http://bauschandlomb.jobs2web.com/go/Bausch-&-Lomb-Pharmaceutical-Scientist-Jobs/13321/ View Bausch & Lomb Pharmaceutical Scientist Jobs at Bausch and Lomb en-us http://basf.jobs2web.com/images/bauschandlomb/logo.gif http://bauschandlomb.jobs2web.com/go/Bausch-&-Lomb-Pharmaceutical-Scientist-Jobs/13321/ 720 Job Title:
Director, Clinical & Scientific Affairs

Req #:
5228BR

Job Description:
Position Summary The Surgical Director of Clinical & Scientific Affairs at Bausch & Lomb is responsible for the development of products in the Surgical medical device category. Leads a group of scientists (MDs and ODs) responsible for clinical trial design, scientific evaluations during the conduct of the trials (monitoring of safety, eligibility, enrollment, and data consistency), and analysis of results. Specific Job Duties . Accountable for product clinical development programs that are of high-quality, but that also lead to timely and cost-effective regulatory approval. . Serves as the leader of the Surgical Global Clinical Development matrixed team in the planning and executions of clinical trials. The team includes operations, statistics, data management, and medical writing, in addition to scientists. . Collaborates and takes clinical leadership role within cross-functional teams, including project managers, preclinical, regulatory, clinical trial materials, etc. . Responsible for the clinical aspects of clinical study reports and responses to regulatory authorities. . Contributes to abstract/manuscript/presentation writing/review, for scientific meetings and internal management reviews. . Maintains responsibility for the clinical input into Business Development due diligences. . Provides medical expertise and medical evaluation of questions regarding ophthalmology clinical practice. . Develops/Maintains relationships with external experts who might be needed to support clinical development programs. . Provides scientific and clinical research expertise in the development of overall strategy of the Surgical business and more specific product clinical development plan. . Performs management functions such as goal setting, individual development plans, and performance evaluations of staff. Identifies training needs to staff and implements training plan. . Proactively evaluates and contributes to process improvement. Management Competencies . Demonstrated knowledge and skill in submission strategies as well as overall Regulatory Science. . Demonstrated experience in leading a team and carrying out performance management and talent processes. . Ability to partner, negotiate, and drive towards win/win outcomes. . Develops effective global internal/external relationships (e.g. cross category, cross functional, etc.) . Excellent oral communication skills (command of English language) and technical writing skills. . Ability to effectively present information in one-on-one and small group situations to internal customers and other employees of the organization. Ability to communicate well with all levels of the organizations. Technical Competencies . Strong questioning and problem-solving skills. . Mathematical skills commensurate with educational background and necessary for describing and summarizing laboratory and/or clinical data in product registration submissions. . Ability to read, analyze and interpret governmental regulations, general business periodicals, professional journals and technical procedures. . Ability to write routine reports and business correspondence. . Computer literate with general office software and internet use.

Qualifications
. Medical Degree (MD / OD) from an accredited US or foreign medical school preferred. PhD with ophthalmic clinical study experience. . At least 5 years of total experience, post-medical training, including clinical practice AND industry experience in the planning, execution, and reporting of clinical trials. . Strong understanding of GCP, ICH, and regulatory compliance. . Knowledge of scientific methods, research design, and medical practices and procedures in ophthalmology.

Work Location CA - Aliso Viejo Relocation Available Yes

Status Full-Time]]> http://bauschandlomb.jobs2web.com/job/ALISO-VIEJO-Director,-Clinical-&-Scientific-Affairs-Job-CA-92653/609162/?utm_source=J2WRSS&utm_medium=rss&utm_campaign=J2W_RSS http://bauschandlomb.jobs2web.com/job/ALISO-VIEJO-Director,-Clinical-&-Scientific-Affairs-Job-CA-92653/609162/?utm_source=J2WRSS&utm_medium=rss&utm_campaign=J2W_RSS Job Title:
Medical Science Liaison - Northwest

