<h3>Job Description</h3>
Job Description
Department
Microbiological Services
Job Title
Microbiologist I
FLSA Status
Exempt
Reports To
Microbiology Manager
1. Role Purpose:
Microbiologist I, will provide practical execution of all activities associated with microbiological testing to support the manufacturing with filled pharmaceutical products, microbial monitoring and oral dose production. This position will engage collaboratively and cross-functionally with other departments to provide microbiological support for activities associated with quality assurance, production, sterilization, facilities maintenance and engineering, method and process validation, product and process development following the cGMP guidelines.
2. Key Duties &amp; Responsibilities:
30% Laboratory Support:
<ul>
<li>Responsible for cGMP compliance in Microbiology Department.</li>
<li>Provide microbiological support to maintain and improve process controls.</li>
<li>Provide secondary support to Quality Assurance programs for the manufacture of aseptically filled and oral dose pharmaceutical products.</li>
<li>Sampling raw materials, in-process material, environment and utilities for microbiological analysis.</li>
<li>Bioburden monitoring of Raw Materials, In-process samples, Manufacturing environment, Utilities and supporting areas.</li>
<li>Sterility Testing of finished products and In-process samples</li>
<li>Bacterial Endotoxin Testing of Raw Materials, Finished products and Container/Closures.</li>
<li>Antimicrobial Effectiveness Testing of finished pharmaceutical products</li>
<li>Cleaning and disinfection.</li>
<li>Stability study support.</li>
<li>Liquid Particulate Matter testing of Finished Drug products.</li>
<li>Container-closure integrity testing.</li>
<li>Colony Morphology, Gram Staining and Microbial Identification.</li>
<li>Assist in Laboratory Investigations related to OOS/OOT results.</li>
<li>Responsible for Laboratory cleanliness and biohazard removal</li>
<li>Actively participates in the Laboratory Training Program</li>
<li>Maintaining Laboratory Inventory (Media, Reagents, Sterile Consumables, Reference Standard and Reference Cultures)</li>
<li>Media preparation and Microbiological Control</li>
<li>Preservation of Microbial Isolates</li>
</ul>
20% Manufacturing Support:
<ul>
<li>Provide support for conducting Gowning Qualification studies to support Aseptic Manufacturing operations</li>
<li>Supports the Aseptic Manufacturing process by conducting Microbial Monitoring of Manufacturing Environment, Surfaces, Personnel and Process utilities (Pharmaceutical Water and Compressed Air)</li>
<li>Trending the Bioburden results obtained from Environment and Utility monitoring on a regular basis</li>
<li>Support Microbial Risk Assessment and mitigation process.</li>
</ul>
20% Validation Support:
<ul>
<li>Support the validation of Steam Sterilization (Pharmaceutical Water and Compressed gases), Manufacturing Area (Air and Surfaces), Personnel, Cleaning and Disinfection and Aseptic Manufacturing Process which includes Aseptic Process Simulations.</li>
</ul>
30% Documentation:
<ul>
<li>Document Microbiological Test details and Results, including in applicable interface (Electronic and Paper Documentation) according to Laboratory procedures.</li>
<li>Initiate Laboratory Investigation in the event of OOS/OOT results.</li>
<li>Excellent written and oral communication skills</li>
<li>MS Office applications</li>
</ul>
3. Typical Supervisory Responsibility:
N/A
4. Education &amp; Experience:
Education Requirement
Specialization (If any)
Bachelor of Science is preferred
Science or related field
Experience Requirement
2-5 years of scientific experience is preferred.
5. Technical competencies/ Certifications/ Licenses:
Technical competencies
<ul>
<li>Strong communication and writing skills including demonstrating proficiency in English.</li>
<li>Will be required to be fully gowned, including eye and facial covering in sterilized garments and be present in a clean room for hours at a time.</li>
</ul>
6. Physical demand and Work environment:
a. Physical demands:
While performing the duties of this job, the employee is required to Alternate Sit/Stand or Walk, Climbing Ramps/Stairs, Hearing Requirements, Keyboarding, Kneeling, Lifting/Carrying, Pushing/Pulling, Reaching At/Below Shoulder Level and Reaching Overhead. The candidate must also be able to Communicating Verbally and effectively.
b. Work environment:
N/A
Company DescriptionPenn Life Sciences 
<h3>Company Description</h3>
Penn Life Sciences

