Abacus Parenteral Drugs Limited

Menu

Careers

Overview

Join the APDL family  and impact more than just your career. Whether you are searching for your first job or the next step in your career, you are invited to join a worldwide ambition to be the chosen manufacturer of pharmaceutical Products . At APDL, we foster an equal opportunity environment for all of our employees and encourage all eligible individuals to apply for any open positions.

Our Culture

At Abacus Parenteral Drugs Limited (APDL), our cultural characteristics are an essential part of who we are and how we live. At the core of all we do is the APDL Way. Every one of our workers exemplifies the following principles in their day-to-day work:.

Career Opportunities

.

Benefits

We have put up a solid employee value proposition so that you not only give us your all, but we also give you a strong promise to do the same. We have devised a variety of perks to help you and your family enjoy life to the fullest while serving with the APDL family. Family to fully enjoy life. Withus life always gets better.....

Application process Tips

Select an opportunity: Find a place that fits your profile. View open positions and requirements.
Job Requirements: Understand key responsibilities and areas of expertise required. Consider required work experience, education and qualifications.
Cultural Appropriateness: Learn about the company’s culture, mission, vision and values. Make sure these align with your own needs and values.

Interview Tips

Be Yourself: Recognize your passions, skills, experience, and learning.
Research the Company: Thoroughly investigate the company's business, performance, and working style.
Leverage Your Experience: Prepare relevant questions to ask during the interview.
Be Prepared: Understand the position’s requirements and match your skills and experiences to them

Job Opportunities

Quality Control Analyst - Chemistry

JOB IDENTIFICATION

Department: Quality Control

Reporting to: QC Team Leader

POSITION PURPOSE:

To ensure effective and timely testing of all samples in accordance with requirements and in line with fast and changing quality procedures and principles, prioritization of testing, management of resources, and effective communication at all levels.

  1. To adhere to procedures on cGMP and GLP and relevant ISO procedures that guide all quality control processes.
  2. Conduct quality control tests on water, bulk, raw materials stability samples and finished products.
  3. Document and prepare reports for all Quality control activities performed online; calibrate and Maintain laboratory equipment as per the plan
  4. Interpret all documents in QC process, revise and prepare SOPs and COAs as required in the process
  5. Work effectively with other analysts and team leaders to achieve shared goals and meet timelines for batch processing and filling processes.
  6. Participate in OOS, OOT investigation, deviation handling, change control, CAPA closure, and quality risk management for continuous improvement.
  7. Participate in training, knowledge sharing, and transfer activities for efficiency and competency.
  8. Sampling of RM, FP, preparation of reagent & standardization of reagent as per production plan requirements.
  9. Calibration of new glassware.
  10. Working standard preparation.
  11. Handling & maintaining Reference standard as per reference standard SOPs, preparation of working standard.
  12. Perform analysis for intermediate sample, finished product sample, Raw material sample, stability sample, PPM & SPM as per work plan ensure it will meet with specification
  13. Perform method validation & verification for the new method and establish specifications.
  14. Proper use and handling of chemicals and consumables
  15. Perform online reporting & keep records.
  16. Timely and proper Communication with staff at all levels while making critical escalation on time
  17. Use provided personal protective gear appropriately.
  18. Proper communication and handling and investigation of all incidences, near misses and accidents

AUTHORITIES

  • Chemical analysis of all types of samples.
  • Signing work reports.
  • Request reports & logbooks.
  • Release intermediate samples.
  • Request for chemical & glassware

COMPETENCIES

  1. Excellent report writing skills, analytical skills, communication skills, and interpersonal skills.
  2. Computer skills, able to learn and adapt to change.
  3. Innovative / creative skills and problem solving

MINIMUM QUALIFICATIONS / REQUIREMENTS

  1. BSc Chemistry or equivalent Degree
  2. Experience in pharmaceutical/healthcare industry is an advantage

Application process

Kindly submit your Cv and Academic credentials to apdlug.careers@abacuspharma.com before 24th. January 2025 by 5 Pm