Req #:
5335BR

Job Description:
* Develop and maintain a wide network of strategic external relationships (KOLs) to build confidence, trust and respect with others, in order to increase competitiveness. * Respond to inquiries to establish and/or further the knowledge of products and related topics. * Facilitate feedback on Ophthalmic-related community needs and opportunities to improve educational and research opportunities. * Serve as the conduit for requests for strategic investigator-initiated studies in the region, and ensure compliance with applicable regulations. * In conjunction with medical communications group, support the development of scientific updates for products' key slides and material, and ensure dissemination (Sales and Presentation to Advisory Boards). * Represent company with formulary presentations. * Design, develop, and deliver scientific presentations to individuals and groups of strategic importance to company. * Assist with educating sales representatives on product knowledge and understanding of technical information within the therapeutic area. * Coordinate the development of roundtables on scientific subjects relevant to B&L's products. * Maintain a thorough and detailed working knowledge of company, its products, current scientific research and publications associated with same. * Identify academic centers and investigators to initiate and/or participate in clinical trials and identify key areas of future research.

Qualifications
*

Education:
M.D., Pharm.D. preferred * Experience: Ophthalmology experience highly preferred. Alternate therapeutic experience: anti-inflamatory, anti-infective. 2+ years experience in the pharmaceutical industry (MSL, medical information, health outcomes, clinical research). *

Special Skills:
Business acumen; self-motivation (position is field-based); excellent presentation skills, as well as the ability to successfully interact with medical professionals at all levels are required. Working knowledge of FDA and OIG requirements, as well as clinical trial design and statistics is required.

Work Location WA - Seattle Relocation Available Yes

Status Full-Time]]> http://bauschandlomb.jobs2web.com/job/SEATTLE-Medical-Science-Liaison-Northwest-Job-WA-98194/653264/?utm_source=J2WRSS&utm_medium=rss&utm_campaign=J2W_RSS http://bauschandlomb.jobs2web.com/job/SEATTLE-Medical-Science-Liaison-Northwest-Job-WA-98194/653264/?utm_source=J2WRSS&utm_medium=rss&utm_campaign=J2W_RSS Job Title:
Medical Science Liaison - North Central

Req #:
5336BR

Job Description:
* Develop and maintain a wide network of strategic external relationships (KOLs) to build confidence, trust and respect with others, in order to increase competitiveness. * Respond to inquiries to establish and/or further the knowledge of products and related topics. * Facilitate feedback on Ophthalmic-related community needs and opportunities to improve educational and research opportunities. * Serve as the conduit for requests for strategic investigator-initiated studies in the region, and ensure compliance with applicable regulations. * In conjunction with medical communications group, support the development of scientific updates for products' key slides and material, and ensure dissemination (Sales and Presentation to Advisory Boards). * Represent company with formulary presentations. * Design, develop, and deliver scientific presentations to individuals and groups of strategic importance to company. * Assist with educating sales representatives on product knowledge and understanding of technical information within the therapeutic area. * Coordinate the development of roundtables on scientific subjects relevant to B&L's products. * Maintain a thorough and detailed working knowledge of company, its products, current scientific research and publications associated with same. * Identify academic centers and investigators to initiate and/or participate in clinical trials and identify key areas of future research.

Qualifications
*

Education:
M.D., Pharm.D. preferred * Experience: Ophthalmology experience highly preferred. Alternate therapeutic experience: anti-inflamatory, anti-infective. 2+ years experience in the pharmaceutical industry (MSL, medical information, health outcomes, clinical research). *

Special Skills:
Business acumen; self-motivation (position is field-based); excellent presentation skills, as well as the ability to successfully interact with medical professionals at all levels are required. Working knowledge of FDA and OIG requirements, as well as clinical trial design and statistics is required.

