<h3>Job Description</h3>
Microbiologist
 
<ul>
<li>Maintain laboratory procedures in accordance with GLP standards of the US FDA.</li>
<li>Strong understanding and in depth knowledge of pharmaceutical microbiological principles, techniques.</li>
<li>Laboratory experience in a cGMP facility</li>
<li>Revision of SOPs</li>
<li>Pharmaceutical Microbiology</li>
<li>QC Chemistry Laboratory</li>
</ul>
 
Are you looking to make a career change to a stable company? This exciting opportunity offers a competitive salary plus an excellent benefits package including medical insurance, dental insurance, vision insurance and paid PTO.Does this position match your future career goals? Then this opportunity could be the right fit for you.
 
Compensation
Full benefits package
Competitive salary
 
Responsibilities include:
<ul>
<li>Keeping up to date with scientific and research developments.</li>
<li>Ensuring that data is recorded accurately in accordance to guidelines.</li>
<li>Observing high health and safety standards.</li>
<li>Maintains quality results by participating in internal audits; reviewing quality control and quality assurance programs.</li>
<li>Follows all safety rules and regulations and conducts periodic safety audits.</li>
<li>Follows all cGMP rules and regulations.</li>
</ul>
 
Requirements:
<ul>
<li>BS degree in Microbiology , Biology or similar.</li>
<li>Laboratory experience in a cGMP facility, including experience with the proper operation of laboratory instrumentation.</li>
<li>This role requires strong analytical skills, attention to detail, and expertise in microbiological testing within a regulated environment.</li>
<li>Test and prepare accurate daily records and documents that report the results of their lab work for lot release.</li>
<li>Analyze, Review and Report test results.</li>
<li>Laboratory experience in a cGMP facility.</li>
<li>Revision of SOPs</li>
<li>Pharmaceutical Microbiology</li>
<li>QC Chemistry Laboratory</li>
<li>Troubleshooting, and the generation and revision of SOPs.</li>
<li>Excellent attention to detail and organizational skills.</li>
<li>Strong analytical and problem-solving abilities.</li>
</ul>
 
 
Jasleen Kaur
<a href="mailto:jasleen@ajuliaexecutivesearch.com" target="_blank">jasleen@ajuliaexecutivesearch.com</a>
Ajulia Executive Search is a search firm specializing in Manufacturing, Finance, IT, Legal and Pharmaceutical positions. This is a confidential search for one of our preferred clients. It is a direct hire position that includes competitive compensation and full comprehensive benefit package.
#ZR

Microbiologist

<h3>Job Description</h3>
Plant Microbiologist
Contract till December 2025
Onsite in Sanford, ME
 
Core Responsibilities: 
<ul>
<li>Perform microbiological testing of water and environmental monitoring samples.</li>
<li>Manage samples, chain of custody, test requests, data review, and release for microbiological samples sent for testing.</li>
<li>Assist with product and equipment validations.</li>
<li>Assist in the maintenance of lab equipment and calibrations.</li>
<li>Complete failure investigations and accurately document Out of Specification results.</li>
<li>Review microbiology documentation.</li>
</ul>
 
Education and Experience: 
<ul>
<li>Bachelor of Science degree in Microbiology, Biology, or a related major.</li>
<li>Minimum of three years’ experience in a GMP laboratory environment (Personal Care, Pharmaceutical, Food, Environmental).</li>
<li>Experience should include working in a manufacturing environment both in a lab and with exposure to plant floor micro control programs.</li>
<li>Familiarity with and ability to execute GMP-compliant failure investigations, CAPA, deviations, and change documentation.</li>
</ul>
 
Competencies: 
<ul>
<li>Solid understanding and practical experience with Good Laboratory Practices (GLPs), including general microbiological laboratory practices, instrumentation (autoclaves, gram staining, water purification systems, etc.), failure investigations of nonconforming products, and general computer skills (Google Suite, MS Word, MS Excel, SPC, SAP, email).</li>
<li>High energy level with a focus on results.</li>
<li>Excellent communication skills—both speaking and writing—to keep team members informed, maintaining lab notebooks and testing documentation.</li>
<li>Proven knowledge of microbiology, validations, cGMP, and instrumentation.</li>
<li>Ability to work independently with initiative, set priorities, and manage multiple tasks within deadlines.</li>
</ul>

