Fat Purification Worker Job Description Sample
Fat Tuesday Model Server
Don't just work. Work Happy.
A career in gaming? At Boomtown Casino we think you'll enjoy an exciting industry, fast-paced days and nights, diverse, enthusiastic co-workers, unlimited growth and support from one of the leaders in the industry.
We are currently seeking a talented individual to become a Fat Tuesday Model Server. An individual could be successful if they possess the following.
Your daily responsibilities include
Provides personalized service and uses guest name.
Resolves service problems according to guidelines.
Serves as ambassador of goodwill while working and at customer and public relations functions; appears in publicity photos.
Promotes casino events and programs.
Provides fast (20 minute or less round time), friendly, professional beverage service to casino guests; carries full trays on every round.
Monitors guest consumption of alcohol and intervenes as needed according to guidelines.
Takes drink orders, communicates with bartender, assists in the preparation of drinks and presents drinks to guests.
Handles money according to procedure.
Works well with others, especially Bartenders, F&B Outlet Supervisors, and all other members of management.
Maintains clean and stocked workstation.
Maintains company-issue uniform in good condition and reports to work in authorized uniform as mandated by organization. This includes maintaining a clean and well-groomed appearance in compliance. with departmental and company dress code standards.
To be successful in this position it will require the following skill set
Must be 21 years of age.
High school diploma or equivalent.
Must successfully complete C.A.R.E training certification course.
Read, write legibly, understand and speak English.
Excellent customer service/communication skills.
Count money and change correctly.
Know or is able to learn tray service, cocktail ingredients.
Available to work required schedule which may include nights, weekends, holidays and overtime as needed.
Must meet professional appearance standards as prescribed by company policy.
Must be physically mobile with reasonable accommodation.
Must be able to respond to visual and oral cues.
Must be able to lift and carry 20 lbs. (full cocktail tray) for extended periods of time.
Able to tolerate second-hand smoke, noise, bright lights.
Able to work at a fast pace in often crowded/noisy environment.
Physically mobile with reasonable accommodations including ability to push, pull, carry and lift up to 25 lbs., and the ability to push, pull, reach, bend, twist, stoop, stack, crouch, kneel and balance when performing job duties in varying work areas such as confined spaces.
Ability to read and interpret documents in English, such as safety rules, operating and maintenance instructions and procedure manuals. Ability to read and communicate verbally in English. Written communication skills in in English may also be required.
Ability to apply commonsense understanding to carry out instructions furnished in written, oral, or diagram form. Ability to deal with problems involving several concrete variables in standardized situations.
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 may be made to enable individuals with disabilities to perform the essential functions.
While performing the duties of this job, the employee is regularly required to stand and use hands to finger, handle, or feel objects, tools, or controls. The employee frequently is required to reach with hands and arms and talk or hear. Specific vision abilities required by this job include close vision, color vision, and peripheral vision.
The employee must regularly lift and/or move up to 10 pounds, frequently lift and/or move up to 25 pounds, and occasionally lift and/or move up to 50 pounds, and must have the ability to push, pull, reach, bend, twist, stoop, stack, crouch, kneel and balance when performing job duties in varying work areas such as confined spaces.
The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. The noise level in the work environment is usually moderate to loud.
Employee could be exposed to an environment containing unrestricted second hand tobacco smoke.
Something to leave you with
Penn National Gaming is more than you may realize. We have properties throughout the United States and Canada and are embarking on an aggressive growth mode. Our departments and areas of opportunity are ideal for just about any skill set. And our company-wide commitment to making sure our guests smile as much as we do means you'll enjoy a fun working environment.
I acknowledge that I have received a copy of my job description and understand my job responsibilities and duties. I further understand that at times I may be assigned and expected to perform duties not listed in the above responsibilities, according to business needs.
Now that you have read about who we are, here is your opportunity to see what we're about!