Work Location IL - Chicago Relocation Available Yes

Status Full-Time]]> http://bauschandlomb.jobs2web.com/job/CHICAGO-Medical-Science-Liaison-North-Central-Job-IL-60684/653265/?utm_source=J2WRSS&utm_medium=rss&utm_campaign=J2W_RSS http://bauschandlomb.jobs2web.com/job/CHICAGO-Medical-Science-Liaison-North-Central-Job-IL-60684/653265/?utm_source=J2WRSS&utm_medium=rss&utm_campaign=J2W_RSS Job Title:
Scientist I

Req #:
5316BR

Job Description:
To provide analytical support to R&D analytical operations by executing methods development and validations, and methods transfer. Supporting site analytical and R&D investigations & process improvement projects. These include, but not limited to finished products and raw materials qualification, analytical method development and validations, testing of process and cleaning evaluations and validations samples; evaluating container and closure systems leachables and extractables. Providing technical support in the designing, specifying, commissioning, overseeing systems, testing and releasing of clinical trial materials. Complying with company cGMP and safety practices and procedures, including, participating in GMP training and FDA audits.

Job Duties:
- Analytical support for analytical method development and validation, and testing of sterile and non-sterile solutions, suspensions, and ointments, nasal and injectable products, and any other product type manufactured at the site, and as deemed necessary by the company. - Develop and validate analytical test method procedures for new and existing products deemed necessary by the company. - Qualify new raw material supplier chemical ingredients, and develop and validate analytical test method procedures for use in releasing them in commercial environment. - Participate or lead analytical method transfer process to QC, other R&D, or CRO labs. - Demonstrate effective technical skills in technical writing, data collection and analysis skills. - Participate in project team environment, and maintain technical skills by keeping up with current analytical training. - Conducting investigations to support R&D projects and commercial product testing. - Other duties not included above, but are required to support the growth and viability of company.

Qualifications


Education:
BS, MS, or PhD in Chemistry, Biology, or related physical sciences. Experience: Minimum of one year experience in analytical chemistry in pharmaceuticals with BS. Entry level for higher level degree.

Special Skills:
Computer literate, and is able to use MicroSoft Office software (Word, XL, PowerPoint, Project, Vision, etc.) Specialized Training: Empower, LIMS experience are positives.

Work Location FL - Tampa Relocation Available No

Status Full-Time]]> http://bauschandlomb.jobs2web.com/job/TAMPA-Scientist-I-Job-FL-33603/644696/?utm_source=J2WRSS&utm_medium=rss&utm_campaign=J2W_RSS http://bauschandlomb.jobs2web.com/job/TAMPA-Scientist-I-Job-FL-33603/644696/?utm_source=J2WRSS&utm_medium=rss&utm_campaign=J2W_RSS Job Title:
Sr. Microbiologist

Req #:
5317BR

Job Description:
The Senior Microbiologist is responsible for providing technical expertise/leadership as subject matter expert in the area of pharmaceutical microbiology. An emphasis will be placed in providing direct support for microbiology investigations, trend analysis metrics, LIMS Support, Validation, training, Environmental and Personnel Monitoring and technical studies for the Microbiology department. This position has no direct reports but at times where the microbiology management may be out of the office, can provide direct support to personnel, as needed. The Sr. Microbiologist provides analytical expertise and informational support to the Global Quality, Research and Development organizations, and other Bausch & Lomb sites on an as needed basis. This position is responsible for creating and executing against strategic goals, providing limited overall direction and oversight in the attainment, measurement and monitoring of established site level performance metrics. Job Duties Include but are not limited to: Responsible for completion of all Microbiology Investigations. . Support implementation of LIMS system. Eventually, the position will administer the system for the laboratory. . Support microbiology validations. Prepare protocols, final report, and technical studies as needed. . Review and or approve sterility testing, bioburden testing, EM data, growth promotion, microbial ID, and other microbiological tests when necessary. . Prepare and analyze trend analysis reports of EM, sterility and other microbiology test data as needed. . Provide/coordinate training, re-

Qualifications
and certification as needed. . Promote a culture a safety in the laboratory. Qualifications

Education:
MS degree in Science, Microbiology, Biology or related discipline. Experience: 4-8 years of microbiology experience in a biopharmaceutical/medical device industry.

Special Skills:
Must have demonstrated expertise and knowledge in microbiological principles and application related to sterility testing, microbial identification, GMP laboratory practices and clean room technology. Must have demonstrated computer literacy skills (e.g. Microsoft Office, Oracle, LOTUS Notes, etc.). Should have demonstrated proficiency in LIMS or other trending database applications. Demonstrated ability in statistical process control is a plus. Specialized Training: Trained in cGMP for laboratory operations and compliance to regulatory guidelines with working knowledge of microbial ID systems, (VITEK 2, Biolog, ect), USP sterility and bioburden test methods to include use of Isolator technology).

