has a single mission: To be a world-class Immunological Services Provider for leading livestock producers and their veterinarians. Medgene is seeking to hire a Process Development and Improvement Associate Scientist for our rapidly growing business and product pipeline.
Purpose: Perform process development and improvement studies as directed by the Process Development and Improvement Leader. Distinguishing Feature: The Process Development and Improvement Associate Scientist is responsible for executing process development and improvement studies for the manufacture of recombinant proteins. The position requires the ability to write, read, and understand standard operating procedures and
be able to execute the procedures to ensure compliance with CVB regulations. Good documentation practices are required while documenting the work that is being performed.
Functions: Read and understand SOPs and Protocols for manufacturing vaccines. Maintains records detailing adherence to established policies. Execute experiments in small scale bioreactors and fermenters to optimize expression and product quality of recombinant biologics. Maintain detailed and accurate laboratory notebooks/batch records. Have proven hands on experience in aseptic techniques. Perform production of buffers, growth media, and solutions. Help maintain laboratory equipment, supplies, and a clean/safe working
environment. Assist with production activities as needed. Work with Production on transfer of products.
Manufacturing of veterinary vaccines in compliance with CVB guidelines and regulations. Maintains appropriate records commensurate with CVB guidelines. Ensures high-quality production standards from culture through bottling. Ensure security of Master Seed, Unreleased, and Released Products. Assist with creating the conditions for increasing productivity by analyzing and improving existing processes as well as improving technology transfers and minimizing losses. Performs other work as assigned. Reporting Relationships: Reports directly to the Process Development and Improvement Leader.
Indirectly reports to the VP of Manufacturing. Challenges and Problems: Challenged to provide effective, safe vaccines to commercial clients in a timely manner. Assist with investigations into poorly-growing cultures, inefficient yields, processing problems. Keeping of detailed records will be an absolute necessity, subject to Audit by the Regulatory and Compliance Officer and Quality Assurance. Decision-Making Authority The Process Development and Improvement Leader is responsible for making experimental decisions involved in the efforts of the position in order to deliver accurate, concise, and timely data.
Decisions may also be delegated to Process Development and Improvement Leader by the Vice President of Manufacturing. Contact with Others: Daily contact with manufacturing, QA, QC, Regulatory, and R&D personnel. Limited contact with Sales and Marketing. Working Conditions: Potential for exposure to human and animal pathogens, including blood-borne pathogens. Exposure to infectious agents, dangerous chemicals, high-voltage equipment, toxic fumes, high-pressure steam, temperature extremes, and potential mutagens. Knowledge, Skills, and Abilities: Knowledge of: BS in Biochemistry, Biology, or equivalent.
Previous experience with fermentation and/or cell culture, chromatography, or other downstream processing techniques. Basic level knowledge and understanding of 9CFR. Basic level knowledge and understanding of hazardous material handling. Aseptic Techniques and good laboratory practices. Good Documentation Practices. Ability to: Follow specific procedures. Work safely with infectious materials and specimens. Operate scientific equipment and computers. Establish and maintain effective working relationships with others. Keep detailed and accurate documentation.
Maintain a safe work environment for self and other employees at all times. Job Posted by Applicant Pro
precisely than previously possible. Medgene Labs has a single mission: To be a world-class Immunological Services Provider for leading livestock producers and their veterinarians. Purpose: Medgene Labs is seeking a Research Scientist to join our growing team and help fully develop our construct bank for viral and bacterial expressed proteins.
The candidate will serve as technical support, providing molecular engineering experience. Primary focus will be to perform daily laboratory assays, maintenance, and optimization of procedures. Distinguishing Feature: The Research Scientist is responsible for support within the Construct Team. Must have a strong background in molecular and immunological
assays, protein production and optimization, and bioinformatics. Coordination and cooperation with Construct Team, Immunological Services, Production, and Quality Assurance departments are essential.
The position requires independent judgement and interpretation under the direct supervisor. Candidates should have a minimum of a Bachelor of Science in Microbiology/Chemistry/Animal Science or related field. Experience preferred, but not required. Functions: Perform molecular cloning efforts by applying molecular biology techniques. Characterization of vaccine candidates by performing molecular biology techniques. Operate and maintain laboratory and experimental equipment. Work collaboratively
with other team members to accomplish project goals and milestones.