Microbiologist I

<h3>Job Description</h3>
Job DescriptionCompany Description 
Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies.
In over just 30 years, Eurofins has grown from one laboratory in Nantes, France to over 47,000 staff across a network of more than 900 independent companies in over 50 countries and operating more than 800 laboratories. Eurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products, as well as providing innovative clinical diagnostic testing services, as one of the leading global emerging players in specialised clinical diagnostics testing
If you’re looking for a rewarding career, apply with us today!&nbsp;&nbsp;
Job Description 
We are seeking a detail-oriented and motivated Microbiologist&nbsp;with experience in water system monitoring, microbiological testing, and environmental monitoring in a GMP-regulated setting. The analyst will be responsible for collecting and testing water and clean steam samples, performing environmental monitoring, and analyzing facility cleaning and in-process samples. Responsibilities could include:
Water system&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;
<ul>
<li>Collection of samples from the facility water and clean steam systems</li>
<li>Microbiological testing of the facility and/or laboratory water purification system samples.&nbsp;&nbsp;</li>
<li>GMP review of data</li>
<li>Qualification and Release of Media</li>
<li>Analytical testing of the facility cleaning samples and Microbial testing of facility In-Process samples</li>
<li>Initiation and follow-up of exceeded alert and action limits per procedure</li>
<li>Participation in the preparation of monthly trending reports</li>
</ul>
Environmental Monitoring
<ul>
<li>Performs plate readings for all environmental monitoring samples as necessary</li>
<li>Performs environmental monitoring, including unmanned Environmental Monitoring in accordance with Sterile Operations schedule</li>
</ul>
Laboratory Support:
<ul>
<li>Logs microbiological testing media and reagents and performs growth promotion</li>
<li>Provides testing support for validation work such as for Validation Maintenance</li>
<li>Provides support for third-party testing, including preparation of documents and shipment of samples, sample tracking, and documentation archiving using LabWare</li>
<li>Provides Microbial Identification support, including documentation, subculturing, Gram stains (where applicable), ensuring chain of custody, review of any vendor report, and interfacing with the vendors</li>
</ul>
Qualifications 
The Ideal Candidate will Have:&nbsp;
<ul>
<li>Experience in a Quality Control Lab or Sterile Suite&nbsp;</li>
<li>Familiarity with cGMP's</li>
<li>Excellent communication (oral and written)</li>
<li>Strong Attention to Detail&nbsp;</li>
<li>A client-focused mindset&nbsp;and a commitment to exceptional service.</li>
</ul>
Minimum Qualificaitons:&nbsp;
<ul>
<li>Bachelor's degree in Biology or Microbiology or Associate’s Degree with a minimum of 1 year of Microbiological experience in the Pharmaceutical Industry</li>
<li>Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude</li>
<li>Ability to work flexible hours at times to support business needs.</li>
<li>Experience with Microsoft Office&nbsp;</li>
<li>Authorization to work in the United States indefinitely without restriction or sponsorship</li>
</ul>
 Additional Information 
What to Expect in the Hiring Process:&nbsp;
<ul>
<li>10-15 Minute Phone Interview with Region Recruiter</li>
<li>45-60 Minute Virtual Interview with Manager and/or Group Leader</li>
</ul>
Additional Details:&nbsp;
The position is full-time, Monday-Friday from 7am-3pm. Candidates living within a commutable distance of King of Prussia, Pennsylvania, and the surrounding areas are encouraged to apply.&nbsp;&nbsp;
Excellent full-time benefits including:
<ul>
<li>comprehensive medical coverage, dental, and vision options</li>
<li>Life and disability insurance</li>
<li>401(k) with company match</li>
<li>Paid vacation and holiday</li>
</ul>
Eurofins Lancaster Laboratories Professional Scientific Services®&nbsp;(PSS) is a global, award-winning insourcing solution that places our people at our clients’ sites dedicated to running and managing laboratory services while eliminating headcount, co-employment, and project-management worries.
We infuse our 55-year track record of scientific and laboratory operations expertise, as well as HR, and a great place to work best practices, to recruit, hire, train, and manage highly qualified scientists to perform laboratory services using our client’s quality systems and equipment.
To learn more about Eurofins Lancaster Laboratories, please explore our website&nbsp;<a href="http://www.eurofinsus.com" target="_blank">www.eurofinsus.com</a>.
Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

