Cell Coverer Job Description Sample
Cell Processing Specialist Car-T Cell Therapy - Morris Plains, NJ
Cell Processing Specialist CAR-T Cell Therapy - Morris Plains, NJ
Novartis is a global healthcare company based in Switzerland that provides solutions to address the evolving needs of patients worldwide. Novartis recently received the first ever FDA approval for a CAR-T cell therapy for children and young adults with B-cell precursor acute lymphoblastic leukemia (ALL) that is refractory or has relapsed at least twice; a novel immunocellular therapy, a one-time treatment that uses a patient's own T cells to fight cancer, and is the first therapy based on gene transfer approved by the FDA. Therapy will be manufactured for individual patients using their own cells at the Novartis Morris Plains, New Jersey facility where Novartis continues to advance its CAR-T manufacturing expertise. The Morris Plains site plans to hire over 300 Quality, Production, Supply Chain and Bioanalytics associates in the next 10-12 months.
Due to the nature of the starting materials (patient cells) the Cell processing Specialist role requires the highest level of proficiency and ownership. The Specialist will be responsible for end to end processing and verification of patient derived clinical and commercial cellular immunotherapy products.
Specific responsibilities will include:
End to end ownership for the processing of the assigned patient starting material in the clean room environment.
Maintain and prepare equipment/environment for use.
Document all steps in the assigned Batch record in line with GMP requirements.
Conduct all necessary processing/verification steps for the assigned lot with the highest skill level of aseptic technique.
Assist on Deviation Investigations, Change Controls, Safety Inspections and CAPAs.
Perform execution of assigned qualification/ validation activities.
Be responsible for successful on time completion of a required training curriculum composed of Global Operating Procedures (GOPs), Standard Operating Procedures (SOPs), Aseptic Techniques, Gowning Qualifications and other relevant training, including HSE for the specific role.
Perform other duties as assigned. Examples might be: successful completion of assigned PU project initiatives and/or work stream tasks, such as process improvements, efficiencies, Innovation Quality Productivity (IQP).
Maintain an "audit ready" module.
Selected associates must:
Be able to gown aseptically and work in a clean room environment (ISO 8, 7 and ISO 5) area for extended periods of time.
Be able to work with automated cell processing equipment such as Elutra, CS5, or Sepax.
Be knowledgeable in the use of production related IT systems such as SAP and MES.
Possess sound cell biological decision making.
Senior Mechanical Engineer – Cell Qualification And Cell R&D
This person's primary role will be ensuring current and future battery cell mechanical designs meet the requirements of Tesla's current and future battery modules, and vice versa. This person will work closely with Tesla's cell characterization and qualification team as well as battery module teams to design and execute mechanical methods that directly impact Tesla's product lifetimes and reliability. This role also involves working with module production teams to ensure cell requirements are met in actuality, not only by design. This person will work to qualify and iterate upon cell mechanical designs based on Tesla's needs and the capabilities of Tesla's cell suppliers. This person must exhibit the knowledge, leadership, and drive needed to not only challenge the status quo, but also define and execute the optimal path forward.