Work Location SC - Greenville Relocation Available Yes

Status Full-Time]]> http://bauschandlomb.jobs2web.com/job/GREENVILLE-Sr_-Microbiologist-Job-SC-29603/644697/?utm_source=J2WRSS&utm_medium=rss&utm_campaign=J2W_RSS http://bauschandlomb.jobs2web.com/job/GREENVILLE-Sr_-Microbiologist-Job-SC-29603/644697/?utm_source=J2WRSS&utm_medium=rss&utm_campaign=J2W_RSS Job Title:
Research Scientist

Req #:
5372BR

Job Description:
Position Summary A biomedical device materials research position that provides exciting opportunities for developing novel ophthalmic products that bring enhanced value to customers Job Duties ?Design and develop new ophthalmic product concepts applying principles of material science and polymer chemistry and processing ?Conduct materials characterization using established analytical techniques such as DSC, DMA, TGA, rheometry, etc. ?Interact / Collaborate with multifunctional groups: Synthesis, Surface Science, Process Development, Engineering ?Draft and implement protocols ?Conduct design of experiment (DOE) studies and perform statistical data analysis

Qualifications


Education:
M.S./Ph.D. in Chemical/Biomedical / Polymer Engineering or Polymer Science Experience: PhD, (0-2 years)/M.S.(4-6 years) in Polymer / Process Chemistry, R&D of polymers, medical devices, including experience in biopolymers, polymer solutions and coatings, polymer processes and characterization methods, expertise in lubrication mechanisms and contact mechanics, etc. Experience in ophthalmic medical device field a plus. .Extensive knowledge of polymer science and engineering including polymerization reactions, polymer processing and extraction methods .In depth knowledge of engineering and thermoplastic resins .Working knowledge of physical/chemical/analytical techniques such as HPLC, GC, UV-VIS, FT-IR, DSC etc .Experience in solution/polymer rheology and thermal characterization techniques such as DCS, TGA, DMA, etc. desirable .Knowledge of wetting measurement techniques such as static contact angles, DCA, etc. .Should possess excellent computer skills including data collection and statistical analysis abilities This individual should be a hands-on person with strong troubleshooting skills and ability to think creatively. A pro-active and results-oriented mindset is a necessary qualification. The candidate must also possess excellent planning abilities and effective communication skills.

Work Location NY - Rochester-One Bausch&Lomb Place Relocation Available Yes

Status Full-Time]]> http://bauschandlomb.jobs2web.com/job/ROCHESTER-Research-Scientist-Job-NY-14673/672388/?utm_source=J2WRSS&utm_medium=rss&utm_campaign=J2W_RSS http://bauschandlomb.jobs2web.com/job/ROCHESTER-Research-Scientist-Job-NY-14673/672388/?utm_source=J2WRSS&utm_medium=rss&utm_campaign=J2W_RSS Job Title:
Manager Library/Information Science

Req #:
5358BR

Job Description:
Bausch & Lomb seeks a creative, technologically savvy, service-oriented information scientist to ensure that the library's information technology supports its mission to provide tools for research and development. This position is part of the library team with responsibility for managing electronic resources, including an integrated library system, link resolvers, electronic journals, desktop databases, technical support, training and web site management. The information scientist will: . Provide leadership in investigating and implementing new information technologies and services . Develop and implement an internal technical report library . Manage electronic library including maintaining link resolver . Catalog electronic and print resources . Supervise one full-time, senior information scientist Will work with the procurement organization to negotiate contracts with vendors. Must be able to generate relevant requirements and metrics. Knowledge of and good working relationships with key vendors such as Thomson, Dialog, ProQuest and CAS is desirable.