<h3>Job Description</h3>
Job Description
WML provides on job training including safety procedures.
Prepare media and broth for use in microbiology testing.
Perform instrumentation maintenance.
Clean up laboratory and autoclave laboratory waste as required.
Data entry using MS excel.
Must maintain neat, accurate and complete records and logs.
Must be able to focus continuous attention to detail with operations requiring some diversification in approach to fairly routine processes.
Customer service, lots of customer interaction on phone and in person.
Other duties that come up, whatever it takes to get the job done.
PDE (Pay Depends on Experience)
Company DescriptionWater Management Laboratories, Inc., is an accredited environmental testing laboratory in Tacoma established in 1976. We are the EPA reference lab for State of WA for multiple procedures in inorganic and organic chemistry and microbiology. Our focus is on drinking water, wastewater, storm water, surface water, soil, solids, and we can do much more. 
<h3>Company Description</h3>
Water Management Laboratories, Inc., is an accredited environmental testing laboratory in Tacoma established in 1976. We are the EPA reference lab for State of WA for multiple procedures in inorganic and organic chemistry and microbiology. Our focus is on drinking water, wastewater, storm water, surface water, soil, solids, and we can do much more.

Microbiologist

About Us
Pace Life Sciences
Pace makes the world a safer, healthier place. We advance the science of our pharmaceutical and biopharmaceutical customers through the drug development process, from early-phase R&amp;D through clinical trials and GMP commercial product support. For customers with in-house manufacturing and labs, Pace provides professional services to support their operations.
 Job Description
 Job Description: We are seeking a skilled and detail-oriented Microbiologist to join our Quality Control team. The ideal candidate will have experience in a sterile fill finish manufacturing environment and a strong background in microbiological testing. This role is essential to ensuring the sterility and safety of our products. 
 Key Responsibilities: 
<ul>
<li> Perform routine and non-routine microbiological testing of raw materials, in-process samples, and finished products. </li>
<li> Conduct environmental monitoring of the manufacturing facility, including air, surface, and personnel monitoring. </li>
<li> Perform endotoxin, bioburden and particulate matter testing. </li>
<li> Develop and validate microbiological methods in compliance with regulatory guidelines. </li>
<li> Maintain and calibrate laboratory equipment and instruments. </li>
<li> Document and review test results accurately and promptly. </li>
<li> Investigate and resolve any microbiological quality issues or deviations. </li>
<li> Collaborate with cross-functional teams to support product development and manufacturing processes. </li>
<li> Ensure compliance with GMP, GLP, and other regulatory requirements. </li>
</ul>
 Qualifications: 
<ul>
<li> Bachelor's or Master's degree in Microbiology, Biology, or a related field. </li>
<li> Minimum of 2-3 years of experience in a microbiology role within a sterile fill finish manufacturing environment. </li>
<li> Proficiency in microbiological techniques such as aseptic techniques, microbial enumeration, and endotoxin testing. </li>
<li> Strong understanding of GMP, GLP, and regulatory requirements. </li>
<li> Excellent attention to detail and problem-solving skills. </li>
<li> Ability to work independently and as part of a team. </li>
<li> Strong communication and documentation skills. </li>
</ul>
 Additional Information
Benefits
80 hrs of paid vacation per year, 7 paid holidays per year, 2 floating holidays per year (prorated based on start date), 40 hrs paid sick time per year, paid bereavement leave (days based on relation to the employee), 8 hrs paid volunteer time per year, parental leave, medical, dental, vision, voluntary short-term disability, long-term disability, life insurance, voluntary supplemental life insurance, traditional 401k and ROTH 401k with a company match, HSA, FSA, employee referral bonus, employee assistance program, tuition reimbursement program, employee recognition program, voluntary ID theft coverage, voluntary legal coverage, voluntary accident insurance, voluntary hospital indemnity insurance, and voluntary critical illness insurance. 
Equal Opportunity Employer
Pace provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, creed, color, religion, genetics, protected veteran status, national origin, sex, age, disability, marital status, sexual orientation, gender identity or expression, citizenship, or any other characteristic protected by federal, state or local laws. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training.
 Work Schedule Mon-Fri dayshift

