Quality Assurance Officer – Abbott


Since 1910, Abbott has been dedicated to helping people in India live healthier lives through a diverse range of science-based nutritional products, diagnostic tools, branded generic pharmaceuticals, and diabetes and vascular devices.

Headquartered in Mumbai, Abbott India Limited, a publicly listed company and a subsidiary of Abbott Laboratories, takes pride in offering high-quality trusted medicines in multiple therapeutic categories such as women’s health, gastroenterology, cardiology, metabolic disorders and primary care.

One of India’s fastest-growing pharmaceutical companies, Abbott India Limited is part of Abbott’s global pharmaceutical business in India.

We have expertise across product development, manufacturing, sales and customer service and are dedicated to providing high-quality, reliable products with the expert clinical support our customers need.

Abbott India Limited believes in providing quality healthcare through a mix of global and local products for people in India. Our in-house development and medical teams undertake product and clinical development tailored to the unique needs of the Indian market. Our employees work to produce high-quality, high-volume formulations using cost efficient processes. And, our trained personnel are dedicated to ensuring compliance with international quality standards.


Analysis and Review of IP, FP.


  • On time analysis & release of raw material, in process samples & finished product samples.
  • Ontime Training completion within predefined timelines.
  • Laboratory standards, chemicals preparation, standardization & stock management.
  • Lab SOP & work instruction review & revision.
  • Lab Equipment calibration & preventive maintenance.
  • Adhere Abbott safety & quality requirements.
  • Lab area 6S, GMP, GLP management• Laboratory consumables stock management etc.

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  • B.Sc/M.Sc. / M.Tech in Chemistry (Dairy / Food) with minimum 1-3 years of relavent experience.
  • Thorough knowledge of general Analytical analysis procedures.
  • Understanding of Quality systems ISO 9001/ISO 22000/ FSSA /BIS / Risk Assessment and exposure for HAZOP/HACCP analysis.

BACKGROUND: 1-3 years of experience in a reputed food processing / pharmaceutical industry. (Out of which at 1-2 years as QA Executive Analytical Laboratory in similar industry is preferrable)

  • Being proficient in Gujarati is advantage.
  • Ability to accurately interpret the quality related problems of ingredients, finished food & process checks in food processing.
  • Ability to conduct trouble shooting studies to resolve the problems encountered w r t Quality and Hygiene/GMP at Site.
  • Ability to handle all type of Analytical quality issues in the entire supply chain.
  • Hands on experience of analytical lab equipment operations. (i.e. HPLC, ICPMS, LCMS, Protein Analyser, Fat Analyser, moisture analyser etc.)




Ensure right product quality is released to market by carrying out  the timely and accurate analysis of all the finished products in shifts and timely feedback (signals) to Production on quality trends.

  • Responsible for analysis of in-process liquid samples & finished product powder for macro & micro nutrients (protein, fat, moisture, minerals, vitamins etc).
  • Responsible for operation, calibration & maintenance of equipments as per Abbott & OEM Guidelines.
  • To maintain and upkeep the hygiene, cleanliness and work place safety in the lab.
  • Laboratory SOP & Work instruction review & revision inline with global AN/AQ policies & other relevent governing documents (Including regulatory documents FSSAI,BIS etc.).
  • Participate in product sensory analysis.
  • Implementing, maintaining and improving the established analytical lab and in-process testing process and methods.
  • Monitoring, analyzing and communicating site analytical testing results and productivity, and recommending improvement actions.
  • Participating in site internal audits, Providing professional analytical inputs when any needs from other functions, such as supplier evaluation, validation etc.
  • Managing the analytical lab to assure the EHS compliance, Maintain safe and healthy working conditions for employees under his/her supervision.
  • Attend EHS training assigned and ensure that employees who report to him/her attend required training.
  • Ensure to submit Near Miss reports and other opportunities to improve the EHS Program. Adhere use of PPE in accordance with all safety rules and practices.
  • Analytical laboratory equipment maintainence and calibration, Analytical reagents, reference standards and glassware procurement and management.
  • Carryout cleaning validations for new equipment and existing equipment and suggest effective methods of cleaning for ensuring right product quality, Support the validation activities in terms of design, operational and performance qualification of the process and laboratory equipment


•To support in preparation of Opex & Capex budgets for Analytical function, making the proposal and  close follow-up of execution of new and exisitng projects.


•Building and Managing analytical team to assure the capability and stability,  Recommending the structure, roles and responsibilities for the analytical  lab,  Recruinting talents,  Behaving as an example of the analytical staff, Communicating the site goals/metrics, Performing people manager’s activities on setting goals, coaching and reviewing performance, Supporting functional head on building the function structure to achive the function goals.

  • Promote and support team development activities.
  • Impart training to workmen and staff on GMP requirements and QMS requirements.


  • Implement BIS method where applicable.
  • Preparation of SOPs and work instructions whenever new QMS requirements become effective. Carryout gap analysis of new QMS documents and take actions for their implementation.
  • Ensure that the laboratory operates with calibrated equipment and carryout performance qualifications of the equipment, as per the frequencies.
  • Meet the requirements of EHS/GPCP in handling of Biohazardous waste generated at the laboratory
  • To support the Analytical compliance of ISO 17025, ISO 9001, ISO 22000 and HACCP, BIS, FSSAI requirements in and around the manufacturing facility by regular interaction with all stakeholders.
  • Ensure all the requirements as per the ISO 9000:2000 / QMS elements and implementing the updated requirements in Quality Assurance to improve & sustain the systems.

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