Total 5 Others job vacancies

Microbiologist (1-Year Contract)

Company: Pharma MNC

Microbiologist (QC Analyst/ Pharma/ Contract)

12 Months Contract

Location : Gul Circle (5 mins walk from MRT)

Basic Salary : Up to $5,500 depending on experience

Industry : Pharmaceutical

Responsibilities

• Executing analytical testing in a timely manner, ensuring adherence to the committed scheduled plans
• Performing his/ her tasks in accordance with cGMP and HSE requirements, and with the associated instructions, procedures, records, related to these tasks
• Recording all expected raw data, calculations, information, related to his/her tasks, to comply with cGMP and data integrity requirements
• Ensuring that is trained and qualified to the assigned analytical testing that requires to be qualified
• Performing the QC data review of executed tests by other analysts in a timely manner, ensuring adherence to the committed scheduled plans
• Informing his/her manager of any quality or HSE event (deviations, OOx,…) in a timely manner to ensure investigation and impact assessment are performed appropriately
• Participating actively to any investigation, where is involved, to ensure investigations and impact assessment are performed appropriately
• Executing assigned CAPAs related to remediation plans, continuous improvements
• Ensuring that his/her lab/facilities, lab instruments are kept in a quality and safety status to ensure that they can be used appropriately.
• Owning assigned stability studies, in compliance with approved stability program
• Ensuring the issuance and review of all deliverables related to assigned stability studies, such as risk assessment, protocols, reports, data trending, deviations, and summary reports
• Ensuring that sampling and testing related to stability is executed in a timely manner and stability results trend performed on time, including reports issuance
• Ensuring that all expected stability data (including events, change control…) are compiled in a proper way, to provide appropriate data trending and statistical analysis of stability studies, in compliance with associated stability protocols

Additional Accountabilities

• Review analytical results and perform audit trail review before batch release.
• Carry out on-the-job training for General and Specific Analytical Method to QC analysts and chemical technicians, by incorporating cGMP and safety aspects of the procedures.
• Perform troubleshooting of equipment in the laboratory and provide guidance to QC analysts on the troubleshooting.
• Trained and work independently on specific testing method
• Ensure availability of workplace risk assessment and safe working procedures for contractors and the quality personnel. Ensure safe working in all areas of work by practicing and communicating safety message at +QDCI Sanofi Manufacturing System (SMS) Awareness, Life Saving Rules (LSR), GMP/Data Integrity Awareness
• Other responsibilities that are not included in the above are related to quality assignments.

Lim Pey Chyi (Apple) - Apple.lim@manpower.com.sg

Recruitment Consultant (R2090579)

Manpower Staffing Services (S) Pte Ltd

EA Licence: 02C3423

Pay: Up to $7,000
Location: Ubi
Work hours: Monday – Friday, office hours

Job Scope

• Lead, design and performs method development and validation of new test procedures for incoming projects.

• Act as Technical Reviewer for A2LA accredited tests and non-accredited tests.

• Evaluates analytical results to interpret data and render opinions for projects.

• Liaison with Customers with regards to technical services and perform site visits where required.

• Prepares documents including methods, procedures, standard operating procedures and summary reports.

• Ensure that SOPs follow ISO 17025, cGMP and other regulatory requirements.

• Provides problem-solving skills for test procedures and investigations within laboratory unit.

• Monitor all proficiency-based testing and ensure compliance.

• Participate in audits conducted by external agencies and authorities and in quarterly management review.

• Drive quality and safety improvement initiatives within the department.

• Coach and mentor technical personnel and provide strong technical leadership.

• Supports the Laboratory Manager in all relevant functions

 Requirements

• Minimum Bachelor of Science or related degree.

• Minimum 6 years relevant QC microbiological experience in regulated laboratory, minimum 2 of which should be in a supervisory role.

• Experience in method validation, method transfer, qualifications activities in regulated laboratory.

• Good knowledge of ISO17025, cGMP and other regulatory guidelines.

If interested, please email me at alexgoh@recruitexpress.com.sg or telegram @alexgohhl

Alex Goh Hock Leong

(CEI.No: R1763413 l Recruit Express Pte Ltd (Healthcare & Life Science) | 99C4599).

Location: Tuas
Salary: $6,500 + 2 months bonus
Working hours: Monday to Friday, Office hours

Job Description:

1. Quality Control & Compliance
Review and approve QC data, ensuring accuracy, data integrity (ALCOA+), and compliance with GMP, QMS, and safety requirements.

2. Microbiological Testing & Monitoring
Oversee and perform microbiological testing (e.g. sterility, bioburden) and environmental monitoring for cleanrooms, ensuring sterility assurance in operations.

3. Investigation & Continuous Improvement
Lead or support investigations (OOS, deviations, CAPA), perform root cause analysis, and drive continuous process and system improvements.