<h3>Job Description</h3>
Wet Lab Associate (Pharmaceutical)
Location: Novato, CA (On-Site)
Pay Rate: $30.80/hr.
Duration: 1-year W-2 contract role (Strong potential to extend or convert to FTE)
Work Schedule: Schedule/ 6:00am-7:00pm (12 hours). Thurs-Sat alternating Wed
 
Job Duties:
<ul>
<li>Learn and execute biopharmaceutical manufacturing processes, including mammalian cell culture, depth filtration, tangential flow filtration, column chromatography, protein purification, and bulk drug substance formulation.</li>
<li>Operate large-scale bioprocess equipment for Cell Culture and Purifications operations.</li>
<li>Prepare buffer and media solutions.</li>
<li>Gain proficiency with automation systems such as LIMS, MES, and PI.</li>
<li>Utilize PCR, Gel Electrophoresis, and Western Blot Techniques.</li>
<li>Support process optimization initiatives.</li>
<li>Laboratory clean-up/ Supplies restock.</li>
</ul>
Quality and Compliance:
<ul>
<li>Understand and adhere to cGMPs within Commercial Operations.</li>
<li>Utilize Quality systems for Deviations, CAPAs, Change Requests, Action/Alert Reports, etc.</li>
</ul>
Education &amp; Experience:
<ul>
<li>Bachelor of Science degree in Biology, Biochemistry, Chemistry, Biotechnology, Molecular Biology, or related field with lab requirements; OR</li>
<li>Associate degree in a science-related field or Biotech certificate with 2+ years of experience in Biotech manufacturing or regulated industry.</li>
<li>PCR experience preferred.</li>
<li>Previous undergraduate lab, internship, or research experience a plus.</li>
</ul>
 
Please submit a copy of your resume in PDF or Word format to be considered.

<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 
<ul>
<li>
<ul>
<li>Accurately and safely perform analytical test methods or related support activities as per procedures or protocols and review that results conform to standards.</li>
<li>Analysts will perform testing in a biological safety cabinet including but not limited to microbial, yeast, and mold counts.</li>
<li>Analyst will perform micro-identification.</li>
<li>Analysts will utilize laboratory software to perform testing.</li>
<li>Analyst will perform endotoxin testing on water samples.</li>
<li>&nbsp;Analyst will perform data entry and review own work for accuracy in accordance with laboratory procedures, standards, and GMP requirements.</li>
<li>Analyst will complete receipt of samples coming into the lab.</li>
<li>Analyst will assist in routine housekeeping, 5S, and documentation review for the laboratory.</li>
</ul>
</li>
</ul>
Qualifications 
<ul>
<li>Strong computer, scientific, and organizational skills</li>
<li>Excellent communication (oral and written) and attention to detail</li>
<li>Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude</li>
<li>Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies</li>
<li>BS in field of Chemistry, Biology or related field, or other related degree concentration, or equivalent directly-related experience (two years of directly related industry experience is equivalent to one full-time year of college in related major)</li>
<li>Authorization to work in the United States indefinitely without restriction or sponsorship</li>
</ul>
 Additional Information 
<ul>
<li>Position is&nbsp;Thursday to Monday (with flexible options as long as it covers weekends) from 10:00 am- 6:00 pm. Overtime as needed.&nbsp; Candidates currently living within a commutable distance of&nbsp;Indianapolis, IN&nbsp;are encouraged to apply.&nbsp;</li>
</ul>
<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>#LI-EB1</li>
<li>Authorization to work in the United States indefinitely without restriction or sponsorship</li>
</ul>
Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

<h3>Job Description</h3>
Job DescriptionEQUAL OPPORTUNITY EMPLOYER
Corden Pharma provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws. Corden Pharma embraces fair hiring practices.
 