Track and document results with Official Documents and Laboratory Notebooks. Creating the conditions for increasing productivity by analyzing and improving existing processes. Monitoring Compliance with aseptic procedures and cleaning schedules as well as occupational health and safety regulations. Ensuring a culture of safety for all employees at VST/Medgene. Performs other work as assigned. Reporting Relationships: Typically reports to the Constructs and Process Development Director, and may provide work direction to Associates, Technicians, and/or students or other staff assigned to the laboratory.
Challenges and Problems: Challenges include performing within established timelines, maintaining accuracy, and consistency due to variance in constructs. Keeping of detailed records will be an absolute necessity, subject to audit by the Regulatory and Compliance. Problems include potential weekend and off-hours work. Decision-Making Authority Decisions include development of specific assays, interpretation of data and communication to appropriate department; what supplies to order; safety and accuracy of equipment; the identity of reference reagents and tests; sources of testing problems; when to contact supervisors for assistance; whether to call service for a piece of equipment; informing management of status of vaccine serials.
Contact with Others: Daily contact with junior technicians, additional staff of VST/Medgene. Working Conditions: Potential for exposure to human and animal pathogens, including blood-borne pathogens. Exposure to infectious agents, dangerous chemicals, high-voltage equipment, toxic fumes, high-pressure steam, temperature extremes, and potential mutagens. Knowledge, Skills, and Abilities: Knowledge of: The methods and techniques of bacterial, viral, mammalian and insect cell culture.
Baculovirus expression vectors and protein production Molecular techniques including transfections, cloning, DNA/RNA extraction and PCR, restriction enzyme digestion Common biochemical and immunological techniques, including SDS-PAGE, UV/Vis spectroscopy, ELISA and western blotting. Laboratory quality controls procedures and appropriate statistical methods. Ability to: Perform various cell culture growth methods, tests, and analyses. Follow specific procedures Work safely with infectious materials and specimens Operate scientific equipment and computers Write detailed SOPs and protocols Identify reference materials Establish and maintain effective working relationships with others Perform various tests, adapt techniques as required, and perform complex computations.
Prepare scientifically accurate and thorough reports. Medgene Core Competencies Accountability and level of Impact Plans and leads completion of project work with team Works autonomously; manages resources; consults with and updates supervisor Technical/Functional Expertise & Application Applies broad knowledge and specialized training in complex scientific principles and techniques Modifies existing processes, procedures and technologies, or develops new ones, as needed May provide training, or technical consultation to others Problem Solving and Innovation Applies methodology and creativity to resolve complex problems to individual accountabilities and project teamwork.
Communication, Collaboration, and People Influence Proactively collaborates and shares information/ better practices within and across Medgene teams, units and departments to influence at the site level. Produces internal written communications; provides input to publications for external use; facilitates team meetings; presents in project teams. Job Posted by Applicant Pro
has a single mission: To be a world-class Immunological Services Provider for leading livestock producers and their veterinarians. Medgene is seeking to hire an R&D Analytical Development Associate Scientist for our rapidly growing business and product pipeline.
Purpose: Perform daily operations within the R&D Analytical Development team. Distinguishing Feature: The position is responsible for developing new analytical assays for use in R&D or QC manufacturing. The analytical team also serves as a resource for troubleshooting or reoptimizing existing assays in R&D or QC manufacturing. Knowledge of basic laboratory procedures within an analytical laboratory and aseptic techniques are required.
Previous experience with immunological assays (including ELISA, Western Blots or Serology) is preferred. Experience with automated Western Blot technology is a plus.
The position requires the ability to read and understand standard operating procedures and be able to execute the procedures to ensure compliance with CVB regulations. Good documentation practices are required. Functions: Assist in design, optimization, and validation of immunological assays for use in R&D and QC manufacturing. Assist in troubleshooting of issues that may arise with current immunological assays. Read and understand SOPs and Protocols for manufacturing vaccines. Maintains records detailing adherence to established
policies. Maintains appropriate records commensurate with CVB guidelines.