4. Laboratory Operations & Support
Manage lab equipment, calibration, maintenance, troubleshooting, sampling plans, and ensure lab readiness for projects and product transfers.

5. Team Leadership & Collaboration
Provide guidance, training, and supervision to team members, support audits/inspections, and collaborate with cross-functional teams on quality and operational initiatives.

Requirements:

• Diploma or Degree in Microbiology, Biotechnology, Life Sciences, or related field.
• Prior experience in pharmaceutical, biologics, or GMP-regulated environment, preferably with aseptic or sterile manufacturing exposure will be an added advantage.
• Familiar with microbiological testing (e.g. sterility, bioburden, environmental monitoring) and aseptic techniques.
• Detail-oriented, strong problem-solving skills, able to work independently and lead or guide junior staff when required.

By submitting your resume, you consent to the collection, use, and disclosure of your personal information per ScienTec’s Privacy Policy (scientecconsulting.com/privacy-policy).

This authorizes us to:

• Contact you about potential opportunities.
• Delete personal data as it is not required at this application stage.
• All applications will be processed with strict confidence. Only shortlisted candidates will be contacted.

Tan Guo Wei (Isaac) - R1655144
ScienTec Consulting Pte Ltd – 11C5781

Job Scope:

• Review/Approve testing documentation and test records. Maintain integrity, accuracy and completeness of QC data and records.
• Meet quality objectives set by management & comply to Alcon, QMS and Safety requirements.
• Timely completion of all compliance activities without overdue, including but not limited to NCI, OOS, CAPA, Effectiveness Check, CR, training, periodic review.
• Timely report non-conformance or out-of-specification events. Lead or assist in root cause analyses for product defects and quality lapses, and take effective actions to prevent recurrence.
• Drive and promote the continuous improvement culture. Challenge current processes, identify improvements and drive the effort to implement lab system/process while maintaining compliance and reducing human Intervention.
• Review and assess external standard and/or regulatory requirements pertaining to quality control activities and implement necessary changes to ensure compliance
• Perform basic equipment troubleshooting.
• Investigate underlying causes, technical faults and issues pertaining to laboratory equipment, method or practices, and take necessary actions to resolve the problems.
• Develop testing protocols and procedures for Quality Control activities
• Develop APQR sub-reports and ensure timely submission of sub-reports without overdue.
• Participate in new product transfer or second sourcing projects and ensure laboratory readiness according to timeline to support the site objectives.
• Determine and implement optimal approach for laboratory equipment calibration, maintenance and operation. Ensure laboratory infrastructure and equipment function as intended.
• Compile data to support business and performance metrics reporting
• Provide guidance, coaching and training to the team as required.
• Participate directly in laboratory inspections, 5-S, internal and external audits
• Develop sampling plans for Quality Control purposes and cascade guidelines for optimal sampling conditions to laboratory personnel
• Analyse data to identify unfavorable trends and address issues with relevant stakeholders and to drive improvement on the method robustness
• Assist in PQR and OPV with cross functions (MS&T, Compliance) and perform related investigation if required.

• Review, report and analyse data to support business and performance metrics reporting
• Monitor the effectiveness of improvements and changes made to QC activities, methods and workflows
• Lead and coordinate with other functions or sites for site/global initiatives
• Backup to the Manager/Supervisor
• Perform any other duties as assigned by Supervisor / Manager according to business needs.
• Supervise / Provide guidance, coaching and required training to the managing team.
• Work together with supervisor to improve competency of the team.
• Coach associates in the areas of technical and professional development. Perform testing and/or inspection on raw material, in-process material, finished products and monitoring activities.
• Certified trainer to conduct on-the-job training
• Coordinate stability samples (e.g. creation of studies in LIMS, sample pulling, sample testing)
• Perform routine calibration and maintenance of laboratory equipment
• Planning/Assigning of tests and activities
• Approve reports for data documentation and analysis
• Review and/or approve investigations, reports, protocols, SOPs/WIs/forms.
• Candidates with prior aseptic manufacturing and testing experience are preferred.
• Plan, execute, and review environmental monitoring programs for cleanrooms (Grades A, B, C, D).
• Perform and oversee – Viable/ Non-viable air monitoring, surface and personal monitoring
• Support aseptic manufacturing operations to ensure ongoing sterility assurance.
• Perform or review results for microbiological tests, including Sterility and bioburden testing
• Ensure microbiology laboratory compliance with Data integrity, ALCOA+ principles and GMP documentation practices
• Support internal audits, health authority inspections, and customer audits.
• Performs any other duties as assigned by functional manager according to business needs.

Requirements:

• Min Degree in Biomedical Science or related discipline
• Able to start within a short notice

Interested candidates please send your resume to anna.chen@recruitexpress.com.sg

Anna Chen jiaxin

CEI No: R25157621

Recruit Express Pte Ltd

EA License: 99C4599