<h3>Job Description</h3>
Job Description
ABOUT UDA:
UDA is a local, family-owned, dairy cooperative committed to serve the needs of our members, community, and customers by providing high quality milk and dairy products. As the only milk marketing co-op in the state, UDA oversees the production, processing, and marketing of Arizona’s finest milk products from farm to Retail in 48 hours or less. From sweet cream and butter to non-fat dry milk, UDA provides milk products to manufactures and supermarket chains throughout the Grand Canyon State.
Our motto at UDA is “United in Excellence.” The dairy industry’s success isn’t built on one dairy or brand, it’s built on the community as a whole - this includes our amazing employees. When you join UDA, you’re not just joining a business, you’re joining a family. Since 1960 UDA has been headquartered, operated, and managed in Arizona. We strive to provide our employees with rewarding career opportunities aimed at long-term stability, growth, and advancement. We put our heart and soul into our products and value our team who show up, every day and do the work.
Job Summary: 
The Microbiologist is responsible for conducting both qualitative and quantitative testing on finished products, in process, water and environmental samples using aseptic techniques.&nbsp; The Microbiologist follows all GLP/GDP guidelines and ensures that test results are accurate and in compliance with company policies. 
MICROBIOLOGIST PRIMARY FUNCTIONS AND RESPONSIBILITIES: 
<ul>
<li>Apply aseptic/microbiological techniques in daily workload and prepare and analyze samples for indicator organisms and pathogens according to acceptable methods.</li>
<li>Keep accurate and legible records and understand GDP.</li>
<li>Independently pursue an assigned series of processes, procedures, or techniques in accordance with the Standard Methods for the Examination of Dairy Products, Quality Manual, Chemical Hygiene Plan, Safety Manual, and approved laboratory procedures.&nbsp;</li>
<li>Accurately perform and read test results and notify QA management of deviations.</li>
<li>Prepare media and reagents as needed for daily microbiological testing.</li>
<li>Maintain a high degree of technical competence by attending professional workshops and being aware of food industry issues and trends&nbsp;</li>
<li>Report inventory and expendable supplies/materials needed for testing requirements. </li>
<li>Assist in quality control duties to by taking incubator temperatures, inoculating control organisms, running media controls etc., and other laboratory quality control procedures including quality control documentation. </li>
<li>Assist with the coordination of sample collection, transport, and receiving. </li>
<li>Maintain a clean and sanitary work area at all times. </li>
<li>Adhere to all SOP’s and HACCP guidelines</li>
<li>Always maintain food safety and quality standards, resolving and/or reporting compliance issues immediately</li>
</ul>
MICROBIOLOGIST - QUALIFICATIONS:
Skills &amp; Abilities:
<ul>
<li>Excellent Aseptic technique and use of biological hood</li>
<li>Versed in GMP/GLP, FDA, SMEDP, ADPI, AOAC and other method reference sources</li>
<li>
Ability to work a variety of 12-hour shifts, which may include nights, weekends, and holidays.
</li>
<li>Competent in the use of Microsoft Office, Outlook, Word, Excel and Teams. </li>
<li>Detail orientated and the ability to conduct laboratory testing in a precise and accurate manner. </li>
<li>Able to prioritize daily workload and meet laboratory deadlines as expected. </li>
<li>Must have good verbal and written communication skills. </li>
<li>Requires ability to read, hear, speak, and comprehend and carry out verbal and written instructions &amp; Standard Operating Procedures (SOP)</li>
</ul>
Experience: (required)
<ul>
<li>1-4 years related experience in similar function or industry, or equivalent combination of education and experience.</li>
</ul>
Experience: (preferred)
<ul>
<li>Experience that includes working in a GMP regulated industry preferred. </li>
<li>1-2 years of Microbiology experience preferred</li>
</ul>
Education/Certifications:
<ul>
<li>Bachelor’s Degree in Microbiology, or related field of study, or equivalent work experience in microbiology in related field. </li>
</ul>
PHYSICAL REQUIREMENTS:
Reasonable accommodations may be made to enable differently abled individuals to satisfactorily perform the essential functions.
<ul>
<li>Requires ability to walk and stand for 12 or more hours at a time. </li>
<li>Requires ability to safely operate equipment. </li>
<li>Requires ability to work safely within the laboratory environment. </li>
<li>Requires ability to visually observe the condition of surroundings. </li>
<li>Requires ability to stoop, bend, reach, lift and carry items up to 55lbs often. </li>
<li>Requires ability to push and pull items frequently up to 55lbs. </li>
<li>Requires ability to hear and speak and frequently hear and speak in very noisy environments. </li>
<li>Requires ability to work in confined spaces occasionally. </li>
<li>Requires ability to work safely with hazardous chemicals.&nbsp;</li>
</ul>
BENEFITS:
<ul>
<li>Medical, Dental &amp; Vision plans</li>
<li>401(k) Retirement Plan with employer match</li>
<li>Disability Insurance</li>
<li>Life Insurance</li>
<li>Employee Assistance Program</li>
<li>Health &amp; Wellness Programs</li>
<li>Paid Time Off</li>
<li>Shift Pay Differential</li>
<li>Education Assistance</li>
<li>On-site Fitness Center</li>
<li>On-Site Health Clinic &nbsp; &nbsp;</li>
</ul>
The duties and responsibilities described are not a comprehensive list; employees may be subject to additional, or altered, tasks and the scope of the role may change as necessitated by business demands. UDA will not consider any application submissions from unauthorized third-parties, consulting, or external staffing firms and will not be held subject, or liable, to any terms, fees, or penalties associated with a submission. 
UDA is an equal opportunity employer. Applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, sexual orientation, gender identity, disability, or protected veteran status. 
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K8MnrA1heX

