Total 49 job vacancies by Sunward Pharmaceutical Private Limited

Summary of Job Scope:

1) Carry out routine general cleaning and housekeeping works as assigned by superior.

2) Perform cleaning activities such as washing drainage, collect trash, sweeping rubbish outside factory compound.

3) Washing toilet and inform and report any damage of toilet or facilities around factory area.

4) Topping up of toiletries

5) Distribute washed uniform to respective worker’s lockers.

6) Collecting used uniform and do recording before vendor’s collection.

7) Mopping and vacuuming of offices’ floor

8) Perform gardening work such as watering all plants and upkeep the flower plants.

9) Wipe down tables and chairs in canteen.

10) Tidying praying altar and assist with offerings.

11) Work according to the supervisor’s instruction

Requirements:

1) Ability to follow supervisor instruction.

2) Ability to work independently with minimum supervision.

3) Ability to cooperate with supervisor.

Responsibilities:

• Perform in process quality check and physical test on in-process materials & finished products
• Prepare Sampling of Intermediate products and finished products and collected send to QC lab for testing
• Perform quality check on Packaging material and physical testing.
• Maintain retention sample for all production batches.
• Housekeeping of In-process laboratory equipment and retention sample.

Requirements:

• ITE / A Level or equivalent of related field
• Able to perform independently in a fast paced environment
• Able to perform multi-task as assigned by superior
• Fresher welcomed
• Willing to do OT
• 1 or 2 years hands on experience in related field will be advantageous

Job Scope:

• Responsible for troubleshooting, repairing and servicing of machinery faults in the production and factory facility area.
• To maintain inspection readiness of the factory equipment to ensure audit compliance with regulatory, safety and engineering standards.
• Perform all tasks in accordance with GMP regulations.

Qualifications and Skills:

• Minimum Nitec certification or its equivalent
• At least 1-3 year of experience in the operation environment
• Knowledge of general maintenance processes and methods
• Good understanding of electrical, pneumatic and mechanical systems with experience with PLC, PCB Board and electrical components
• Working knowledge of tools, common appliances and devices
• Good physical condition and strength with a willingness to work overtime and occasional night shift

Responsibilities:

• Coordinate and oversees the planning, organizing, and delegating of work to Store personnel
• Will be responsible for making sure that all Store policies and SOPs are followed

Job Scope:

• Plan, organize, direct and control the day to day Store operation
• Provide training and ensure Store personnel follow work instruction and procedures set up in compliance with GMP
• Ensure store environment is conducive for storage of goods
• Liaise with Planner / Production Pharmacist / QC Dept / Customer Service Executive / Accounts to ensure a smooth operation
• Any other ad hoc assignment & duties by HOD

Requirements :

• GCE 'O' /Diploma holder are welcome
• Basic Computer Skills
• Ability to work independently within deadlines

Summary of Job Scope:

Responsible for technical enhancement of quality control and analytical development in QC Laboratory functions.

• Work allocation and arrangement for daily QC routine work
• Finish Product Quality Control
• Checking Report of "In-Process control of Tablet"
• In process quality control of intermediates (IPQC)
• Review and evaluation of Analyst test report and data to ensure test result is up-to date and accurate.
• Review and ensure QC Records and BMR are up-to-date, complete and accurate.
• Supervision of quality control check on raw material dispensing
• Management, Monitering and testing on sample.
• Monitor retained samples and waste of tested sample of intermediates and finished products.
• Environment monitoring and recording for retention sample room.
• Supervision and training of laboratory technicians and laboratory assistant and chemist in carrying out their duties.
• Responsibe to revise of SOP for IPQC and FPQC and relevant section.
• Verify and approve test result in absence of QC Manager.
• Calibration of laboratory equipment and apparatus.
• Ensure Good Laboratory Practice (GLP) & Lab Safety.
• Optimization of usage of laboratory equipment.
• Support in the investigation and management of product complaints.
• Participate in process and cleaning validation.