Design, develop, prototype, and execute mechanical test and characterization methods for battery cells and cell components
From first principles and experimental data, determine cell mechanical requirements such as maximum loads, limits of plastic deformation
Manage cell and cell-module interface requirements and work with validation teams
Be familiar with finite element methods (FEA) for mechanical modeling; work with FEA/modeling engineers to validate models and extract material parameters from mechanical tests that you have designed and performed
Produce meaningful and compelling analyses and data visualizations beyond Excel
Author technical presentations and summarize high-impact technical findings
Work in a laboratory and/or production environment, not just at a desk
Collaborate with and proactively build professional relationships with engineers, scientists, and technicians across different groups
Degree in Mechanical Engineering or similar
MS or PhD with 2+ years professional experience
BS with 4+ years professional experience
CAD; drafting; GD&T; tool / fixture / jig design
Design and execution of mechanical characterization experiments
Mechanical load frame operation, e.g. Instron, MTS, stress, strain, and creep measurements
Working with machine shops, rapid prototyping, and additive manufacturing
Building test fixtures using extruded aluminum framing and electromechanical parts e.g. pneumatic or solenoid actuators
Data acquisition systems; analog and digital signals
Extensive working knowledge of precision dimensional inspection tools
Working knowledge & relevant coursework in finite element analysis (FEA) methods
Ability to break down complex technical topics and deliver visual technical presentations (e.g. PowerPoint) to groups of engineers, scientists, and technicians
MATLAB, Python, LabVIEW, R
Mechanical testing of composite materials
Other materials test laboratory equipment
Ability to demonstrate a strong interest or passion for lithium-ion battery technology
Experience with mechanical testing of batteries
Knowledge of safety hazards of working with and mechanical testing of lithium and lithium-ion batteries
Please send most current resume and cover letter to PEControls@tesla.com
Cell Processing Associate Car-T Cell Therapy Morris Plains, NJ
Cell Processing Associate CAR-T Cell Therapy
The Cell Processing Associate is responsible for intermediate processing of patient derived clinical and commercial cellular immunotherapy products. Due to the nature of the starting material (patient cells) this role requires basic proficiency and ownership of the process.
Intermediate ownership for the processing of the assigned Patient starting material in the clean room environment.
Ability to gown aseptically and work in a clean room environment (ISO 8, 7 and ISO 5) areas for extended periods of time.
Maintains and prepares equipment/environment for use.
Ability to work with automated cell processing equipment such as the wave bioreactor.
Ability to perform in process operations such as: bioreactor sampling, static sampling and in process environmental monitoring.
Knowledgeable in the use of production related IT systems such as SAP and MES.
Documents all steps in the assigned Batch record in line with GMP requirements.
Conduct all necessary processing steps for the assigned lot with highest skill level of aseptic technique.
Assist with deviation investigations and inspections.
Participation in assigned qualification/ validation activities, as necessary.
Responsible for successful on time completion of required training curriculum comprising of the necessary Global Operating Procedures (GOPs), Standard Operating Procedures (SOPs) and Aseptic Techniques, Gowning Qualifications and other relevant training including HSE for the specific role.
Maintains an "audit ready" module.
Perform other duties as assigned; ie. batch record review, process streamline improvements, safety walk-thrus.
Mold Cell Oper STP
MOLD CELL OPERATOR STP
West Pharmaceutical Services, Inc. is a leading manufacturer of packaging components and delivery systems for injectable drugs and healthcare products. Working by the side of its customers from concept to patient, West creates products that promote the efficiency, reliability and safety of the world's pharmaceutical drug supply. West is headquartered in Exton, Pennsylvania, and supports its customers from locations in North and South America, Europe, Asia and Australia. West's 2016 sales of $1.5 billion reflect the daily use of approximately 112 million of its components and devices, which are designed to improve the delivery of healthcare to patients around the world.
MOLD CELL OPERATOR
2ND & 3RD SHIFT SCHEDULE
2:30 PM - 10:30 PM
10:30 PM - 6:30 AM
HIRE RATE: $18.46/HR.
3 MON MID RATE: $19.38/HR.
6 MON TOP RATE: $20.30/HR.
MUST ATTACH RESUME WITH WORK HISTORY WHEN APPLYING TO BE CONSIDERED
Certified to perform all job functions of a Molder, Trimmer and Finisher within the cell.
Essential Duties and Responsibilities:
Prepare stock to load press.
Apply mold release, load and unload product.
Inspect and process molded panels.
Statistically monitor product quality levels.
Make minor adjustments to press set-up as required.
Maintain appropriate set-up and data in press computer. Monitor for proper setting and alarms.
Complete daily production summary reports.
Do safety checks on V&O.
Check for correct solution in tank & place panels in solution.
Seat panels in die, trim and call for trim check.
Washer and Tilt Table – wash item and then cool on tilt table.
