Ipca Laboratories Limited, a leading pharmaceutical company, is currently seeking highly motivated and skilled individuals to join our team in Indore. We offer a dynamic and rewarding work environment where you can contribute to the development and manufacturing of high-quality pharmaceutical products. We are committed to fostering a culture of innovation, collaboration, and continuous improvement.
Available Positions at our API (Active Pharmaceutical Ingredient) Plant in Pologround, Indore:
We are actively recruiting for several key positions within our API plant. If you possess the relevant experience and qualifications, we encourage you to apply. Below are the detailed descriptions of each role:
1. Chemist / Sr. Chemist (Quality Assurance)
Qualifications & Experience:
- UG/PG degree in a relevant field (Chemistry, Pharmacy, etc.)
- Minimum 2 years (Chemist) / 4 years (Sr. Chemist) of experience in Quality Assurance within a pharmaceutical manufacturing environment.
Job Description:
This role involves ensuring stringent compliance with regulatory guidelines (WHO, MHRA, USFDA) and company Standard Operating Procedures (SOPs). Key responsibilities include:
- Documentation & Audits: Thorough review of documentation, conducting internal and external audits, and maintaining robust quality management systems (QMS).
- Deviation & CAPA Management: Handling deviations, change controls, and Corrective and Preventive Actions (CAPA).
- Regulatory Compliance: Ensuring ongoing compliance with all relevant regulatory requirements.
2. Chemist / Sr. Chemist / Quality Control Technician (API)
Qualifications & Experience:
- ITI/Diploma/12th/UG/PG in a relevant field (Chemistry, Pharmacy, etc.)
- Minimum 2 years (Technician) / 2 years (Chemist) / 4 years (Sr. Chemist) of experience in API quality control.
Job Description:
This position requires a strong understanding of analytical techniques and cGMP principles. Responsibilities encompass:
- Analytical Testing: Performing analysis and review of in-process and intermediate samples using techniques such as HPLC and GC (with Chromeleon 7.2 software proficiency preferred).
- Instrumentation: Proficient use of equipment including pH meters and Karl Fisher titrators.
- Data Management: Experience with Electronic Data Management Systems (EDMS) and Laboratory Information Management Systems (LIMS).
- Investigation & CAPA: Investigation of Out-of-Specification (OOS) and Out-of-Trend (OOT) results, and subsequent CAPA implementation.
3. Executive/Sr. Executive – Production (Powder Processing Area)
Qualifications & Experience:
- UG/PG degree in a relevant field (Chemistry, Pharmacy, Engineering, etc.)
- Minimum 6 years of experience in production, preferably within the pharmaceutical API industry, with a focus on powder processing.
Job Description:
This role is critical to efficient production operations within our powder processing area. Key responsibilities include:
- Production Planning & Scheduling: Planning and executing packing schedules according to production requirements.
- cGMP & Safety Compliance: Ensuring strict adherence to cGMP guidelines and all safety protocols within the Powder Processing Area (PPA).
- System Operation: Operating the Computerized System for Manufacturing (CSM) for the punching of packing and raw materials.
- Validation & Documentation: Preparing, reviewing, and approving validation activities for products and equipment. Initiating and managing Critical Control Points (CCPs), Temporary Critical Control Points (TCCPs), and preparing Batch Production Records (BPRs), SOPs, and other documentation.
- Deviation Management: Handling deviations, OOS/OOT results, and CAPA management utilizing Trackwise (or similar software).
4. Apprentice Production (BSc./MSc. Chemistry)
Qualifications & Experience:
- BSc./MSc. in Chemistry.
- Prior experience in a production environment is beneficial but not mandatory. This is an excellent opportunity for recent graduates to gain practical experience in a leading pharmaceutical company.
Job Description:
This role involves providing support to the production team. Key responsibilities include:
- Production Support: Assisting in various production activities.
- Process Monitoring: Monitoring production processes and maintaining accurate records.
- Quality Assurance: Supporting the maintenance of quality standards throughout the production process.
Important Considerations:
- Desired Candidate Profile: Candidates with prior experience in WHO, MHRA, and USFDA-approved pharmaceutical API plants are highly preferred.
- Application Process: Interested candidates are requested to submit their resumes to lalit.jangid@ipca.com.
- No Recruitment Fees: Ipca Laboratories does not solicit any payments from prospective candidates and has not authorized any agency or individual to collect recruitment fees. Please be wary of any such requests.
We offer a competitive salary and benefits package, along with excellent opportunities for professional development and career growth. Join our team and be a part of a company that is dedicated to improving global health. We look forward to receiving your application!