<h3>Job Description</h3>
Job DescriptionCompany Description 
Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.
The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products.
In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.
In 2021, Eurofins generated total revenues of EUR 6.72 billion, and has been among the best performing stocks in Europe over the past 20 years.
Job Description 
Position Responsibilities:
<ul>
<li>Endotoxin and bioburden testing</li>
<li>Environmental Monitoring sampling</li>
<li>Water sampling (potentially including animal facility)</li>
<li>Compressed gas sampling</li>
<li>General lab duties (cleaning, stocking, cold room 5S, etc.)</li>
</ul>
Qualifications 
Basic Minimum Qualifications:
<ul>
<li>Bachelor or Master degree in science or other related degree concentration</li>
<li>3+ years related experience</li>
<li>Standard microbiological methods and aseptic laboratory technique experience</li>
<li>Knowledge of cGMP preferred</li>
<li>Experience with LIMS and Electronic laboratory notebooks</li>
<li>Ability to work in a fast paced team-oriented setting</li>
<li>Excellent communication (oral and written) and attention to detail</li>
<li>Authorization to work in the United States indefinitely without restriction or sponsorship</li>
</ul>
 Additional Information 
This position is Full-Time,&nbsp;Monday - Friday, 8:00 a.m. - 5:00&nbsp;p.m. with overtime as needed and the potential for some off shift hours as dependent on project.&nbsp;Candidates currently living within a commutable distance of&nbsp;West Point, PA&nbsp;are encouraged to apply.
<ul>
<li>Excellent full time benefits including comprehensive medical coverage, dental, and vision options</li>
<li>Life and disability insurance</li>
<li>401(k) with company match</li>
<li>Paid vacation and holidays</li>
</ul>
Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

