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CGMP Biomanufactuirng Training Specialist
Job in
Madison, Dane County, Wisconsin, 53786, USA
Listed on 2026-07-12
Listing for:
Kelly Services
Full Time, Seasonal/Temporary
position Listed on 2026-07-12
Job specializations:
-
Business
Regulatory Compliance Specialist
Job Description & How to Apply Below
* Job Title:
** CGMP Biomanufactuirng Training Specialist
** Location** :
Madison, WI- ONSITE
** Duration:
** 4-6 months with possible extensions
** Pay:** $29.81 /HR.
** Shift:
** MON-FRI 8AM - 5PM.
** Position Overview*
* + This position works with Training Manager, cGMP Biomanufacturing to organize and present in-person training sessions on SOPs, cGMP processes, compliance and Environmental Health and Safety to cGMP Bio Manufacturing Group
+ Assists with developing content and formatting training materials, developing and administering training programs for employees.
+ Assesses training and development needs for the cGMP Bio Manufacturing Group
+ Helps individuals and groups develop skills, safety and knowledge
+ Creates training manuals, monitors training for effectiveness.
** Responsibilities:*
* + Track/monitor training and provide timely, accurate information and reports to Training
+ Manager including metrics actions needed to ensure compliance
+ Actively lead training sessions
+ Assist in conducting needs assessment to determine training requirements.
+ Works with managers to address learning issues, instruction problems, or new educational needs regarding specific employees or groups
+ Assist in developing qualifications/evaluations to ensure training effectiveness in the MFG department
+ Assist to design and develop training including structured job specific tasks, SOP training, FDA cGMP, Environmental Health & Safety regulations, and general work skills as needed
+ Revises materials based on assessment/evaluation findings/outcomes
+ Partners/collaborates with Subject Matter Experts to identify need, target audience and desired performance standards
+ Assists in improvements for safety and provides on the floor manufacturing support.
+ Assist Quality Assurance department with SOP training as needed
+ Participate in team meetings
+ Track/review training records for accuracy and completeness.
+ Informs personnel of communications, decisions, policies and all matters that affect their performance, attitudes and results.
+ Maintain effectiveness of Quality system as it pertains to cGMP and training requirements
+ Assists in general cleanroom housekeeping and adherence to 5S standards
+ Assist in execution of equipment qualification/validation protocols, as required
+ Ability to work scheduled shift and other off-shift coverage as required
+ Other duties as assigned
*
* Education:
*
* + B.S./B.A. in Biology, Chemistry or other related scientific field, with minimum of 1-2 years' experience in related laboratory work
*
* Required Experience:
*
* + Bio Manufacturing or other Pharmaceutical/Medical Device experience
+ Clean room, aseptic technique, and/or general lab equipment experience
+ cGMP, Good documentation practices (GDP), Good Laboratory Practices (GLP) knowledge
Following standard operating procedures
+ Experience operating, maintaining and troubleshooting Biomanufacturing-related equipment
** Preferred Experience*
* + Commercial Bio Manufacturing experience or other Pharmaceutical/Medical Device experience
+ Prior ISO 6/7/8 cleanroom experience
+ Prior dedicated training experience
+
Experience with Trackwise, Compliance Wire or other electronic tracking software
** Technical Requirements:*
* + Ability to work within ISO 6/7/8 clean room environments
+ Ability to use Excel, Word, and other MS Office applications
+ Ability to add, subtract, multiply, divide and to record, balance, and check results for accuracy
+ Ability to peer review data to ensure data is well organized with complete documentation
+ Ability to understand and independently apply cGMPs to everyday work with regards to documentation and equipment use
+ Ability to operate within a clean room environment (ISO 6/7/8) and provide on the floor support.
** Why Kelly?*
* Kelly® puts you in charge of your career, with access to cutting edge projects and technologies in industry leading organizations. Top companies throughout the world have trusted Kelly as a premier source of engineering & scientific talent and services since 1965. And Engineering & Scientific job seekers know Kelly® as a firm with an unmatched reputation for quality, integrity and professionalism.
Whether you seek the variety and flexibility of working on short-term project engagements or prefer contract-to-hire or direct hire placement with our clients, apply with Kelly® to explore opportunities that suit your specific professional interests.
As a Kelly Services employee, you will have access to numerous perks, including:
+ Exposure to a variety of career opportunities as a result of our expansive network of client companies
+ Career guides, information and tools to help you successfully position yourself throughout every stage of your career
+ Access to more than 3,000 online training courses through our Kelly Learning Center
+ Weekly pay and service bonus plans
+ Group-rate insurance options available immediately upon hire
* As part of our promise to talent, Kelly supports those who work with us through a variety of…
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