Micro QC Analyst I
$35 per hourjob summary:
The Micro QC Analyst I is dedicated to the Microbiology Laboratory and EM Monitoring Program. The role of the Micro QC Analyst I will be that of various Microbial testing, EM monitoring of the aseptic production areas, ordering and stocking supplies, creating/reviewing SOPs, investigation writing, data entry. location: Ridgefield, New Jersey
job type: Contract
salary: $35 - 38 per hour
work hours: 9 to 5
education: Bachelors responsibilities:
- The candidate must have previous quality control microbiology experience. Experience in bioburden testing, membrane filtration, sterility isolator testing, conductivity, total organic carbon or endotoxin assays is preferred - Basic knowledge of aseptic manufacturing environmental monitoring of Grade A-D Areas. - SOP review, creation and approval is preferred - OOS investigations writing is preferred - Basic knowledge of compliance with all cGMP standards, safety and environmental regulations and company SOPs. - Data entry of EM sampling results, LIMS, logbooks, and other miscellaneous lab data. - Interact with Project Teams and cross-functional groups related to site operations - Cohesive Micro player in the Micro department who is willing to assist or help a fellow analyst. Analyst Qualifications: - Act for Change: Embrace change and innovation and initiate new and improved ways of working. - Cooperate transversally: Collaborate effectively with peers, stakeholders and partners across the organization to positively impact business results. - Develop People: Take responsibility for developing one's self and mentor other Micro Personnel in anticipation of future business needs or to assist the micro department. HSE - It is required that individuals care for their own safety and wellbeing. Individuals must promote a safe working environment for employees and contractors working in their area of responsibility. - Individuals must complete all required HSE trainings. Everyone is required to report all accidents and incidents and support investigations in their areas of responsibility. Individuals must ensure timely closure of HSE actions owned by their departments. qualifications:
- BA/BS in Microbiology/Biology with 2+ years' experience in CGMP, pharma or lab environment is required. - Practical experience in general microbiology laboratory techniques working with bacteria, yeast and mold. - Prior experience with data review, authoring SOPS, Change Controls, out of specification investigations and report writing is recommended. - Working knowledge of cGMPs in pharmaceuticals/biological/aseptic/medical device manufacturing - Excellent technical writing skills - Ability to collaborate effectively with personnel and between departments - Problem-solving skills - Strong communicator - Works independently - Working knowledge of Word, Excel and PowerPoint - Physical Requirements include the capacity to lift and carry up to 20 pounds, kneel, reach and stretch, and to stand for at least 4 hours. skills: Microbiology, Laboratory Information Management Systems (LIMS), SOP Development, Good Manufacturing Practices (GMP)
Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact View email address on randstadusa.com.
Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including: medical, prescription, dental, vision, AD&D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility).
This posting is open for thirty (30) days.
The Micro QC Analyst I is dedicated to the Microbiology Laboratory and EM Monitoring Program. The role of the Micro QC Analyst I will be that of various Microbial testing, EM monitoring of the aseptic production areas, ordering and stocking supplies, creating/reviewing SOPs, investigation writing, data entry. location: Ridgefield, New Jersey
job type: Contract
salary: $35 - 38 per hour
work hours: 9 to 5
education: Bachelors responsibilities:
- The candidate must have previous quality control microbiology experience. Experience in bioburden testing, membrane filtration, sterility isolator testing, conductivity, total organic carbon or endotoxin assays is preferred - Basic knowledge of aseptic manufacturing environmental monitoring of Grade A-D Areas. - SOP review, creation and approval is preferred - OOS investigations writing is preferred - Basic knowledge of compliance with all cGMP standards, safety and environmental regulations and company SOPs. - Data entry of EM sampling results, LIMS, logbooks, and other miscellaneous lab data. - Interact with Project Teams and cross-functional groups related to site operations - Cohesive Micro player in the Micro department who is willing to assist or help a fellow analyst. Analyst Qualifications: - Act for Change: Embrace change and innovation and initiate new and improved ways of working. - Cooperate transversally: Collaborate effectively with peers, stakeholders and partners across the organization to positively impact business results. - Develop People: Take responsibility for developing one's self and mentor other Micro Personnel in anticipation of future business needs or to assist the micro department. HSE - It is required that individuals care for their own safety and wellbeing. Individuals must promote a safe working environment for employees and contractors working in their area of responsibility. - Individuals must complete all required HSE trainings. Everyone is required to report all accidents and incidents and support investigations in their areas of responsibility. Individuals must ensure timely closure of HSE actions owned by their departments. qualifications:
- BA/BS in Microbiology/Biology with 2+ years' experience in CGMP, pharma or lab environment is required. - Practical experience in general microbiology laboratory techniques working with bacteria, yeast and mold. - Prior experience with data review, authoring SOPS, Change Controls, out of specification investigations and report writing is recommended. - Working knowledge of cGMPs in pharmaceuticals/biological/aseptic/medical device manufacturing - Excellent technical writing skills - Ability to collaborate effectively with personnel and between departments - Problem-solving skills - Strong communicator - Works independently - Working knowledge of Word, Excel and PowerPoint - Physical Requirements include the capacity to lift and carry up to 20 pounds, kneel, reach and stretch, and to stand for at least 4 hours. skills: Microbiology, Laboratory Information Management Systems (LIMS), SOP Development, Good Manufacturing Practices (GMP)
Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact View email address on randstadusa.com.
Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including: medical, prescription, dental, vision, AD&D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility).
This posting is open for thirty (30) days.
Vacancy posted 2 days ago
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