Equal Opportunity Employer
Process Development Engineer Purification Development
Known for its scientific and operational excellence, Regeneron is a leading science-based biopharmaceutical company that discovers, invents, develops, manufactures, and commercializes medicines for the treatment of serious medical conditions. Regeneron commercializes medicines for eye diseases, high LDL-cholesterol, atopic dermatitis and a rare inflammatory condition and has product candidates in development in other areas of high unmet medical need, including rheumatoid arthritis, asthma, pain, cancer and infectious diseases.
We are seeking a process development engineer who enjoys working on projects collaboratively and is also capable of recognizing when someone needs to take the lead, and is equally comfortable doing so. This role is a hands-on junior management position within the Purification Development group within Preclinical Manufacturing and Process Development (PMPD). This engineer will be involved in the full scope of the department's work supporting our robust pipeline from preclinical evaluation all the way through commercial licensure and life cycle management of the processes providing important medications to our patients with unmet medical needs.
This position includes leading and performing Quality by Design (QbD) driven, state of the art downstream process development, based on Regeneron's suite of proprietary technologies. This engineer will be relied upon to support technology transfer of these processes to our GMP manufacturing facilities around the world. This position will also have a highly visible role within the department while driving the group's technical development priorities forward.
This individual would be entrusted with the career development of junior engineers and would be given the resources, time and training to effectively mentor and develop them. The ideal candidate would not only be an effective leader of their own subgroup, but be willing to be a non-positional leader within their larger group.
Development of Innovative Polishing chromatography separations, within a cross functional team of other SME's to deliver a final process that has been prospectively developed using the principals of QbD to ensure robust, uninterrupted supply of safe medicines for our patients.
Utilizes subject matter expertise in field of chromatography to design, lead, and react to experiments/projects independently.
Experienced leader that knows when and how to delegates tasks, inspires individuals whether direct reports or project team members, and demonstrates strong leadership and poise in approach to their work and the management of their group.
Analyzes data and interprets experimental results within context of "project" goals and makes recommendations to management. Use of statistics, such as ANOVA, nonlinear least square regression, and well-designed DoE's, etc. to characterize design space and generate statistical models of process performance, variation and failure rate.
Communication with all levels in the organization, demonstrating meticulous organization and high attention to detail. Conduct research and development in area of subject matter expertise with minimal guidance. Makes Science-based recommendations by novel incorporation of learning from internal and external (literature) sources.
Potential additional responsibilities include participation in viral clearance studies for clinical and commercial drug candidates and process transfer to Regeneron's manufacturing facilities. The position may require travel (5-10%) and occasional work on weekends.
The ideal candidate will have a degree in Chemical Engineering or Biochemical Engineering.
PhD. 0-2 years of experience, M.S.c with 5-7 years' experience, or B.Sc. with 8-10 years of experience.
Relevant experience with:
Akta Explorer/Avant, Akta Pilot, BioProcess Skid, Depth Filtration, Tangential Flow Filters, Normal Flow Filters, Chromatographic Columns, HPLC, UPLC, Diafiltration Skid , Laminar Flow Hood, Chemical Fume Hood, Empower, Unicorn, JMP, LlMS, Tech Transfer Experience to GMP Manufacturing. Small Scale Purification Model Development.
Level will be commensurate with experience
This is an opportunity to join our select team that is already leading the way in the Pharmaceutical/Biotech industry. Apply today and learn more about Regeneron's unwavering commitment to combining good science & good business.
To all agencies: Please, no phone calls or emails to any employee of Regeneron about this opening.
All resumes submitted by search firms/employment agencies to any employee at Regeneron via-email, the internet or in any form and/or method will be deemed the sole property of Regeneron, unless such search firms/employment agencies were engaged by Regeneron for this position and a valid agreement with Regeneron is in place. In the event a candidate who was submitted outside of the Regeneron agency engagement process is hired, no fee or payment of any kind will be paid.
Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, sexual orientation, gender identity, disability status, protected veteran status, or any other characteristic protected by law.
We are looking for a driven individual to join our enzyme manufacturing team as a Purification Scientist in Madison, Wisconsin. In this role you will be responsible for manufacturing the enzyme reagents used in the Illumina sequencers. You will work closely with other purification scientist within an industry setting to produce highly purified enzyme reagents.
Purify of a variety of molecular biology enzymes and nucleic acid binding proteins to aid in our growing product lines.
Work as part of a scientific team and participate in team meetings and initiatives.
Identify and implement continues improvement ideas within Production process.
Complete in-process assays, including SDS-PAGE gels as well as standard protein characterization assays and contamination assays.
Execute inventory control of reagents, chemicals, and supplies using proper labeling and computerized systems.
Maintain general lab organization (6S) of lab supplies, equipment and reagents.
Other duties that may be determined by management.
3+ years of experience in protein purification or related biochemistry areas.
Hands-on experience in purification at various industrial scales using both non-automated methods and automated FPLC systems (e.g. the AKTA platform), as well as homogenization, batch purification, precipitation, dialysis, and tangential flow filtration.
Experience with buffer preparation including pH and conductivity measurements.
High level of technical proficiency, initiative, independent thought, and collaborative ability.
Excellent laboratory, organizational, and analytical skills.
Experience writing SOPs and Work Instructions.
Additional experiences that are desired, but not mandatory:
Purification experience within an industry setting
CGMP Experience and Good Documentation practices (GDP)
Experience working in an Operational Excellence Culture
Computerized Inventory Control ERP systems (e.g. SAP)
Computerized Compliance systems (e.g. EtQ Reliance)
- B.S. in biochemical engineering, biochemistry, protein biochemistry or related field
Illumina believes that everyone has the ability to make an impact, and we are proud to be an equal opportunity employer committed to providing employment opportunity regardless of sex, race, creed, color, gender, religion, marital status, domestic partner status, age, national origin or ancestry, physical or mental disability, medical condition, sexual orientation, pregnancy, military or veteran status, citizenship status, and genetic information. If you have a disability or special need that requires accommodation, please contact us at email@example.com. To learn more, visit: https://www.dol.gov/ofccp/regs/compliance/posters/pdf/eeopost.pdf
Intern / Master's Thesis Student In The Field Of Bioproduct Purification
Discover a world of opportunities. #HumanChemistry
See what chemistry can do for your career: careers.evonik.com
Exploring opportunities. Growing together.
VACANCY REFERENCE NUMBER 19646
Intern / Master's thesis student in the field of bioproduct purification
The term of employment is limited to 3 - 6 months.
Location: Germany : Hanau
Function: Engineering; Production & Technology
Career Level: Students
Legal Entity: Evonik Industries AG
Business Line: Technology & Infrastructure
What we offer
You will work on exciting and challenging topics together with a team in an ultra-modern, innovative and creative environment. Intensive on-the-job training with expert colleagues guarantees you will quickly become familiar with your duties and perform them independently. Performance related pay and the opportunity for personal and professional development are of course part of the package. Since 2009 Evonik Industries AG has been certified as a family-friendly company by the German Hertie Foundation.
MEET THE TEAM - Learn more about Evonik from our employees
Screening and evaluation of adsorbents
Simulation and application of (continuous) chromatographic separation processes
Experimental validation of purification processes on a laboratory and pilot plant scale
Scale-up, process and plant design
Documentation and presentation of results
Measuring and modeling of phase equilibria
Plan, set up, conduct and evaluate batch and continuous crystallization on a laboratory and pilot plant scale
Evaluation and optimization of in-situ measuring techniques with respect to regulation issues
Characterization of particle properties in collaboration with various specialist departments
Documentation and presentation of results
Design optimized purification processes by interlinking appropriate procedures such as ultrafiltration, chromatography, adsorption,
crystallization and others
Benchmarking and optimization, as well as comparison, of process variants from a technical and business viewpoint
Documentation and presentation of results
A minimum of 120 ECTS points in a Bachelor program – preferably in the field of process engineering/biological and chemical engineering
Interest in dealing with issues surrounding the purification of biotechnologically produced products
Experience in the named fields would be an advantage
Good knowledge of English
Basic software skills (MS Office)
Excellent communication skills and ability to work in a team Initiative, good sense of responsibility, flexible
To ensure the fastest process of your application and to protect the environment, please apply online via our careers portal at https://careers.evonik.com.
