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Be ready on sampling plans, system suitability, OOS handling, change control, and how you would document a failed assay without data integrity risk. Ask which products and methods run at Dahej and how QC partners with QA and production.
Best fit for candidates who want hands-on pharmaceutical QC in an Indian manufacturing environment, care about patents and compliance culture, and are comfortable with shift/plant discipline at a site like Dahej.
As Officer QC at Troikaa’s Dahej setup, expect a regulated pharma quality lab day: sample receipt and identity checks, in-process and finished-product testing to approved methods, instrument readiness, and ALCOA-style documentation. You flag OOS/deviations, support investigations with production, and clear batches only when specs and records align—accuracy and traceability matter more than speed.
Strengthen HPLC/GC basics, wet chemistry, pharmacopoeial monographs (IP/BP/USP as used on site), GMP documentation, and deviation/CAPA literacy. No certification catalog or costs were supplied for this role family.
No. The listing is on-site in India (Dahej referenced in the title), not remote.
Public news frames Troikaa Pharmaceuticals as an Indian generics-focused pharma firm with defended drug IP and active corporate leadership moves.
No verified salary figures or employee-review ratings were provided in the source data for this listing.
Troikaa Group Officer QC DahejIndia Role Overview The role of an Officer Quality Control (QC) at Troikaa Group in Dahej, India, involves performing accurate and reliable analysis of various samples as per method of analysis or protocol. This includes raw materials, finished products, in-process samples, stability samples, validation samples (process and cleaning validation), packaging material, and water sample analysis. Key Responsibilities To perform accurate and reliable analysis of Raw material, Finished Products, In-process samples, stability sample, validation samples (process and cleaning validation), Packaging material and water sample analysis as per method of analysis or protocol. To record the procedure of the test performed and observations contemporaneously. Requirements No specific requirements mentioned in the source text. However, candidates should possess strong analytical skills, attention to detail, and experience in quality control practices within the pharmaceutical or related industries. Why Join Troikaa Group Troikaa Group offers a robust work environment with opportunities for professional growth and development. The company is committed to excellence in quality management and provides a supportive team atmosphere where employees can contribute to the success of the organization. Applying for This Role To apply, complete your application directly on this page, or you'll be redirected to the employer's application platform to finish submitting there. Ensure all details are accurate and comprehensive to increase your chances of being considered for the position.
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