Qualifications
A bachelor degree required, Master's Degree in Library/Information Science from an ALA accredited program or equivalent preferred. Experience in a corporate or Scientific/R&D library. Experience with management of integrated library systems, electronic resources, website layout/delivery preferred. Management experience is preferred. Familiarity with patron authentication/user security access is desirable.

Work Location NY - Rochester-1400 N Goodman Street Relocation Available Yes

Status Full-Time]]> http://bauschandlomb.jobs2web.com/job/ROCHESTER-Manager-Library-Information-Science-Job-NY-14673/671368/?utm_source=J2WRSS&utm_medium=rss&utm_campaign=J2W_RSS http://bauschandlomb.jobs2web.com/job/ROCHESTER-Manager-Library-Information-Science-Job-NY-14673/671368/?utm_source=J2WRSS&utm_medium=rss&utm_campaign=J2W_RSS Job Title:
Senior Research Scientist: Lens Care Formulations Development

Req #:
5361BR

Job Description:
Position Summary: Working in the Lens Care Formulations Development Department, this position requires a self-motivated, scientifically curious individual capable of designing and developing formulations for new lens care products. This individual will be responsible for supporting R&D activities in the Vision Care business. The position includes working with other scientists and technical people from various scientific disciplines (i.e. microbiology, process development, non-clinical safety, analytical chemistry, clinical research etc.) on establishing feasibility for new lens care products. Specific

Job Duties:
The candidate will design and develop complex innovative new lens care product formulations against specific objectives. The ideal candidate will have experience in product development with emphasis on formulations development, scale-up, and technical manufacturing support. The individual must be able to perform functional activities of a Senior Research Scientist that may include but not be limited to: 1. Development or improvement of new or existing lens care products (liquid formulations) 2. Take initiative to evaluate and champion new ingredients/technologies that provide superior consumer benefits 3. Scientific understanding of and experience working with surfactants, polymers, and antimicrobial agents/preservatives, 4. Ability to utilize basic laboratory techniques to carry out work responsibilities as well as develop new methods to enhance product development efforts 5. Work on a cross-functional project team to establish feasibility for new lens care products 6. Analyze/interpret complex technical data from multiple scientific disciplines to make decisions about new formulation candidates 7. Prepare necessary documentation/presentations to support technical communication of research and development activities. 8. Supervise/guide scientists and technicians.

Qualifications
Preferred Qualifications: - PhD or equivalent degree in chemistry or chemical engineering or relevant discipline with 0- 2 years experience in the medical device, personal care, or pharma/biotech industry or a M.S. degree in a related field with extensive product development experience Thorough understanding of the scientific principles of formulation, ingredient chemistry and industry trends - A track record and the ability to be a high performing individual and a team player - Experience in taking initiative in organizing and completing assignments on time and strong problem solving skills - Work effectively with internal and external customers/colleagues - Must exhibit excellent oral and written communication skills as well as good interpersonal skills - Skilled in Microsoft office software and laboratory software - Familiar with FDA regulatory requirements on lens care products and OTC products

Work Location NY - Rochester-1400 N Goodman Street Relocation Available Yes

Status Full-Time]]> http://bauschandlomb.jobs2web.com/job/ROCHESTER-Senior-Research-Scientist-Lens-Care-Formulations-Development-Job-NY-14673/669161/?utm_source=J2WRSS&utm_medium=rss&utm_campaign=J2W_RSS http://bauschandlomb.jobs2web.com/job/ROCHESTER-Senior-Research-Scientist-Lens-Care-Formulations-Development-Job-NY-14673/669161/?utm_source=J2WRSS&utm_medium=rss&utm_campaign=J2W_RSS Job Title:
Head of Clinical & Scientific Affairs

Req #:
5367BR

Job Description:
Position Summary: The Head of Pharmaceutical Clinical & Scientific Affairs at Bausch & Lomb is responsible for the development of products in the Rx, OTC, Generics, and Nutraceuticals categories. Leads a group of scientists (MDs and ODs) responsible for clinical trial design, scientific evaluations during the conduct of the trials (monitoring of safety, eligibility, enrollment, and data consistency), and analysis of results.

