Troikaa Pharmaceuticals Hiring Executive – Regulatory Affairs (Compliance) in Ahmedabad
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(Troikaa Pharmaceuticals Hiring Executive) |
Introduction
If you are searching for Regulatory Affairs jobs in Ahmedabad with strong exposure to GMP compliance, QC documentation review, and pharmaceutical data integrity, this opportunity can be highly valuable for your career growth.
Troikaa Pharmaceuticals is currently inviting applications for the position of Executive – Regulatory Affairs (Compliance). This role is ideal for professionals with 1–3 years of experience in Regulatory Affairs, Quality Control (QC), and pharmaceutical compliance functions. Candidates with hands-on experience in COA review, stability data evaluation, audit trail review, and OOS/OOT investigations will find this position aligned with their expertise.
This is a full-time, permanent pharma job offering exposure to finished products, in-process samples, microbiological documentation, and stability studies within a regulated pharmaceutical manufacturing environment.
About The Company – Troikaa Pharmaceuticals Ltd
Troikaa Pharmaceuticals Ltd is a well-established Indian pharmaceutical company known for its innovative drug delivery systems and specialized therapeutic products. The company was founded in 1983 and is headquartered in Ahmedabad, Gujarat, India.
Troikaa operates in multiple therapeutic segments and has built a strong presence in domestic and international markets. The company focuses on research-driven pharmaceutical formulations and compliance with global regulatory standards.
Headquarters: Ahmedabad, Gujarat, India
Founded: 1983
Industry: Pharmaceutical & Biotechnology
Employees: 2,000+ professionals (approx.)
Global Presence: Exports to multiple regulated and semi-regulated markets
Troikaa is recognized for maintaining strict GMP compliance, regulatory documentation standards, and data integrity practices across its manufacturing facilities.
Job Overview Summary
The Executive – Regulatory Affairs (Compliance) role at Troikaa Pharmaceuticals focuses primarily on regulatory compliance oversight and Quality Control (QC) documentation review. The selected candidate will be responsible for verifying finished product documentation, reviewing stability data, evaluating audit trails, and ensuring data integrity compliance in line with GMP and regulatory requirements.
This position plays a critical role in ensuring that laboratory results, COAs, instrument calibration records, and investigation reports meet regulatory standards and internal compliance policies.
Vacancy Details (Official Information)
Role: Executive – Regulatory Affairs (Compliance)
Company: Troikaa Pharmaceuticals Ltd
Location: Ahmedabad, Gujarat
Industry: Biotechnology / Pharmaceutical
Department: Legal & Regulatory
Employment Type: Full-Time, Permanent
Experience Required: 1–3 Years
Application Mode: Online
Responsibility Explanation
The Executive – Regulatory Affairs (Compliance) will perform comprehensive QC documentation review and regulatory verification tasks. The major responsibilities include:
Finished Product Review
The candidate will review and approve Certificates of Analysis (COA), verify electronic data review checklists, and cross-check raw analytical data. They must ensure instrument calibration compliance, verify working and reference standards, and confirm acceptance criteria as per specification and Method of Analysis (MOA).
In-Process Sample Review
This involves reviewing QC results for in-process materials, checking instrument performance, validating calibration records, and ensuring documentation accuracy in accordance with regulatory standards.
Stability Sample Evaluation
The role requires reviewing stability COAs, trending reports, and electronic checklists while ensuring compliance with ICH stability guidelines. The candidate must confirm documentation integrity and regulatory alignment for stability studies.
Microbiological & Trending Documentation
The executive will review microbiological reports, analyze product quality trends, and ensure regulatory documentation approval before final release.
Investigation & Compliance Oversight
The job includes evaluation of OOS (Out of Specification) cases, OOT (Out of Trend) investigations, laboratory deviations, and incident reports. The candidate must conduct audit trail reviews of QC instruments such as HPLC, GC, and UV systems and ensure strong data integrity compliance.
This role requires close attention to detail, analytical thinking, and regulatory awareness.
Eligibility (Official)
Experience: 1–3 years in Regulatory Affairs / QA / QC (Pharmaceutical Industry)
Strong knowledge of:
QC instruments (HPLC, GC, UV, etc.)
Audit trail review
GMP compliance
Regulatory standards
Data integrity practices
COA approval
Laboratory investigations
Finished product and stability documentation
Skills Required
To succeed in this Regulatory Affairs Compliance job, candidates must have:
Strong analytical skills for reviewing QC raw data
Knowledge of GMP and regulatory compliance frameworks
Understanding of ICH stability guidelines
Expertise in audit trail verification and data integrity
Ability to handle OOS and OOT investigations
Good documentation and report writing skills
Familiarity with pharmaceutical manufacturing processes
Cross-functional coordination ability with QA, QC, and production teams
Salary Estimate
Based on the Ahmedabad pharmaceutical job market and compliance-focused roles, the expected salary range for this position is:
₹4,20,000 – ₹6,50,000 per annum
Salary may vary depending on:
Professionals with strong regulatory compliance exposure may negotiate higher packages.
Interview Details (Official)
Interview details are not publicly disclosed. Shortlisted candidates will be contacted by the HR or recruitment team of Troikaa Pharmaceuticals for further selection rounds.
Selection may include:
Required Documents
Candidates should keep the following documents ready:
Updated CV / Resume
Educational qualification certificates
Experience certificates
Latest salary slips (if applicable)
ID proof
Passport-size photographs
Regulatory or audit exposure documents (if available)
How to Apply
Interested candidates can apply through the official job listing portal:
Application Link:
Candidates are advised to apply as early as possible since pharma regulatory roles receive high application volumes.
Frequently Asked Questions (FAQs)
Q1. Is this a QC job ora Regulatory Affairs job?
This is a Regulatory Affairs (Compliance-focused) role that involves QC documentation review and GMP compliance oversight.
Q2. What instruments knowledge is required?
Candidates should have knowledge of HPLC, GC, UV, and other QC analytical instruments.
Q3. Is prior OOS investigation experience mandatory?
Experience in handling OOS/OOT investigations is strongly preferred.
Q4. Is this suitable for freshers?
No, a minimum of 1–3 years of pharmaceutical industry experience is required.
Q5. What is the career growth in this role?
Candidates can grow into Senior Regulatory Executive, Compliance Manager, or Data Integrity Lead roles.
Final Conclusion
The Executive – Regulatory Affairs (Compliance) position at Troikaa Pharmaceuticals offers a strong opportunity for professionals aiming to build a long-term career in pharmaceutical regulatory compliance and data integrity management.
With exposure to COA review, stability evaluation, audit trail verification, and GMP compliance, this role enhances technical expertise in regulatory affairs and QC oversight. Ahmedabad continues to be a major pharma hub, and working with an established company like Troikaa Pharmaceuticals can significantly strengthen your regulatory career profile.
If you have 1–3 years of experience in QC or Regulatory Affairs and want to work in a structured, compliance-driven environment, this is a promising pharma job opportunity.
Note: Pharma Duniya does not charge any money for job information. Candidates are advised to verify details from the official company website.
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