H-1B Visa Quality Control Microbiologist Jobs
Quality Control Microbiologist roles qualify as H-1B visa specialty occupations because they require at minimum a bachelor's degree in microbiology, biology, or a closely related field. Pharmaceutical, biotech, and food safety employers sponsor H-1B visas for this role, and many file LCAs under SOC code 19-1022.
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SGS is the global leader and innovator in inspection, verification, testing and certification services. Founded in 1878, SGS is recognized as the global benchmark in quality and integrity. With over 97,000 employees in 130 countries and operating a network of more than 2,400 offices and laboratories, we provide services to almost every industry by assuring quality and safety of products and services.
Trusted all over the world, SGS is a market leader because we put 100% passion, pride and innovation into everything we do. We encourage new ideas. We welcome people who challenge the way we do things. And we will be 100% committed to helping you reach your full potential.
Job Description
Microbiologist II - SGS North America, Inc., Fairfield, New Jersey.
- Mentoring and training new microbiologists as needed (5% of time)
- Accessing appropriate technical references and documenting data in notebooks and LIMS (5% of time)
- Data entry, receiving/returning calls, sending/receiving information, copying of documents, and processing assignments (5% of time)
- Being accountable for quality assurance tasks vital to the position, including, but not limited to, lab area monitoring, media qualification, incubator, instrument and equipment calibration, and maintenance and sterilization procedures (15% of time)
- Scheduling analyses so that completion deadlines are met but also so that analyses are thoroughly and thoughtfully conducted (5% of time)
- Responsible for accurate and timely recordkeeping, diligently following standards for analysis and SOPs (5% of time)
- Conducting analyses of samples in accordance with USP, EP ASTM, AOAC, FDA, EPA, or other compendia procedures, procedures supplied by the client, and other non-routine procedures as encountered (20% of time)
- Practicing aseptic techniques and disinfection per laboratory Standard Operating Procedures (SOPs) (10% of time)
- Conducting Assays to find working concentrations and potencies using microbiological methods for Antibiotic testing (10% of time)
- Performing Sterility tests as per the compendia requirements and client methods (5% of time)
- Preparing media and reagents required for the conduct of microbiological analyses (5% of time)
- Designing and executing R&D experimental frameworks within cGMP-regulated laboratory environments while providing technical governance and procedural oversight to ensure data integrity, regulatory compliance, and reproducibility across project deliverables (10% of time)
Qualifications
Must have a Bachelor’s degree in Microbiology, Biology, or a related field plus two (2) years of experience in the job offered or related occupation. Experience must include:
- One (1) year of experience creating unique login identification in LIMS for each sample submittal, entering sample records and generates labels using LIMS in accordance with chain of custody; applying labels to all samples
- One (1) year of experience logging samples into LIMS by assigning the appropriate analytical test codes to each sample in accordance with the chain of custody
- Six (6) months of experience with accountability for quality assurance tasks vital to laboratory operations, including, but not limited to, monitoring laboratory area, maintaining media qualification, calibration of incubators, instruments and equipment and maintenance and sterilization procedures
- Six (6) months of experience conducting analyses of samples in accordance with USP, EP ASTM, AOAC, FDA, EPA or other compendia procedures, procedures supplied by the client, and other non-routine procedures as encountered; accessing appropriate technical references and documenting data in notebooks and LIMS
- One (1) year of experience reviewing and completing all COC discrepancies/client communication documentation in a timely manner
5 days/40hrs/wk; $63,378.00/Yr.
Additional Information
SGS is an Equal Opportunity Employer, and as such we recruit, hire, train, and promote persons in all job classifications without regard to race, color, religion, sex, national origin, disability, age, marital status, sexual orientation, gender identity or expression, genetics, status as a protected veteran, or any other characteristics protected by law.
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily with or without reasonable accommodations. The requirements listed above are representative of the knowledge, skills, and/or abilities required.
This job description should not be construed as an exhaustive statement of duties, responsibilities or requirements, but a general description of the job. Nothing contained herein restricts the company’s rights to assign or reassign duties and responsibilities to this job at any time.