Job Duties:
* Accountable for product clinical development programs that are of high-quality, but that also lead to timely and cost-effective regulatory approval. * Serves as the leader of the Pharmaceutical Global Clinical Development matrixed team in the planning and executions of clinical trials. The team includes operations, statistics, data management, and medical writing, in addition to scientists. * Collaborates and takes clinical leadership role within cross-functional teams, including project managers, preclinical, regulatory, clinical trial materials, etc. * Responsible for the clinical aspects of clinical study reports and responses to regulatory authorities. * Contributes to abstract/manuscript/presentation writing/review, for scientific meetings and internal management reviews. * Maintains responsibility for the clinical input into Business Development due diligences. * Provides medical expertise and medical evaluation of questions regarding ophthalmology clinical practice. * Develops/Maintains relationships with external experts who might be needed to support clinical development programs. * Provides scientific and clinical research expertise in the development of overall strategy of the Pharmaceutical business and more specific product clinical development plan. * Performs management functions as goal setting, individual development plans and performance evaluations of staff. Identifies training needs to staff and implements training plan. * Proactively evaluates and contributes to process improvement.

Qualifications
Qualifications: * MD required - Ophthalmology experience strongly preferred. * Experience: Minimum 7-10 years research, clinical trial, or related experience. Must have excellent communication, organizational, and writing skills. *

Special Skills:
Experience with ophthalmic pharmaceuticals for the treatment of glaucoma and dry eye preferred.

Work Location NJ - Madison Relocation Available Yes

Status Full-Time]]> http://bauschandlomb.jobs2web.com/job/MADISON-Head-of-Clinical-&-Scientific-Affairs-Job-NJ-07940/669167/?utm_source=J2WRSS&utm_medium=rss&utm_campaign=J2W_RSS http://bauschandlomb.jobs2web.com/job/MADISON-Head-of-Clinical-&-Scientific-Affairs-Job-NJ-07940/669167/?utm_source=J2WRSS&utm_medium=rss&utm_campaign=J2W_RSS Job Title:
Scientist II, Microbiology

Req #:
5338BR

Job Description:
Conduct collaborative antimicrobial research and method development experiments, including (1) development of antimicrobial assays against protozoa, fungi, and bacteria (2) independent design/execution/optimization of new and ongoing studies, and (3) presentation/communication of results and conclusions to internal/external scientists and to project teams. Specific Job Duties (bulleted list of detailed job responsibilities in order of importance) . Responsible for design, development, and implementation of new in vitro microbiology methods and antimicrobial efficacy tests for vision care pipeline technology projects (80%). . Generate timely, accurate experimental summaries and draft reports for review by senior scientific staff (10%). . Participate in drafting and presentation of project support and method development activities to internal and external scientists, including presentations at scientific conferences and publication in peer reviewed literature (10%).

Qualifications
.

Education:
B.A/B.S. in Microbiology, Biochemistry, Molecular Biology, Cell Biology, Biotechnology or other related biological discipline. Master's level education is highly desired but not required for this position. . Experience: Minimum 2 - 4 years post bachelor's full time laboratory experience in health care related R&D, including demonstrated success in conducting independent experiments with minimal to moderate direction from senior scientific staff. .

Special Skills:
(1) Independent laboratory experience with protozoa, tissue culture, or other microbial culture/testing systems. (2) Strong scientific, mathematical, and interpersonal skills for conducting robust experiments, generating accurate experimental summaries, and communicating effectively with peers, senior scientific staff, and external colleagues. (3) Multitasking skills and demonstrated success in rapid acquisition of practical knowledge in new scientific areas as needed to support evolving project needs.

Work Location NY - Rochester-1400 N Goodman Street Relocation Available Yes

Status Full-Time]]> http://bauschandlomb.jobs2web.com/job/ROCHESTER-Scientist-II,-Microbiology-Job-NY-14673/664780/?utm_source=J2WRSS&utm_medium=rss&utm_campaign=J2W_RSS http://bauschandlomb.jobs2web.com/job/ROCHESTER-Scientist-II,-Microbiology-Job-NY-14673/664780/?utm_source=J2WRSS&utm_medium=rss&utm_campaign=J2W_RSS