Silicone-stoppers are silicone coated per customer specifications.
Oxiglaze and Pep II-stoppers treated in chemical solution.
Metal detect-stoppers are scanned for metal particles.
Check routing slip for disposition of trimmed parts.
Reinspection of Final QC rejects.
Use good housekeeping practices to maintain a clean, orderly and safe work area.
Follow all safety rules and safety procedures.
Performs other duties, as assigned based on business needs.
Conforms with and abides by all regulations, policies, work procedures, instruction, and all safety rules.
Exhibits regular, reliable, punctual and predictable attendance.
Education and Experience:
High School or equivalent
0 - 3 Years of experience
Successfully complete all training programs and certification requirements. Previous experience preferred. Some basic computer skills required.
Knowledge, Skills and Abilities:
Able to be aware of all relevant SOPs as per Company policy as they are related to the position covered by this Job Description
Support and contribute in Lean Sigma programs and activities towards delivery of the set target
Able to comply with the company's safety policy at all times
List any safety requirements applicable to role within your country
Able to comply with the company's quality policy at all times.
List any quality requirements applicable to role within your country
- Non-US only where required for certain levels
Physical and Travel Requirements
- Must be able to lift up to 35 lbs. continuously and up to 50 lbs. occasionally.
West is an equal opportunity employer and we value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status. If you have a disability or special need that requires accommodation, please let us know. Where permitted by law, an offer of employment with West Pharmaceutical Services, or any of its subsidiary or affiliate companies, is contingent upon the satisfactory completion of background screening and/or a pre-employment drug screening.
Regulatory Affairs CMC Senior Manager - Cell And Gene Therapy
Independently, provide strategic and operational global CMC regulatory direction and documentation for projects/products within responsibility covering development, registration and approval/post approval activities as assigned.
1.Formulate, lead and drive global CMC regulatory strategy for development projects or marketed products with a focus on creativity and innovation, maximizing the business benefit balanced with regulatory compliance. 2. Proactively communicate CMC regulatory strategy, key issues and any other critical topics throughout the life cycle in an adequate and timely manner to interdisciplinary project teams and to appropriate management level in regulatory, technical development and technical operations departments as appropriate. 3. Lead and implement all global CMC submission activities (planning, authoring, reviewing, coordination, submission) for assigned projects/products, while applying the global strategy into submissions. Make quality regulatory decisions, balancing risks and benefits. 4. As early as possible, identify the required documentation and any content, quality and/or timeliness issues for global submissions and negotiate the delivery of approved technical source documents in accordance with project timelines. 5. Author high-quality CMC documentation for HA submission, applying CMC global regulatory strategies, assuring technical congruency and regulatory compliance, meeting agreed upon timelines and e-publishing requirements. 6. Establish and maintain a single point of contact with FDA or country affiliates, RA regional and TA groups for all communication on development and marketed products. Establish and maintain sound working relationships with partners and customers. 7. Initiate and lead Health Authority interactions and negotiations as appropriate; setting objectives, preparing briefing books, coordinating and planning rehearsals and risk mitigation plans. 8. Lead and drive cross-functional CMC Health Authority Response Teams (HARTs) for assigned development projects and/or marketed products, and prepare CMC responses, as appropriate. 9. Lead, prepare and communicate CMC risk management assessments (RMA), contingency plans and Lessons Learned exercises on major submissions and escalate to management as appropriate. 10. Keep knowledge up to date with regard to regulatory guidelines and requirements in all global regions as well as for new technical trends. 11. Represent own department on due diligence teams for in-licensing and divestment opportunities. 12. Represent own department on teams for continuous improvement within the department. 13. Provide advice and direction within the department within specialized assignments as assigned.
