- Maintainthe laboratory quality management system to ensure compliance withcGMP.
- Audit the Quality ControlLaboratory to ensure compliance to SOPs.
- Investigate, assess, andtroubleshoot test and/or equipmentproblems.
- ReviewOut-of-trend/Out-of-specification results and participate ininvestigations to determine root cause andCAPA.
- Ensure analytical equipment iscalibrated and well maintained at alltimes.
- Ensure that laboratorypersonnel training requirements are met and that training recordsare current.
- Interview, hire, andtrain new staff.
- Provideconstructive feedback and retraining asneeded.
- Handles discipline ofemployees in accordance with companypolicy.
- Maintainthe laboratory quality management system to ensure compliance withcGMP.
- Establish product test methodsand specifications. This includes raw materials, in-processproduct, finished products and stabilitysamples.
- Audit the Quality ControlLaboratory to ensure compliance to SOPs.
- Maintain appropriate laboratoryinventory to ensure timely release ofmaterials.
- Participate in methodqualifications, validations, andtransfers.
- Other duties asassigned.
- Excellentverbal and written communication skills inEnglish.
- Excellent management andteamwork skills.
- Excellentorganizational skills and attention todetail.
- Excellent time managementskills with a proven ability to meetdeadlines.
- Ability to function wellin a high-paced and at times stressfulenvironment.
- Ability to understandand follow all Standard Operating Procedures and current GoodManufacturing Practices provided by theCompany.
- Knowledge and control ofanalytical equipment including calibration andmaintenance.
- Understanding ofquality systems including change control, deviations andCAPAs.
- Ability to handle multipletasks concurrently and complete them in a timelymanner.
- PharmaceuticalLabatory Manager: 5 years(Required)
- Chemistry/Pharmaceutical:5 years(Required)
- CGMP:5 years(Required)
- FDAregulations: 5 years(Required)
- Chemistry, Biology, or a relateddiscipline.
- Experiencein computer software, such as Microsoftapplications.
- Goodknowledge and understanding of quality control, SOPs, cGMPs, OSHA,and FDA policies andregulations.
- 10+years of management experience in a pharmaceutical laboratorysetting.
- Pharmaceuticalexperiencerequired.
- Abilityto walk, stand, or sit 8 or more hours aday.
- Ability to lift heavy items upto 40 lbs. or more.
- Dentalinsurance
- Healthinsurance
- Lifeinsurance
- Paidtimeoff
- Visioninsurance
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Assistant Professor of Spanish Language - Doha, دولة قطر - Qatar university
وصف
Allen Spolden isactively recruiting for a Quality Control Laboratory Manager. Thisis a perm (Direct Hire) opportunity. Relocation assistancewill beprovided.Location:Gulfport, MS (100% onsite isrequired.)
WorkSchedule: M-F, flexible start (4am up to11am).
Salary:Dependent on experience.
JobSummary:
The Quality ControlManager is responsible for managing laboratory personnel andmaintaining the laboratory to ensure all products and proceduresmeet the requirements of 21CFR210, 21CFR211, Regulatory Agencies,and customerexpectations.
SupervisoryResponsibilities:
Duties/Responsibilities:
RequiredSkills/Abilities:
Experience:
Requirements
EducationandExperience
PhysicalRequirements:
JobType: Full-time
Pay: $80,000or more depending onexperience
Benefits
Benefits:
Education and Experience B.S. in Chemistry, Biology, or a relateddiscipline. Experience in computer software, such as Microsoftapplications. Good knowledge and understanding of quality control,SOPs, cGMPs, OSHA, and FDA policies and regulations. 10+ years ofmanagement experience in a pharmaceutical laboratory setting.Pharmaceutical experience required. Physical Requirements: Abilityto walk, stand, or sit 8 or more hours a day. Ability to lift heavyitems up to 40 lbs. or more. Job Type: Full-time Pay: $80,000 ormore depending on experience