<h3>Job Description</h3>
Job DescriptionCompany Description 
The work we do at Eurofins Professional Scientific Services matters, and so do our employees. At Eurofins PSS, we put a focus on your professional growth. We provide our employees the ability to break into the biopharmaceutical industry and grow from the bottom up. We have the supportive teams and tools available to invest in you while also affording you work-life balance and a competitive benefits package.
Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies.
If you’re looking for a rewarding career, a place to call home, apply with us today!
Job Description 
Primary Duties:
The Quality Control Microbiologist will be primarily responsible for sampling and testing of clean utilities and clean rooms to support the commissioning, qualification, and startup of a new manufacturing facility, the Gene Therapy Innovation Center (GTIC).&nbsp; Other responsibilities will include conducting method qualification, method suitability testing, validation and routine testing of microbiological and compendial assays in compliance with all applicable quality systems and current cGMPs within the Quality Control Operations organization.&nbsp; They will support the departmental goals and contribute to general operations of the microbiology laboratory.&nbsp; &nbsp;This role will contribute to the development and implementation of new programs that govern general and microbiology specific laboratory practices, participate in OOS and Alert / Action Investigations, generate deviation documentation and trend reports, and assist with audit preparation and participation. They will author, review, and revise SOP’s, reports, technical documents, and attend cross-functional team meetings as a QC Microbiology representative.
In addition, the Quality Control Microbiologist will perform cGMP testing to support microbiological testing of raw materials, in-process, finished product, and stability samples. Testing will include but is not limited to: environmental monitoring and plate reads, gowning qualification, endotoxin, bioburden. They will ensure compliance with current regulatory requirements (USP, EU, ISO, ICH and FDA guidance), good documentation practices (cGDP) and industry best practices for manufacturing (cGMP).
Job Description:
<ul>
<li>Train on assigned SOPs and perform OJT/Qualification as applicable</li>
<li>Perform environmental monitoring (EM), which requires gowning qualification, routine EM sampling, plate incubation/enumeration</li>
<li>Support method transfers and method qualification/suitability</li>
<li>Perform required on-site microbiology, compendial, and raw material testing, which includes but not limited to:&nbsp; Bioburden, Endotoxin, ID, Growth Promotion, pH, Osmolality, and Appearance.</li>
<li>Participate in laboratory investigations, deviation investigations.</li>
<li>Identify areas for continuous improvement and complete document revisions.</li>
<li>Author and Lead Technical Protocols and Technical Reports</li>
<li>Data entry, scanning, filing, and trending</li>
<li>Order QC supplies to support testing</li>
<li>Initiate Work Order as required for laboratory equipment</li>
<li>Represent the department in cross functional meetings and projects</li>
</ul>
Qualifications 
Basic Minimum Responsibilities:
<ul>
<li>BS or MS degree in Biology/Microbiology required</li>
<li>Minimum 5 years of related experience in the Biotechnology/Medical Device/ Pharmaceutical manufacturing laboratory industry</li>
<li>Experience working in a GMP environment is required</li>
<li>Must have hands on experience performing Microbiological testing such as: growth promotion, endotoxin and microbial limits/bioburden testing.</li>
<li>Hands on experience sampling in Clean Room environments and aseptic technique</li>
</ul>
 Additional Information 
Position is&nbsp;Full Time, Monday-Friday, 8am-5pm with overtime as needed.&nbsp;Candidates currently living within a commutable distance to&nbsp;Philadelphia, PA&nbsp;are encouraged to apply.
What we offer:
<ul>
<li>Excellent full time benefits including comprehensive medical coverage, dental, and vision options</li>
<li>Life and disability insurance</li>
<li>401(k) with company match</li>
<li>Paid vacation and holidays</li>
<li>Yearly goal-based bonus &amp; eligibility for merit-based increases</li>
</ul>
Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Senior QC Microbiologist

