Hartland, WI · On-site
$73K - $110K/yr
Masters of Science in Chemistry, Biology, Biotechnology, Chemical Manufacturing, Biomedical Engineering, or Engineering. * Six Sigma certification. * 3 years of validation experience in a cGMP Device ...
Hartland, WI · On-site
$73K - $110K/yr
Masters of Science in Chemistry, Biology, Biotechnology, Chemical Manufacturing, Biomedical Engineering, or Engineering. * Six Sigma certification. * 3 years of validation experience in a cGMP Device ...
Milwaukee, WI · On-site
$105K - $130K/yr
Our total rewardsapproach includes an annual performance bonus (subject to eligibility criteria) in ... Understandingof Investment Managementdata domainsincluding Security Masters, Reference data,Indexes ...
Milwaukee, WI · On-site
$105K - $130K/yr
Our total rewardsapproach includes an annual performance bonus (subject to eligibility criteria) in ... Understandingof Investment Managementdata domainsincluding Security Masters, Reference data,Indexes ...
B.S. in life science, biology, business or marketing - MBA preferred * 2-3 years of direct account management experience in a molecular diagnostic setting with a history of proven past performance ...
B.S. in life science, biology, business or marketing - MBA preferred * 2-3 years of direct account management experience in a molecular diagnostic setting with a history of proven past performance ...
B.S. in life science, biology, business or marketing - MBA preferred * 2-3 years of direct account management experience in a molecular diagnostic setting with a history of proven past performance ...
B.S. in life science, biology, business or marketing - MBA preferred * 2-3 years of direct account management experience in a molecular diagnostic setting with a history of proven past performance ...
$10.55 - $15.95
8% of jobs
$18.60 is the 25th percentile. Wages below this are outliers.
$15.95 - $21.34
34% of jobs
The median wage is $23.47 / hr.
$21.34 - $26.74
20% of jobs
$26.74 - $32.13
13% of jobs
$32.36 is the 75th percentile. Wages above this are outliers.
$32.13 - $37.53
6% of jobs
$37.53 - $42.92
9% of jobs
$42.92 - $48.31
4% of jobs
$48.31 - $53.71
3% of jobs
$53.71 - $59.10
1% of jobs
$59.10 - $64.50
0% of jobs
$64.50 - $69.89
1% of jobs
$10
$30
$69
Jobs that require a master's degree in biology include those in education, science, medicine, pharmaceuticals, and a host of other technical positions within agriculture and government land management. Your specific duties and responsibilities differ depending on your job. For example, if you are a biology instructor at a community college, your tasks include grading, making assessments, and helping students master the material. On the commercial side, pharmaceutical sales positions require you to have a strong technical knowledge of the products you are selling to other medical professionals. You can also find research positions in which you conduct experiments for a variety of purposes.
| Aspect | Masters In Biology | Biological Technician |
|---|---|---|
| Required Credentials | Master's degree in Biology or related field | Bachelor's degree in Biology or related field |
| Work Environment | Research labs, academic institutions, environmental agencies | Laboratories, field sites, research facilities |
| Employer & Industry Usage | Universities, research institutions, government agencies | Research labs, biotech companies, environmental organizations |
| Common Search & Comparison | Yes | No |
The Masters In Biology typically involves advanced coursework and research, preparing individuals for higher-level roles in research or academia. Biological Technicians support research projects through data collection and lab work, often requiring a bachelor's degree. While both roles work in biological settings, the Masters In Biology offers more specialized knowledge and opportunities for independent research, making it suitable for those seeking advanced careers or further education.
The top searched job categories for Masters In Biology jobs in Milwaukee, WI are:
$73K - $110K/yr
Full-time
Medical, Life, Retirement, PTO
Re-posted 10 days ago
7.6
Based on 251 frontline employees who took The Breakroom Quiz
231st of 545 rated manufacturers
Job Summary
Responsible for the validation of facility utilities, and equipment processes for cGMP products such as pharmaceuticals, medical devices, and cosmetic products to adhere to 21 CFR 211/210, 21 CFR 820, and other applicable regulatory requirements. Assist in authoring and executing protocols to demonstrate that manufacturing processes are executed with consistent quality and results within a controlled environment. Responsible for managing and or performing revalidation, engineering studies to evaluate new products or components, change control assessments, and coordination of computer and test method validations of applicable products.Job Description
Validate new and revalidate as appropriate existing equipment used in OTC/Cosmetic and medical device manufacturing.