If you are applying for a position within the United States and you have difficulty completing the on-line employment application because of a disability, please call 201-508-3149 for assistance and leave a message. You will receive a call back. Please note, this phone number is not for general employment information, but is only for individuals who are experiencing difficulty applying for a position due to a disability.
Company Description
SGS is the global leader and innovator in inspection, verification, testing and certification services. Founded in 1878, SGS is recognized as the global benchmark in quality and integrity. With over 97,000 employees in 130 countries and operating a network of more than 2,400 offices and laboratories, we provide services to almost every industry by assuring quality and safety of products and services.
Trusted all over the world, SGS is a market leader because we put 100% passion, pride and innovation into everything we do. We encourage new ideas. We welcome people who challenge the way we do things. And we will be 100% committed to helping you reach your full potential.
Job Description
Microbiologist II - SGS North America, Inc., Fairfield, New Jersey.
- Mentoring and training new microbiologists as needed (5% of time)
- Accessing appropriate technical references and documenting data in notebooks and LIMS (5% of time)
- Data entry, receiving/returning calls, sending/receiving information, copying of documents, and processing assignments (5% of time)
- Being accountable for quality assurance tasks vital to the position, including, but not limited to, lab area monitoring, media qualification, incubator, instrument and equipment calibration, and maintenance and sterilization procedures (15% of time)
- Scheduling analyses so that completion deadlines are met but also so that analyses are thoroughly and thoughtfully conducted (5% of time)
- Responsible for accurate and timely recordkeeping, diligently following standards for analysis and SOPs (5% of time)
- Conducting analyses of samples in accordance with USP, EP ASTM, AOAC, FDA, EPA, or other compendia procedures, procedures supplied by the client, and other non-routine procedures as encountered (20% of time)
- Practicing aseptic techniques and disinfection per laboratory Standard Operating Procedures (SOPs) (10% of time)
- Conducting Assays to find working concentrations and potencies using microbiological methods for Antibiotic testing (10% of time)
- Performing Sterility tests as per the compendia requirements and client methods (5% of time)
- Preparing media and reagents required for the conduct of microbiological analyses (5% of time)
- Designing and executing R&D experimental frameworks within cGMP-regulated laboratory environments while providing technical governance and procedural oversight to ensure data integrity, regulatory compliance, and reproducibility across project deliverables (10% of time)
Qualifications
Must have a Bachelor’s degree in Microbiology, Biology, or a related field plus two (2) years of experience in the job offered or related occupation. Experience must include:
- One (1) year of experience creating unique login identification in LIMS for each sample submittal, entering sample records and generates labels using LIMS in accordance with chain of custody; applying labels to all samples
- One (1) year of experience logging samples into LIMS by assigning the appropriate analytical test codes to each sample in accordance with the chain of custody
- Six (6) months of experience with accountability for quality assurance tasks vital to laboratory operations, including, but not limited to, monitoring laboratory area, maintaining media qualification, calibration of incubators, instruments and equipment and maintenance and sterilization procedures
- Six (6) months of experience conducting analyses of samples in accordance with USP, EP ASTM, AOAC, FDA, EPA or other compendia procedures, procedures supplied by the client, and other non-routine procedures as encountered; accessing appropriate technical references and documenting data in notebooks and LIMS
- One (1) year of experience reviewing and completing all COC discrepancies/client communication documentation in a timely manner
5 days/40hrs/wk; $63,378.00/Yr.
Additional Information
SGS is an Equal Opportunity Employer, and as such we recruit, hire, train, and promote persons in all job classifications without regard to race, color, religion, sex, national origin, disability, age, marital status, sexual orientation, gender identity or expression, genetics, status as a protected veteran, or any other characteristics protected by law.
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily with or without reasonable accommodations. The requirements listed above are representative of the knowledge, skills, and/or abilities required.
This job description should not be construed as an exhaustive statement of duties, responsibilities or requirements, but a general description of the job. Nothing contained herein restricts the company’s rights to assign or reassign duties and responsibilities to this job at any time.