Clinical Director, Sickle Cell Center Of Excellence, Section Of Hematology And Medical Oncology, Department Of Medicine, Busm/Bmc (9945/D0318)
We are seeking a BE/BC hematologist to serve as the Clinical Director of the Sickle Cell Center of Excellence, within the Section of Hematology/Oncology at Boston University and Boston Medical Center. The Sickle Cell Center is the largest of its kind in New England, serving a population of over 400 patients, and builds on a long tradition of innovative basic and clinical research in sickle cell disease at Boston University.
The Clinical Director will lead clinical care initiatives in a multi-disciplinary clinic that includes a dedicated nurse practitioner, patient navigator, and medical subspecialists. The director will, in addition, lead a rapidly expanding clinical trials program focused on novel therapies for sickle cell disease, and will collaborate with both internal and external laboratory-based investigators pursuing a range of basic and translational research projects. Successful candidates will have had training and demonstrated expertise in the care of patients with sickle cell disease and in clinical investigation; however, outstanding candidates at the beginning of their careers will be also be considered. Academic rank will be based on qualifications and experience.
We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law. We are a VEVRAA Federal Contractor.
DO NOT APPLY THROUGH THE BOSTON UNIVERSITY HR WEBSITE.
Interested applicants should forward a CV and cover letter to: Matthew Kulke MD, Chief, Hematology/Oncology and Deputy Director, Cancer Center at Boston University and Boston Medical Center.
Email to: Carol-Ann Collins at Carolfirstname.lastname@example.org.
Scientist I Single Cell Transcriptomic Approaches To Cell Types In The Mouse Nervous System
The Allen Institute for Brain Science, located in Seattle, Washington, is committed to understanding how the brain works and helping to unlock the mysteries of neurological diseases and disorders affecting millions worldwide.
The Allen Institute is seeking an exceptional candidate who will be part of a Seattle-based multidisciplinary team within the Cell Types Program. The successful candidate will participate in high-throughput single cell transcriptome data generation and analysis to support the effort funded by the newly awarded BRAIN grant from the NIH, which aims to define all cell types in the adult mouse brain. The candidate will be a Ph.D. graduate in life sciences or computational biology and will possess strong experimental and computational skills. She/he will collaborate with several other departments on the identification and classification of cell types in the mouse nervous system.
Work within the Molecular Genetics team on experimental design, execution, and research associate training in order to generate large-scale single cell transcriptome datasets.
Work with Modeling, Analysis and Theory team to timely and iteratively analyze single cell data from the internal single cell transcriptomics pipeline and facilitate generation of cell type taxonomy.
Design and execute validation and follow-up experiments to place the transcriptomics results in the neurobiological context.
Write and publish manuscripts, grant progress reports and grant applications.
Present work internally and externally at conferences.
Evaluate new single cell RNA-seq platforms and techniques.
Work with Electrophysiology and Neuroanatomy teams to facilitate data organization and integration in an effort to create multimodal neuronal taxonomy.
Ph.D. in life sciences or computational biology (e.g., Neuroscience, Genomics, Genetics, or related field).
Knowledgeable in genomic data generation from primary tissues (rodent handling, dissection, single cell collection, molecular biology, and next generation sequencing).
Knowledgeable about developmental neurobiology and systems neurobiology
Knowledgeable about RNA-seq, ATAC-seq and/or ChIP-seq data
Proficiency in R and Linux shell scripting.
2+ years of experimental experience in genomic data generation from primary tissues (rodent handling, dissection, single cell collection, molecular biology, and next generation sequencing).
2+ years of experience working in a rodent model system studying a neurobiological problem in vivo (e.g., developmental neurobiology, systems neurobiology).
2+ years of computational experience working with RNA-seq, ATAC-seq and/or ChIP-seq data, preferably at the single cell level.
Ability to develop, test, implement, and share new experimental and computational tools quickly, in an iterative manner, after feedback from experimental, data production, and analysis teams.
Experience with additional programming languages (Perl, Python, Matlab) preferred.
Exceptional oral and written communication skills.
Ability to work independently as well as part of a team to meet aggressive timelines in a collaborative environment.
It is the policy of the Allen Institute to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by federal, state or local law. In addition, the Allen Institute will provide reasonable accommodations for qualified individuals with disabilities.