<h3>Job Description</h3>
Job DescriptionDescription:
SHINE Technologies is immediately seeking a QC Microbiologist who will have primary focus on performing routine microbiological benchwork and environmental sampling of multiple manufacturing cleanroom spaces. This position will also help to ensure all QC microbiological equipment remains in a state of validation and calibration and will support the production of Lutetium-177 by performing the daily responsibilities within the QC microbiology laboratory, sterility suite, and manufacturing cleanrooms. This role will also perform a variety of data workup, review, analysis, and trending as assigned.
 
This new position will transition to 4 10-hour shifts after completing 3 months of 1st shift training (8 hours Monday-Friday)
Shift: Tuesday - Friday 6:00am - 4:00pm
The base salary range for this position is $30/hour-$38/hour plus a comprehensive compensation package. Our salary ranges are determined by role, level, and location. 
 
Duties and Responsibilities:
Specific duties and responsibilities of the QC Microbiologist include, but are not limited to:
<ul>
<li>Evaluate and report the microbiological quality of finished goods and ensure compliance with established specifications while maintaining compliance to approved methods.</li>
<li>Perform daily/weekly environmental monitoring testing (cleanroom monitoring, water testing), sterility and endotoxin testing of final product for release. </li>
<li>Review and execute microbiological tests/procedures.</li>
<li>Set up and operate Quality Control lab equipment (microbiological).</li>
<li>Participate in Out of Specification investigations and Environmental Excursions as needed.</li>
<li>Sample raw materials per the material specifications and perform in-house testing, including growth promotion testing of media. Coordinate testing and shipping to contract laboratories for external lab testing.</li>
<li>Ensure preventative maintenance and calibration activities for microbiological lab equipment are carried out to schedule.</li>
<li>Perform data entry of environmental monitoring results.</li>
<li>Ensure QC Laboratory is maintained in a clean and compliant manner.</li>
<li>Comply with Good Manufacturing Practices, Good Laboratory Practices and Good Documentation Practices.</li>
<li>Other duties as assigned.</li>
</ul>
 
Requirements:
<ul>
<li>Minimum: 2-4 years of experience in a cGMP/GLP laboratory.</li>
<li>Preferred: BS in Microbiology with 0-2 years of experience in Pharmaceuticals, Medical Device or Radiopharmaceuticals, cleanroom experience and knowledge related to radiation pharmaceuticals, ability to conduct analytical assays with knowledge of cGMP, ICH, SP and other global compendial regulations and guidance.</li>
<li>Willingness to be “hands on” and understand new technology required for success.</li>
<li>Strong experience in attention-to-detail and following specific written and oral instructions.</li>
<li>Competency in understanding and a willingness to learn a variety of mathematical analyses.</li>
<li>A self-directed, laboratory-focused mindset with a desire to achieve timely results.</li>
<li>A investigative mindset is preferred.</li>
</ul>
Eligibility for employment is conditioned on the applicant’s ability to qualify for access to information subject to U.S. Export Controls. Additionally, applicant’s eligibility may be conditioned based upon meeting the Nuclear Regulatory Commission requirements for access to Safeguards Information, which typically requires a pre-employment drug screen, fingerprinting and criminal background check.
 
SHINE values diversity in all its forms as a critical component of innovation, which is fundamental to our success. Every member of the SHINE community benefits from the talents and experiences of our peers, from the mutual respect we exercise, and from the responsibility we take for our actions.
 
SHINE Technologies is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status.
 
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