CAREERS AT NAVESTA

Investing in our talent means investing in the future of Navesta.

At Navesta Pharmaceuticals, we believe that our employees are our most valuable asset. The contribution of each individual is never small as we believe that each person plays a vital role in shaping the future of the company.

Our culture is one which welcomes new ideas and suggestions to improve our processes and investments. Fresh eyes see new opportunities for Navesta, pushing the company to continually improve, change, and innovate.

Navesta doesn't believe in recruiting just the best on paper. We believe in giving chances and opportunities to our employees so that they grow and develop into the best. After all, we believe that each and every person is fully capable of achieving great things if they are given the resources and opportunities to do so.

All current vacancies are located in Sri Lanka.

Responsibilities

  • Handling regulatory audits such as US FDA / EU GMP / PICs.
  • Well conversant knowledge and experience in good laboratory practices. (GLP)
  • Hands on experience in all laboratory instruments such as HPLC, GC, FTIR, UV/ Vis Spectro, TOC Analyser etc. and troubleshooting of the same
  • Knowledge in analytical method validations, instrument validations, analyst qualifications etc.
  • Experience in laboratory information management systems. (LIMS)
  • Experience in sterile manufacturing facility would be preferred.

Personal Profile

  • Bachelor’s degree in Pharmacy / Chemistry / Biochemistry or related discipline.
  • Min 4 -6 years of experience in pharma manufacturing environment with minimum 2 years in managerial exposure of handling a chemical lab.

On offer

  • Attractive remuneration package
  • Career development opportunity in a pioneering venture
  • Excellent working environment

To apply please send your CV, cover letter, and references to [email protected].

Responsibilities

  • Report to Production manager or Head of Production for all matters pertaining to manufacturing & packaging process.
  • Responsible for execution of production schedule at manufacturing & packaging floor.
  • Assist the production & QA Manager in enforcing and ensuring GMP compliance and Good Documentation Practice, on the production floor.
  • Responsible in enforcing and ensuring Safety and Health compliance in the work place.
  • Assist the Production Manager in continuous training of packaging staff.
  • Responsible for review and establishment of the production procedure (SOP).
  • Ensure that all BMR/ BPR and other documents are completed in time immediately upon completion of the batch.
  • Responsible to prepare minute of every production deviation meeting.
  • Coordinate with the continuous improvement team in improvements on the manufacturing & packaging process lines.
  • Coordinate with the maintenance department for trouble-shooting, investigation and preventive maintenance of all manufacturing & packaging equipment.
  • Responsible for participation in any activities pertaining to training, safety, First-aid and fire-fighting organized by the company for the benefits of staff and company.
  • Maintain production areas to the required standard using defined cleaning procedures

Personal Profile

  • Degree in Science (B Pharm, BSc Pharmacy or Chemistry) or equivalent
  • Minimum 1-2 years working experience in Pharmaceutical manufacturing environment. (Fresher may also apply)
  • Good leadership and communication skill with the ability to interact well with all parties concerned.
  • Able to work under pressure to meet tight deadline with minimum supervision.

On offer

  • Attractive remuneration package
  • Career development opportunity in a pioneering venture
  • Excellent working environment

To apply please send your CV, cover letter, and references to [email protected].

Responsibilities

  • Report to Supervisor/Production Executive on all matters pertaining to daily operations in the sterile areas.
  • Adhere strictly to approve company procedures, plant and personal hygiene as well as safety precautions aligned with current Good Manufacturing Practices (cGMP) and Safety Policy.
  • Attend training and practical on-job training that is related to sterile area operations.
  • Record all activities clearly in the respective room or equipment log book.
  • Understand accurately all processes including disinfecting/sanitization and other activities related to sterile area.
  • Ensure machines in aseptic manufacturing areas are operated in full compliance to standard operating procedures.
  • Understand accurately all processes including disinfecting/sanitization and other activities related to sterile area.

Personal Profile

  • Minimum GCE A/L (Science stream)
  • Age between 20 to 30 years old.
  • At least 1 year working experience in food industry, Electronics or pharmaceutical.
  • Preference will be given to those with experience working in Clean Room environment.

On offer

  • Attractive remuneration package
  • Career development opportunity in a pioneering venture
  • Excellent working environment

To apply please send your CV, cover letter, and references to [email protected].

Interested in working for Navesta in our Sri Lanka facilities but don't see any job openings that are in line with what you're looking for? Email us your CV and why you want to work for Navesta and we might just make a position for you. Otherwise, please inquire about any questions you may have.

NAVESTA HR

29/3 Kirimandala Mawatha
Nawala, Rajagiriya
Sri Lanka

[email protected]

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