If you are applying for a position within the United States and you have difficulty completing the on-line employment application because of a disability, please call 201-508-3149 for assistance and leave a message. You will receive a call back. Please note, this phone number is not for general employment information, but is only for individuals who are experiencing difficulty applying for a position due to a disability.
See all H-1B Visa Quality Control Microbiologist Jobs
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Get Access To All JobsTips for Finding H-1B Visa Sponsorship in Quality Control Microbiologist
Align your credentials to SOC 19-1022
Your degree field must directly match the Quality Control Microbiologist job description for USCIS to approve the specialty occupation requirement. A degree in microbiology, biochemistry, or a closely related life science is the strongest match.
Search LCA filings for QC microbiology roles
Use the OFLC Wage Search to find employers who have filed Labor Condition Applications specifically for microbiologist or quality control scientist positions. This confirms H-1B sponsorship history before you apply.
Target FDA-regulated industries over general employers
Pharmaceutical, medical device, and biologics manufacturers hire QC Microbiologists under GMP compliance requirements, making sponsorship common. Employers in these sectors already have immigration counsel and established H-1B filing processes.
Use Migrate Mate to filter by sponsorship history
Search Quality Control Microbiologist roles on Migrate Mate to see employers with verified DOL LCA filing history for this occupation. You skip the guesswork of cold-applying to employers who don't sponsor.
Confirm your wage tier before accepting an offer
Your offered salary must meet the prevailing wage for your work location under DOL guidelines. Check the OFLC Wage Search for the Level I through Level IV wage tiers for SOC 19-1022 in your target city before negotiating.
Ask about cap-exempt status during offer negotiations
Hospitals, university research labs, and nonprofit research institutions may qualify as cap-exempt H-1B employers, letting you file outside the annual lottery. Clarify your prospective employer's cap status early so you understand the filing timeline.
H-1B Visa Quality Control Microbiologist: Frequently Asked Questions
Does a Quality Control Microbiologist role qualify as an H-1B specialty occupation?
Yes. USCIS treats Quality Control Microbiologist as a specialty occupation because the position normally requires at minimum a bachelor's degree in microbiology, biology, biochemistry, or a directly related field. Employers must document that the specific role requires that degree field in the LCA and I-129 petition. Roles that list a degree as preferred rather than required can draw an RFE, so confirming the job description language before filing matters.
Which industries are most likely to sponsor H-1B visas for this role?
Pharmaceutical manufacturers, biologics companies, medical device firms, and food and beverage producers operating under FDA or USDA regulatory frameworks hire QC Microbiologists in volume and commonly sponsor H-1B visas. Contract research organizations and contract manufacturing organizations are also frequent sponsors. These employers already maintain immigration counsel, which reduces your internal friction during the petition process. You can browse sponsoring employers by industry on Migrate Mate.
How does the prevailing wage requirement work for QC Microbiologist H-1B petitions?
Your employer must pay you at least the prevailing wage for SOC code 19-1022 in your specific work location, as determined by the DOL. Wage levels run from Level I for entry-level to Level IV for senior specialists. Your employer certifies this wage in the LCA before filing the I-129 with USCIS. If the offered salary falls below the certified wage level, USCIS can deny the petition, so confirming wage compliance before signing an offer letter protects both parties.
Can I transfer my H-1B to a new QC Microbiologist role without waiting for the lottery again?
Yes. H-1B portability under AC21 lets you transfer an approved H-1B to a new employer in the same or a substantially similar occupation without re-entering the cap lottery. A Quality Control Microbiologist role at a new employer generally qualifies as substantially similar to your existing petition if the SOC code and core duties align. Your new employer files an H-1B transfer petition and you can start work as soon as the receipt notice is issued.
What documentation strengthens an H-1B petition for a QC Microbiologist?
A degree transcript showing a major in microbiology, biology, or biochemistry is the foundation. If your degree is from outside the U.S., a credential evaluation from a NACES-member organization confirming equivalency to a U.S. bachelor's degree is required. Published research, laboratory certifications such as ASM credentials, and a detailed employer job description that explicitly requires a specific degree field all reduce the risk of a USCIS Request for Evidence.