Abacus Parenteral Drugs Limited

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

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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

Production Officer-Sterilization -01
Reporting to: Team Leader-Sterilization
Job Purpose
To supervise staff, monitor, and coordinate process control measures specifically in the sterilization section so as to ensure efficient output.
JOB ROLES AND EXPECTATIONS:
  1. To ensure continuous quality production by proper supervision of manpower, activities, and status of working machines in the department.
  2. To ensure proper batch-wise production & separation in the pre- & post-sterilisation areas by ensuring proper line clearance and status labeling.
  3. To follow up on the regular maintenance, validation, & calibration of production machinery.
  4. To ensure proper implementation of the cGMP guideline for all staff and support staff.
  5. To ensure adherence to good housekeeping practices and also monitor the cleanliness of equipment.
  6. To regularly plan and avail all materials required for daily operations of the section
  7. To participate in the process of preparing and reviewing SOPs and ensuring its implementation all the time.
  8. To ensure proper filling of information in the corresponding documents like BMR, sterilization logbooks, leak test logbooks, cleaning logbooks, and positive pressure records.
  9. To ensure good understanding & implementation of good documentation practices all the time
  10. To participate in the process of preparing and reviewing SOPs and ensuring its implementation all the time.
  11. To ensure proper filling of information in the corresponding documents like BMR, sterilization logbooks, leak test logbooks, cleaning logbooks, and positive pressure records.
  12. To ensure good understanding & implementation of good documentation practices all the time
  13. To efficiently plan for sterilization of products appropriately in case more than one product is in the process cycle.
  14. To ensure sterilization of clean room and dispensing garments within the clean room area
  15. To ensure minimum wastage of utilities like steam, cooling water, compressed air, electricity, etc.
  16. To conduct trainings for all new recruits in the department.
  17. To regularly conduct routine on-the-job trainings for all temporary employees and also update them on GMP guidelines.
  18. Ensure that any other duty assigned by the supervisor is executed to Management expectations
AUTHORITIES
  • Reviewing the headcount of contract laborers shift wise and authorizing manpower in coordination with team leader.
  • Executing and documenting all sterilization activities online.
  • Training of casual workers before they are involved in production activities.
  • Stoppage of filling machine if any out of specification results observed and confirmed in coordination with section head- filling.
  • Instructing the BFS operators to rectify if any quality defect bottles are produced.
  • Co-ordination with different sections in production for smooth running of activities.
COMPETENCIES
  • Advanced science background
  • CGMP knowledge
  • Product knowledge
  • Budget & planning
Behavioral / Attitude Competencies
  • Analytical skills
  • Effective communication
  • Result oriented
  • Team work
  • Mature & assertive
MINIMUM QUALIFICATIONS / REQUIREMENTS
  • Bachelor’s degree in Industrial Chemistry, Pharmacy, Chemical Engineering, Biological Sciences or any other related field.
  • 2 years’ experience working in relevant / similar company
  • Ability to work with senior people.
  • Excellent report-writing skills
For the Job Application Process

Submission Details:

Attach your CV and Academic Credentials. Late applications will not be considered.

We look forward to receiving your applications.