Job Description

• Overseas entire manufacturing facilities, schedule and flow of work or between departments to expedite production
• Review master production schedule and work orders and revises schedule according to work order specifications, establish priorities and availability or capacity of workers, material, machine and equipment.
• Reschedule identical processes to eliminate duplicate machine set-up, to develop cost-effective measures
• Review distributes work order to departments, donating quantity, type and proposed completion date of units to be produced.
• Review documents such as production schedule, work orders and staffing tables to determine personnel and material requirements and material priorities
• Liaise with department supervisors to determine progress of work and provide information on processing
• Compile reports concerning of work and downtime due to failure of machine and equipment and to explain on production delays.
• Maintain inventory of materials needed to complete productions.

Requirements

• At least bachelor degree, post graduate diploma in any science, engineering, management or others filed related to planning and job arrangement.
• Minimum 2 year experience in Production Planning preferably in manufacturing environment
• Well versed in computer skill especially in excel and other Microsoft office skills and knowledge in Navision is preferred.
• Close attention to details is essential
• Must be able to perform each essential duty satisfactory and in timely manner
• Independent & communication skills

Responsibilities:

• Managing and organising inter departmental meetings and appointments.
• Coordinates projects by contractor or department by capturing timeline of ongoing projects and delivering progress updates.
• Take accurate and comprehensive notes at meetings.
• Liaising with staffs, contractors, or any other external organizations.
• Carrying out projects or task or understudy to observe and improve the efficiency of departmental workflow.
• Implementing and maintaining procedures that can improve workflow in departmental process.
• Proper documentation of the implementation/understudy/observation
• Handling ad-hoc duties from direct supervisor from time to time

Requirements:

• Minimum educational level of Diploma and above
• Must have basic computer skills
• Good with minutes writing
• Documentation and filing of records
• Attention to details, possess good planning, organisation and administrative skills
• Ability to multi-task, self-motivated, independent, meticulous & discipline
• Possess industrial manufacturing background will be preferred

Responsibilities:

1. Involve in manufactory processes

• Supervise process flow control
• Supervise machine/equipment setting control
• Quality Control in between processes
• Monitor issues and matters on manpower

2. Provide positive suggestions on improvement on process

3. Suggest machines/equipment alteration for better control and preventive maintenance programme

4. Ensure strict GMP control and guidelines

5. Any other assignment by Management

Requirement:

· Diploma in Pharmaceutical Technology

Summary of Job Scope:

Assist production HOD to ensure that BMR and NAV closure and updating is online and real time.

• Ensure on time closure of BMR

• Ensure that all NAV entry at each stages is on time

• Preparation and submission of daily production reports

Assist production HOD to control processes and manpower

• Ensure GMP is adhere in production

• Ensure all processes are in order and following BMR

• Ensure on- time filling and closure of any deviation or IPIR; and issue investigation

• Ensure all manpower are trained properly

Overall supervision of production personnel & production procedures

Job Objective

• To ensure that each department operates smoothly during office hours / OT.
• To ensure that better quality of products are produced.
• To ensure that all production personnel operates according to current Good Manufacturing
• Practice (cGMP) standards.

Responsibility

• Responsible for checking the quality of all the products manufactured.
• Recognize the importance of production process control.
• Report immediately to HOD and relevant personnel of any technical and disciplinary problems encountered during production.
• Seek approval from HOD before troubleshooting.
• In-charge of safekeeping of keys to main gate and ensuring that the gate is always locked after office hours.
• In-charge of the keys to the raw materials room and intermediate room when the Controller is absent.
• To check that the production procedure is followed and report any deviation from standard practice stated in the BMR.
• Report any non-compliant behavior according to GMP standards.
• Be well-trained in GMP standards.
• Provide suggestions for improvement of production work flow and its control.
• Willingness to learn all the production processes and operation and control of each piece of equipment.
• Perform the required administrative duties such as submitting the daily report, monitor the flow of BMR.
• Train new or existing production personnel according to training schedules from HOD.
• Assist the HOD with the production work flow.
• Duties as and when assigned by the Company.

