Remote Community Health Research Scientist

and analytical services to solve your most difficult development challenges in Biologics. The Upstream Process Development team is responsible for the development and implementation of upstream processing methodologies and analytical procedures that can be easily transferred to the c GMP Manufacturing Team.

This position will perform multiple complex projects in Upstream Process Development while maintaining project timelines. The position will serve as a technical lead for the development of robust, high performing upstream processes with emphasis on transferability to c GMP manufacturing. This individual's knowledge will result in working independently on assigned tasks/projects, developing

and overseeing project plans to improve processes, and acting as a technical backup to the Director. This position plans and conducts work requiring independent judgment in the evaluation, selection, and substantial adaptation/modification of standard techniques, procedures and criteria.

This is a fulltime role working Days; Monday - Friday Catalent is committed to a Patient First culture through excellence in quality and compliance, and to the safety of every patient, consumer and Catalent employee. The Role: Provides expertise in process development for numerous mammalian cell lines. Initiates, directs and executes scientific development for innovation and process improvements. Acts

as the technical lead for Client development projects, communicates project status and effectively provides technical explanation/rationalization.

Researches and develops existing and new technologies/process improvements. Critically analyzes complex data, interprets and integrates experimental results with project objectives. The Candidate: Education: Ph. D. in Biotechnology, or related field with at least 4 years of laboratory experience in an industrial setting. MS in Biotechnology or related field with at least 8 years of industry laboratory experience. B. S/B. A. in Biotechnology, or related field with at least 10 years of industry laboratory experience.

Experience: Extensive mammalian cell culture experience Operating, maintaining, and troubleshooting stirred vessel bioreactors or fermenters preferably in an industrial setting Strong knowledge of latest upstream process development strategies Knowledge of the optimization of mammalian cell production through media and feed improvements Experience in Tech transfers Good documentation practices (GDP) Experience writing standard operating procedures Experience mentoring junior staff regarding laboratory procedures Why you should join Catalent: Fast tracked career growth, with annual performance review and feedback process Competitive base salary with other compensation incentives including yearly incentive plan Medical, Dental, Vision, and 401K are all offered on day one of employment 19 days of Paid Time Off (152 hours PTO) + 8 paid holidays Onsite gym, Catalent corporate discount perks, paid volunteer time off program and other benefits too numerous to mention!

Defined career path and annual performance review and feedback process Catalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world.

Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference. Catalent is committed to the health and safety of its employees, visitors and the customers and patients we serve. As a result of the global pandemic, we have modified many of our recruitment and on-boarding processes to maintain everyone's safety.

The Human Resources teams will communicate all necessary safety processes and procedures throughout each stage. personal initiative. dynamic pace. meaningful work. Visit Catalent Careers to explore career opportunities. Catalent is an Equal Opportunity Employer, including disability and veterans. If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to xyz X@.

This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U. S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process. Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent.

No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you. Important Security Notice to U. S. Job Seekers: Catalent NEVER asks candidates to provide any type of payment, bank details, photocopies of identification, social security number or other highly sensitive personal information during the offer process, and we NEVER do so via email or social media. If you receive any such request, DO NOT respond- it is a fraudulent request.

Please forward such requests to xyz X@ for us to investigate with local authorities. California Job Seekers can find our California Job Applicant Notice HERE.

of all skill levels to learn and master new skills. Cabling experience preferred, but there is no experience necessary for this position! All candidates will be considered, and we will provide on-the-job training where you will learn new skills. We are hiring a fiber-optic installer for areas surrounding the state of Wisconsin.

This job will involve working on a team retrofitting existing buildings with fiber optic cables, splicing fiber, and testing fiber. It will also involve installing fiber optic cables in new construction buildings when it is just the framework on active construction sites. We will fully train all employees on customer service, fiber optic handling, splicing, testing,

basic construction, and safety. Summary of Essential Job Functions: Fiber optic splicing Fiber optic testing Multi-story wall fishing Structured cabling and general routing of fiber Working with and maintaining hand tools and power tools Working from heights and on ladders Accessing and working in attics, basements, and crawl spaces The following skills are a bonus but not necessary to start: Structured cabling Basic understanding of how a building is constructed Familiarity working and maneuvering through tight or hazardous areas including attics, crawl spaces, and basements.

Familiarity with hand tools and power tools Customer service Working as part of a team The following traits are

preferred: Eager to learn new things Interest in new technologies Comfortable in an always changing environment Benefits Paid holidays Paid vacation 401(k) Physical Requirements & Working Conditions 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 that do not cause an undue hardship on the company may be made to enable individuals with disabilities to perform this job, if that would not hinder or prevent the performance of duties or be a safety concern. Company Culture At Kemp Communications LLC we pride ourselves in a friendly work environment, responsive management and a company culture that fosters personal growth and learning new skills.