Corden Pharma is a leading full-service contract development and manufacturing organization (CDMO) of active pharmaceutical ingredients (APIs), excipients, and pharmaceuticals Drug Products (DP) and packaging capabilities with &gt; 2,600 employees across the world. Our services enable pharmaceutical and biotech companies to manufacture medicines with the ultimate goal of improving people’s lives.
Our network in Europe and the U.S. offers flexible and specialized solutions across five technology platforms: Peptides, Lipids, &amp; Carbohydrates; Injectables; Highly Potent &amp; Oncology; and Small Molecules. We strive for excellence in supporting this network and are committed to providing the highest quality products for the well-being of patients.
 SUMMARY
Studies growth, structure, development, and general characteristics of bacteria and other micro-organisms by performing the following duties.
 ESSENTIAL DUTIES AND RESPONSIBILITIES
Include the following. Other duties may be assigned.
<ul>
<li>Isolates and makes cultures of significant bacteria or other micro-organisms in prescribed or standard inhibitory media, controlling factors such as moisture, aeration, temperature, and nutrition</li>
<li>Identifies micro-organisms by microscopic examination of physiological, morphological, and cultural characteristics</li>
<li>Performs endotoxin analysis using turbidimetric and gel clot methods on water and product samples</li>
<li>Maintains the Micro Lab including supply ordering, sterilization, instrument maintenance, and calibration</li>
<li>Generates methods and standard operating procedures relevant to the Micro Lab</li>
<li>Attends and participates in QC Team meetings</li>
<li>Performs Air sampling and testing </li>
<li>Performs Site water activities</li>
<li>Performs water sampling testing</li>
<li>Performs investigation samples</li>
<li>Performs API samples for lot release for all products</li>
<li>Performs Micro program and Micro improvements in the Micro Area</li>
<li>Train QC Staff on new procedures and processes</li>
<li>Qualify new media</li>
</ul>
LEADERSHIP &amp; BUDGET RESPONSIBILITIES
None.
SAFETY &amp; ENVIRONMENTAL RESPONSIBILITIES
Every individual is personally responsible for the safety and environmental aspects of their activities in the workplace. Each employee is expected to perform their job duties in a safe manner utilizing all their knowledge, training, ability, and experience.
QUALITY RESPONSIBILITIES
Corden Pharma Colorado (CPC) is a manufacturer of a variety of pharmaceutical products. In following Current Good Manufacturing Practices (cGMP), Corden Pharma Colorado manufactures in accordance with the US Food and Drug Administration (FDA), International Council for Harmonisation Q7 (ICH), and other global regulations as applicable. This is critical as it is our mission to not place patients at risk due to inadequate safety, quality, or efficacy. CPC’s Quality Management System, which incorporates cGMP, is designed to deliver this quality objective. Attainment is produced through the requisite participation and commitment of all staff across departments and at all levels within the company. 
cGMP is the part of Quality Management System ensuring products are consistently produced to accurate quality standards. Adherence to clearly defined procedures, in compliance with the principles of cGMP, is required when performing operations across Corden Pharma Colorado.
QUALIFICATIONS
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
EDUCATION and/or EXPERIENCE
Bachelor's Degree (BA) from a four-year college or university; or one year of related experience and/or training; or equivalent combination of education and experience.
LANGUAGE SKILLS
Ability to read and interpret documents such as safety rules, operating and maintenance instructions, and procedure manuals. Ability to write routine reports and correspondence. Ability to speak effectively before groups of customers or employees of an organization.
MATHEMATICAL SKILLS
Ability to calculate figures and amounts such as proportions, percentages, area, and volume. Ability to apply concepts of basic algebra.
REASONING ABILITY
Ability to solve practical problems and deal with a variety of concrete variables in situations where only limited standardization exists. Ability to interpret a variety of instructions furnished in written, oral, diagram, or schedule form.
CERTIFICATES, LICENSES, REGISTRATIONS
None.
PHYSICAL DEMANDS
The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
While performing the duties of this job, the employee is regularly required to work with hands and talk or hear. The employee frequently is required to stand, walk, and sit. The employee is occasionally required to reach above shoulder height; climb or balance; stoop, kneel, crouch, or crawl; and taste or smell. The employee must occasionally lift and/or move up to 50 pounds. Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception, and ability to adjust focus.
WORK ENVIRONMENT
The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
While performing the duties of this job, the employee is occasionally exposed to fumes or airborne particles, low levels of toxic or caustic chemicals, and outside weather conditions. The noise level in the work environment is usually moderate.
CORE COMPETENCIES
These are the specific areas of knowledge, skill and ability that are important for successful job performance. They must be job related and consistent with business necessity.
<ul>
<li>Strong math, reading, and comprehension skills</li>
<li>Analytical skills and knowledge of general or biochemistry</li>
<li>Analytical skills and knowledge of general or organic chemistry</li>
<li>Mechanical aptitude with lab equipment</li>
<li>Support senior level QC Staff with general lab duties</li>
<li>Perform basic methods on test samples</li>
<li>Good communication skills and computer skills</li>
<li>Ability to work closely with team members to a common goal</li>
<li>Attention to detail</li>
<li>Ability to work on 12-hour rotating shifts, night or day; weekends and holidays required</li>
</ul>
SALARY
Actual pay will be based on your skills and experience.
BENEFITS
<ul>
<li>401(k) matching - Corden Pharma will contribute 100% of the first 6% - 100% vested after 2 years of service </li>
<li>Accident Plan</li>
<li>Critical Illness Insurance</li>
<li>Dental Insurance</li>
<li>Disability Insurance</li>
<li>Employee Assistance Program</li>
<li>Flexible Spending Account</li>
<li>Health Insurance PPO/HSA</li>
<li>Hospital Indemnity Plan</li>
<li>ID Theft Protection</li>
<li>Life Insurance</li>
<li>Paid Maternity/Paternity Leave</li>
<li>Tuition Reimbursement</li>
<li>Wellness Program</li>
<li>Vacation – Three Weeks 1st Year</li>
<li>Vision Insurance</li>
</ul>
This post will expire on July 19, 2025