Duties & Responsibilities:

• Ensuring compliance with regulations set by Health Sciences Authority of Singapore
• Keeping up to date with changes in regulatory legislation and guidelines
• Liaising and negotiating with regulatory authorities
• Gathering, evaluating, organizing , managing, collating information for submission to authorities
• Obtaining and maintaining licences related to manufacturing of pharmaceuticals in Singapore
• Providing advice on the requirements for labelling, storage and packaging
• Ad hoc task assigned by Management

Requirement:

· Graduate, holding a degree in Pharmacy

· Registered with the Singapore Pharmacy Council (SPC) preferred

· Pharmacist experience in ACDT, ICH, and ASEAN guideline for registration

· Knowledge in Quality Management System is added advantage

Job Scope:

• The entire operational aspects to established SOP, GMP, GDP and GLP practices and regulatory requirements.
• Handling issues from cross functional departments like QC/ Production/ Warehouse/ Engineering etc.
• Ensure procedures and practices are adhered in accordance with cGMP requirements.
• Conducting Risk Assessment, collect sample during validation process and qualification.
• Involve and provide expertise in vendor audit, evaluation/qualification and assessment and ensure proper execution of validation (IQ, OQ, PQ etc.).
• Advisory on Corrective and Preventive Action (CAPA) arisen out of External/Internal audits, Unusual Occurrences/Incidents, Failures and Market complaints.
• Advisory on documentation and management of deviations, critical process steps parameters.

Duties and Responsibilities

• Establish R&D procedures and work processes.
• Development of new and/or improved product formulation to meet pharmacopeia requirements.
• Development of suitable manufacturing process for the product formulation.
• Produces sample batch in lab scale and pilot scale.
• Responsible for effective technology transfer and upscaling to commercial scale batches.
• Participates in process validation for the R&D batches.
• Provides training to production personnel on improved formulation and manufacturing processes.
• Ensures suitable test method is developed and validated for the new/improved products.
• Trouble-shooting in the areas of formulation and process for routine production.
• Participation in the investigation of product complaints (if applicable).
• Monitors the progress of stability study for R&D samples.
• Establishment of technical information e.g. specifications of raw material, packaging materials, finished products.
• Provides documentation to support registration of products with regulatory authority.
• To ensure the quality of product is in accordance with the specification.
• To review and feedback if there is any improvement needed for the process of manufacturing.
• To ensure that products are produced, stored according to the appropriate documentation and monitor storage conditions for materials and product in order to obtain or maintain the required quality.
• To inspect, investigate and take samples in order to monitor factors which may affect product quality.
• To ensure all products, in process materials, production facilities and process are in accordance to codes of Good Manufacturing Practice (GMP) requirement through proper monitoring procedures, effective training program and up to date documentations.
• To monitor drugs manufacturing activities and ensure company is always in compliance with the latest PICS & GMP guideline.
• To ensure that company is always updated with the latest guideline required.
• Review and make recommendation for improvement in area of manufacturing processes, safety, environment, sanitation and hygiene.
• To approve the instruction relating to production operations and to ensure their strict implementation.
• To ensure the qualification and maintenance of his department, premises and equipment.
• To ensure that the appropriate validations are conducted timely and accordingly.
• To ensure all GMP quality related record are kept properly

Requirement

• Bachelor Degree/Master in Pharmacy/Pharmaceutical Sciences
• Minimum 2 - 5 years’ experience in pharmaceutical industry
• Minimum 2 years’ experience in drug development and formulation as well as manufacturing process/technologies

• Min Form 5 or N Level
• Computer Literate (preferred)
• Able to commit OT when required
• Able to understand, read simple English
• Forklift License (preferred)
• Able to carry 25kg
• Able to do calculation/credit in Mathematics
• Full-time/permanent job
• 中五或N level
• 会操作电脑 （优先考虑）
• 可以加班
• 可以读和写基本英文
• 叉车执照（优先考虑）
• 可以扛重物（25kg)
• 可以算数/算数有达到至少C成绩
• 全职工

基本薪资： $1,100.00至$1,400.00（每月 ）

Basic Salary : $1,100 to $1,400 (per month)

Job Description

1. To do material dispensing according to weekly dispensing schedule and BMR

2. To do cleaning before and after dispensing

3. To check all raw materials receive from store.

4. To ensure loose bags are being weighed before & after dispensing.

5. To comply to GMP requirements

6. To ensure all records are accurate and up to date

7. Participate in stock-take.

8. Maintain tidiness and cleanliness of dispensing and store areas.

Requirements

· Minimum N/O/A Level with good mathematic calculation

· Fresh graduated from school are encourage to apply