Vacancy Announcement TIME Pharmaceutical 

Vacancy Announcement TIME Pharmaceutical 

Vacancy Announcement TIME Pharmaceutical 

TIME Pharmaceutical  is committed to deliver the best of health care services to every individual for a healthier life which has constantly inspired our people to innovate, excel and set new benchmarks. Marching towards excellence, TIME Pharmaceutical with a world-class manufacturing unit produces therapeutic products portfolio that matches international class and offers the best services which is required in the better health care delivery system.

TIME Pharmaceutical focused towards extending our product portfolio, improving the existing products as well as drug delivery systems and expanding product applications with an appropriate update of latest technologies and upgrading facilities by technical collaboration with the MNC.

TIME Pharmaceutical Announces Vacancy for following post:

1. QUALITY ASSURANCE OFFICER 

Job Description: 

Job Title: Quality Assurance Officer

Department: Quality Assurance

Reports to: Head of Department Quality Assurance

Status: Regular

Duty Station: Factory Office, Gaindakot, Nawalparasi

Authority: Exercises authorities as delegated by seniors that are related to QA Department within the norms and policies of the company

Functional Relationship: Work with/for the Factory pertaining to QA Department

Accountable to: Customers, Time Pharma Employees, Board of Directors and Shareholders of the company

Job Purpose

The QA Officer will work directly in support of the HOD QA on all activities related to Quality Assurance Department.

The QA Officer is a member of the Time Pharmaceuticals (P.) Ltd. team assisting for the improved and sustained performance and productivity of the company.  The Officer must be able to demonstrate that the QA Department is a worthwhile component to contribute to achieve the Corporate Mission of the Company.

Essential Job Functions

 The QA Officer shall perform the following job:

• • To achieve quality goals with contribution in continual improvement.
  • To perform routine jobs related to issue of Batch Manufacturing record (BMR), Formats, Log sheets, line clearance, crosscheck of BMR, Analytical worksheets and Finished products to ensure quality in product.
  • To participate in the internal audit as auditee as per schedule and responsible for the follow up for the timely closure of the non conformances.
  • To provide On-job and GMP trainings to employees, induction training to new employees and in plant training to trainees and assess their understanding of training and complete re-training wherever necessary.
  • To actively participate in periodic QA activities such as calibrations, Air Handling Unit Validation.
  • To actively participate in the implementation and documentation of deviation, change control, CAPA, Incidents, OOS, Customer complaints and nonconformities.
  • To initiate preparations of documents such as MFRs, BMRs, Validations and Qualifications along with forms, templates and protocol and assist Head of Quality for their approvals.
  • To prepare Weekly status report (QA), Monthly reports and to participate in evaluation of Key Performance Indicators of GMPs, Annual Product Review.
  • To take periodic rounds in the Warehouse, Production, QC Lab, Maintenance and factory premises to verify that logs, BMRs and other data entries are concurrent with the process, operational data within the specifications and also GMPs/ GLPs/ GWPs and GHPs are followed.
  • To perform online entry of DAMS-DDA as a part of regulatory requirement for registration of drug products.
  • To support Risk Analysis projects through active participation.
  • To evaluate affectivity of current SOPs and update them as necessary.
  • To supervise and provide technical guidance to the subordinates of QA department.
  • To assist Head of Quality Assurance analyze data to identify areas for improvement in the quality system.

Compliance to policies, rules/regulations and guidelines

Adheres relevant policies, rules, regulations and guidelines of company (Personnel, Financial, Administrative policies, Security Guideline, Sexual Harassment Policy; Code of Conduct against Corruption etc.).

Required Competencies:

• • Bachelor’s degree / Master’s degree in Pharmacy with 2 to 3 years of experience.
  • Basic knowledgeable of GMP.
  • Ability to work independently as well as collaboratively in a fast-paced environment
  • Demonstrated ability to deal with confidential and highly sensitive information
  • Good organizational skills with a demonstrated ability to work on multiple priorities at one time.
  • Good knowledge and understanding of laws of Nepal related to employment;
  • Good conflict resolution skills;
  • Good communication and listening skills;
  • Good knowledge in MS Office – Excel, Word, PPT, Outlook

Language skill: Good verbal and written English and Nepali language;

Job Description:  (Fresh QA) 

Job Title: Quality Assurance Officer

Department: Quality Assurance

Reports to: Head of Department Quality Assurance

Status: Regular

Duty Station: Factory Office, Gaindakot, Nawalparasi

Authority: Exercises authorities as delegated by seniors that are related to QA Department within the norms and policies of the company

Functional Relationship: Work with/for the Factory pertaining to QA Department

Accountable to: Customers, Time Pharma Employees, Board of Directors and Shareholders of the company

Job Purpose

The QA Officer will work directly in support of the HOD QA on all activities related to Quality Assurance Department. 

The QA Officer is a member of the Time Pharmaceuticals (P.) Ltd. team assisting for the improved and sustained performance and productivity of the company.  The Officer must be able to demonstrate that the QA Department is a worthwhile component to contribute to achieve the Corporate Mission of the Company.

Essential Job Functions

The QA Officer shall perform the following job:

To achieve quality goals with contribution in continual improvement.

• • To perform routine jobs related to issue of Batch Manufacturing record (BMR), Formats, Log sheets, line clearance, crosscheck of BMR, Analytical worksheets and Finished products to ensure quality in product.
  • To actively participate in the implementation and documentation of deviation, change control, CAPA, Incidents, OOS, Customer complaints and nonconformities.
  • To prepare Weekly status report (QA), Monthly reports and to participate in evaluation of Key Performance Indicators of GMPs, Annual Product Review.
  • To take periodic rounds in the Warehouse, Production, QC Lab, Maintenance and factory premises to verify that logs, BMRs and other data entries are concurrent with the process, operational data within the specifications and also GMPs/ GLPs/ GWPs and GHPs are followed.
  • To evaluate affectivity of current SOPs and update them as necessary.
  • To supervise and provide technical guidance to the subordinates of QA department.

