Pharmaceutical Quality Control Analyst at Puerto Life Sciences Job
Puerto Life Sciences Pvt. Ltd. is an innovative pharmaceutical organization dedicated to ensuring quality, safety, and compliance at every step of manufacturing life-saving solutions. Operating with advanced technical infrastructure, the company fosters a quality-driven and culture-first workspace ecosystem. They are currently looking to onboard experienced quality professionals to join their state-of-the-art facility located in Neemrana, Rajasthan.
Puerto Life Sciences Hiring for Below Positions
1. Department: Quality Control
Designation: Reviewer & GLP
Experience: 6+ Years (6+ years pharmaceutical QC experience with strong Data Review & GLP exposure mandatory)
Qualification: B.Pharm / M.Pharm / M.Sc or relevant qualification
Vacancies: 1 Position
Key Responsibilities:
• Review of analytical raw data; chromatograms; worksheets; calculations; System suitability; analytical reports; data integrity and ALCOA+ compliance; GLP/GMP review; OOS/OOT review; deviation/CAPA review; Stability data review; RM/Finished Product data review; Method validation/verification documentation; Identification of compliance gaps; audit support; Guidance/training to QC personnel; Ensuring laboratory documentation and GLP compliance.
• Technical Requirements: Analytical raw data & chromatogram review; GLP, GMP & Data Integrity (ALCOA+); Method validation / verification; Stability studies (RM & Finished Product); Deviation, CAPA, OOS/OOT handling; Audit preparation & compliance support; Training & mentoring QC team; Strong documentation & reporting skills.
2. Department: Quality Control
Designation: Officer – QC Analytical / HPLC
Experience: 2+ Years (Hands-on pharmaceutical HPLC experience mandatory)
Qualification: B.Pharm / M.Pharm / B.Sc / M.Sc or relevant qualification
Vacancies: 2 Positions
Key Responsibilities:
• HPLC operation and troubleshooting; Assay; Related Substances/Impurity testing; Identification; Sample and standard preparation; Chromatographic data handling & analytical method execution; Method validation/verification support; Stability testing; RM and Finished Product testing; Instrument calibration/qualification; Analytical documentation; OOS/OOT; deviations; CAPA; GMP/GLP; ALCOA+ and data integrity; laboratory SOP compliance.
• Technical Requirements: HPLC operation & troubleshooting; Analytical method execution; Assay & impurity analysis; System suitability & chromatographic data handling; Method validation & verification support; Stability, RM & Finished Product testing; Instrument calibration / qualification; GMP/GLP, ALCOA+ & data integrity; Documentation & compliance (SOP, OOS/OOT, CAPA).
Who Can Apply
- Candidates holding a foundational degree in Pharmacy (B.Pharm/M.Pharm) or Science (B.Sc/M.Sc) matching the role profiles.
- Analytical professionals possessing mandatory, hands-on pharmaceutical experience with HPLC instruments or advanced data review practices.
- Quality experts deeply familiar with global laboratory regulatory standards such as GLP, cGMP, and data integrity (ALCOA+) frameworks.
Career Growth at Puerto Life Sciences Pvt. Ltd.
Building a professional pathway with Puerto Life Sciences offers analytical professionals immense core technical and regulatory development. Operating inside a high-compliance quality control ecosystem builds comprehensive mastery over chromatographic data systems, strict validation protocols, and critical laboratory investigations (OOS/OOT, CAPA). Senior roles get directly involved in internal audit compliance planning, identifying gap closures, and mentoring junior chemists. This robust operational exposure expands your core analytical competence, driving steady upward mobility toward laboratory management or senior quality auditing tracks.
How To Apply Puerto Life Sciences Jobs
Send your CV at email
Work Location: Neemrana, Rajasthan
Email Address: share cv on hr@puerto.in
Frequently Asked Questions
1. What specialized testing workflows are handled by the Officer QC Analytical profile?
The technical vacancy centers extensively on executing liquid chromatography runs, managing standard preparation protocols, conducting assay testing, and tracking impurity/related substance profiles for raw materials and finished products.
2. Is a working familiarity with data integrity frameworks mandatory for the reviewer position?
Yes, the company explicitly mandates that the Reviewer & GLP expert must possess deep operational experience in handling data integrity guidelines, maintaining ALCOA+ compliance metrics, and monitoring analytical raw data or chromatograms.
3. How many active positions are open for hiring across these two listed Quality Control streams?
The recruitment notification outlines a total of three vacancies: one position is available for the senior Reviewer track, while two positions are actively open for the Officer QC Analytical/HPLC stream.
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| Puerto Life Sciences Hiring for QC Analytical Department in Neemrana |
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