We look forward to hiring individuals who share our values of taking pride in ones work and providing an excellent customer experience. Pay Starting wages are $18-$24/hour depending on existing skills and experience. We pay every week on Friday. DISCLAIMER: We are an Equal Opportunity Employer for any employee or applicant, irrespective of race, color, religion, interaction, age, marital status, interactionual orientation, gender identity, genetic information, national origin, veteran status, disability, or any other legally protected characteristic.

All employees must be authorized to work in the United States. We are a drug-free work environment. Employment with the Company is contingent on the successful completion of a drug test, reference check, and MVR check Job Posted by Applicant Pro

to be a vital member of our team. Responsibilities: Perform solid phase synthesis, purification, and characterization of oligonucleotides and oligonucleotide conjugates Analyze, interpret, and communicate synthetic and analytical results Present results at group meetings to Sr.

Staff Troubleshoot and optimize current procedures Multitask and work on several different projects concurrently Maintain inventory of reagents and consumables Requirements : B. S. /M. S. Chemistry or Biochemistry with understanding of organic and analytical chemistry Experience working in a chemistry lab Experience with High-performance liquid chromatography Desire to work in a fast-paced and dynamic startup environment

Applicants must have authorization to work in the U. S. Preferred Experience: 1 - 7 years of relevant work experience, preferably in solid phase synthesis Experience with RPIP-HPLC, AEX-HPLC, UV, NMR, LCMS, MALDI, and HRMS is highly desired Analytical or purification method development experience using RPIP-HPLC and AEX-HPLC Individual compensation decisions will be based on various factors, such as primary work location, complexity and responsibility of role, job duties/requirements, and relevant experience and skills.

We offer a wide range of benefits including a retirement savings plan (with company match), paid vacation, holidays, and health benefits to include medical, prescription

drug, dental and vision coverage in accordance with the terms and conditions of the applicable plans.

About Empirico: Empirico is a biotechnology company focused on the discovery and development of novel medicines which mimic the effects of naturally-occurring genetic variants that confer favorable effects on health and disease. Empirico’s two foundational technology platforms - the Precision Insights Platform™ for genetically-validated target discovery and the si RCH™ platform for the discovery and development of si RNA medicines - are used separately and in tandem to enable Empirico and our collaborators from the discovery and validation of novel targets to clinically-viable therapeutics.

Empirico’s exceptional internal capabilities, augmented by those of its partners, are driving the advancement of a growing and differentiated pipeline of wholly-owned and partnered programs. Empirico is headquartered in San Diego, CA with a major second site in Madison, WI. We’re striving to build a strong culture of inclusivity, transparency and collaboration at Empirico, where our diverse and equitable workforce is empowered to contribute to our mission. We always seek the best candidate for the position and encourage you to apply even if your experience or qualifications don’t match up exactly with the job description.

Empirico is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, interaction, national origin, interactionual orientation, gender identity, disability status, protected veteran status, or any other characteristic protected by law. To All Agencies: Please do not contact any employee of Empirico about this position. All resumes submitted by agencies to any employee of Empirico via-email or in any form and by any method will be deemed the sole property of Empirico, unless such agencies were engaged by Empirico for this position and a valid agreement is in place.

Investigator for non-regulated, GLP-regulated, and GCP-regulated bioanalysis studies. Additional responsibilities include: Lead and direct scientific work to support internal methods and experiments. Develop and review protocols and sample analysis plans.

Review data with the method development team to ensure methods are ready for validation. Approve validation methods and reviews sample analysis methods. Independently review and approve raw data. Evaluate data and tables to ensure regulatory guidelines and expectations are met. Review reports for scientific accuracy and completeness. Provide technical support as needed. Assist with efforts to troubleshoot and solve assay problems. Assist

with client communications regarding scientific direction. Work with the client to determine project requirements. Assist with scientific directives for the study team.

Identify scientific issues or scope changes within the study. Communicate and monitor scientific expectations with scientific staff and clients. Promote quality within the study team. Provide a technical resource for less experienced team members. Education and Experience: Bachelor of Science (BS) degree in science or related field; Masters (MS) degree in science or related field preferred 2-3 years of experience in the job discipline Excellent communication and interpersonal skills Proven ability to prioritize and manage

time Excellent attention to detail Able to utilize word processing, database, spreadsheet, and specialized software Experience and skill with Watson, Nautilus, and Analyst preferred Knowledge of regulatory agency guidelines Labcorp is proud to be an Equal Opportunity Employer: As an EOE/AA employer, Labcorp strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind.

We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, interactionual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic.

We encourage all to apply. For more information about how we collect and store your personal data, please see our Privacy Statement. For more details: jobs-search. org/information-technology_madison-c451678/associate-lead-scientist-bioa-lc-ms-madison_i1976183195