Job Description
VACANCIES
Sands Active (Pvt) Limited is (a subsidiary of Melwa Group) a BOI approved state of the art pharmaceutical manufacturing company by partnering with the State Pharmaceutical Manufacturing Corporation Sri Lanka with the intention to fulfill local pharmaceutical related demand.
EXECUTIVE – QUALITY CONTROL
Duties and Responsibilities
- Perform routine analysis of raw materials, excipients, packing materials, water analysis and finished products.
- Preparation of COA and SPEC / STP SOP preparation.
- Knowledge of OOS / OOT/ incident / deviation investigation procedure.
- Review of routine analysis date & stability data and SPEC and STP.
- Follow the test procedure as per QC compliance.
- Perform analytical method development and validation for drug products and preparation of AMV protocols and report.
- Analysis of formulation development trails, routine stability & drug excipient compatibility samples.
- Perform assay, related substances, dissolution test by HPLC and UV instrument.
- Execute HPLC & GC development.
- Execute water content, identification test by IR instrument.
- Review documents and release materials.
- Perform calibration of analytical instruments & stability sample analysis.
- Possessing knowledge in GLP & CGMP.
Qualifications and Experience
- B.Pharm or Chemistry full qualification.
- 02 – 03 years’ experience in a pharmaceutical manufacturing QC lab or similar laboratory experience.
- Ability work independently by meeting deadlines.
- Must be a good team player with positive attitudes.
- Excellent communication skills in English.
EXECUTIVE – QUALITY ASSURANCE
Duties and Responsibilities
- To develop efficient filing system of all QA documents by assigning file numbering system, prepare master index, lists of documents and ensure correct filing of documents.
- Preparation of SOPs.
- Preparation & Review of batch manufacturing records and batch packing records.
- Assist in execution of validation and qualification activities.
- Review of filled BMR/BPR.
- To monitor IPQA activities on shop floor.
Qualifications and Experience
- Bsc Science or B.Pharm full qualification.
- 02 – 03 years’ experience in a pharmaceutical manufacturing environment.
- Ability work independently by meeting deadlines.
- Must be a good team player with positive attitudes.
- Excellent communication skills in English.
PRODUCTION OFFICER
Duties and Responsibilities
- Enough knowledge to operate and maintain all process equipments.
- Able to prepare BMR,BPR,SOPs related to production.
- Co-ordination with QC/QV Engineering, Warehouse and other department for smooth functioning.
- Maintaining online documentation, GMP and GDP in area.
- Maintain the compliance/Aftercare on shop floor with respect to Standard procedures.
- Ensure the shift, daily, weekly and monthly production plan schedule adheres as per the supply plan from the respective department.
- Periodic checks of granulation, tablet compression manufacturing and packing.
- Perform validation protocol execution of machineries, equipments and process.
- Improve and monitor the efficiencies of machineries, materials and people against the industry best practices.
- Maintain the daily production report and comparison of actual vs planned to achieve the production KPIs and analyze any deviations and taking corrective actions.
Qualifications and Experience
- Bsc Science or B.Pharm full qualification.
- Must be a good team player.
- Ability to work with minimum supervision.
QA OFFICER
Duties and Responsibilities
- Responsible for performing and supervising IPQA activities at every stage of manufacturing and packing.
- Ensure proper cleaning, maintenance, and verification of equipment, production areas, and dispensing processes.
- Oversee the dispensing of raw and packing materials and review related manufacturing and packing documents.
- Conduct sampling, challenge tests, and hold time studies as per approved validation protocols.
- Prepare, review, and update Standard Operating Procedures (SOPs) and ensure compliance with documentation practices.
- Manage the review and closing of batch records (BMR/BPR) and ensure online completion of documentation.
- Perform in-process checks and sampling of semi-finished and finished goods.
- Execute responsibilities such as line clearance, team training.
Qualifications and Experience
- Bsc Science or B.Pharm full qualification.
- 02 – 03 years’ experience in a pharmaceutical manufacturing environment.
- Ability work independently by meeting deadlines.
- Must be a good team player with positive attitudes.
- Excellent communication skills in English.
An attractive remuneration package inclusive of other fringe benefits and excellent career development opportunities await for the selected candidates.
If you feel that you are the right candidate that we are looking for, please send us your CV to info@sandsactive.lk including details of two non-related referees to reach us within 07 days of this advertisement.
Manager - HR & Administrations, Sands Active (Pvt) Limited