Perform engineering studies to determine if projects are feasible.
Assist with measurement system analysis including Gage R&R.
Support product/design transfer activities including validations and creation of updates to documentation needed to manufacture OTC cosmetic and medical devices.
Support Change Assessment activities including assessment and qualification of changes to existing product components and implementation of products into manufacturing lines.
Support root cause investigations for non-conformances related to manufacturing validations.
Develop, prepare and install equipment and revise test validation procedures/protocols to ensure that a product is manufactured in accordance with appropriate regulatory agency validation requirement and current industry practices.
Responsible for IQ/OQ and PQ phases and implementation of validated SOPs.
Coordinate projects directly with vendors and service providers to ensure that all validation and installation requirements are being satisfied during the execution of protocols.
Develop timelines for all projects and ensure that deadlines and goals are being met. Frequently update management and team on progress.
Proactively work with members of the division or project team to identify issues that might delay the project; make recommendations to improve time lines for project completion.
Compile and analyze validation data, prepare reports, and make recommendations for changes and/or improvements.
Maintain all of the documentation pertaining to qualification and validation of assigned projects and equipment/systems.
REQUIRED EXPERIENCE
Education
Bachelor of Science Degree in Biology, Chemistry, or Engineering.
Work Experience
At least 2 years of validation experience in a cGMP Device or Drug environment.
Experience with validations of controlled environments or equipment validations in a regulated environment.
Experience with validation documentation and related change control.
Strong ability to manage multiple priorities, self-starter attitude, good oral and writing skills and the ability to work independently and as a team in an efficient manner.
PREFERRED QUALIFICATIONS
Masters of Science in Chemistry, Biology, Biotechnology, Chemical Manufacturing, Biomedical Engineering, or Engineering.
Six Sigma certification.
3 years of validation experience in a cGMP Device or Drug environment.
Process validation experience in a pharmaceutical or Medical Device manufacturing environment.
Experience with validation of various product types such as liquid products, solid dosage products, and multi-component products.
Experience in FDA regulated environment.
Experience with ISO 13485 and ISO 11607 standards.
Experience with Measurement System Analysis.
Experience with Minitab statistical analysis software.
Experience with root cause analysis.
Medline Industries, LP, and its subsidiaries, offer a competitive total rewards package, continuing education & training, and tremendous potential with a growing worldwide organization.
The anticipated salary range for this position:
$73,000.00 - $110,000.00 AnnualThe actual salary will vary based on applicant's location, education, experience, skills, and abilities. This role is bonus and/or incentive eligible. Medline will not pay less than the applicable minimum wage or salary threshold.
Our benefit package includes health insurance, life and disability, 401(k) contributions, paid time off, etc., for employees working 30 or more hours per week on average. For roles where employees work less than 30 hours per week, benefits include 401(k) contributions, paid time off, as well as access to the Employee Assistance Program, Employee Resource Groups and the Employee Service Corp. For a more comprehensive list of our benefits please click here.
We're dedicated to creating a Medline where everyone feels they belong and can grow their career. We strive to do this by seeking diversity in all forms, acting inclusively, and ensuring that people have tools and resources to perform at their best. Explore our Belonging pagehere.
Medline Industries, LP is an equal opportunity employer. Medline evaluates qualified individuals without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, age, disability, neurodivergence, protected veteran status, marital or family status, caregiver responsibilities, genetic information, or any other characteristic protected by applicable federal, state, or local laws.
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Medline Industries, LP is the leading nationwide supplier of medical, surgical and pharmaceutical products to hospitals, nursing homes, HME providers, surgery centers, physician offices and home care/hospice settings.
Medical equipment and supplies manufacturing
10,000+ Employees
Winnetka, IL, US
1966
