Role & responsibilities - Review of Batch Manufacturing Records (BMR), Batch Packaging Records (BPR), and other related documentation. Implementation and monitoring of cGMP compliance across departments. Handling of deviations, CAPA, and change controls. In-process checks and line clearance during production activities. Conduct internal audits and support external regulatory audits (USFDA, EDQM, WHO, etc.). Review and preparation of SOPs and other quality documents. Training of personnel on GMP, GDP, and SOPs. Ensuring data integrity and documentation control. Preferred candidate profile 2 to 5 years of QA experience in An API manufacturing Unit Good communication and documentation Skill
Department: ADL Experience: 5+ Years Qualification: M.Sc. (Analytical Chemistry) Location: Vadodara Job Description: We are looking for an experienced Executive in the Analytical Development Laboratory (ADL) to support R&D activities. The role involves method development, validation, analytical testing, and ensuring regulatory compliance of pharmaceutical products. Key Responsibilities: Develop and validate analytical methods for pharmaceutical substances and products. Conduct analytical testing using HPLC, GC, UV, Mass Spectrometry, etc . Troubleshoot analytical issues and ensure data accuracy and reliability. Adhere to quality control protocols and support audits (Customer/Regulatory). Maintain and calibrate lab instruments and stay updated with new analytical technologies. Follow QMS, SOPs, and safety standards. Skills Required: Strong knowledge of analytical chemistry techniques. Experience in pharmaceutical R&D. Good documentation and communication skills.
Department: EHS Experience: 8+ Years Location: Dahej, Gujarat Qualification: B.Sc/M.Sc in Environment / ADIS / PDIS Job Summary: Looking for an experienced EHS Manager to lead and manage Environment, Health, and Safety (EHS) programs across our operations. The role involves policy development, regulatory compliance, safety management, training, audits, and continuous improvement to ensure a safe, compliant, and sustainable workplace. Key Responsibilities: Develop and implement EHS policies and procedures in line with regulations and industry standards Ensure compliance with OSHA, EPA, and other regulatory bodies Conduct risk assessments, incident investigations, and EHS audits Manage environmental impact, sustainability initiatives, and occupational health programs Deliver safety training and address skill gaps Support cross-functional teams on EHS matters for projects, expansions, and new processes Lead emergency preparedness planning and drills Key Skills: EHS Management, Safety Audits, Regulatory Compliance, Risk Assessment, Environmental Sustainability, Training & Development, Incident Investigation, Emergency Preparedness
Role & responsibilities 1. Quality Assurance (QA) : Assist in reviewing SOPs, BMRs, and BPRs. Support documentation for regulatory compliance (GMP, WHO, USFDA, etc.) Help with internal audits and CAPA implementation. Monitor and maintain quality management systems (QMS). 2. Quality Control (QC) : Perform basic sampling, testing, and analysis under supervision. Operate analytical instruments like HPLC, UV, Dissolution Tester, etc. (training provided). Assist in preparation of reagents, volumetric solutions, and reports. Follow Good Laboratory Practices (GLP) and ensure compliance. 3. Production : Understand the manufacturing process of tablets, capsules, ointments, etc. Learn operations of granulation, compression, coating, and packing machines. Follow safety and GMP norms on the shop floor. Support documentation such as BMRs and logbooks. 4. Research & Development (R&D) : Assist in formulation development and pilot batch trials. Conduct lab experiments under supervision. Maintain experimental records and data sheets. Preferred candidate profile Freshers or candidates with up to 1 year of experience. Basic understanding of pharma manufacturing / QA / QC / R&D / Production. Willingness to work in shifts (if required). Good communication skills and a keen interest in learning.
Job Title : Marketing Executive Department: Marketing Location: Vadodara, Gujarat (Candidate must be willing to relocate) Qualification: Any Graduate / MBA (Preferred) Experience: 2 to 6 years Industry Preference: API Intermediates / Specialty Chemicals Job Summary: We are seeking an experienced and dynamic Marketing Executive to join our team. The ideal candidate will have a strong background in API and specialty chemicals sales, client and product handling, and business development in both domestic and non-regulated international markets. The role involves strategic market development, sales target management, and coordination across internal and external stakeholders to ensure smooth operations and business growth Key Responsibilities: Support existing business by understanding customer requirements and ensuring continuity. Generate new leads and expand the customer base in both domestic and international markets. Build and maintain strong relationships with customers and distribution partners. Ensure timely and effective communication and services to customers and channel partners. Coordinate with internal departments such as Production, Quality, PPIC, etc., for seamless execution. Plan, organize, and manage marketing activities, define priorities, monitor progress, and ensure high-quality performance within the assigned region. Monitor and manage credit control in line with company policies. Adhere to QMS (Quality Management System), SOPs, training modules, and compliance standards for customer and regulatory audits. Key Skills Required: Strong communication and interpersonal skills Proven track record in B2B marketing, especially in Pharma API or Intermediate segment Lead generation and client retention Strategic thinking and team coordination Knowledge of regulatory compliance in Pharma sector
Role & responsibilities 1. Quality Assurance (QA) : Assist in reviewing SOPs, BMRs, and BPRs. Support documentation for regulatory compliance (GMP, WHO, USFDA, etc.) Help with internal audits and CAPA implementation. Monitor and maintain quality management systems (QMS). 2. Quality Control (QC) : Perform basic sampling, testing, and analysis under supervision. Operate analytical instruments like HPLC, UV, Dissolution Tester, etc. (training provided). Assist in preparation of reagents, volumetric solutions, and reports. Follow Good Laboratory Practices (GLP) and ensure compliance. 3. Production : Understand the manufacturing process of tablets, capsules, ointments, etc. Learn operations of granulation, compression, coating, and packing machines. Follow safety and GMP norms on the shop floor. Support documentation such as BMRs and logbooks. 4. Research & Development (R&D) : Assist in formulation development and pilot batch trials. Conduct lab experiments under supervision. Maintain experimental records and data sheets. Preferred candidate profile Freshers or candidates with up to 1 year of experience. Basic understanding of pharma manufacturing / QA / QC / R&D / Production. Willingness to work in shifts (if required). Good communication skills and a keen interest in learning.
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