Please address your application to Marvin Botthof. If you have any questions regarding the application process, please contact our Recruiting Center Team at 0800 2386645 (germany only) or +49 201 177 4200.
VACANCY REFERENCE NUMBER 19646
Please note that Evonik will not accept any unsolicited application documents sent by staffing firms. Evonik works in conjunction with preferred service providers and will not pay any fee to staffing firms in the absence of an appropriate framework agreement. Should Evonik receive a candidate profile from a staffing firm with which it has no framework agreement, and should this candidate subsequently be considered in the recruitment process or offered employment, no claims from the staffing firm will be entertained in this regard.
[Not translated in selected language]
Protein Purification Technician I
The Protein Purification Technician I performs assigned manufacturing and process development duties in a ISO 13485 environment.
Job performance will involve a variety of activities including:
Executes development and production scale purification protocols as directed.
Works with standard scientific equipment as described in relevant procedures; AKTA Purifier and AKTA Pilot, UV spectrophotometer, balances, chromatography columns, PAGE, autoclaves, pH meter, refrigerators, freezers, biohazard safety cabinets.
Records results in laboratory notebooks; required to have meticulous organization and record keeping skills.
Prepares buffers and solutions.
Communicates as a team member with other functional groups, via face to face, email and written reports.
Assists with investigations, root cause analysis, and corrective action/preventative action (CAPA) implementation.
Maintains protein purification batch records to ensure quality standards are met.
Maintains and operates machinery used in manufacturing based on specific procedures.
Cleans work area, machinery and equipment and maintains work area in an orderly manner.
Stocks lab areas with supplies as needed, inventories supplies and places orders.
Keeps up-to-date with required training and development and improve job skills.
Interprets operating requirements and monitors gauges and instrumentation.
Additional duties as assigned.
- Bachelor's degree from four year college or university and/or combination of experience and training.
- 1-2 years related life sciences experience or equivalent combination of education and experience.
Drive and Determination.
Ability to participate with others as a member of the team to ensure that demanding and difficult projects are handled smoothly and cooperatively to enhance success of project and maintain strong relationships within all parts of company.
Strong communication skills.
Ability to work flexible hours to complete tasks as required.
We are an Equal Opportunity Employer and do not discriminate against any employee or applicant for employment because of race, color, sex, age, national origin, religion, sexual orientation, gender identity, status as a veteran, and basis of disability or any other federal, state or local protected class.
Senior Scientist, Downstream Processing / Purification
Janssen Research & Development, L.L.C., a division of Johnson & Johnson's Family of Companies is recruiting for an Senior Scientist, located in Malvern, PA.
At the Janssen Pharmaceutical Companies of Johnson & Johnson, what matters most is helping people live full and healthy lives. We focus on treating, curing and preventing some of the most devastating and complex diseases of our time. And we pursue the most promising science, wherever it might be found.
Janssen Research & Development, LLC discovers and develops innovative medical solutions to address important unmet medical needs in oncology, immunology, neuroscience, infectious diseases and vaccines, and cardiovascular and metabolic diseases. Please visit http://www.janssenrnd.com/ for more information.
We are Janssen. Our mission drives us. Our patients inspire us. We collaborate with the world for the health of everyone in it.
Thriving on a diverse company culture, celebrating the uniqueness of our employees and committed to inclusion. Proud to be an equal opportunity employer.