Manager, Cell Therapy And Cell Engineering Facility (Ctcef)
At Memorial Sloan Kettering (MSK), we're not only changing the way we treat cancer, but also the way the world thinks about it. By working together and pushing forward with innovation and discovery, we're driving excellence and improving outcomes.
For the 28th year, MSK has been named a top hospital for cancer by U.S. News & World Report. We are proud to be on Becker's Healthcare list as one of the 150 Great Places to Work in Healthcare in 2018, as well as one of Glassdoor's Employees' Choice Best Place to Work for 2018. We're treating cancer, one patient at a time. Join us and make a difference every day.
The Operations and QA Manager, Cell Therapy and Cell Engineering Facility (CTCEF) directs, plans and actively participates in daily functions of the Cell Therapy and Cell Engineering Facility to ensure efficient and effective operations and compliance with all aspects of quality assurance and facility operations in a highly regulated environment. The CTCEF is responsible for the production of clinical cellular products for Phase I/II clinical trials.
Responsible for maintaining the CTCEF facility in GMP compliance
Supervises a team of 5 staff members who operate the facility, including the facility manager
Oversees gowning and personnel monitoring procedures
Oversees environmental monitoring procedures
Oversees operation and validation of equipment
Oversees qualification and quarantine of raw material
Oversees the database for the management and inventory of raw materials and clinical products.
Oversees and contributes to inspections, audits and certification of suppliers
Oversees and coordinates the multi-user GMP facility operations
Oversees facility user's qualifications (e.g training, workflow, reagents qualifications, SOPs, process validations)
Oversees the integration of multi-users raw material inventory supplies for manufacturing
Oversees production scheduling and facility turnover (e.g cleaning, room and equipment certifications)
Oversees the Equipment monitoring alarm 24/7 (> 400 units) including on-site and off-site storage of cellular clinical products
Responsible for developing and maintaining the CTCEF quality management system to ensure that the facility and processes are compliant with cGMP/FDA regulations.
Supervises one Technical writer who operates MasterControl
Develops and maintains the CTCEF quality manual
Develops and maintains the CTCEF quality management system to ensure facility and processes compliance with current 21CFR/FDA regulations and FACT/ Immune Effector Cells regulations
Oversees operation and maintenance of MasterControl: controlled documentation life cycle (e.g SOPs, MPCRs), training, deviation, change control, quality improvement, validation, audit
Oversees completion and documentation of training and on-going competency
Oversees and supports non-compliances
Prepares the facility for external audit
Oversees and conducts internal audits
Insures readiness of facility for FDA inspections
Contributes to Gene Transfer and Somatic Cell Engineering (GTF) user group production runs related documentation
Supervises a team of 2 staff members who coordinate production runs and related compliant documentation
Supports issuance of Batch Production and Controlled Records (BPCR)
Supports and coordinates the assembly, timely completion and reviewing of the BPCR
Contributes to MPCR approval
Development and implementation of new manufacturing procedures
Liaise with the Director, the Production manager and the Research and Technology Mgmt group for effective integration and FDA compliance of new procedures in the core facility.
Assists production teams with process qualifications and validations documentation
Contributes to the preparation of documents including the CMC section of INDs submitted to the FDA
Delivery of cellular products for infusion of cellular products
Helps the QA Coordinator, QC and Production staff members to coordinate tthe release and delivery of cellular products to the hospital staff in compliance with FACT/IEC regulations
Prepares budgets, chargeback invoices, facility user invoices and helps establish contract manufacturing services
Master's Degree with 5-10 years of related experience in cGMP operations, laboratory management or work in controlled therapeutic manufacturing environments is highly preferred.
