Process Engineer

3 weeks ago

Canada, CA Dr. Reddy’s Laboratories Ltd Full time
Company Description

Dr. Reddy’s Laboratories Ltd. is a leading multinational pharmaceutical company based across global locations. Each of our 24,000 plus employees comes to work every day for one collective purpose: to accelerate access to affordable and innovative medicines because Good Health Can’t Wait.

We started in 1984 with a modest investment, 20 employees and a bold vision. Today, we have research and development centres, manufacturing facilities or a commercial presence in 66 countries.

For nearly four decades, we have stood for access, affordability and innovation based on the bedrock of deep science, progressive people practices and robust corporate governance. As the pharmaceutical industry evolves and undergoes disruption, we see an opportunity to strengthen our core further and to build the future.

Dr Reddy’s maintains a work environment free from discrimination and is an equal opportunity employer. We treasure every talent and recognize merit and diversity in our organization.


Job Description

Job Summary
We are seeking a dynamic and experienced scientist in Process Engineering in Active Pharmaceutical Ingredient (API) development with proven expertise in scaling up or down technologies to meet production demands. Proficient in Process and Chemical Engineering, adept at troubleshooting complex projects, facilitating technology transfer, and optimizing operations. Demonstrated experience in unit operations including crystallization, filtration, drying, and size reduction, with a strong commitment to quality and regulatory compliance.

Roles & Responsibilities

  • You will be responsible for development and Scale-up of processes for new products, Technology Transfer & Process Validation of the product at plant scale.
  • You will be responsible to work in collaboration with Chemistry team & provide necessary inputs during Design of Experiments (DoE) studies & further process optimization.
  • You will be responsible to develop detailed process understanding & ensure scale-up feasibility using fundamental studies of reaction kinetics, Crystallization, Process Safety, Process analytical technology (PAT).
  • You will be responsible to ensure appropriate facility/equipment/technology mapping at in house/SBP plants.
  • You will be responsible to draft the process for scale up i.e Kilo lab, Critical Process Parameter (CPP) and validation batches in co-ordination with Cross Functional Teams.
  • You will be responsible for Technology Transfer & Scale-up of Active Pharmaceutical Ingredient (API) and engineering optimization studies with minimal guidance.
  • You will be responsible for supporting Drug Master Filing (DMF), address regulatory queries related to process engineering, and demonstrate awareness of process validation, GMP, and GLP aspects to facilitate smooth regulatory filing.
  • Your role will involve staying familiar with the Intellectual property (IP) landscape and relevant literature, participate in industry forums, and disseminate knowledge within PE teams, applying existing knowledge and technologies during development.
  • You will be responsible for proactive planning & timely completion of Process Engineering tasks in alignment with project goals.
  • You will be working collaboratively in cross functional team to drive Process Engineering activities.

Qualifications

Educational qualification: B.Tech in Chemical Engineering

Minimum work experience: 7 years of experience in Process development & scale up of at least 6-8 products.

Skills & attributes:
Technical Skills

  • Have work experience on Process scale up of Active Pharmaceutical Ingredients.
  • Knowledge of core chemical engineering like Heat & mass transfer, reaction engineering, fluid dynamics, separation technologies etc. for process optimization & scale up.
  • Experience in Operational Excellence, Scale-up process.
  • Knowledge of product Development, basic understanding of Chemistry, analytical, RA and IP.
  • Experience in Technology Transfer.
  • Should be well versed with Current Good Manufacturing Practice (CGMP) practices & quality systems in Pharma industry.
  • Familiarity with tools for engineering optimization like Design of Engineering (DoE), dynochem.

Behavioral Skills

  • Excellent communication and interpersonal skills.
  • Strong analytical and problem-solving abilities.
  • Ability to work collaboratively with own team and cross-functional teams.

Additional Information

About the Department

Integrated Product Development Organisation

We integrate our deep science capabilities and cutting-edge technology to develop innovative, accessible and affordable therapies for patients worldwide. We are a science-driven, innovation-focused pharmaceutical company committed to accelerating access to healthcare solutions to patients around the world.


Benefits Offered
At Dr. Reddy’s we actively help to catalyse your career growth and professional development through personalised learning programs. The benefits you will enjoy at Dr. Reddy’s are on par with the best industry standards. They include, among other things, joining & relocation support, family support (Maternity & Paternity benefits), learning and development opportunities, medical coverage for yourself and your family, life coverage for yourself.

Our Work Culture
Ask any employee at Dr. Reddy’s why they come to work every day and they’ll say, because Good Health Can’t Wait. This is our credo as well as the guiding principle behind all our actions. We foster a culture of empathy and dynamism. People are at the core of our journey over the last few decades. #J-18808-Ljbffr

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