The candidate for this position will lead and perform processdevelopment for the antibody purification processes within the API-LargeMolecule group in Malvern, PA. The candidate's primary responsibilities willinclude leading and participating in the design of experiments, executing theplanned experiments, and optimizing the process steps to the target processscale. This will include laboratory and occasional pilot-scale scalechromatography and filtration. Additional responsibilities include but are not limited to the following:
Lead the design and executionof development studies to identify and determine appropriate conditions andranges of (critical) process parameters for chromatographic purification &separation and several types of filtration
Record andanalyze experimental data, verify data integrity and accuracy, andreport/summarize findings to the project team, and also draft technicaldocuments and perform technology transfer to collaboration partners.
Work in a team environment as well as contributingindividually to meet project timeline and objectives
A PhD in Chemical Engineering or Biological Sciences or Biochemistrywith at least 3 years of relevant post-doctoral experience OR MS in ChemicalEngineering or Biological Sciences or Biochemistry and with at least 12 yearsof relevant experience OR a BS in Chemical Engineering or Biological Sciencesor Biochemistry and with at least 15 years of relevant experience isrequired
Knowledge and hands-on experience in downstream processing andpurification of antibodies/recombinant protein therapeutics, in particularchromatography and filtration, are required
Exposure to analytical method development for in-processmethods is preferred
Experience maintaining written records of work in the formof (electronic) notebooks, technical reports and protocols is required
Data reporting, ability to present findings to management,and experience with team-based collaborations is a must
Occasional weekend work may be required
Manufacturing Associate I/Ii - Protein Purification
MacroGenics is a leader in the discovery and development of innovative medicines that utilize our next generation antibody-based technologies. Our team of 300+ dedicated individuals is advancing a pipeline of product candidates to treat patients with cancer as well as various autoimmune disorders and infectious diseases. Our products and platforms have attracted multiple partnerships with leading pharmaceutical companies around the globe.
The Company considers its employees to be its most valuable asset and we are committed to providing opportunities for individuals to learn and grow as a means to further their professional development. MacroGenics' corporate culture promotes an atmosphere of innovation, open communication and teamwork where employees can see firsthand how they contribute to the success of the organization.
Summary of Position
The Manufacturing Associate I/II participates in the manufacturing of biopharmaceutical drug product to support MacroGenics' multiple clinical programs in the Protein Purification area. This position will work in the manufacturing suite under GMP (Good Manufacturing Practices) to ensure that materials manufactured meet required specifications and regulatory requirements.
Responsibilities and Job Duties
Participate in hands-on production in the manufacturing of material for clinical trials in a GMP environment by conducting purification operations including filtration, chromatography, titrations, column packing, and ordering and accounting for consumption of raw materials and components.
Contribute to the creation and revision of Batch Records, Work Instructions, Standard Operating Procedures, Material Specifications, and other GMP documents.
Adhere to all SOPs and execute batch records under GMP regulations documenting all manufacturing activities clearly and accurately, including preparation records, testing records, equipment use records, and laboratory notebooks.
Maintain adequate supplies and perform routine equipment maintenance.
Maintain manufacturing area in a clean, neat, and orderly condition at all times.
Participate in a variety of projects designed to improve the quality, and efficiency of the manufacturing team.
Follow all related safety rules and procedures when working with hazardous materials.
Education & Experience
Manufacturing Associate I
- High School Diploma or equivalent with exposure to science and math coursework and a minimum of three years of related experience in the biotech/pharmaceutical industry
- Associate's degree in a related discipline with no experience
Manufacturing Associate II
- High School Diploma or equivalent and a minimum of five years of related biopharmaceutical manufacturing experience in FDA regulated, controlled production environment
Associate's degree in a related discipline and a minimum of one year of related biopharmaceutical manufacturing experience in FDA regulated, controlled production environment
Prior experience following GMP rules and procedures
Knowledge, Skills and Abilities
Knowledge of protein purification techniques
Ability to write and revise technical documents
Ability to lift up to 30 lbs.
