Puerto Life Sciences Pvt. Ltd. has announced recruitment for Quality Control (QC) Analytical and Reviewer & GLP positions at its Neemrana, Rajasthan location. The company is looking for qualified candidates with pharmaceutical industry experience in analytical testing, HPLC operations, quality control documentation, data integrity, and GLP/GMP compliance.

Candidates with relevant pharmaceutical qualifications and hands-on laboratory experience can apply for these opportunities by submitting their updated CV to the company’s recruitment email address.

Job Details

• Company Name: Puerto Life Sciences Pvt. Ltd.
• Job Location: Neemrana, Rajasthan
• Department: Quality Control (QC) – Analytical
• Job Type: Company recruitment
• Application Mode: Email
• Official Website: www.puertolifesciences.com
• Email for Application: hr@puerto.in

1. Reviewer & GLP

Number of Vacancies: 1 Position

Experience Required: 6+ Years

Qualification: B.Pharm, M.Pharm, M.Sc., or a relevant qualification.

Mandatory/Preferred Experience: Candidates should have at least six years of pharmaceutical QC experience, with strong data review and GLP exposure.

Key Responsibilities

• Review analytical raw data, chromatograms, worksheets, and calculations.
• Check system suitability, analytical reports, data integrity, and ALCOA+ compliance.
• Review GLP/GMP documentation, OOS/OOT results, deviations, and CAPA records.
• Review stability data and raw material/finished product analytical data.
• Support analytical method validation and verification documentation.
• Identify compliance gaps and support audits.
• Guide and train QC personnel.
• Ensure proper laboratory documentation and GLP compliance.

Technical Requirements

• Analytical raw data and chromatogram review.
• Knowledge of GLP, GMP, and data integrity requirements, including ALCOA+.
• Method validation and verification.
• Stability studies involving raw materials and finished products.
• Handling deviations, CAPA, OOS, and OOT investigations.
• Audit preparation and compliance support.
• Training and mentoring QC team members.
• Strong documentation and reporting skills.

2. Officer – QC Analytical / HPLC

Number of Vacancies: 2 Positions

Experience Required: 2+ Years

Qualification: B.Pharm, M.Pharm, B.Sc., M.Sc., or a relevant qualification.

Mandatory/Preferred Experience: Candidates must have hands-on pharmaceutical HPLC experience.

Key Responsibilities

• Operate and troubleshoot HPLC instruments.
• Perform analytical assays and related substances/impurity testing.
• Prepare samples and standards for analytical testing.
• Handle chromatographic data and execute analytical methods.
• Support analytical method validation and verification.
• Perform stability testing of raw materials and finished products.
• Carry out instrument calibration and qualification activities.
• Maintain analytical documentation and handle OOS/OOT results, deviations, 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 testing and analysis of raw materials and finished products.
• Instrument calibration and qualification.
• GMP/GLP compliance and data integrity.
• Documentation and compliance with SOPs, OOS/OOT procedures, and CAPA requirements.

How to Apply for Puerto Life Sciences Jobs

Interested and eligible candidates should prepare an updated CV highlighting their educational qualifications, relevant pharmaceutical experience, technical skills, and current employment details.

Candidates should also mention their current CTC and notice period while applying.

Send your CV to: hr@puerto.in

Company Website: www.puertolifesciences.com

Applicants should ensure that their qualifications and experience match the requirements of the position before submitting their applications.

5 Technical Frequently Asked Questions (FAQs)

1. What is the role of a Reviewer & GLP professional in pharmaceutical QC?

A Reviewer & GLP professional reviews analytical raw data, chromatograms, calculations, laboratory worksheets, and analytical reports. The role also involves checking data integrity, GLP/GMP compliance, stability data, deviations, CAPA, and OOS/OOT investigations.

2. What is ALCOA+ in pharmaceutical data integrity?

ALCOA+ is a set of principles used to maintain reliable and trustworthy data. ALCOA stands for Attributable, Legible, Contemporaneous, Original, and Accurate. The additional principles include Complete, Consistent, Enduring, and Available.

3. What are the main responsibilities of an HPLC analyst?

An HPLC analyst operates and troubleshoots HPLC instruments, prepares samples and standards, performs assay and impurity testing, checks system suitability, reviews chromatographic results, and maintains analytical records according to approved methods and laboratory SOPs.

4. What are OOS, OOT, and CAPA in pharmaceutical quality control?

OOS means Out of Specification, referring to a result outside established acceptance criteria. OOT means Out of Trend, referring to a result that deviates from an expected trend. CAPA stands for Corrective and Preventive Action, which addresses identified problems and helps prevent their recurrence.

5. What is the importance of method validation and stability testing?

Method validation demonstrates that an analytical procedure is suitable for its intended purpose. Stability testing evaluates how the quality of a drug substance or product changes over time under specified environmental conditions. Both activities support product quality, safety, and regulatory compliance.

Conclusion

Puerto Life Sciences Pvt. Ltd. is inviting applications for Reviewer & GLP and Officer – QC Analytical/HPLC positions at Neemrana, Rajasthan. Candidates with the required pharmaceutical qualifications, analytical skills, and relevant experience can apply by sending their updated CV, current CTC, and notice period to hr@puerto.in.

Apply only if your qualifications and experience meet the requirements of the relevant position.