Apotex Careers: Executive Job | MSc Chemistry Graduates Apply Now
Are you looking for an Executive job in analytical research or Chemistry jobs in Bangalore with a global pharmaceutical organization? Apotex is hiring for an Executive – Analytical Research & Development (NOS) role in Bangalore, offering a strong opportunity for professionals seeking growth-focused Apotex careers. This role is ideal for candidates experienced in analytical method development, validation, and GMP-regulated environments.
About Apotex Inc.
Apotex is a Canadian-based global health company. We improve everyday access to affordable, innovative medicines and health products for millions of people worldwide, with a broad portfolio of generic, biosimilar, innovative branded pharmaceuticals and consumer health products. Headquartered in Toronto, with regional offices globally, including in the United States, Mexico, and India, we are the largest Canadian-based pharmaceutical company and a health partner of choice for the Americas for pharmaceutical licensing and product acquisitions.
- Job Post: Executive – Analytical Research & Development (NOS)
- Location: Bangalore
- Education: MinimumMSc/BPharm or any equivalent degree.
- Experience: Minimum 3 to 6 years of experience in GMP regulated Pharmaceutical Industry.
Job Summary
Execution of analytical method optimization/development, validation/verification of analytical test methods related to Compendia, In-house developed methods, Site transfer methods, Regulatory queries, Method Life
Cycle Management (MLCM) studies, supplier-driven changes (SDC), and other procedural updates. Preparation of method validation/verification protocols and reports.Job Responsibilities
- Execution of Method optimization/development studies. Method validation/verification of In-house methods, Compendia, SDC, MLCM, and Cleaning Analytical methods by adhering to the regulatory procedures.
- Preparation of Method verification/Method transfer Protocols and reports.
- Execution of Method transfer analysis and reporting.
- Execution of analytical studies related to Regulatory queries/submission requirements.
- Perform all work in accordance with all established regulatory compliance and safety requirements.
- Responsible for the activities in the Quality Control Laboratory, including cGLP, documentation, and implementation of the departmental quality system.
- Works safely and collaborates as a team member to achieve all outcomes.
- Demonstrate behaviours that exhibit our organizational Values: Collaboration, Courage, Perseverance, and Passion.
- Ensure personal adherence with all compliance programs, including the Global Business Ethics and Compliance Program, Global Quality policies and procedures, Safety and Environment policies, and HR policies.
- All other relevant duties as assigned.
Knowledge, Skills, and Abilities
- Command on Microsoft-Office (Word, Excel).
- Knowledge in Method optimization/development activities.
- Best inthe effective completion of work activities to meet the timelines.
- Able to perform multi-parameter analysis on an HPLC instrument.