Maintenance of laboratory equipment, facility, and standards within the Analytical team. Ensure compliance with aseptic procedures and cleaning schedules. Performs other work as assigned. Reporting Relationships: Reports directly to Analytical Manager. Challenges and Problems: Challenged to develop and validate assays used for quantification of proteins in an independent setting. Assist with different problems such as mechanical/equipment failure, contamination, or poorly growing cultures. Keeping of detailed records subject to Audit by the Regulatory and Compliance and Quality Assurance, will be an absolute necessity.
Decision-Making Authority Decisions will be made in conjunction with Analytical team. Contact with Others: Daily contact with R&D, Manufacturing, QA, and QC personnel. Limited contact with Regulatory, Sales and Marketing, personnel. Working Conditions: Potential for exposure to human and animal pathogens, including blood-borne pathogens. Exposure to infectious agents, dangerous chemicals, high-voltage equipment, toxic fumes, temperature extremes, and potential mutagens. Knowledge, Skills, and Abilities: Knowledge of: Immunological assays used for quantification of proteins.
Aseptic Techniques and good laboratory practices. Good Documentation Practices. Experience with ELISA, Western Blot or other immunological assays preferred. Ability to: Develop and follow specific procedures. Work safely with infectious materials and specimens. Operate scientific equipment and computers. Establish and maintain effective working relationships with others. Keep detailed and accurate documentation. Maintain a safe work environment for self and other employees at all times. Job Posted by Applicant Pro
lives of everyone we touch, and we re always looking for people like you to join our mission. And making a difference isn t the only perk of traveling with us. Start your medical travel career with Fusion Medical Staffing and gain access to competitive pay packages, comprehensive benefits, corporate discounts and perks, a clinical team to support you along your journey, and a recruiter determined to help you succeed.
We ve got your back so you can focus on what you do best: helping others. _______________________________________________________Registered Nurse - Operating Room Position: Registered Nurse Specialty: Operating Room Lic/Certs: ACLS, BLS13 week Operating Room Registered Nurse
travel assignment Client in Montevideo, MN is looking for a Operating Room Registered Nurse to help them out for 13 weeks. At Fusion Medical, we truly believe that as people taking care of people, together we can do anything.
Benefits Include: Paid Time Off (PTO) after 1560 hours Highly competitive pay Best in the industry Medical, Dental, and Vision Short term disability 401(k) Aggressive Refer-a-friend Bonus Program Your recruiter is available 24-7 Reimbursement for licensure and CEU s Qualifications/Requirements: One to three years experience as a Registered Nurse preferred Other certifications may be required for this position Critical thinking, service excellence and good interpersonal
communication skills, ability to read/comprehend written instructions, ability to follow verbal instructions, PC skills Physical Abilities: Remain in a stationary position, move about, move equipment (50-100lbs), pushing, pulling, bending.
The following is a summary of the major job duties of this job. Other duties may be performed, both major and minor, which are not mentioned below. Specific activities may change from time to time. Communicates and collaborates with physicians and other health team members. Provides and coordinates patient care with other health team members. Monitors patients' responses to interventions and reports outcomes. Administers medications as ordered with appropriate documentation.
Monitor and evaluates patients before, during, and post procedure depending on unit. Shares on-call responsibilities with a 30-minute response time if required. Maintains cleanliness of rooms and adequate stock of supplies. Transports patients as needed. Performs other duties as assigned. Required Essential Skills: Interpersonal Skills - to work effectively with a variety of personnel (professional and ancillary) to present a positive attitude and a professional appearance. Technical/Motor Skills - Ability to grasp, fine manipulation, pushing/pulling and able to move about when assisting with procedures and/or using department equipment.
Mental Requirements - Must be able to cope with frequent contact with the general public, customers, and meeting deadlines under pressure. Must be able to work under close supervision occasionally as well as working without assistance from other personnel. Must be able to contend with irregular activity schedules occasionally and continuous concentration to detail. Sensory - Visual acuity, ability to effectively communicate Fusion is an EOE/E-Verify Employer About Fusion Medical Staffing: Fusion Medical Staffing provides career opportunities to healthcare professionals by helping medical facilities fill their staffing needs.
