Careers

Experience: 15 – 20 Years

Qualification: M Pharm., M.Sc. – Chemistry, B.Sc. – Chemistry, B. Pharm

Brief Job Description:

• Preparation and Submission of the dossiers for domestic (CDSCO) and export market (Asian/African/LATAM/CIS) as per the latest guidelines.
• Preparation and submission of dossiers for EU/South Africa/UK/Brazil and regulated markets is desirable.
• Review of dossiers as per regulatory guidelines to ensure speedy registration and approval.
• Review of source documents and data like BMR, BPR, PV, AMV, Analytical data, stability data, DMF, etc.
• Handling the queries of the respective markets sent by local representatives OR the regulatory body of that country.
• Collection, review and collating the data required for regulatory submissions.
• Maintaining the life cycle of the product.
• Review of Artworks and preparation of Package insert, SmPC, PIL of Generics with respect to Innovator information and guidelines.
• Preparation and review of pharmacovigilance documentation like PSUR, RMP, PMF, etc.
• Responding to requests from Internal teams like marketing Domestic and International marketing. Maintaining tracker sheets for regulatory status (Registration, submission and targeted submission, etc.) updated up to the date.

Experience: 10 – 12 Years

Qualification: Engineering in Chemical and Mechanical

Brief Job Description:

• Must have expertise in machinery and CAPEX procurement, ensuring optimal selection and cost-effectiveness.
• Should be well-versed in costing analysis and URS for equipment purchases.
• Experience in handling procurement processes specific to API and formulation units is essential.
• Should have a strong understanding of vendor assessment, price negotiation, and regulatory compliance in capital purchases.
• Ability to coordinate with cross-functional teams for technical evaluation and budget alignment in procurement decisions.

Experience: 11 – 15 Years

Qualification: M.Sc. + M.B.A. / M.Pharm. + M.B.A./ B.Pharm. + M.B.A

Brief Job Description:

• Overseeing end-to-end project lifecycle, understanding of API mfg. from lab development upto commercial mfg.
• Coordination with various teams to ensure that the defined milestones of API development are achieved as per plan.
• Knowledge of regulatory requirements of US/EU/ROW markets (APIs).
• Awareness of technology transfer process from R&D to plant scale and batches execution at plant.
• Expertise in MS Excel and Power point.
• Should have sound analytical skills, capability of business data interpretation.
• Excellent verbal & written communication skills.
• Communicating project progress & status to stakeholders.
• Experience of budgeting of products.
• Should be able to visit mfg. sites / CMOs as & when required.

Experience: 10 – 15 Years

Qualification: B.Pharm/B.sc., M.Pharm/ Msc/MBA – Marketing

Brief Job Description:

• Researching and analyzing international markets like LATAM, GCC, Iraq to identify opportunities and develop tailored marketing strategies for pharmaceutical formulations.
• Ensuring compliance with local regulations and guidelines in the target countries.
• Managing the lifecycle of pharmaceutical formulations in international markets, including product registration, launch, and ongoing optimization.
• Tracking and analyzing marketing performance, identifying areas for improvement, and implementing corrective actions.

Experience: 10 – 15 Years

Qualification: B.Pharm/B.sc., M.Pharm/ Msc/MBA – Marketing

Brief Job Description:

• Deep understanding of the API market landscape, including regulations, customer base, and competitive dynamics in different international regions like MENA, Turkey.
• Creating and implementing effective international marketing plans, including targeted campaigns, promotions, and digital marketing initiatives.
• Conducting thorough market research to identify opportunities, analyze competitors, and understand customer trends.

Experience: 0 – 2 Years

Qualification: Any Graduate

Brief Job Description:

• Preparing order processing
• Pre-shipment documentation
• Post shipment documentation
• Bank documents — letter of credit , CAD , DA , Advance Payment
• Preparing Proforma invoice
• Certificate of origin / AIFTA
• Insurance certificate
• MIS reports

Experience: 2 Years

Qualification: B.Sc./ M.Sc.

Brief Job Description: 

• Preparation and review of SOP, API development report, SLP, Lab Validation Report, Technology Transfer Report, Analytical Development Report, Process and Analytical Validation Report of R&D.

Experience: 4 Years

Qualification: B.Sc./ M.Sc.

Brief Job Description: 

• Preparation and review of SOP, API development report, SLP, Lab Validation Report, Technology Transfer Report, Analytical Development Report, Process and Analytical Validation Report of R&D, Justification report for Specification & analytical method & impurity profiling etc.
• Good knowledge of various analytical technics and chemical process development. Practical exposure of GLP, Schedule-M of Indian Drugs and cosmetic acts, ICH Guidelines and Safety and other quality guidelines.

Experience: 3 – 6 Years

Qualification: M.Sc./ Ph.D.

Brief Job Description: 

• Method development of new molecules, method validation, Stability related all activities, review for Daily analysis of R & D samples.
• Wet Analysis, and review of R & D samples.
• Daily analysis of R & D samples by HPLC, GC. Calibration of instruments.

Experience: 7 Years

Qualification: M.Sc./ Ph.D.

Brief Job Description: 

• Good experience and qualification on analytical chemistry, NMR, IR, TGA, DSC etc. high-end analytical techniques, data interpretation for RMs, KSMs, impurities, intermediates and APIs.
• Good knowledge in literature search, reference compilation, qualification and ICH and safety etc. guidelines for analytical development.
• Excellent understanding track record of Analytical method development, trouble shootings, impurity profiling and validation calibrations of HPLC, LCMS, IR, Polarimeter, Head space GLC, potentiometer and KF Titrator etc.
• To perform wet analysis/ instrumental analysis for raw materials/in-process/ intermediates, Stability and APIs.
• Preparation of reports, specification, standard test procedure and COAs of raw materials/in-process/ intermediate/ finished products etc.
• LNB writing, data compilation for standards and impurities.
• To adhere to all SOPs and Regulatory guidelines while working in laboratory.
• Use Personal Protective Equipment and practice all safety norms and Good Laboratory Practices.
• Appraise and seek guidance of project leaders to deliver the desired results timely.