Applicants must be familiar with the principles of quality assurance and FDA regulations.
excellent communication, interpersonal skills and organizational skills
- team leader, strong supervisory and leadership skills
- project management
- equipment qualification and validation
- writing reports and computer software skills #LI-SB1
MSK is an equal opportunity and affirmative action employer committed to diversity and inclusion in all aspects of recruiting and employment. All qualified individuals are encouraged to apply and will receive consideration without regard to race, color, gender, gender identity or expression, sexual orientation, national origin, age, religion, creed, disability, veteran status or any other factor which cannot lawfully be used as a basis for an employment decision.
Federal law requires employers to provide reasonable accommodation to qualified individuals with disabilities. Please tell us if you require a reasonable accommodation to apply for a job or to perform your job. Examples of reasonable accommodation include making a change to the application process or work procedures, providing documents in an alternate format, using a sign language interpreter, or using specialized equipment.
Production Cell Leader
Req ID: 22271
Receives no instructions on routine work, general instructions on new assignments. Tasks are moderately complex in nature where judgment is required in resolving problems and making recommendations.
Decisions/actions may cause a minor impact on the work unit operations or schedules. Works under general Supervision. Situations not covered by standard processes, procedures and methods are referred to expert resource.
May demonstrate work methods to new employees. Deals directly with immediate supervisor, co-workers and team members; engages in exchanges of factual information and provides some explanation; interactions with external contacts, if applicable, require exchanging factual information and providing some explanation.
Performs tasks such as, but not limited to, the following: ,
Provides task leadership, balances personnel and facilitates the movement of product(s) through designated area of responsibility. Monitors the conduct, performance and contribution of cell members.
Performs hand soldering; manual assembly; setup, operation, and basic maintenance of custom and standard semiautomatic and/or automated assembly equipment and tools; operation of automated and operation of functional test units. Moves from one operation and/or product to another as schedule dictates. Inspects product using visual, automated, electronic and mechanical inspection procedures.
Uses automated and non-automated diagnostic programs to perform electronic product testing and functional testing. Troubleshoots, highlights and communicates issues relating to routine and/or basic defects.
Has foundation skills, is competent in a range of skills associated with their primary work area and possesses and actively uses coaching and some additional key skills outside of their primary work area. Knowledge/Skills/Competencies: ~Must possess specific certifications as defined by site operations.
~General knowledge of product process flow.
~Knowledge of product quality and soldering specifications and quality improvement processes.
~Knowledge of manufacturing information systems.
~Ability to recognize problems in the assembly process or with assembly components and to address those problems.
~Ability to learn established quality and quantity requirements. Ability to manually assemble components and produce high quality products in defined time periods.
~Ability to work effectively with team members and lead the team to high quality production within tight deadlines.
~Knowledge of electrical, electromechanical and pneumatic systems and principals of operation.
~Ability to analyze equipment and systems, make appropriate adjustments within area of defined job scope or highlight highlight/communicate problems to Team Leader.
~Knowledge of personal computers and ability to learn and use applications specific to this area
~Ability to maintain detailed, accurate and organized records.
~Ability to effectively communicate with a variety of internal customers.
~Basic manufacturing system knowledge. Physical Demands: ~Duties of this position are performed in a manufacturing environment with occasional to frequent exposure to elements such as noise, dust, chemicals, operating machinery, temperature extremes, etc.
~Duties of the position require periodic light physical effort and exertion including prolonged repetitive motions requiring manual dexterity and precise hand/eye coordination, sitting in confined workspaces, using tools and equipment, and moving and handling materials.
~Duties may require periodic heavy manual effort including lifting objects
~Duties require extended periods of sustained visual concentration on detailed documentation and product assemblies.
~Above demands are carried out within the Company and statutory Health and Safety guidelines Typical Experience: Three to five years' relevant experience.
Typical Education: High school diploma and additional courses after high school, or an equivalent combination of education and experience.
Educational Requirements may vary by geography Notes: This job description is not intended to be an exhaustive list of all duties and responsibilities of the position.
Employees are held accountable for all duties of the job. Job duties and the % of time identified for any function are subject to change at any time.
Celestica (NYSE, TSX: CLS) is a US$5.6 billion global leader in the delivery of end-to-end product lifecycle solutions.