Ability to work occasional weekends or overtime as needed
Ability to follow detailed instructions and to maintain accurate records and notes
Ability to work effectively in a team environment
Ability to successfully perform multiple tasks, when required
Skills in problem solving and troubleshooting
Ability to safely operate production equipment in accordance with established practices
MacroGenics is proud to be an equal opportunity employer. Employment selection and related decisions are made without regard to race, color, national origin, sex, gender identity, sexual orientation, religion, age, disability, protected veteran status, or any other characteristic protected by federal, state or local law. We are committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the employment process, please email firstname.lastname@example.org or call (301) 354-3566 and/or 711 for TTD/TTY service. Equal Opportunity Employer/Veterans/Disabled
For more information about our commitment to equal employment opportunity, please click here.
Plant Maintenance Mechanic-Water Purification Plant
Performs skilled & Semi-skilled maintenance duties as they relate to equipment repair and upkeep. Perform manufactures recommended preventative maintenance to equipment at the Water Purification Plant.
Essential Job Duties:
Repairs equipment including pumps, chemical feeders, valves and specialized equipment.
Performs preventative maintenance on plant equipment according to manufacturer's recommendations.
Performs annual maintenance at plants including but not limited to cleaning and painting of water treatment basins and painting of equipment.
Performs electrical repairs including wiring of electric motors, switches, and panels.
Troubleshoots electrical problems including checking and repairing control circuits.
Serves as a shift relief as needed, assuming full authority, duties and responsibilities of position that is being filled.
Performs related duties as required.
Physical and Environmental Conditions:
Ability to sit, stand and transport self from building to building. Ability to drive a vehicle to and from various work sites.
Employee will work in a seasonal temperatures bending, kneeling, twisting and climbing. Employee can work with potential mechanical, chemical and electrical hazards. Employee may be exposed to communicable diseases while handling raw sewage.
Must be able to lift in excess of 50 lbs, climb stairs and open access hatches. Must be able to climb 50 ft ladders and work effectively at that height. Must be able to wear an SCBA.
Employee communicates with other employees and the public, as necessary.
Skill in observing, reading and interpreting written materials. Knowledge of plant operations and maintenance.
Skill in performing mathematical calculations. Ability to use testing and measuring equipment. Skill in the use of hand tools, test equipment, and welding tools. May work rotating shifts.
High school diploma or equivalent required. One to three years experience in a related field preferred.
Must receive and retain a valid 'C" Water license within 3 years of employment. Must receive Hazmat Awareness level and SCBA certifications within 1 year of employment. Must remain qualified to wear SCBA. Must posses a valid Texas Class 'B' CDL or have the ability to obtain license within a reasonable amount of time.
Scientist I - Protein Purification
PROTEIN PURIFICATION SCIENTIST NEEDED IN CARLSBAD!
Responsible for manufacturing product(s) in a lab setting following standard operating procedures. Will utilize basic laboratory techniques, calculations, materials measurement, operation of laboratory equipment and record keeping necessary to manufacture products.
Will perform column purification/ chromatography, buffer preparation, SDS-Page Analysis, Western Blotting, and other protein characterization techniques. Responsible for Batch Data Records, notebooks, customer reports and work order documents.
Utilize specialized technical knowledge and skills to make detailed observations and analyze data to ensure within operating parameters.
Advise manager of factors that may affect quality of product. Suggest options/ideas for corrective actions.
Maintain equipment, product inventories and related records as assigned. Note variances on manufacturing documents; audit and evaluate process documents and propose revisions.
Complete, distribute and file records as required in accordance with Document Control Practices. Identify potential issues in the production process; report findings to team management and members for resolution or participate in troubleshooting.