<h3>Job Description</h3>
Job Description MicrobiologistResponsibilities: 
<ul>
<li>Create SOP for microbiological validation and development of new procedures</li>
<li>Generate IQ, PQ, and OQ for new procedures</li>
<li>Conduct microbiological testing on samples on manufactured products.</li>
<li>Isolate, culture, and identify microorganisms using standard microbiological techniques.</li>
<li>Analyze and interpret test results; prepare technical reports and present findings.</li>
<li>Maintain and calibrate laboratory equipment and ensure proper laboratory protocols are followed.</li>
<li>Perform environmental monitoring and sterility testing as needed.</li>
<li>Ensure compliance with regulatory requirements (e.g., FDA, USDA, EPA, ISO, GMP/GLP).</li>
<li>Collaborate with cross-functional teams including R&amp;D, QA/QC, and production.</li>
<li>Maintain detailed records of procedures, observations, and data.</li>
<li>Contribute to continuous improvement of lab processes and standard operating procedures (SOPs).</li>
</ul>
Requirements:
<ul>
<li>Bachelor’s degree in Microbiology, Biology, or a related field required.</li>
<li>Master’s degree or Ph.D. is a plus (especially for research-focused roles)</li>
<li>1–3 years of experience in a laboratory setting preferred.</li>
<li>Experience in [industry-specific microbiology, e.g., clinical, pharmaceutical, food safety] is a plus.</li>
</ul>
Salary: $25/hr

<h3>Job Description</h3>
Job Description
At Sheffield Pharmaceuticals, the home of the original Sheffield Toothpaste, we offer exclusive, quality, branded products to promote wellness and relief to our customers. Our wellness and first aid products include a variety of creams and ointments, nasal products, and toothpaste all made in the USA since 1850.
We are currently seeking a QC Microbiologist with experience working in an analytical or quality control lab for a 1st Shift opening. Based in our New London, CT facility, and under the Supervision of the Lab Supervisor, the QC Microbiologist performs quality control analysis, testing and related functions within a Manufacturing QC Lab environment, as outlined below.
Key Responsibilities:
<ul>
<li>Responsible for performing total aerobic microbial count, microbial limit testing, total combined molds and yeast count, and preparatory testing;</li>
<li>Maintenance and preparation of inoculums, antibiotic determination, environmental auditing, DI Water testing and stability testing;</li>
<li>Responsible for cGMP's and SOP's;</li>
<li>Performs quality control analysis on finished products including stability testing and in process goods and incoming materials;</li>
<li>Routine, repetitive checking and testing of production product, including visual and sample inspections of parts used, weights and measures;</li>
<li>Inspect filling equipment for various Q.C. aspects;</li>
<li>Maintain proper documentation for filling quality control as required;</li>
<li>Assists in experiments relative to the discovery and development of new products;</li>
<li>Makes pilot batches of experimental products;</li>
<li>Create processing batch sheets from work orders, and create packaging batch records (PBR's), check artwork, crimp code, log sheets, &amp; shipping requirements;</li>
<li>Prepare artwork ingredient lists;</li>
<li>Complete Certificate of Analysis for customer orders;</li>
<li>Send letters and samples to outside contract laboratories;</li>
<li>Create Bulk labeling stickers;</li>
<li>General electronic and hard copy file maintenance;</li>
<li>Housekeeping with respect to records control;</li>
<li>Maintain and update as needed the NS database and MSDS log;</li>
<li>Maintain cleanliness and appearance of department;</li>
<li>Maintain proper liaison with all departments to contribute to the team philosophy;</li>
</ul>
<ul>
<li>Responsible for following all safety regulations and complying with S.O.P.'s, DEP, EPA, OSHA, FDA, and cGMP's while performing duties;</li>
<li>Other assigned tasks as necessary assigned by Management;</li>
<li>Follow all Environmental and OSHA requirements. Attend in-house training sessions.</li>
</ul>
Qualifications:
Bachelors degree in Microbiology or Biology and 2-5 years of experience preferred. Associates Degree with additional experience will also be considered. Minimum of one-year experience in analytical or quality control laboratory preferred.
Sheffield Pharmaceuticals is an Equal Employment Opportunity employer. We provide equal opportunity to employees and applicants for employment without regard to race, creed, color, religion, sex, age, national origin, physical or mental disability, sexual orientation, marital or familial status, genetic information, protected veteran status, or other basis protected by law.