Our customers trust us to deliver the most advanced design, engineering and manufacturing expertise for their highly sophisticated and complex products. From advanced medical devices, to highly engineered aviation systems, to next-generation hardware solutions for the Cloud, at Celestica we manage the complexity for our customers and set the bar for quality and reliability in their markets. Our customer portfolio includes leaders in the enterprise computing, communications, aerospace and defense, industrial, smart energy, healthtech and semiconductor markets. Headquartered in Toronto, our global network spans 13 countries with 26,000 employees throughout the Americas, Europe and Asia.
Nearest Major Market: Allentown
Job Segment: Electrical, Engineer, Information Systems, Inspector, Cloud, Engineering, Technology, Quality
Assistant Editor, Molecular Cell/Cancer Cell
Cell Press is seeking a full-time scientific editor to work jointly on Molecular Cell and Cancer Cell. As an editor, you would be responsible for moving the journals forward by:
Recruiting exciting research studies and review material
Assessing submitted research papers
Overseeing the peer review process
Establishing relationships with researchers
As an editor, you will also travel to scientific conferences and research institutions to directly engage with scientists and to keep abreast of recent research developments. You will also have the opportunity to contribute to broader Cell Press initiatives to shape the future of science communication.
Broad interests, love of science, and desire to learn. As an editor, you will need to understand the diverse science covered by Molecular Cell and Cancer Cell, and you will need to appreciate the issues and questions that drive different fields.
A talent for clear communication. Good editors help authors make their message clear, concise, and compelling, so readers know why the science is important and how it will impact their work.
Interest in digital communication and publishing trends.
Creativity, willingness to experiment, and desire to improve.
The ability to organize, prioritize, and focus.
Great interpersonal skills. Collaboration and networking are core aspects of the job.
PhD in relevant discipline. We will consider candidates with expertise in any topic area covered by Molecular Cell or Cancer Cell. Post-doctoral experience preferred. Previous editorial experience is not necessary (training will be provided). Applicants with a professional background such as running a research group or working in industry are also encouraged to apply.
This is a full-time in-house editorial position, based at the Cell Press office in Cambridge, Massachusetts. Cell Press offers an attractive salary and benefits package and a stimulating working environment. Applications will be held in the strictest of confidence.
Applications will be considered on a rolling basis. Please include a cover letter describing why you are interested in the job and how your skills and knowledge could contribute to the journals.
Elsevier is a global information analytics business that helps institutions and professionals progress science, advance healthcare and improve performance for the benefit of humanity. We help researchers make new discoveries, collaborate with their colleagues, and give them the knowledge they need to find funding. We help governments and universities evaluate and improve their research strategies. We help doctors save lives, providing insight for physicians to find the right clinical answers, and we support nurses and other healthcare professionals throughout their careers.
Elsevier provides digital solutions and tools in the areas of strategic research management, R&D performance, clinical decision support, and professional education; including ScienceDirect, Scopus, SciVal, ClinicalKey and Sherpath. Elsevier publishes over 2,500 digitized journals, including The Lancet and Cell, more than 35,000 e-book titles and many iconic reference works, including Gray's Anatomy. Elsevier is part of RELX Group, a global provider of information and analytics for professionals and business customers across industries.
Elsevier employs over 7,000 people in more than 70 offices worldwide. We are an employer of choice, attracting and developing talented and creative people who thrive in a challenging and fast-paced environment. We offer an excellent compensation and benefits package as well as a real opportunity for career growth in a growing organization. Elsevier is an equal opportunity employer: qualified applicants are considered for and treated during employment without regard to race, color, creed, religion, sex, national origin, citizenship status, disability status, protected veteran status, age, marital status, sexual orientation, gender identity, genetic information, or any other characteristic protected by law. If a qualified individual with a disability or disabled veteran needs a reasonable accommodation to use or access our online system, that individual should please contact 1.877.734.1938 or email@example.com.
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