job Role & Responsibilities
Quality Control Analytical Department
The QC Analytical department handles analytical testing, laboratory data review, documentation, and compliance activities. Candidates should have relevant pharmaceutical quality control experience and knowledge of applicable laboratory procedures.
Reviewer & GLP Role
The Reviewer & GLP position involves reviewing analytical data, chromatograms, laboratory documentation, stability data, and method validation records. The role also includes compliance support, audit preparation, and guidance for QC personnel.
QC Analytical / HPLC Role
The Officer – QC Analytical / HPLC position involves operating HPLC systems, performing analytical testing, handling chromatographic data, supporting method validation, and maintaining laboratory documentation.
Eligibility & Qualifications
Candidates should possess the relevant educational qualifications and professional experience specified for their preferred position.
Educational Qualifications
- B.Pharm
- M.Pharm
- B.Sc.
- M.Sc.
- Other relevant qualifications, as applicable to the position.
Experience Requirements
- Reviewer & GLP: 6+ years of pharmaceutical QC experience, with strong data review and GLP exposure.
- Officer – QC Analytical / HPLC: 2+ years of experience, with mandatory hands-on pharmaceutical HPLC experience.
Additional Skills
- Knowledge of pharmaceutical quality control procedures.
- Understanding of GMP, GLP, and ALCOA+ data integrity principles.
- Experience with analytical documentation and laboratory compliance.
- Knowledge of method validation, stability studies, and deviation management, where applicable.
- Familiarity with OOS/OOT investigations and CAPA documentation.
Location & Salary
Job Location
Puerto Life Sciences Pvt. Ltd.
Neemrana, Rajasthan, India.
Salary Details
The recruitment poster does not specify salary figures. Compensation may vary according to the position, qualifications, and relevant experience.
How to Apply
Interested candidates can submit their updated CV to the recruitment email address provided by Puerto Life Sciences.
Email: hr@puerto.in
Company Website: www.puertolifesciences.com
Application Instructions
- Mention the position you are applying for: Reviewer & GLP or Officer – QC Analytical / HPLC.
- Highlight relevant pharmaceutical QC experience.
- For the HPLC position, clearly mention hands-on HPLC experience.
- Include relevant analytical testing, data review, GLP/GMP, and documentation skills in your CV.
- Mention your current CTC and notice period, as requested in the recruitment poster.
Important Instructions
- The Reviewer & GLP position has one vacancy and requires 6+ years of experience.
- The Officer – QC Analytical / HPLC position has two vacancies and requires 2+ years of experience.
- Hands-on pharmaceutical HPLC experience is mandatory for the Officer – QC Analytical / HPLC position.
- Candidates should ensure that their qualifications and experience match the selected role.
Frequently Asked Questions
1. Which company is hiring for QC Analytical positions?
Puerto Life Sciences Pvt. Ltd. is recruiting for QC Analytical positions at its facility in Neemrana, Rajasthan.
2. Which positions are available?
The openings are for Reviewer & GLP, with one vacancy, and Officer – QC Analytical / HPLC, with two vacancies.
3. Which qualifications are accepted?
The recruitment poster lists B.Pharm, M.Pharm, B.Sc., M.Sc., or other relevant qualifications, depending on the position.
4. How much experience is required?
Reviewer & GLP requires 6+ years of pharmaceutical QC experience. Officer – QC Analytical / HPLC requires 2+ years of experience and hands-on pharmaceutical HPLC experience.
5. What salary is offered?
The recruitment poster does not specify salary details. Candidates should confirm compensation during the recruitment process.
6. How can candidates apply?
Candidates can send their updated CV to hr@puerto.in.
Job Summary
| Category | Details |
|---|---|
| Company | Puerto Life Sciences Pvt. Ltd. |
| Vacancies | Reviewer & GLP; Officer – QC Analytical / HPLC |
| Required Education | B.Pharm, M.Pharm, B.Sc., M.Sc., or relevant qualification |
| Experience | Reviewer & GLP: 6+ years; Officer – QC Analytical / HPLC: 2+ years |
| Location | Neemrana, Rajasthan |