Kamla Group of Companies Recruitment: Quality Control Jobs in Injectable Manufacturing

Kamla Group of Companies has announced new job openings for experienced pharmaceutical professionals in its Quality Control Department. The company is hiring for multiple positions at its injectable manufacturing facility located in Boisar, Tarapur.

Candidates with qualifications such as B.Pharm, M.Pharm, or M.Sc. in Chemistry/Pharmaceutical Sciences and relevant experience in Quality Control, analytical instruments, analytical method development, and regulatory compliance can apply.

This recruitment drive offers opportunities for experienced candidates seeking pharmaceutical jobs in HPLC analysis, Analytical Development Laboratory (ADL), QC review, and injectable manufacturing.

Kamla Group Recruitment – Job Overview

Particulars Details

Company Name

Kamla Group of Companies

Industry

Pharmaceutical / Injectable Manufacturing

Department

Quality Control

Job Location

Boisar, Tarapur

Positions

HPLC / Analysis Officer, ADL Head, Reviewer

Total Vacancies

8

Experience Required

2 to 12 Years, depending on the position

Qualification

B.Pharm / M.Pharm / M.Sc. (Chemistry / Pharmaceutical Sciences)

Application Mode

Email

Official Website

https://www.kamlagroup.co.in/

Available Positions and Experience Requirements

HPLC / Analysis Officer

Kamla Group is hiring 5 candidates for the position of HPLC / Analysis Officer.

Experience Required: 2–6 Years

Candidates should have hands-on experience in pharmaceutical Quality Control laboratories and the operation of analytical instruments such as HPLC, GC, UV Spectrophotometer, Karl Fischer apparatus, and dissolution testing equipment.

ADL Head

The company has announced 1 vacancy for the ADL Head position.

Experience Required: 10–12 Years

Applicants should possess extensive experience in Analytical Development Laboratories, analytical method development, method validation, method transfer, regulatory compliance, data integrity, and management of analytical laboratory activities.

Reviewer

Kamla Group is recruiting 2 candidates for the Reviewer position.

Experience Required: 8–12 Years

Candidates should have strong knowledge of Quality Control documentation, analytical data review, chromatographic data assessment, Good Manufacturing Practices (GMP), data integrity principles, and regulatory requirements.

Educational Qualification

Candidates applying for Kamla Group Quality Control jobs should possess one of the following educational qualifications:

B.Pharm (Bachelor of Pharmacy)

M.Pharm (Master of Pharmacy)

M.Sc. in Chemistry

M.Sc. in Pharmaceutical Sciences

Applicants should also have knowledge of cGMP, WHO-GMP, regulatory requirements, laboratory documentation, data integrity, and analytical instruments.

Key Skills and Requirements

Candidates should have relevant experience working in an injectable manufacturing facility.

Applicants are expected to have hands-on knowledge of analytical instruments, including HPLC, GC, UV Spectrophotometer, Karl Fischer titration equipment, and Dissolution Apparatus.

Knowledge of analytical method development, analytical method validation, and method transfer is important, particularly for senior-level positions.

Candidates should understand regulatory compliance requirements and data integrity principles such as ALCOA+.

Strong documentation, communication, teamwork, and time-management skills are also required.

Job Location

Boisar, Tarapur

Candidates should carefully consider the job location before submitting their applications.

How to Apply for Kamla Group Recruitment

Interested and eligible candidates can send their updated CV/resume to the email address mentioned below.

Email: anjali.yadav@kamlagroup.co.in

Contact Numbers: 8956480712 / 7972964497

Official Website: https://www.kamlagroup.co.in/

While sending your application, use a clear email subject line such as:

Application for HPLC Analysis Officer – Your Name – Total Experience

or

Application for ADL Head / Reviewer – Your Name

Candidates should mention their current organization, total experience, current CTC, expected CTC, notice period, and current location in the application email where appropriate.

Important Note for Candidates

Candidates should verify the job information and application details before applying. Never pay money to any individual or agency in exchange for a job offer. Recruitment processes and requirements may be changed, closed, or updated by the employer at its discretion.

Technical FAQs for Kamla Group Quality Control Jobs

1. What is the principle of HPLC, and why is it widely used in pharmaceutical Quality Control?

Answer: High-Performance Liquid Chromatography (HPLC) separates the components of a mixture based on their differential interactions with the stationary phase and mobile phase. In pharmaceutical Quality Control, HPLC is commonly used for assay determination, impurity profiling, content uniformity, dissolution sample analysis, stability studies, and related substances testing because of its high accuracy, sensitivity, and reproducibility.

2. What is analytical method validation, and which parameters are evaluated?

Answer: Analytical method validation demonstrates that an analytical procedure is suitable for its intended purpose. Depending on the method and applicable regulatory guidance, validation parameters may include accuracy, precision, specificity, linearity, range, detection limit, quantitation limit, robustness, and system suitability.

3. What is the difference between analytical method validation and method transfer?

Answer: Analytical method validation establishes documented evidence that a method performs reliably for its intended analytical purpose. Analytical method transfer demonstrates that the receiving laboratory can successfully perform an established analytical procedure according to predefined acceptance criteria.

4. What is ALCOA+ in pharmaceutical data integrity?

Answer: ALCOA refers to data being Attributable, Legible, Contemporaneous, Original, and Accurate. ALCOA+ expands these principles to include Complete, Consistent, Enduring, and Available. These principles help ensure that laboratory and manufacturing data remain reliable, traceable, and compliant throughout the data lifecycle.

5. What should a QC reviewer check while reviewing HPLC analytical data?

Answer: A QC reviewer should check sample preparation and calculations, instrument calibration and qualification status, chromatographic sequence, system suitability results, integration parameters, audit trails where applicable, deviations, out-of-specification or atypical results, compliance with approved test procedures, and the completeness and accuracy of laboratory documentation.

Conclusion

Kamla Group of Companies Recruitment provides career opportunities for experienced pharmaceutical professionals seeking roles in the Quality Control Department of an injectable manufacturing facility. With openings for HPLC / Analysis Officers, ADL Head, and Reviewers, candidates with relevant educational qualifications, analytical laboratory experience, regulatory knowledge, and strong data integrity practices can apply by sending their updated resumes to the official recruitment email address provided in the job advertisement.