<h3>Job Description</h3>
Job DescriptionDescription:
Provides microbiological support for all manufacturing and support activities. Participates in activities such as environmental monitoring, media fills, microbiological and chemical sampling of utilities and services, and other tasks as assigned. Performs microbiological and related testing including, but not limited to, bio burden BET, MLT, Microbial Identification, Sterility, TOC, pH, Conductivity, Utility Monitoring, and Growth Promotion. Perform quarterly and annual data analysis, archiving and trending of Environmental Monitoring and utilities data. Serves as mentor to member(s) of the Microbiology staff. 
Requirements:
<ul>
<li>Understand and perform microbiological techniques including, but not limited to, Bio burden, Sterility, Endotoxin, TOC, Water Testing, Environmental Monitoring, Growth Promotion and visual inspections.</li>
<li>Create or revise departmental SOPs.</li>
<li> Maintain the quarterly report for the Microbiology lab tracking all Alerts, Actions, or OOS.</li>
<li>Perform all relevant microbiology tests and reports</li>
<li>Maintain, review and approve all equipment log books associated with the Microbiology Lab.</li>
<li>Keep Microbiology area in a tidy, organized and in a sanitary condition at all times.</li>
<li>Ensure that all supplies related to microbiological monitoring and testing are maintained in sufficient quantities and within shelf-life.</li>
<li>Create, execute and compile verification protocols and reports related to Microbiology.</li>
<li>Leads laboratory investigations for out of specification (OOS) microbiological testing results, and other microbiological laboratory non-conformances.</li>
<li>Prepare deviations, investigations, OOS, change control, work orders and test reports.</li>
<li>Excellent verbal and written communication skills.</li>
<li>Assist in ordering/inventory of lab supplies.</li>
<li>Subject Matter Expert regarding aseptic technique and processing and contributes to related training.</li>
<li>Optimize procedures and methods in relation to microbiological monitoring.</li>
<li>Maintains microbiological results and reports, tracks, trends and metrics ad hoc and per established schedules.</li>
<li>Monitor compendia and other standards to ensure procedures and processes are current with industry standards.</li>
<li>At the request of Quality Assurance Department, assist in vendor audits.</li>
<li>Maintains currency with FDA, EMA and other CGMP standards and industry trends. </li>
</ul>
Education and Experience Required:
<ul>
<li>B.S. in a scientific discipline. </li>
<li>Minimum 3 to 5 years working in a FDA/EMA regulated environment. </li>
<li>Excellent writing skills, judgment, integrity, investigation (as in OOS), ability to work independently.</li>
</ul>
This job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee. Duties, responsibilities and activities may change or new ones may be assigned at any time with or without notice.

