QC Micro Analyst
Company Name:
Regeneron
Job Summary and
Essential Functions:
Known for its scientific and operational excellence, Regeneron is a leading science-based biopharmaceutical company that discovers, invents, develops, manufactures, and commercializes medicines for the treatment of serious medical conditions. Regeneron markets medicines for eye diseases, colorectal cancer, and a rare inflammatory condition and has product candidates in development in other areas of high unmet medical need, including hypercholesterolemia, oncology, rheumatoid arthritis, allergic asthma, and atopic dermatitis.
Summary:
This is a level IV second shift position.
Performs testing to ensure cGMP compliance in the manufacturing facility. Responsible for assessing the microbiological quality of products, manufacturing equipment, manufacturing process areas, and facility utilities.
Essential Duties and Responsibilities include, but are not limited to, the following:
Reviews and updates SOPs.
Performs peer review of data.
Performs laboratory investigation reports.
Participates in training of other employees.
Performs microbial identification procedures.
Maintains laboratory supplies, media, and reagents inventory.
Participates in the overtime and weekend schedule as required.
Performs bioburden and endotoxin testing of products and raw materials.
Performs microbiological testing of in-process and final product materials.
Performs biological and endotoxin indicator testing used in the validation of manufacturing equipment.
Updates microbiological environmental monitoring results database and prepares monthly report.
Performs acceptance testing of commercially prepared microbiological culture media.
Assists in coordinating equipment maintenance and calibration.
Uses Laboratory Information Management System (LIMS) for sample and sample test result tracking.
Performs all duties relevant to the Quality Control Microbiology Technician position as required.
Additional responsibilities for Analysts II-IV include, but are not limited to:
Increasing involvement in the training of employees.
Increasing responsibilities for reviewing documents and data.
Microbiology representation and participation in cross functional site meetings.
Administration of programs such as gowning, training, ordering, calibration, etc.
Technical writing assignments such as SOPs, protocols, final reports, trend reports, risk assessments, laboratory investigations, etc.
Experience and Required Skills:
Education and
Experience:
Requires BS/BA in Life Sciences or equivalent along with 8 plus year's relative experience, preferably in the pharmaceutical or biotechnology industries.
Will substitute relevant work experience in lieu of degree requirement.
This is an opportunity to join our select team that is already leading the way in the Pharmaceutical/Biotech industry. Apply today and learn more about Regenerons unwavering commitment to combining good science & good business.
To all agencies: Please, no phone calls or emails to any employee of Regeneron about this opening. All resumes submitted by search firms/employment agencies to any employee at Regeneron via-email, the internet or in any form and/or method will be deemed the sole property of Regeneron, unless such search firms/employment agencies were engaged by Regeneron for this position and a valid agreement with Regeneron is in place. In the event a candidate who was submitted outside of the Regeneron agency engagement process is hired, no fee or payment of any kind will be paid.
Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.
Apply online at:
http://careers.regeneron.com/united-states/auditing/jobid5153004-qc-micro-analyst-jobsEstimated Salary: $20 to $28 per hour based on qualifications.
Regeneron
Job Summary and
Essential Functions:
Known for its scientific and operational excellence, Regeneron is a leading science-based biopharmaceutical company that discovers, invents, develops, manufactures, and commercializes medicines for the treatment of serious medical conditions. Regeneron markets medicines for eye diseases, colorectal cancer, and a rare inflammatory condition and has product candidates in development in other areas of high unmet medical need, including hypercholesterolemia, oncology, rheumatoid arthritis, allergic asthma, and atopic dermatitis.
Summary:
This is a level IV second shift position.
Performs testing to ensure cGMP compliance in the manufacturing facility. Responsible for assessing the microbiological quality of products, manufacturing equipment, manufacturing process areas, and facility utilities.
Essential Duties and Responsibilities include, but are not limited to, the following:
Reviews and updates SOPs.
Performs peer review of data.
Performs laboratory investigation reports.
Participates in training of other employees.
Performs microbial identification procedures.
Maintains laboratory supplies, media, and reagents inventory.
Participates in the overtime and weekend schedule as required.
Performs bioburden and endotoxin testing of products and raw materials.
Performs microbiological testing of in-process and final product materials.
Performs biological and endotoxin indicator testing used in the validation of manufacturing equipment.
Updates microbiological environmental monitoring results database and prepares monthly report.
Performs acceptance testing of commercially prepared microbiological culture media.
Assists in coordinating equipment maintenance and calibration.
Uses Laboratory Information Management System (LIMS) for sample and sample test result tracking.
Performs all duties relevant to the Quality Control Microbiology Technician position as required.
Additional responsibilities for Analysts II-IV include, but are not limited to:
Increasing involvement in the training of employees.
Increasing responsibilities for reviewing documents and data.
Microbiology representation and participation in cross functional site meetings.
Administration of programs such as gowning, training, ordering, calibration, etc.
Technical writing assignments such as SOPs, protocols, final reports, trend reports, risk assessments, laboratory investigations, etc.
Experience and Required Skills:
Education and
Experience:
Requires BS/BA in Life Sciences or equivalent along with 8 plus year's relative experience, preferably in the pharmaceutical or biotechnology industries.
Will substitute relevant work experience in lieu of degree requirement.
This is an opportunity to join our select team that is already leading the way in the Pharmaceutical/Biotech industry. Apply today and learn more about Regenerons unwavering commitment to combining good science & good business.
To all agencies: Please, no phone calls or emails to any employee of Regeneron about this opening. All resumes submitted by search firms/employment agencies to any employee at Regeneron via-email, the internet or in any form and/or method will be deemed the sole property of Regeneron, unless such search firms/employment agencies were engaged by Regeneron for this position and a valid agreement with Regeneron is in place. In the event a candidate who was submitted outside of the Regeneron agency engagement process is hired, no fee or payment of any kind will be paid.
Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.
Apply online at:
http://careers.regeneron.com/united-states/auditing/jobid5153004-qc-micro-analyst-jobsEstimated Salary: $20 to $28 per hour based on qualifications.
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