Job Summary: We are seeking a Project Manager with a Mechanical/Electrical Engineering background to oversee the execution of pharmaceutical manufacturing facility projects at our Karakapatla site. The ideal candidate will have 5–10 years of relevant experience in handling process and utility equipment, HVAC systems, and machinery used in semi-finished or finished dosage formulations. Key Responsibilities: Manage end-to-end project execution including installation and commissioning of: (i) Process equipment; (ii) Utility systems; and (iii) HVAC systems Coordinate with consultants, vendors, and cross-functional teams for timely project execution. Review equipment specifications, layouts, piping and ducting drawings, and ensure compliance with pharma standards. Monitor progress on-site, resolve technical issues, and ensure adherence to timelines and budgets. Ensure compliance with cGMP, Revised Schedule M, safety, and environmental standards. Prepare and maintain project documentation, installation qualification records, and handover reports. Qualifications: B.E. / B.Tech in Mechanical/Electrical Engineering 5–10 years of experience in pharmaceutical industry Hands-on experience with formulation machinery (semi-finished / finished) Strong understanding of process flow, utility systems, and cleanroom HVAC Good communication, planning, and vendor management skills Familiarity with regulatory norms and project documentation requirements
Location: Karakapatla, Biotech Park Phase-III, Telangana Department: Projects / Engineering / Validation Reporting To: Senior Management Experience Required: 3–8 years Salary Offered: ₹25,000 to ₹60,000 per month (based on experience and skills) Job Summary: Rashmi Pharma Pvt Ltd is looking for a qualified Project & Validation Engineer with a Mechanical or Electrical Engineering background to manage the execution and validation of key systems at our pharmaceutical manufacturing facility in Karakapatla. The role involves supervising building commissioning, equipment installation, coordinating project execution, and handling qualification/validation activities in compliance with GMP and regulatory norms. Key Responsibilities: Oversee execution and commissioning of mechanical systems including: (i) Process equipment (ii) Utility systems (iii) HVAC systems Execute IQ/OQ/PQ protocols for equipment and systems as per validation plan Review engineering layouts, utility drawings, and equipment documentation Coordinate with vendors, contractors, consultants, and internal departments Ensure compliance with cGMP and Revised Schedule M standards Support preventive and breakdown maintenance planning during and after execution Maintain all validation records, calibration logs, and documentation for audits/inspections Qualifications: Diploma / B.E. / B.Tech in Mechanical or Electrical Engineering 3–8 years of experience in pharmaceutical project execution and equipment validation Working knowledge of process equipment, utilities, HVAC, and cleanroom setups Experience with commissioning, IQ/OQ/PQ, and GMP documentation Awareness of safety, environmental, and maintenance requirements Good coordination, troubleshooting, and communication skills
Location: Rashmi Pharma Pvt Ltd – Cherlapally, Hyderabad Department: Marketing & Business Development Experience Required: 0–2 years Salary Offered: ₹15,000 to ₹20,000 per month Job Summary: We are hiring a Business Development Executive to support marketing and client acquisition efforts for our pharmaceutical manufacturing business. This is a great opportunity for fresh MBA graduates or junior professionals with a flair for communication, market research, and lead generation. Key Responsibilities: Assist in identifying new business opportunities in domestic and international markets Support marketing campaigns, email outreach, and digital presence Coordinate with prospective clients, prepare proposals and company profiles Maintain client database, follow-up on leads, and generate inquiries Assist in creating marketing material and presentations for exhibitions or client meetings Conduct basic market research and competitor benchmarking Qualifications: MBA 0–2 years of experience in pharma marketing or business development Strong communication, presentation, and interpersonal skills Good command over MS Office and email writing Interest in pharmaceutical manufacturing and regulatory context is an advantage
1. QA Executive – Junior Level Experience Required: 2–4 years Salary Offered: ₹20,000 per month Job Summary: We are seeking motivated QA Executives with 2–4 years of experience to support daily quality assurance activities in a GMP-regulated pharmaceutical facility. The role will focus on documentation review, QA activities, and ensuring compliance with regulatory standards. Key Responsibilities: Review batch manufacturing and packing records Line clearance for production and packaging activities Support in handling deviations, change controls, CAPA, and incident reports Ensure compliance with cGMP and Revised Schedule M requirements Participate in in-process checks and quality monitoring Assist in preparation and review of SOPs, logbooks, and other controlled documents Support internal audits and regulatory inspection readiness Qualifications: B.Pharm / M.Pharm / B.Sc / M.Sc (Life Sciences/Chemistry) 2–4 years of experience in QA in a pharmaceutical company Good understanding of cGMP and QMS principles Strong documentation and communication skills 2. QA Executive – Mid-Level Experience Required: 4–8 years Salary Offered: ₹30,000 per month Job Summary: We are looking for experienced QA Executives with 4–8 years of experience to take responsibility for advanced QA functions, including compliance management, documentation oversight, and training of junior QA staff. Key Responsibilities: Review and approval of batch records, logbooks, and controlled documents Oversee line clearance, in-process checks, and QA compliance Lead and investigate deviations, OOS, OOT, change controls, and CAPA Coordinate with production, QC, and engineering for quality compliance Handle document control, issuance, archival, and retrieval systems Support vendor qualification and raw material quality compliance Prepare for and participate in internal audits and regulatory inspections Mentor and guide junior QA team members Qualifications: B.Pharm / M.Pharm / B.Sc / M.Sc (Life Sciences/Chemistry) 4–8 years of QA experience in a pharmaceutical manufacturing unit Strong knowledge of QMS, regulatory compliance, and cGMP Experience in facing audits (USFDA/WHO/other regulatory bodies is an advantage) Excellent analytical, communication, and leadership skills
1. QA Executive Junior Level Experience Required: 24 years Salary Offered: 20,000 per month Job Summary: We are seeking motivated QA Executives with 24 years of experience to support daily quality assurance activities in a GMP-regulated pharmaceutical facility. The role will focus on documentation review, QA activities, and ensuring compliance with regulatory standards. Key Responsibilities: Review batch manufacturing and packing records Line clearance for production and packaging activities Support in handling deviations, change controls, CAPA, and incident reports Ensure compliance with cGMP and Revised Schedule M requirements Participate in in-process checks and quality monitoring Assist in preparation and review of SOPs, logbooks, and other controlled documents Support internal audits and regulatory inspection readiness Qualifications: B.Pharm / M.Pharm / B.Sc / M.Sc (Life Sciences/Chemistry) 24 years of experience in QA in a pharmaceutical company Good understanding of cGMP and QMS principles Strong documentation and communication skills 2. QA Executive Mid-Level Experience Required: 48 years Salary Offered: 30,000 per month Job Summary: We are looking for experienced QA Executives with 48 years of experience to take responsibility for advanced QA functions, including compliance management, documentation oversight, and training of junior QA staff. Key Responsibilities: Review and approval of batch records, logbooks, and controlled documents Oversee line clearance, in-process checks, and QA compliance Lead and investigate deviations, OOS, OOT, change controls, and CAPA Coordinate with production, QC, and engineering for quality compliance Handle document control, issuance, archival, and retrieval systems Support vendor qualification and raw material quality compliance Prepare for and participate in internal audits and regulatory inspections Mentor and guide junior QA team members Qualifications: B.Pharm / M.Pharm / B.Sc / M.Sc (Life Sciences/Chemistry) 48 years of QA experience in a pharmaceutical manufacturing unit Strong knowledge of QMS, regulatory compliance, and cGMP Experience in facing audits (USFDA/WHO/other regulatory bodies is an advantage) Excellent analytical, communication, and leadership skills Show more Show less