Write technical documents which may include standard operating procedures and batch records. May lead process improvement projects or product transfer projects May perform other related duties as required and/or assigned
Minimum Qualifications (must have): Must have a bachelor's degree in Biology, Chemistry, Biochemistry, or other related discipline. Master's degree is a plus.
Requires a minimum of 3 years relevant experience demonstrating laboratory techniques in a manufacturing environment or research laboratory. Demonstrated proficiency in the use of scientific laboratory techniques, equipment and materials required.
Experience in the use of basic laboratory techniques, including buffer preparation, column purification/ chromatography, SDS-Page Analysis, Western Blotting, and other protein characterization techniques are beneficial.
Familiar with GE AKTA FPLC protein chromatography equipment and Unicorn software. Experience with different modes of chromatography such as: affinity, ion-exchange, size exclusion, hydrophobic interaction.
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Senior Scientist/Engineer -Downstream Process Development/ Protein Purification
Bristol-Myers Squibb is a global biopharmaceutical company whose mission is to discover, develop and deliver innovative medicines that help patients prevail over serious diseases.
One shared journey is moving us forward at Bristol-Myers Squibb. Around the world, we are passionate about making an impact on the lives of patients with serious disease. Empowered to apply our individual talents and ideas so that we can learn and grow together. Bristol-Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees the resources to pursue their goals, both at work and in their personal lives.
Bristol-Myers Squibb has consolidated early biologics process development organization comprising Molecular biology, Cell Line Development, Upstream and Downstream development, and Process Analytics collocated with a large Analytical Development organization in New Jersey. BMS Hopewell site is part of New Jersey's "Biopharmaceutical Life Sciences Cluster," a concentrated area of biotechnology, medical device, and pharmaceutical companies.
The Senior Scientist/Engineer will be working in a dynamic team setting with the opportunity to lead development of downstream process with cutting-edge technologies and with a growing biologics portfolio. The Scientist/Engineer candidate in purification process development will be responsible for conducting research and development that leads to efficient and scalable recovery and purification processes for therapeutic proteins.
Lead a process development team to develop protein purification strategies to meet established timelines
Design and execute experiments utilizing HTS, FMEA and DOE to produce a robust process
Implement purification process development, optimization, scale up of biologic manufacturing processes and support as needed process characterization and PPQ activities of therapeutic proteins
collaborate with internal and external partners
Identify technical issues, troubleshoot, solve problems and achieve clear resolution
Write technical reports and lead project reviews on a regular basis in matrix organization
Transfer processes from Development labs to BMS production facilities and CMO
Author process description and development reports, review manufacturing batch records and facility fit documents, and provide support with identification and troubleshooting of manufacturing process issues
Research new equipment/technology and contribute to platform improvement
Trains others on procedures, operations, new technology, methods and mentors new scientist
Provide effective management for planning, coordinating and executing tasks and projects in a given time frame
Follow safety procedures
Maintains laboratory notebook meeting corporate standards
PhD in Chemical/Biochemical Engineering, Biotechnology, Protein Chemistry or Biochemistry with minimal 4 years of industrial experience in Process Development/Purification Process Development, or MS with minimal 10 years; or BS with minimal 13 years of relevant industrial experience.
Track record experience with all aspects of purification strategies including protein A, Ion Exchange, HIC, mixed mode, UF/DF, viral clearance, centrifugation etc.
Extensive experience with process optimization for product purity, recovery, impurity removal, cost reduction
Extensive experience in technology transfer and interaction with CROs and CMOs
Experience with scale-up/down process models
Experience with high throughput experimentation and mechanistic modelling is desirable
Experience in leading teams and managing projects
Working knowledge of design of experiments and use of statistics for data analysis
Working knowledge of upstream and analytical sciences
Experience with CMC writing and IND filing preferred
Understanding of current trends of ICH and regulatory agencies
Bristol-Myers Squibb is an equal opportunity employer - M/F/Vet/Disability
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