QC Microbiology Specialist
- Employer
- Integrated Resources, Inc
- Location
- Westborough, Massachusetts, US
- Salary
- Competitive
- Closing date
- Dec 1, 2021
View more
- Sector
- Consultancy/Private Sector
- Field
- Conservation science
- Discipline
- Biology
- Salary Type
- Salary
- Employment Type
- Full time
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Job Description PURPOSE & Product: AIRM is seeking a highly motivated individual to join us as a QC Microbiology Specialist (temp). This position provides Quality Control Microbiology support to all aspects of a GMP environmental monitoring program and product testing. Looking for experience with environmental monitoring in a GMP setting. Position is Tuesday through Saturday.
JOB RESPONSIBILITIES:
Performing environmental monitoring sampling in manufacturing cleanrooms.
Organization and completion of assay documentation and entering data into QC database.
Assist in the trending of environmental monitoring data.
Write, revise and review Standard Operating Procedures and Forms.
Lab maintenance and updates on equipment calibrations and equipment use logbooks according to cGMP standards.
Assist in conducting and documenting laboratory investigations.
Sample submissions in a timely manner to various contract testing vendors.
Perform other lab duties as required.
This position interacts with QC, QA and Manufacturing personnel and management.
REQUIRED SKILLS
Bachelors degree in Life Science, Microbiology, Biochemistry or related discipline with 1-2 years of relevant biotech or pharmaceutical industry experience.
Knowledge of GMP, SOPs and quality control process.
Proficient in MS Word, Excel, Power Point and other applications.
Strong written and verbal communication skills.
Ability/Flexibility to work weekends is required
PREFERRED SKILLS:
Experience in the biotech and/or pharmaceutical industry.
JOB RESPONSIBILITIES:
Performing environmental monitoring sampling in manufacturing cleanrooms.
Organization and completion of assay documentation and entering data into QC database.
Assist in the trending of environmental monitoring data.
Write, revise and review Standard Operating Procedures and Forms.
Lab maintenance and updates on equipment calibrations and equipment use logbooks according to cGMP standards.
Assist in conducting and documenting laboratory investigations.
Sample submissions in a timely manner to various contract testing vendors.
Perform other lab duties as required.
This position interacts with QC, QA and Manufacturing personnel and management.
REQUIRED SKILLS
Bachelors degree in Life Science, Microbiology, Biochemistry or related discipline with 1-2 years of relevant biotech or pharmaceutical industry experience.
Knowledge of GMP, SOPs and quality control process.
Proficient in MS Word, Excel, Power Point and other applications.
Strong written and verbal communication skills.
Ability/Flexibility to work weekends is required
PREFERRED SKILLS:
Experience in the biotech and/or pharmaceutical industry.
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