Fusion staffs a variety of specialties within the nursing and allied healthcare fields. We offer competitive pay packages and benefits that travelers deserve. At Fusion, you can seriously choose your own adventure! Fusion's purpose is to ensure that everyone we touch has a better life. We strive to be humble, driven and positive in all our actions! Specialty Fields: Cardiopulmonary Cath Lab Home Health Laboratory Long Term care Nursing Radiology Therapy Associated topics: ambulatory, asn, cardiothoracic, care unit, domiciliary, infusion, intensive, maternal, nurse, staff nurse
traveler with Uniti Med you work with one recruiter creating a solid relationship that always has your best interest in mind. Your recruiter will be a true champion to provide you with a unique travel experience, place you in premier locations around the U. S.
and match you to the right assignment for YOU. Who doesn t love that? Uniti Med offers competitive pay packages and a full benefits package for healthcare workers in the nursing, long term care, home health, radiology, therapy, laboratory, and cardiopulmonary fields. Associated topics: ambulatory, care, care unit, intensive, maternal, nurse, psychatric, registered nurse, transitional, unit
Medgene Labs has a single mission: To be a world-class Immunological Services Provider™ for leading livestock producers and their veterinarians. POSITION SUMMARY Medgene Labs seeks a Quality Assurance Technician, who is responsible for Quality Assurance functions for a veterinary vaccine production company.
The successful candidate will be responsible for developing, improving, and adhering to quality assurance goals and systems, including prioritization, and providing quality oversight for a manufacturing facility. This position will report to the Quality Assurance Manager. Professional and experienced in handling a wide range of Quality Assurance responsibilities. Able to work independently
with little or no supervision. JOB DUTIES The Quality Assurance Technician, as a member of the Compliance Team, is responsible for ensuring quality assurance by ensuring processes and personnel activities are compliant with company policy and governing regulations.
Operations Provide document support to team members who produce batches and serials releases. Perform production batch and serial releases. Generation and quality approval of deviation investigation and auditing records Review of regulatory documentation such as Outlines of Production, Special Outlines, and labels. Communicate between departments to ensure projects are started, executed, and finished according to regulations
and company policies. Coordinate with Regulations regarding facility documentation and equipment to ensure compliance.
Support the document management system related to manufacturing. Auditing functions of facilities, processes, and inventories as prescribed Review of internal Master Documents Process improvement Management of the internal training program Management and internal release of raw materials Assist in internal and external audits. Organization Manage regulated labels including production and inventory. Support Manufacturing in the movement of products through computer systems Provide support in Quality Assurance activities such as Change Controls, Deviations, and Document Management Develop and implement workflows and processes.
Manage the internal inventory system of inputs and final products. Review end-user records for the accuracy of implemented operations Training and Support Conduct a review of the adequacy and effectiveness of the Quality Management System Support and encourage a Quality Culture. Create, monitor, and train internal processes. Perform additional duties as required. MINIMUM QUALIFICATIONS: Knowledge of: Interest in vaccine licensing practices and procedures Interest in science and biotechnology Proven office management, administrative, or assistant experience Knowledge of office management responsibilities, systems, and procedures Excellent time management skills and ability to multi-task and prioritize work.
Attention to detail and problem-solving skills. Excellent written and verbal communication skills Strong organizational and planning skills Proficient in MS Office Knowledge of data and administrative management practices and procedures Knowledge of clerical practices and procedures Ability to: Follow detailed directions and instructions. Communicate information clearly and concisely. Establish and maintain effective relationships with coworkers. Job Posted by Applicant Pro
and develop, produce and market innovative medicines, solutions and services in more than 110 countries and regions. FIRST SHIFT HOURS & EXCELLENT BENEFITSContact Joey at 919-308-xyz X or email joey. benefield@NEW GRADS WELCOME! Seeking Registered Nurse or Licensed Practical Nurse for Plasma Donation Center Are you looking for something different?