Compliance to policies, rules/regulations and guidelines

Adheres relevant policies, rules, regulations and guidelines of company (Personnel, Financial, Administrative policies, Security Guideline, Sexual Harassment Policy; Code of Conduct against Corruption etc.).

Required Competencies:

Bachelor’s degree / Master’s degree in Pharmacy.

• • Basic knowledgeable of GMP.
  • Ability to work independently as well as collaboratively in a fast-paced environment
  • Demonstrated ability to deal with confidential and highly sensitive information
  • Good organizational skills with a demonstrated ability to work on multiple priorities at one time.
  • Good knowledge and understanding of laws of Nepal related to employment;
  • Good conflict resolution skills;
  • Good communication and listening skills;
  • Good knowledge in MS Office – Excel, Word, PPT, Outlook

Language skill: Good verbal and written English and Nepali language;

2. QUALITY CONTROL OFFICER 

Job Title: Quality Control Officer

Department: Quality Control

Reports to: Quality Control Manager

Status: Regular

Duty Station: Factory Office, Gaindakot, Nawalparasi.

Authority: Exercises authorities as delegated by Supervisor that are related to Quality Control (QC) Department within the norms and policies of the company

Functional Relationship: Work with/for the Factory Office pertaining to QC Components.

Accountable to: Customers, Time Pharma Employees, Board of Directors and Shareholders of the company

Job Purpose

The QC Officer will work directly in support of the Quality Control Manager on all activities related to Quality Control Department.

The QC Officer is a member of the Time Pharmaceuticals Pvt. Ltd. team assisting for the improvement and sustained performance and productivity of the company.  The Officer must be able to demonstrate that his presence in QC Department is a worthwhile component to achieve Corporate Mission of the Company.

Essential Job Functions

 The QC Officer shall perform the following job:

To achieve quality goals with contribution in continual improvement.

• • • To perform routine jobs related to QC Department which includes instrument calibration, water analysis, Sampling of finished products, intermediate products, packing materials and raw materials.
    • Analyze the raw material and packing material in accordance with the established analytical procedures and prepare reports.
    • Dispensing of raw materials and packing materials.
    • Prepare reagents and standard solution for analysis.
    • Responsible for cleanliness and discipline in the working areas.

Compliance to policies, rules/regulations and guidelines

Adheres relevant policies, rules, regulations and guidelines of company (Personnel, Financial, Administrative policies, Security Guideline, Sexual Harassment Policy; Code of Conduct against Corruption etc.).

Required Competencies:

• • • Bachelors / Master’s degree in Pharmacy. M.Sc., Chemistry.
    • 2 to 3 years of experience in related field may apply for senior positions and fresh candidate can also apply.
    • Basic knowledgeable of GMP.
    • Ability to work independently as well as collaboratively in a fast-paced environment
    • Demonstrated ability to deal with confidential and highly sensitive information.
    • Good organizational skills with a demonstrated ability to work on multiple priorities at one time.
    • Good knowledge and understanding of laws of Nepal related to employment;
    • Good conflict resolution skills;
    • Good communication and listening skills;
    • Good knowledge in MS Office – Excel, Word, PPT, Outlook

Language skill: Good verbal and written English and Nepali language;

3. PRODUCTION OFFICER

Job Title: Production Officer

Department: Production

Reports to: Head of Department Production

Status: Regular

Duty Station: Factory Office, Gaindakot, Nawalparasi

Authority: Exercises authorities as delegated by seniors that are related to Production Department within the norms and policies of the company

Functional Relationship: Work with/for the Factory pertaining to Production Department.

Accountable to: Customers, Time Pharma Employees, Board of Directors and Shareholders of the company

Job Purpose

The Production Officer will work directly in support of the HOD Production on all activities related to Production Department.

The Production Officer is a member of the Time Pharmaceuticals (P.) Ltd. team assisting for the improved and sustained performance and productivity of the company.  The Officer must be able to demonstrate that the Production Department is a worthwhile component to contribute to achieve the Corporate Mission of the Company.

Essential Job Functions

 The Production Officer shall perform the following job:

1. To achieve quality goals with contribution in continual improvement.
2. Organize and ensure that drug products are produced in accordance with the established production procedure and schedule.
3. Ensure that the drug products are produced in accordance with the batch manufacturing record so as to improve production output.
4. Ensure that all required equipments are always ready for use, clean and in good condition.
5. Maintains cleanliness of equipments and working areas.
6. Maintains the subordinate discipline, favorable working environment and assists the subordinates on technical matters.
7. Contributes to continual improvement initiatives aimed at improving the efficiency/ effectiveness of GMP operation.

Compliance to policies, rules/regulations and guidelines

Adheres relevant policies, rules, regulations and guidelines of company (Personnel, Financial, Administrative policies, Security Guideline, Sexual Harassment Policy; Code of Conduct against Corruption etc.).

Required Competencies:

• • Bachelor’s degree / Master’s degree in Pharmacy.
  • Basic knowledge of GMP.
  • Ability to work independently as well as collaboratively in a fast-paced environment
  • Demonstrate ability to deal with confidential and highly sensitive information
  • Good organizational skills with a demonstrated ability to work on multiple priorities at one time.
  • Good knowledge and understanding of laws of Nepal related to employment;
  • Good conflict resolution skills;
  • Good communication and listening skills;
  • Good knowledge in MS Office – Excel, Word, PPT, Outlook

Language skill: Good verbal and written English and Nepali language;

For more information about vacancy or apply click here https://timepharma.com/career

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