JOB DESCRIPTION
KEY TASKS:
Performs microbial testing of raw materials, packaging materials, intermediate, bulk, finished
product, lab trial and stability samples using current
pharmacopoeias and established procedures. Ensures all analysis is completed, reviewed and
approved within agreed turn around times.
Performs routine environmental monitoring; air
sampling, bio-trace swabbing of machinery and
equipment, swabbing of personnel as necessary.
Performs other duties which may be assigned by
Quality Manager, for which training and/or an
explanation has been provided and understood.
3.1 Finished Product inspection
3.2 Returned Goods inspection
3.3 cGMP audit
3.4 Validation activities
3.5 Quality Control Processes (Raw Material, In- Process, Packaging, Finished Goods)
3.6 In-line Inspection
4. Performs routine testing on water purification
system in line with company and regulatory
specifications. Trends associated data.
5. Performs microbial identification to ensure
compliance with procedure and regulatory
requirements.
6. Organizes and maintains standard procedures and
microbial test records in an organized system for
easy retrieval.
7. Maintains and coordinates calibration of measuring
equipment in the area of assignment.
8. Ensures that procedures are carried out carefully, accurately, and complying with Good Laboratory
Practices (GLP) and Good Microbiological
Practices to eliminate errors.
9. Ensures that Good Manufacturing practices (GMP)
are being implemented in production line and in
the plant premises at all times.
10. Performs quality control on incoming media and
maintains inventory of reagents. Ensures lab is
supplied with consumables. Prepares request for
purchase.
JOB QUALIFICATION
Education & Training:
Minimum of Bachelor’s degree in Microbiology, Biology, Chemistry, Pharmacy
Work Experience Requirements:
At least one (1) year relevant experience of micro analysis and
operation experience in a cosmetic, pharmaceutical or biotech
environment.
Skill/Knowledge & Other Requirements:
Have an understanding of techniques used in microanalysis.
Has knowledge in Good Laboratory Practices and Good Manufacturing
Practices.
Strong computer skills.
Good in oral and written communication.
Have initiative, high attention to detail, and the ability to multi-task.
OTHER JOB REQUIREMENTS
Education
Bachelor's/College Degree
Field of study
Biology, Chemistry, Pharmacy/Pharmacology
Specialization
Quality Assurance
JOB BENEFITS
Basic Computer Proficiency
KEY TASKS:
Performs microbial testing of raw materials, packaging materials, intermediate, bulk, finished
product, lab trial and stability samples using current
pharmacopoeias and established procedures. Ensures all analysis is completed, reviewed and
approved within agreed turn around times.
Performs routine environmental monitoring; air
sampling, bio-trace swabbing of machinery and
equipment, swabbing of personnel as necessary.
Performs other duties which may be assigned by
Quality Manager, for which training and/or an
explanation has been provided and understood.
3.1 Finished Product inspection
3.2 Returned Goods inspection
3.3 cGMP audit
3.4 Validation activities
3.5 Quality Control Processes (Raw Material, In- Process, Packaging, Finished Goods)
3.6 In-line Inspection
4. Performs routine testing on water purification
system in line with company and regulatory
specifications. Trends associated data.
5. Performs microbial identification to ensure
compliance with procedure and regulatory
requirements.
6. Organizes and maintains standard procedures and
microbial test records in an organized system for
easy retrieval.
7. Maintains and coordinates calibration of measuring
equipment in the area of assignment.
8. Ensures that procedures are carried out carefully, accurately, and complying with Good Laboratory
Practices (GLP) and Good Microbiological
Practices to eliminate errors.
9. Ensures that Good Manufacturing practices (GMP)
are being implemented in production line and in
the plant premises at all times.
10. Performs quality control on incoming media and
maintains inventory of reagents. Ensures lab is
supplied with consumables. Prepares request for
purchase.
JOB QUALIFICATION
Education & Training:
Minimum of Bachelor’s degree in Microbiology, Biology, Chemistry, Pharmacy
Work Experience Requirements:
At least one (1) year relevant experience of micro analysis and
operation experience in a cosmetic, pharmaceutical or biotech
environment.
Skill/Knowledge & Other Requirements:
Have an understanding of techniques used in microanalysis.
Has knowledge in Good Laboratory Practices and Good Manufacturing
Practices.
Strong computer skills.
Good in oral and written communication.
Have initiative, high attention to detail, and the ability to multi-task.
OTHER JOB REQUIREMENTS
Education
Bachelor's/College Degree
Field of study
Biology, Chemistry, Pharmacy/Pharmacology
Specialization
Quality Assurance
JOB BENEFITS
Basic Computer Proficiency
Submit profile
Dermessé Inc.
About the company
Dermessé Inc. jobs
199 J.P. Rizal St., Brgy Poblacion II, Silang Cavite Philippines , 4118
Quality Control Supervisor ( Slaughter house )
BENCHSTONE ENTERPRISE INCORPORATED
SAR 2,700.00 - 3,000.00 per month
Position Quality Control micro analyst recruited by the company Dermessé Inc. at , Joboko automatically collects the salary of , finds more jobs on Quality Control Micro Analyst or Dermessé Inc. company in the links above
About the company
Dermessé Inc. jobs
199 J.P. Rizal St., Brgy Poblacion II, Silang Cavite Philippines , 4118