Gracure Hiring QC Stability/FG Officer
- Company Overview
- Job Role & Responsibilities
- Key Technical Responsibilities
- Instrument Exposure Required
- Eligibility / Qualifications
- Location & Work Details
- Application Process
- Why Consider a QC Stability Role at Gracure?
- Frequently Asked Questions (FAQs)
- 1. Is HPLC experience mandatory?
- 2. Can freshers apply?
- 3. What type of QC experience is preferred?
- 4. Is this a regulatory plant?
- 5. How to apply for the QC Officer role?
- Job Summary Table
B.Pharm, M.Sc QC Officer 4 Vacancies Bhiwadi
B.Pharm, M.Pharm, M.Sc with 1–4 yrs hiring for QC Stability/FG Officer roles in Bhiwadi at Gracure Pharmaceuticals Ltd.
Gracure Pharmaceuticals Ltd. is inviting applications for Quality Control (QC) Stability and Finished Goods (FG) roles at its Bhiwadi, Rajasthan facility. This opportunity is ideal for pharmacy and science graduates with hands-on analytical experience in regulated pharmaceutical manufacturing environments. If you are currently working in QC HPLC analysis, assay testing, dissolution studies, or stability sample evaluation, this role offers structured exposure to GMP-compliant quality control systems in a growing formulation company.
Professionals searching for QC HPLC jobs in Rajasthan, pharmaceutical stability testing careers, or quality control officer vacancies in formulation plants will find this opening aligned with long-term regulatory and analytical career growth.
Company Overview
Gracure Pharmaceuticals Ltd. is a recognized name in the Indian pharmaceutical manufacturing sector, known for its commitment to quality formulations and regulatory compliance. The company operates with a strong focus on finished dosage forms and maintains structured Quality Management Systems (QMS) aligned with cGMP guidelines.
The Bhiwadi manufacturing facility plays a critical role in ensuring finished product quality, stability monitoring, and regulatory documentation support. In today’s pharmaceutical industry, Quality Control departments are central to data integrity, batch release approval, and global regulatory submissions. Gracure’s QC team supports product lifecycle management through analytical method validation, stability testing, and finished goods evaluation.
Working in QC Stability and FG analysis strengthens expertise in pharmaceutical analytical chemistry, regulatory documentation practices, and instrument handling under GLP/GDP environments.
Job Role & Responsibilities
Department: Quality Control – Stability / Finished Goods
Designation: Officer / Senior Officer
Experience Required: 1–4 Years
The selected candidates will be responsible for analytical testing and stability monitoring of finished pharmaceutical products.
Key Technical Responsibilities
- Performing HPLC analysis for Assay and related substances
- Conducting Dissolution testing as per pharmacopeial standards
- Handling UV and IR spectroscopy for routine analysis
- Ensuring System Suitability testing before sample analysis
- Performing Finished Goods (FG) testing and documentation
- Conducting stability sample analysis as per stability protocol
- Reporting and investigating laboratory incidents and deviations
- Maintaining analytical data integrity and documentation compliance
- Supporting audit readiness and regulatory inspections
Instrument Exposure Required
- HPLC systems
- UV Spectrophotometer
- IR Spectroscopy
- Dissolution Apparatus
Candidates must be comfortable with chromatographic data analysis, calibration checks, and laboratory documentation practices aligned with GMP, GLP, and regulatory compliance standards.
QC Stability professionals directly contribute to determining product shelf life, monitoring degradation patterns, and ensuring therapeutic efficacy over time. This role has a direct impact on patient safety and regulatory approvals.
Eligibility / Qualifications
Educational Qualification:
- B.Pharm
- M.Pharm
- M.Sc. (Analytical Chemistry / Chemistry / Pharmaceutical Sciences)
Relevant Courses Include:
Pharmaceutics, Pharmaceutical Analysis, Pharmaceutical Chemistry, Analytical Chemistry, Organic Chemistry, Industrial Pharmacy, Life Sciences.
Experience Requirement:
1 to 4 years of experience in pharmaceutical Quality Control, specifically in stability testing or finished goods analysis within GMP-compliant manufacturing units.
Candidates must have hands-on exposure to HPLC-based assay testing, dissolution studies, and laboratory documentation systems.
Freshers are not eligible for this position.
Location & Work Details
Company: Gracure Pharmaceuticals Ltd.
Location: Bhiwadi, Rajasthan
Bhiwadi is an emerging pharmaceutical manufacturing zone with strong industrial infrastructure and proximity to major logistics networks. Professionals working in this cluster gain exposure to regulated manufacturing practices and stability-driven product development processes.
Salary will be based on experience, technical competency in QC analytical testing, and current industry standards.
Application Process
Interested and eligible candidates can send their updated resume to:
Ensure your CV clearly mentions:
- Total years of QC experience
- Experience in Stability or Finished Goods testing
- Instrument exposure (HPLC, UV, IR, Dissolution)
- Current CTC and notice period
Shortlisted candidates will be contacted by the HR team for technical evaluation and further interview rounds.
Why Consider a QC Stability Role at Gracure?
- Direct involvement in stability program execution
- Exposure to regulatory-compliant analytical testing
- Hands-on HPLC and dissolution testing experience
- Career growth in pharmaceutical quality assurance and regulatory compliance domains
- Strong foundation in analytical method validation and data integrity systems
Quality Control Stability is one of the most technically demanding and high-growth segments within pharmaceutical manufacturing. Professionals with strong analytical expertise often transition into regulatory affairs, quality assurance leadership, or analytical R&D roles over time.
Frequently Asked Questions (FAQs)
1. Is HPLC experience mandatory?
Yes. Hands-on experience in HPLC assay and dissolution testing is essential.
2. Can freshers apply?
No. The role requires 1–4 years of relevant QC experience.
3. What type of QC experience is preferred?
Stability testing, finished goods analysis, assay testing, system suitability checks, and handling laboratory incidents in GMP environments.
4. Is this a regulatory plant?
The facility operates under GMP-compliant systems supporting finished dosage manufacturing and stability programs.
5. How to apply for the QC Officer role?
Send your updated resume to manisha.birla@gracure.com.
Job Summary Table
| Company | Gracure Pharmaceuticals Ltd. |
|---|---|
| Vacancies | QC Officer, QC Senior Officer (Stability / Finished Goods) |
| Required Education | B.Pharm, M.Pharm, M.Sc. (Analytical Chemistry / Pharmaceutical Sciences) |
| Experience | 1–4 Years in QC Stability / FG Analysis |
To apply for this job email your details to manisha.birla@gracure.com
