Gracure Pharmaceuticals Limited, a leading Delhi-based pharmaceutical company established in 1992 by Mr. A.S. Bhargava, is committed to providing world-class, affordable medicines. With a strong focus on research and development, Gracure boasts a state-of-the-art, EU-GMP approved manufacturing unit located in Bhiwadi, Rajasthan. We are a forward-thinking organization dedicated to innovation and excellence in the pharmaceutical industry, and we are currently seeking talented and dedicated individuals to join our growing team.
Our Commitment to Quality and Affordability:
At Gracure Pharmaceuticals, our mission extends beyond simply producing medications. We are deeply committed to improving global health access by ensuring high-quality, affordable pharmaceutical products are readily available. This commitment drives our research efforts and shapes our manufacturing processes, ensuring that every product leaving our facility meets the highest standards of efficacy and safety. Our EU-GMP certification reflects this unwavering dedication to quality and compliance. We are proud of our legacy and excited about the future of pharmaceutical innovation, and we invite you to be a part of it.
Current Job Openings in Bhiwadi, Rajasthan:
Gracure Pharmaceuticals is currently hiring for several key positions within our Quality Assurance, Quality Control, and Production departments. These roles offer excellent opportunities for career growth within a dynamic and rewarding environment. Below is a detailed description of each opening:
1. Quality Assurance Department:
- Position: Senior Officer – Qualification / Validation
- Qualification: M.Sc. or B.Sc. in Pharmacy
- Experience: 2 to 4 years of relevant experience in Qualification/Validation within the pharmaceutical industry. Experience with regulatory compliance (e.g., EU GMP, WHO GMP) is highly desirable.
- Responsibilities: This role involves the planning, execution, and documentation of qualification and validation activities for equipment, processes, and systems. You will play a crucial role in ensuring compliance with regulatory guidelines and maintaining the highest standards of quality throughout the manufacturing process. Specific duties include but are not limited to: authoring validation protocols and reports, executing qualification and validation studies, and managing validation documentation.
2. Quality Control Department:
- Position: Executive – Reviewer (Analytical Data Review)
- Qualification: M.Sc. or B.Sc. in Pharmacy
- Experience: 5 to 7 years of relevant experience in analytical data review within the pharmaceutical industry. Experience with chromatographic techniques (HPLC, GC) and spectroscopic methods (UV-Vis, IR) is essential. A strong understanding of regulatory requirements and data integrity principles is crucial.
- Responsibilities: The primary responsibility will be the comprehensive review and approval of analytical data generated during the testing of raw materials, in-process materials, and finished products. This includes evaluating the accuracy, precision, and reliability of the data, ensuring compliance with established SOPs and regulatory guidelines. This role demands a keen eye for detail, strong analytical skills, and an unwavering commitment to data integrity.
- Position: Officer – Microbiology
- Qualification: M.Sc. or B.Sc. in Microbiology or related field.
- Experience: 2 to 3 years of experience in a pharmaceutical or related industry laboratory setting. Experience with microbiological testing methods (e.g., sterility testing, bioburden testing, environmental monitoring) is preferred. Knowledge of GMP principles is essential.
- Responsibilities: This position is responsible for performing microbiological testing of raw materials, in-process materials, and finished products. The role also involves maintaining the cleanliness and sterility of the laboratory environment and ensuring compliance with all relevant regulatory guidelines and internal SOPs.
3. Production Department:
- Position: Operator – Compression/Coating/Liquid Manufacturing
- Qualification: ITI or Diploma in relevant field (e.g., Pharmacy, Chemical Technology).
- Experience: 4 to 7 years of experience in pharmaceutical manufacturing, specifically in compression, coating, or liquid manufacturing operations. Experience with operating and maintaining relevant machinery is essential. Knowledge of GMP is also crucial.
- Responsibilities: This role involves operating and maintaining pharmaceutical manufacturing equipment, ensuring consistent product quality and adhering to strict GMP guidelines. Responsibilities include setting up equipment, monitoring production processes, performing quality checks, and documenting all relevant production parameters.
How to Apply:
Interested and qualified candidates are encouraged to submit their resumes and cover letters to the following email addresses:
- shivani.singh@gracure.com
- aakansha.agarwal@gracure.com
- manisha.birla@gracure.com
Gracure Pharmaceuticals offers a competitive salary and benefits package, along with excellent opportunities for professional development and growth. We are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status. Join our team and contribute to our mission of providing affordable, world-class healthcare solutions.