Microbiologist I

<h3>Job Description</h3>
Job Description
Certified Group is a leading North American provider of laboratory testing and audit and certification services. The Certified Group of companies includes Food Safety Net Services (FSNS), Certified Laboratories, EAS Consulting Group, Labstat International Inc., Advanced Botanical Consulting &amp; Testing (ABC Testing Inc.), Microconsult Inc. and Micro Quality Labs Inc. The Certified Group provides analytical testing and regulatory guidance services in the food &amp; beverage, dietary supplements &amp; NHP, cosmetics, OTC, personal care, tobacco, cannabis, nicotine and hemp industries. 
We are currently looking for a Microbiologist to join our growing team!
ESSENTIAL RESPONSIBILITIES
<ul>
<li>Study the growth, characteristics and effects of bacteria and other microorganisms to better understand their relation to human, plant and animal health.</li>
<li>Perform sterility testing</li>
<li>Perform API strips &amp; troubleshoot issues and concerns regarding cross-contamination</li>
<li>Adapt and understand the procedures from CTFA, AOAC and others as needed. </li>
<li>Perform Total Plate Counts, Enrichments, Preservative Effectiveness Testing, raw material testing, bulk testing, water testing and other tests.</li>
<li>Perform other duties as assigned.</li>
</ul>
MINIMUM QUALIFICATIONS
<ul>
<li>Must have a B.S. in Microbiology </li>
<li>Knowledge of current CTFA/PCPC, AOAC and other industry standard methods and procedures.</li>
<li>Understanding of pharmaceutical, cosmetic and nutritional microbiology.</li>
<li>Understanding and knowledge of the European, United States, Japanese and other Pharmacopeias.</li>
<li>Experience performing microbial testing on pharmaceutical, cosmetic and nutritional raw materials, water samples, bulk &amp; finished products. Example of these tests are: Total Plate Count (TPC), Yeast &amp; Mold, Enrichments and Preservative Effectiveness Testing (PET).</li>
<li>At minimum, 2 or more years of microbiological testing experience in the cosmetic, nutritional or pharmaceutical industries. </li>
<li>Computer literate. Be able to work with Microsoft programs, search engines, basic spreadsheets, etc.</li>
<li>Able to handle multiple tasks and work in a fast paced environment.</li>
<li>Able to adapt to changes to improve company process.</li>
<li>May assist in overseeing work performed by Microbiology Technician.</li>
</ul>
Benefits: 
<ul>
<li>Progressive 401k Retirement Savings Plan</li>
<li>Employer Paid Short- Term and Long-Term Disability, and Life Insurance</li>
<li>Group Medical</li>
<li>Tuition Reimbursement</li>
<li>Flexible Spending Accounts</li>
<li>Dental</li>
<li>Paid Holidays and Time Off</li>
<li>Many positions which qualify for the company bonus program</li>
</ul>
Certified Group values diversity in its workforce. The company is firmly committed to a policy of Equal Opportunity and will administer its policies in a manner that treats each employee and applicant for employment on the basis of merit. Certified Group will take affirmative action to seek out qualified applicants without regard to race, color, religion, sex, national origin, age, handicap, or veteran status.
 Wednesday through Sunday, 9:00 AM to 5:30 PM

<h3>Job Description</h3>
Job Description
Microbiologist within Medical Device ﻿
Offers Benefits | Prestigious Medical Device Company | Opportunity for Advancement 
Description:
The Microbiologist in this role is responsible for ensuing microbiological quality of the completed device. This includes providing technical support for the facility as it pertains to environmental monitoring and microbiological methods, routine and non routine specification investigations, environmental disturbance reports, and annual controlled access environment reports, routine release of manufactured product, and data analysis of sterilization process.
Responsibilities: 
<ul>
<li>Review and analyze routine microbiological test records.</li>
<li>Provide technical support for facility issues related to environmental monitoring and microbiological methods.</li>
<li>Develop microbiological specifications for incoming components</li>
<li>Conduct investigations for out-of-specification (OOS) results.</li>
<li>Develop and execute qualifications for controlled access environments, DI water, and compressed air systems.</li>
<li>Assess manufacturing process changes for microbial impact.</li>
<li>Complete environmental disturbance reports and annual controlled access environment reports.</li>
<li>Sterilization and Laboratory Methods Support</li>
<li>Support routine release of manufactured products through microbiological and sterilization data analysis.</li>
<li>Write protocols and reports for sterilization and microbiological method qualifications.</li>
<li>Provide technical training to laboratory technicians on new equipment and test procedures.</li>
<li>Deliver training on sterilization validation and processes.</li>
<li>Collaborate with cross-functional teams to support company initiatives and continuous improvement.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>5years of experience in medical device or pharmaceutical industry with a Bachelors Degree</li>
<li>2 years of experience in medical device or pharmaceutical industry with a Master's Degree</li>
</ul>
Pay and Benefits
The pay range for this position is $30.00 - $35.00/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
 • Medical, dental &amp; vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in Plymouth,MN.
Application Deadline
This position is anticipated to close on Jul 7, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email <a href="mailto:actalentaccommodation@actalentservices.com" target="_blank">actalentaccommodation@actalentservices.com</a> for other accommodation options.

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