Did you know that your skill set/experience makes you a valuable candidate for a Center Medical Specialist position in one of our plasma donation centers? Grifols prides itself on its family-like culture. Our company has more than tripled its workforce in the last 10 years — we’re growing, and you can grow with us! For more information visit:
What’s In It for You Competitive Pay Career Growth/Promotions Geographic mobility among our more than 300 donation centers No Third Shift Incredible Comprehensive Benefits Package Including: Medical, Dental, Vision, up to 5% 401K match, Tuition Reimbursement, PTO, Holiday Pay, Opportunity to participate in Company Bonus Program About the Job Perform physical examination and establish medical history to determine donor suitability Build rapport with donors to ensure overall customer satisfaction Ensure donor and staff confidentiality Responsible for donor awareness to potential hazards Provide donor education regarding general health and provide counseling regarding unacceptable test results Evaluate
& manage donor injuries and adverse events Perform evaluations of any history of illness or medications to ensure continued donor suitability Assist in employee training Administer employee Hepatitis Vaccine program Job Requirements Educated and currently certified/licensed in the state of employment and according to state requirements as a Registered Nurse, Licensed Practical Nurse, Licensed Vocation Nurse, Paramedic, or EMT.
Current CPR certification required. EEO Minorities/Females/Disability/Veterans#biomatusa#app Location: NORTH AMERICA : USA : SD-Brookings: USBRK - Brookings SD-22nd Ave S-BPC Learn more about Grifols For more details: jobs-search. org/advertising_brookings-c446757/lpn-or-rn-brookings_i1960776193
Company is upgrading plant-based commodities, such as soybean meal and distillers' grain, to sustainable, high-quality ingredients and their applications for use in aquaculture and other specialty animal feeds. We are looking for an applicant who can start working part-time (15-20 hours/week) immediately while classes are still in session with the opportunity to work 40-hour weeks this summer.
Work scheduling is flexible and can accommodate any class schedule. Applicants may have the opportunity to be hired full-time after graduation. JOB DUTIES As a key member of the Houdek team, this role will report to the Feed Research Manager and will be responsible for the following: Full responsibility
for machine operations including reading and analyzing feed production orders. Tasks include weighing and mixing feed ingredients, feed extrusion, grinding, sieving, oil coating feeds, and maintaining a clean work area.
Inspecting final feeds, and making modifications, to ensure our high standards of quality. Maintain clear and accurate feed production records. Accurately count and report inventory of raw materials and finished goods Assist with new product development including research and development projects. Safely operate a forklift Consistently maintain speed and quality within operating guidelines Adhere to established company safety protocols. Effectively communicate and interact
with others across multiple departments. MINIMUM 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. High school diploma or equivalent (GED) required. Must be detail-oriented and have excellent troubleshooting skills. Ability to manage multiple tasks in a fast-paced environment. Ability to use a variety of hand and power tools. Must be able to work as a member of a team. Able to safely lift to 55 lbs unassisted. Job Posted by Applicant Pro
quality ingredients used in aquaculture and other animal feeds. JOB DUTIES The Aquaculture Nutrition Associate participates in the routine maintenance of aquaculture systems, equipment, and facilities of the aquaculture department, and assists with the collection of data for research activities.
This position reports to the Aquaculture Research Manager. Responsibilities include but are not limited to the following: Provide assistance the Aquaculture group in all aspects of facility maintenance and operation as directed. Assist with tasks related to the collection of data for research activities. Assist with husbandry activities and harvest of aquatic animals. Assist with routine maintenance
of life support equipment. Weekend and holiday work will be required periodically. MINIMUM 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. Ability to communicate effectively, both verbally and written. Must be in good physical health and must be able to lift 5O pounds. Experience with construction, machine operation, carpentry, plumbing, PVC pipe repair, pump installation and maintenance, and compressor installation and maintenance is desirable but NOT required. Should have a working knowledge of MS Windows 7 and
be able to use both MS Word and MS Excel. Successful applicant will be self-motivated, enthusiastic, responsible, creative, and able to follow directions.
Must be highly organized, analytical, accurate and detail oriented. Job Posted by Applicant Pro
