Job summary
Job post source
This job is directly from Glenmark Pharmaceuticals
Job overview
The Analytical Quality Assurance Specialist at Glenmark Pharmaceuticals ensures quality and compliance in microbiology and chemistry lab activities, supporting CGMP and data integrity for product testing and batch disposition.
Responsibilities and impact
The role involves monitoring QC processes, troubleshooting quality issues, overseeing sample custody, supporting method validation, documenting activities, identifying training needs, compiling and interpreting QC data, and ensuring compliance with data integrity and cGMP standards.
Experience and skills
Requires a minimum BS/BA in Pharmaceutical Sciences, Chemistry, or Microbiology with 2-3 years of Quality Control experience, strong analytical skills, knowledge of CFRs, communication and interpersonal skills, and problem-solving abilities; quality certifications are a plus.
Company information
Glenmark Pharmaceuticals is a global pharmaceutical company with over 10,000 employees, multiple manufacturing and R&D facilities, and a strong presence in generics and innovative markets, focusing on new chemical and biological entities.
Work environment and culture
The company is in a phase of significant growth, emphasizing teamwork, compliance, and quality in a regulated environment, with a focus on innovation and integrated research.
Company overview
Glenmark Pharmaceuticals is a global pharmaceutical company focused on developing, manufacturing, and marketing generic formulations, specialty products, and active pharmaceutical ingredients (APIs). They generate revenue through the sale of these products across various therapeutic areas, including dermatology, oncology, and respiratory. Founded in 1977 by Gracias Saldanha, the company has grown significantly, establishing a presence in over 80 countries. Key milestones include the launch of innovative drugs and strategic partnerships to enhance their research and development capabilities.
How to land this job
Tailor your resume to highlight your experience in Quality Control and your expertise in microbiology and chemistry laboratory activities, focusing on your knowledge of CGMP and data integrity compliance.
Emphasize your skills in troubleshooting quality issues, method validation, and your ability to review and interpret QC analytical data, including handling OOS results.
Apply through multiple platforms such as Glenmark Pharmaceuticals' corporate career site, LinkedIn, and other job portals where the position is listed to maximize your exposure.
Connect with current employees in Glenmark's Quality Control or Analytical Quality Assurance teams on LinkedIn; start conversations by referencing recent company growth or by asking about their experiences working on CGMP compliance and data integrity practices.
Optimize your resume for ATS by incorporating keywords from the job description like 'CGMP,' 'data integrity,' 'quality control,' 'method validation,' and 'OOS,' ensuring clear, concise formatting and relevant certifications.
Use Jennie Johnson's Power Apply feature to automate your tailored applications across multiple platforms and to identify and connect with relevant Glenmark professionals, saving you time and increasing your chances of success.
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